Accelerated Partial Breast Irradiation (APBI): A review of available techniques
© Njeh et al; licensee BioMed Central Ltd. 2010
Received: 15 June 2010
Accepted: 4 October 2010
Published: 4 October 2010
Breast conservation therapy (BCT) is the procedure of choice for the management of the early stage breast cancer. However, its utilization has not been maximized because of logistics issues associated with the protracted treatment involved with the radiation treatment. Accelerated Partial Breast Irradiation (APBI) is an approach that treats only the lumpectomy bed plus a 1-2 cm margin, rather than the whole breast. Hence because of the small volume of irradiation a higher dose can be delivered in a shorter period of time. There has been growing interest for APBI and various approaches have been developed under phase I-III clinical studies; these include multicatheter interstitial brachytherapy, balloon catheter brachytherapy, conformal external beam radiation therapy and intra-operative radiation therapy (IORT). Balloon-based brachytherapy approaches include Mammosite, Axxent electronic brachytherapy and Contura, Hybrid brachytherapy devices include SAVI and ClearPath. This paper reviews the different techniques, identifying the weaknesses and strength of each approach and proposes a direction for future research and development. It is evident that APBI will play a role in the management of a selected group of early breast cancer. However, the relative role of the different techniques is yet to be clearly identified.
Breast cancer is a worldwide problem, accounting for 10.4% of all cancer incidence among women, making it the second most common type of non-skin cancer (after lung cancer) and the fifth most common cause of cancer death. In the USA, breast cancer has the highest incidence among all cancer types in females with one in every eight to ten women being affected during her lifetime ; it is estimated that 192,370 women will be diagnosed with, and 40,170 women will die of, cancer of the breast in 2009 [2–4].
Breast cancer is the most common cancer in the UK among women although it is rare in men. In 2006 there were 45,822 new cases of breast cancer diagnosed in the UK: 45,508 (over 99%) in women and 314 (less than 1%) in men. Breast cancer is by far the commonest cancer in women in the UK accounting for 31% of all cases. The next most common cancer in women is lung cancer, with 16,647 cases (11% of total) in 2006. So nearly, a third of all new cancers in women are breast cancers. It has been estimated that the lifetime risk of developing breast cancer is 1 in 1,014 for men and 1 in 9 for women in the UK. These were calculated using incidence and mortality data for 2001-2005 .
Early stage breast cancer is defined as stage II or less; on the basis of the lack of lymph node, metastasis and clinical lesion size of 2 cm or less . The 'surveillance, epidemiology and end results' (SEER) program reported that in 2006, 60% of diagnosed breast cancers are early stage [2, 3]. Similarly in Japan, the fraction of early stage breast cancer was reported to be 40.6% in 1996 . With the increasing use of breast cancer screening by mammography, more and more patients will have their breast cancer diagnosed at the early stage. Hence, there is a need for proper clinical management of early stage breast cancer is required. Most women who are newly diagnosed with early-stage breast cancer have a choice of: breast-conserving surgery (such as lumpectomy), a mastectomy (also called a modified radical mastectomy), radiation therapy and systemic treatments.
Rationale for Breast Conservation
Breast conservation therapy (BCT) is the procedure of choice for the management of the early stage breast cancer. BCT consists of resection of the primary breast tumor (lumpectomy, segmental mastectomy or wide local excision) followed by whole breast irradiation (WBI). A total dose of 45-50 Gy is delivered to the entire breast over 5 to 6 weeks (1.8 to 2 Gy per fraction). In most patients, a boost dose of 10-16 Gy to the tumor bed is added. The establishment of BCT as the standard of care resulted from many years of prospective studies such as the National Surgical Adjuvant Breast and Bowel Project (NSABP) B-06 studies [7–9]. These studies found equivalent survival and local control rates among women treated with BCT compared to those treated with mastectomy.
The value of radiation therapy as a breast conservation component has been further validated by studies comparing lumpectomy alone to lumpectomy and radiation therapy. These studies demonstrate a threefold reduction in recurrence with the use of radiation therapy following breast conserving surgery [7, 10–13]. For patients with ductal carcinoma in situ (DCIS), randomized studies comparing lumpectomy alone to lumpectomy plus radiation therapy, conducted by the NSABP and European organization for research and treatment of cancer (EORTC) found a 55% and 47% reduction in the ipsilateral breast cancer events respectively, with the addition of radiation therapy [13, 14]. These and other studies have been recently pooled-analysed by Clarke et al.  and Vinh-Hung et al. . Vinh-Hung's analysis found that the relative risk of ipsilateral breast tumor recurrence after breast-conserving surgery, comparing patients treated with or without radiation therapy, was 3.00 (95% confidence interval [CI] = 2.65 to 3.40). Further, the relative risk of mortality was 1.086 (95% CI = 1.003 to 1.175), corresponding to an estimated 8.6% (95% CI = 0.3% to 17.5%) relative excess mortality if radiation therapy was omitted. BCT is well tolerated with minimal long-term complications, favorable cosmetic outcome and reduced psychological trauma [7, 9]. Radiation therapy therefore is an essential component of BCT. It not only decreases local recurrence but improves overall survival [11, 12]. Because of these excellent results and the better cosmetic outcome, the United States National Institute of Health released a consensus statement, recommending breast conserving treatment as the preferable option for women with early-stage breast cancer .
Rationale for Accelerated Partial Breast Irradiation (APBI)
Despite the advantages of BCT, its utilization remains a problem . It has been reported that many women who are candidates for BCT do not receive it, only 10% to 80% of patients actually receive it [17–19]. In addition 15% to 30% of patients who undergo lumpectomy do not receive radiation therapy [20–22]. Similarly in Japan radiation therapy is performed in approximately 70% of patients following breast conservation surgery . The under utilization of BCT has been associated with the fact that some women cannot, or will not, commit to the usual 6- 7 week course of adjunct conventional radiation therapy that is part of the BCT package . It has been further hypothesized that convenience, access, cost and other logistical issues are major contributing factors. Other logistical issues include: distance from the radiation therapy facility, lack of transportation, lack of social support structure and poor ambulatory status of the patient [18, 25, 26]. Other reasons that may steer women away from BCT that have been identified include physician bias, patient age and fear of radiation treatments . There has been a desire therefore to identify a subset of women who may not benefit from the addition of radiation therapy after lumpectomy for early stage breast cancer; however, no such subset of women has been identified .
Another criticism of BCT relates to consumption of resources; while radiation therapy facilities in the USA have largely kept up with demand for post-lumpectomy radiation therapy, breast irradiation may constitute 25%-30% of patient visits and can stress a health-care delivery system. However, not all countries have such adequate resources. For example Palacios Eito et al.  reported that the number of external irradiation units available in Spain in 2004 (177) was clearly lower than the number desirable (266-316). There is significant shortage of radiation therapy equipment in most of Asia and pacific regions , Latin America , Africa  and Eastern Europe . In Africa, the actual supply of megavoltage radiation therapy machines (cobalt or linear accelerator) was only 155 in 2002, 18% of the estimated need . In 12 Asia-Pacific countries with available data, 1147 megavoltage machines were available for an estimated demand of nearly 4000 megavoltage machines .
The question that arises therefore is 'can similar rates of local control be achieved with radiation therapy delivered only to the area at highest risk for recurrence?' If so, radiation could be delivered in a significantly shortened period, thereby potentially making the BCT option available and attractive to more women. This is the concept of accelerated partial breast irradiation (APBI) [26, 33, 34].
The stronger case for APBI has come from both retrospective and prospective studies; reporting that 44% to 86% of local recurrence occurs close to the tumor bed [10, 35–37]. Ipsilateral breast recurrences in areas other than the tumor bed occurred rarely in 3% to 4% of the cases . An update of the NSABP B-06 trial also confirmed this pattern of local recurrence, with 75% of recurrences at, or near, the lumpectomy site with other site ipsilateral breast recurrence rates similar to the recurrence of contra-lateral second primary breast cancer . Based upon this evidence, BCT, with whole breast irradiation has been criticized as an over-treatment. Whole breast treatments incorporate the entire breast (including the surgical cavity), overlying skin, lower axilla and even small portions of the heart and lung in the treatment fields; this may introduce avoidable toxicity  whereas partial breast irradiation spares more normal tissue.
An additional theoretical advantage of APBI is a decreased dose to normal tissue. With a smaller target volume, it may be expected that adjacent organs such as the heart and lungs will receive less radiation. Radiation-induced lung injury after treatment for breast cancer, such as pneumonitis, lung fibrosis and pulmonary function test changes, are well documented in the literature [40, 41]. An increase in lung cancer incidence and mortality after irradiation for breast cancer has also been reported in large studies [42–45]. It worth noting that the increase risk of long-term cardiac-related mortality after BCT may not be significant with modern breast radiation therapy.
A number of pathology studies have also researched local breast recurrence [46, 47]. In the study by Holland et al., mastectomy specimens from more than 300 women diagnosed with invasive breast carcinoma, who fulfilled the criteria for breast conserving therapy, were systematically investigated . They found that of the 282 invasive cancers, 105 (37%) showed no tumor foci in the mastectomy specimen around the reference mass. In 56 cases (20%) tumor foci were present within 2 cm, and in 121 cases (43%) the tumor was found more than 2 cm from the reference tumor . This study justified the concept that whole-breast treatment either with surgery or radiation therapy is necessary to achieve local control. Supporters of APBI argue that this study was flawed in its patient selection and that the quality of mammography used at the time may have missed radiographic evidence of multicentric disease that would today be detected . Contrary to Holland's data, recent studies from women considered appropriate for breast-conservation therapy reveal that the microscopic extension of malignant cells is unlikely to be beyond 1 cm [49–51].
Accelerated Partial Breast Irradiation (APBI) Techniques
APBI is an approach that treats only the lumpectomy bed plus a 1-2 cm margin, rather than the whole breast. By increasing the radiation fraction size and decreasing the target volume, this technique allows the treatment to be accomplished in a shorter period. APBI is generally defined as radiation therapy that uses daily fraction doses greater than 2 Gy delivered in less than 5 weeks. There are a number of approaches now available for the implementation of APBI, these include: multi-catheter interstitial brachytherapy, balloon catheter brachytherapy, 3D-CRT (conformal radiation therapy) and intra-operative radiation therapy (IORT). Each of these techniques is vastly different from one another in terms of degree of invasiveness, radiation delivery, operator proficiency, acceptance between radiation oncologist and length of treatment. It is important to review the basic principles of radiobiology, as well as critical aspects of patient selection, surgical endpoints and radiotherapy treatment planning. This paper reviews the different techniques, identifying the weaknesses and strength of each approach and proposes a direction for future research and development.
Multi-catheter Interstitial Brachytherapy (MIB) Treatment Technique
Multiple catheters are placed in the breast using a free-hand or template-guided approach. The configuration of the catheters and their relation to the tumor target volume are crucial for effective treatment. Catheter insertion requires a high level of experience to produce an implant of excellent quality. The incorporation computed tomography (CT) based 3D planning and image-guidance has made a significant impact on the quality of the implants . Determination of optimal catheter configuration prior to the procedure (virtual planning) would reduce the dependence of implant quality on the expertise of the physician .
In MIB either low dose rate (LDR) or high dose rate (HDR) brachytherapy may be used. With LDR, sources of Ir-192 sources are implanted for approximately 2 to 5 days while the patient is admitted as an inpatient. HDR however is an outpatient procedure, fractionated over the course of a week, with each treatment varying between seconds to minutes. The proposed dose of 34 Gy in 10 fractions BID (twice daily) for HDR was based on equivalence of the BED (biological effective dose) of this schema to 45 Gy in 4.5 days of the LDR regimen used in early APBI trials .
Results of recent clinical experience with Interstitial brachytherapy with more than 5 years follow up
No of cases
Follow up interval (years)
Dose rate/pt no
Total dose (Gy)
5-year LR (%)
Strnad et al.
PDR = 0.6 Gy/hr
HDR = 4 Gy x8
PDR = 50 Gy
HDR = 32 Gy
Antonucci et al. 
LDR 0.52 Gy/h × 96 hours
HDR = 4 Gy x8
HDR = 3.4 Gyx10
LDR = 50 Gy
HDR = 32 Gy
HDR = 34 Gy
Johansson et al.
Arthur et al.
LDR = 3.5 -5 days
HDR = 3.4 × 10
45 Gy (LDR)
34 Gy (HDR
Polgar et al.
5.2 × 7
King et al 
LDR = 4 days
45 Gy (LDR)
32 Gy (HDR)
Otto et al. 
PDR 5 days, 0.6 Gy/hr
HDR = 4 Gyx8
49.8 Gy (PDR)
32 Gy (HDR)
Polgar et al.
4.33 × 7
5.2 × 7
Balloon-Based Brachytherapy Devices
The balloon based brachytherapy include Mammosite, Axxent electronic brachytherapy, and Contura.
The MSB radiation therapy device generally delivers 34 Gy over 10 fractions (3.4 Gy per fraction, twice daily (BID)). The prescription point is 1 cm from the balloon surface with a minimum of 6 hours between fractions on the same day.
Results of some of the recent clinical experience with Mammosite Brachytherapy System with more than a year follow up.
No of cases
Median follow up interval(months)
Benitez et al.
Niehoff et al 
Patel et al.
Vicini et al.
Chen et al.
Belkacemi et al. 
Voth et al.
Dragun et al. 
Vicini et al.
Jeruss et al. 
2. Axxent Electronic Brachytherapy
This approach implies that a specifically shielded radiation room or an HDR afterloader unit are not required, both of which are needed for treatment with brachytherapy using Ir-192. The elimination of these requirements potentially open-up this APBI approach to a wider usage, particularly for patients who do not live in close proximity to a radiation center with a HDR after-loader unit. Since a shielded room is not required for treatment and the eB device is very portable, the number of setting in which the device can be used increases. It has also been suggested to use the device for intra-operative radiation therapy  and 11 patients have successfully had IORT using the eB device . eB received FDA clearance for the treatment of breast cancer in January of 2006.
One inherent problem with MSB techniques is the high skin dose when the excision cavity is near the skin surface; that can result in late effect skin toxicity. The Axxent source model S7500 has pronounced anisotropy resulting in decreased dose at the proximal portion of the balloon ; this can be used as an advantage to optimize skin dose, particularly, if the cavity to skin distance is small. This anisotropy can also be accounted for by placing a dwell position outside the balloon surface along the proximal end of the catheter .
Being a relatively new device, there is a dearth in clinical experience and hence there are no clear recommendations on clinical use, for example, the surface-to-skin distance using electronic brachytherapy. Chen et al. recently reported a case report of radiation recall associated with the eB device and docetaxel administration . They argued that the prescription of 34 cGy at 1 cm may result in a higher skin dose (when the skin to balloon distance is less than 1 cm) for eB because of the relatively higher fall off rate of the 50 KVp photon compared to Ir-192. The patient that they reported had a surface-to-skin distance of 7.5 mm, greater than the 7 mm MammoSite guideline. The calculated dose to the skin was approximately 537 cGy per fraction. If an 192Ir source had been used instead, the skin dose would have been approximately 470 cGy per fraction, corresponding to a relative dose increase for the electronic source of approximately 14%.
Another potential contributing factor is the increase in relative biologic effectiveness (RBE, the ratio of doses for photons of differing energies required to produce the same biologic effect) related to the lower energy of the photons emitted by the electronic brachytherapy source. It is well established that the biological effectiveness of low-energy photons is large compared with higher-energy gamma rays, because of the dominance of photoelectric absorption at low energies . The RBE for a 40 kVp source (very similar to the Axxent photon spectrum) has been calculated to be 1.28 greater than. an 192Ir source ; hence, the dose from the 192-Ir source must therefore be 1.28 times greater than that of the low energy photon source to produce the same effect (e.g., skin ulceration).
MSB has the longest duration in follow up and new APBI devices compare its clinical efficacy to that of MammoSite. A recent study by Wilder et al.  evaluated one hundred and eighty-two women with early breast carcinoma treated with post lumpectomy brachytherapy using Contura (n = 45) and MammoSite (n = 137) devices with a median follow-up of 16 months. A Contura catheter did not require explantation in 16% (7 of 45) of patients where balloon-to-skin spacing was only 3-6 mm and 11% (5 of 45) of patients where there was an air/fluid pocket greater than 10% of the planning target volume for plan evaluation. A MammoSite catheter was explanted in 10% of cases where the minimum balloon-to-skin distance was <7 mm and in 13% of cases where there was a large air/fluid pocket next to the balloon. They observed incidence rates of acute toxicity with a Contura device similar to those with a MammoSite device . Brown et al.  have also reported similar improvements in dosimetric capabilities (i.e., reduced skin and rib doses and improved PTV_EVAL coverage) with the Contura device.
Hybrid Brachytherapy Devices
Hybrid devices were developed to take advantages of the versatility and dosimetric conformity of multicatheter interstitial brachytherapy with the convenience and aesthetics of a single entry device. There are currently two devices in this category namely the Struts Adjusted Volume Implant (SAVI) and the ClearPath.
1. Strut Adjusted Volume Implant (SAVI)
The SAVI device is surgically implanted on an outpatient basis by the treatment radiation oncologist using ultrasound guidance with the patient under local anesthesia. A CT scan is acquired immediately following the implant surgery, both for the verification of the proper deployment of the device, and for treatment planning. It was recommended by Scanderbeg et al , that although the device does not move independently to the body, one should always try to attain a position as close to the planned patient position due to breast deformation. They found a breast board to be best for patient setup because of its ease of setup and reproducibility.
2. ClearPath (CP)
CP is a relatively new device and hence no clinical outcome data have been reported. However, retrospective dosimetric analysis has been reported [90, 91]. Dickler et al.  found that MSB and CP offered comparable target volume coverage, but CP allowed significantly more normal-tissue sparing. Similarly, Beriwal et al. simulated a phantom study and the parameters of the CP catheter were superimposed on the MSB planning CT scans. The authors found that the median maximum skin dose was 161% for MSB and 113% for CP of the prescription dose .
External Beam Radiation Therapy (EBRT)
The technique is non-invasive and the patient is not subjected to a second invasive surgical procedure or anesthesia, thereby reducing the potential risk of complications. The treatment can wait until completion of pathological analysis about the original tumor and the status of the resection margins are available.
The technique has potential for widespread availability since most radiation therapy centers already perform 3D-CRT for other cancers.
It is likely that an external beam approach will be easier for radiation oncologists to adopt than brachytherapy techniques because the technical demands and quality assurance issues are much simpler.
Treatment results with external beam may be more uniform between radiation oncologists because the outcome depends less on the experience and operative skills of the person performing the procedure than for brachytherapy (especially using interstitial implantation).
It seems less likely that technical issues arising during external beam radiation therapy will require the procedure to be aborted as is not infrequently the case when brachytherapy techniques are used.
External beam is intrinsically likely to generate better dose homogeneity and thus may results in a better cosmetic outcome when compared with bracytherapy techniques.
Despite the above appeal of EBRT APBI, many issues and unanswered question remain. These include breathing motion, treatment setups variation, and the fractionation scheme adopted. The target may move during breathing and the patient may be positioned differently for different fractions. To avoid missing the planned target, a large treatment volume is used. A prone patient position has been suggested by Formenti et al. to minimize target tissue movement during breathing. The prone position also provides exceptional sparing of the heart and lung tissues. Unfortunately, the prone position is not widely used because it requires a special immobilization device and is uncomfortable for some patients.
The use of multiple treatment fields in 3D-CRT/IMRT can increase the volume of normal tissue irradiated to low or moderate doses (i.e increase in integral dose). Also, 3D-CRT delivers higher doses to normal breast tissue since the PTV around the lumpectomy cavity is increased to account to breathing and setup errors .
The identification and contouring of the lumpectomy cavity (LC) is another issue with 3D-CRT APBI. LC determination is critical because treatment delivery is delayed after breast surgery. Furthermore, the GTV and CTV are generally defined as the contouring of a seroma within the lumpectomy cavity, expanded by some margin, usually 1 cm . However, the delineation of the seroma could vary among different observers and even among experienced ones . It has been suggested by Dzhugasvili et al.  that the use of surgical clips as fudicial markers may reduce such observer variability.
Accelerated partial breast irradiation clinical studies using external beam radiation
No of cases
Follow up (months)
Vicini et al
3.85 Gy × 10 (bid)
Vicini et al.
3.85 Gy × 10 (bid)
Chen et al. 
3.85 Gy × 10 (bid)
Taghian et al.
3.2 Gy × 4 (bid)$
Formenti et al.
5.0, 5.5, 6.0 Gy × 5 (10 days)
Formenti et al.
6.0 Gy x5 (10 days)
Magee et al.
5.0 - 5.31 Gy × 8 (10 days)&
Leonard et al. 
3.85 cGy x10 (bid)
Hepel et al.
3.85 Gy × 10 (bid)
Jagsi et al.
3.85 Gy × 10
Intra-Operative Radiation Therapy Techniques
Intra-operative radiation therapy (IORT) refers to the delivery of a single fractional dose of irradiation directly to the tumor bed during surgery. These techniques have been reviewed by Reitsamer et al. , Vaidya et al. [113, 114] and Orecchia and Veronesi . Older intra-operative radiation therapy devices were technically cumbersome, commonly relying on the transportation of the patient from the operating theatre to the radiation therapy unit during surgery, or require custom-built intra-operative radiation therapy theatres . These technical and financial limitations to delivery of intra-operative radiation therapy have prevented widespread use of the approach. Advances in miniaturization technology have enabled the development of mobile intra-operative radiation therapy devices. Intra-operative radiation therapy was first used in 1998 with a device called the Intrabeam, since then, two other mobile linear accelerators have become available (the Mobetron and Novac-7 systems). These systems either generate megavoltage electrons (Mobetron and Novac-7) or kilovoltage photons (intrabeam).
The potential advantages of IORT include delivering of the radiation before tumor cells have a chance to proliferate. Furthermore, tissues under surgical intervention have a rich vascularization, with aerobic metabolism, which makes them more sensitive to the action of the radiation (oxygen effect). Also, the radiation is delivered under direct visualization at the time of surgery. IORT could minimize some potential side effects since skin and the subcutaneous tissue can be displaced during the IORT to decrease dose to these structures, and the spread of irradiation to lung and heart is reduced significantly . IORT eliminates the risk of patients not completing the prescribed course of breast radiotherapy (a well-recognized risk of conventional breast radiotherapy) and allows radiotherapy to be given without delaying administration of chemotherapy or hormonal therapy . IORT has the potential for accurate dose delivery: by permitting delivery of the radiation dose directly to the surgical margins, IORT eliminates the risk of geographical miss in which the prescribed radiation dose is inaccurately and incompletely delivered to the tumor bed. Geographical miss may result from patient movement, inconsistent patient setup, and difficulty identifying the tumor site weeks or months postoperatively and is estimated to occur in up to 70% of patients receiving conventional breast boost radiotherapy . There is potential for decreasing healthcare cost because it is one fraction as opposed to 25 fractions.
With IORT the final pathology reports arrives days post-festum. This has been one of the major criticisms of the technique. So recently a novel handheld probe (Dune Medical Devices, Caesarea, Israel) has been developed for intra-operative detection of positive margins  Such a device can help reduce re-excision rate and improve acceptance of IORT technique.
1. INTRABEAM (X-rays)
The X-ray system produces low-energy photons (30- 50 KVp) with a steep dose fall-off in soft-tissue; no special shielding is therefore required in the room . Dosimetry varies by applicator tip size with the commonly used 3.5 cm applicator sphere delivering 20 Gy at a radius of 1 mm from the surface, 5 Gy at 10 mm and 1 Gy at 27 mm in about 20 minutes . Treatment time lasts for approximately 20 to 45 minutes, depending on the size of the lumpectomy cavity, the size of the selected applicator, and the prescribed dose.
Treatment can be carried out in unmodified operating rooms with minimal exposure to the staff and patient; rapid dose fall-off in the tissue around the applicator guarantees minimal exposure of the surrounding tissue such as the lung and cardiac tissue in the patient.
The physics, radiobiology, dosimetry, and early clinical applications of this low energy x-ray device have been fully evaluated, and the device has received Federal Drug Administration approval for use in any part of the body since 1999 . The RBE for this low-energy x-rays have been estimated to be 1.5 . It has been suggested that the biologically weighted dose (physical dose × RBE) decreases with depth less quickly than physical dose  Therefore despite the steep gradient in physical dose, an effective uniform biological dose is distributed inside a rim of about 15 mm around the most often used intrabeam applicator . Another potential advantage of Intrabeam is that, because normal tissues can repair their damaged DNA within a few minutes but cancer cells with poor DNA- repair machinery may be unable to repair quickly. So treatment given over a long time (intrabeam is between 25-35 minutes) may have a higher therapeutic index than giving similar doses over 2 to 3 minutes .
Some clinical studies using Intra-operative radiation therapy (IORT).
2. MOBETRON (electrons)
3. NOVAC-7 (electrons)
The NOVAC-7 system (Figure 13b) (Hitesys, Latina, Italy) delivers electrons with the use of a mobile dedicated linear accelerator; its radiating head can be moved by an articulated arm that can work in an existing operating room. It is based on a compact S-band standing wave electron beam linear accelerator utilizing a patented auto-focusing structure which eliminates the need of focusing solenoids. The accelerator is moved by six axis robotic arm. It delivers electron beams at four different nominal energies (3, 5, 7 and 9 Mev) . Beam are collimated by means of a hard docking system, consisting of cylindrical perspex applicators available in different diameters (4 to 10 cm) and angles of the head (perpendicular or oblique 15° to 45° with respect to their axis).
A phase III, prospective randomized trial called ELIOT (electron intraoperative therapy) began in 2000 in Italy. A single dose of 21 Gy with energies up to 9 MeV, biologically equivalent to 58-60 Gy in standard fractionation is applied to the tumor bed. The dose of 21 Gy was established from a dose-escalating phaseI/II study . The electron energy used is determined from the depth of the tissue to be irradiated. The accelerators used have been designed to have a dose rate (15-20 Gy per minute) higher than conventional and can deliver 21 Gy in less than 2 min . The entire procedure last for about 15 to 20 minutes. Unnecessary radiation to the underlying normal tissue can be avoided by mobilizing the mammary gland during surgery and placing a lead plate for shielding on its dorsal surface.
The costs of the mobile linear accelerator with a robotic arm, used in intra-operative radiation therapy, are prohibitive for poor countries. Frasson et al.  evaluated the feasibility of ELIOT in the accelerator room of the radiation therapy service for early breast cancer treatment; demonstrating that intra-operative radiation therapy with electrons can be safely performed in an accelerator room with a conventional machine.
A systematic review by Cuncins-Hearn et al.  concluded that the short-term results were similar for both BCT and IORT in terms of local recurrence, disease-free and overall survival. The current evidence base is however poor, making definitive assessment on IORT very difficult. They suggested that further research is required to clarify several issues such as identification of the most appropriate subgroups of patients for IORT, a comparison of the currently available mobile IORT technologies, establishing whether IORT is most appropriate as a boost replacement dose or replacement for all postoperative radiation therapy, the examination of how biological repair processes may differ between the two treatment modalities and determining precisely where local recurrences originate with respect to the original tumor site.
The IORT approach has the advantage of shortening the treatment course further, conveniently delivering the entire course of local therapy at the time of initial excision. However, IORT also presents significant technical challenges, not the least due to the need for accuracy of target definition and treatment delivery inherent in a single dose radiotherapy delivery. One issue is the accuracy of tumor bed definition when tissues are re-approximated following excision. Another is the variable margin of normal tissue irradiated in the re-opposed tissues. IORT may be complicated in patients who are determined to have positive surgical margins and need re-excision. This may not have been a significant issue in the Versonesi studies , as all patients received generous resections with quadrantectomies.
Comparison of the current available APBI techniques (adapted from Sarin ), MIB = multicatheter Interstitial brachytherapy, IORT = intraoperative radiation therapy, RCT = randomized Clinical trials, OAR organ at risk
Balloon based brachytherapy
Hybrid based brachytherapy
1.5 - 2 cm
1.5 - 2 cm
1.5 - 2 cm
10- 30 mm
Coverage of target volume
Sparing of OAR
Suitability for various tumor size, location and shape
Not suitable if inadequate tissue or near axilla
Not suitable for large/irregular cavities or at the periphery
Not suitable Large cavities
Not suitable Large cavities
Not suitable Large cavities
Not suitable Large cavities
May not be suitable for small breast
Not suited for deep seated cavities in large breast
Not suitable for tumors near brachial plexus/axilla or skin
Not suitable for large irregular cavities or at the periphery of breast
Potential for wide spread use
Clinical outcome data
11 years case studies
5 years case studies
4.5 years case studies
8 years case studies
4 years Case studies
4 years RCT
High expertise required and QA
Stringent QA is required
Cavity, shape and size
Cavity shape and size
Cavity shape and size
Treatment planning complex
Treatment planning complex
Setup and breathing errors
High skin Dose
Expensive and 2nd neutrons
Pathology not available
Pathology not available
ASTRO and GEC-ESTRO suitable patient recommendation selections for APBI outside of clinical trials
Suitable group by ASTRO 
Low Risk group by GEC-ESTRO 
> 60 y
BRCA 1, 2 Mutation
< 2 cm
< 3 cm
Negative by at least 2 mm
Negative by at least 2 mm
Unifocal with total size of < 2 cm
IDC, mucinous, tubular and colloid
IDC, mucinous, medullary, colloid
pN0 (by SN Bx or ALND
pN0 (by SLNB or ALND)
One concern regarding APBI is the proliferation of approaches; this inherently makes it difficult to elucidate the generic effect of APBI from the specific effect of a particular technique. As described within this review, many dosing schemes have been used; the different fractionation schemes and different BED make it possible for a failure to occur due to inappropriate dosing rather than the fact that only a partial region of the breast had been irradiated using APBI. Taking the 3D-CRT approach as an example, (see Table 3) many dosing schemes have been reported; for example, in the ELIOT studies, three different dose levels were used: 20 Gy (seven patients), 22 Gy (20 patients), and 24 Gy (20 patients) . Further, the use of soft x-rays as in Intrabeam and Xoft approaches introduce another concept of relative biological effectiveness; thereby introducing another variable when trying to determine the effectiveness of the dosing.
The basic tenet of radiation therapy is the delivery of a tumorcidal dose to the clinical target volume. In terms of applying APBI, there are questions of the appropriate target volume; is 1 cm or 2 cm enough margin for the irradiation of residual tumor? Depending on the particular technique, the delineation of this target can be problematic. It has been well documented that inappropriate target delineation will result in under dosing of the tumor or irradiating excessive volumes of normal tissues and organ at risk . For non-brachytherapy techniques, substantial differences in delineation of the lumpectomy cavity have been observed, even by dedicated breast radiation oncologists . The definition of the CTV is influenced by clinical features in the breast such as dense breast parenchyma, benign calcifications, low seroma clarity score, small volume and proximity to the pectoralis muscles . To facilitate the contouring, surgically placed clips after lumpectomy have demonstrated strong radiographic surrogates of the lumpectomy cavity [99, 144]. Also, written guidelines for contouring CTV have been shown to significantly reduce the inter-observer variability and minimize the volumes for radiation .
Clinical Trial Evidence
As seen in tables 1, 2, 3, 4, the longest follow-up for APBI is with multi-catheter interstitial brachytherapy (MIB). Vicini et al.  have shown local recurrence rates of 3.6% at 10 years. More recently, Polgar et al.  reported a 12 year prospective study using MIB; four (8.9%) ipsilateral breast tumor recurrences were observed, for a 5-, 10- and 12 year actuarial rate of 4.4%, 9.3% and 9.3% respectively. The other techniques have shorter follow-up, with no local recurrence rates at 5 years follow up for MammoSite brachytherapy (MSB) , no reported recurrences in 10 to 28 months with single institution studies of 3D-CRT and 1.3% at 19 months in a single-institution study of intra-operative radiation therapy (IORT) .
It is now accepted that critical evaluation of clinical studies is appropriately done in terms of evidence based medicine. There are a few methodologies for reviewing the quality of the evidence including SORT (strength of recommendation taxonomy), Grade (grades of recommendation, assessment, development and evaluation) and CEBM (center for evidence based medicine). This critical evaluation is usually done under the umbrella of a systematic review and meta-analyses. The present review was not designed as a systematic review, but as a detailed analysis focussed towards providing the details and nuances of the different techniques. Nonetheless, an evaluation of a particular technique will not be complete without some assessment of its clinical validity. In terms of the SORT approach of clinical evidence, RCT provides level 1 clinical evidence of efficacy and validity. There are currently four reported APBI RCT [63, 123, 150, 151]. However, not all of these studies met the SORT recommendation of quality, quantity and consistency. The YBCG (Yorkshire Breast Cancer Group) and Christie Hospital trials lack consistency in terms of patient selection and appropriate target definition, So, these two trials only provides level 3 evidence of efficacy. The Hungary trial  lacks the sample size to detect a difference. Hence, the only RCT that provides level 1 evidence is the recently published TARGIT study. Case control studies provide level 3 evidence of efficacy and validity. Hence, for the other APBI techniques (MIB, Mammosite, 3DCT, and electron IORT) there is currently only level 3 evidence of efficacy.
APBI technique (Experimental Arm)
≥ 45 years
T1 small T2, N0, 1, Ductal
WBI as per institutional guidelines
IORT, Low energy X-rays 50 KV, 20 Gy/1 fraction
Started March 2000, completed enrollment march 2010
≥ 48 years
T ≤ 2.5 cm, pN0, Quadrantectomy
WBI, 50 Gy/25 fractions + optional 10 Gy Boost
IORT 21 Gy/1 fraction, electrons up to 9 MeV
Started in Dec 2000
Non-inferiority, non-irrelevant, 3% difference
≥ 40 years
stages O-II ductal/lobular carcinoma
T ≤ 3 cm, pNO-pNmi, margin ≥ 2 mm
WBI 50- 50.4 Gy/25-28 fractions + optional 10 Gy boost
MIB, 32 Gy/8 fractions HDR, 30.3 Gy/7 fractions HDR, 50 Gy PDR
≥ 18 years
stage 0, I, II (T < 3 cm)
DCIS or invasive adenocarcinoma, ≤ 3 nodes positive, Margin negative
50-50.4 Gy/25-28 fractions, optional 10- 16 Gy boost
Mammosite 34 Gy/10 fractions (5-10 days)
3D EBCRT 38.5 Gy/10 fractions (5-10 days)
Started in 2005 (accrual now closed to low risk patients)
≥ 40 years
DCIS or invasive carcinoma
T< 3 cm, margin negative, node negative, not BRCA 1/BRCA 2
WBI 42.5 Gy/16 fractions/22 days (small breast)
50 Gy/25 fractions/35 days (large breast plus optional boost 10 Gy/4-5 fractions
3D CRT 38.5 Gy/10 fractions (5-8 days)
Minimum daily fraction separation 6 -8 hours
Started in January 2006
≥ 50 years
invasive adenocarcinoma (not lobular) T ≤ 3 cm, margin ≥ 2 mm, node negative
40 Gy/15 fractions/21 days
Arm 1 40 Gy/15 fractions to primary tumour region + 36 Gy/15 fractions to low risk region
Arm 2 40 Gy/15 fractions to primary tumour region
Started in 2006
≥ 49 years
pT1-2 (< 3 cm)
Margins ≥ 2 mm
45 Gy/18 fractions, or 50 Gy/25 fractions, or 50,4 Gy/28
38.5 Gy total in 10 fractions (3.85 Gy per fraction), twice a day
with an interval of at least 6 hours
Started in 2007
APBI in Asia
Breast Conservation Therapy (BCT) in the Asia region has not observed the level of interest and growth observed in the western countries. In Hong Kong, the limited usage of BCT has been associated with limited number of radiation therapy facilities . However, because of the increasing local experience in the administration of BCT, increasing numbers of young patients in the population and increasing efforts to promote breast cancer awareness in recent years, the use of BCT is steadily increasing . For example, in Western Australia the proportion of women under going initial BCT doubled from 33% in 1982-1985 to 72% in 1998-2000 . One will further expect that APBI to increase the use of BCT in the management of early breast cancer. However, there is another issue in the application of APBI to the Asian population which is breast size. Asian women generally have smaller breast compare to European. Some of the APBI techniques might be challenging to apply to this patient group. In Japan for example, excision involving 2 cm free margin from the tumor is most commonly performed. In many cases mammary gland tissue does not remain on the dermal or pectoralis muscle sides of the tumor. The target of irradiation is only the lateral stump . Hence APBI techniques like the Mammosite will not be very applicable in the Asian population, because of potential excessive radiation dose to the skin. Maybe more conformal techniques like the SAVI or Clearpath might be appropriate. However, treatment results have not yet been published.
3D-CRT APBI also has similar limitations in the Asia region. When irradiation is performed in the supine position, flat extension of the breast reduces the distance between the target of the irradiation and the skin, leading to excessive exposure of the skin. However, using the 4field technique of 3D-CRT, Kosata et al.  demonstrated that in Japanese women, patients with a laterally located small tumor can be candidates for APBI, although patients with medially located tumor cannot. They also noted that a new beam arrangement using a combination of photons and electrons (a three-field technique that consisted of opposed, conformal tangential photons and enface electrons) recently proposed by Massachusetts General Hospital  may be more suited to Japanese women than that of the NSABP B-39/RTOG 0413 protocol .
IORT is also been explored as a way to provide APBI to the Japanese population. A phase I study designed using a scheme of dose-escalation from 19, 20, and 21 Gy at 90% isodose has been reported by Sawaki et al.. The IORT treatment was well tolerated in Japanese women, with a prescription dose of 21 Gy was recommended.
The coverage of the target varies depending on the technique. There are limited studies evaluating multiple techniques . Weed and colleagues compared 3D-CRT, mammosite and interstitial brachytherapy; they found that at the coverage at 90% of the prescribed dose, no difference was observed between 3D-CRT and MammoSite (which were both better than interstitial). 3D-CRT resulted in better coverage of the PTV compared with MammoSite or interstitial brachytherapy techniques. Better PTV coverage with 3D-CRT came at the cost of a higher integral dose to the remaining normal breast. Dosimetrically, the best partial breast irradiation technique appears to depend on the clinical situation.
Quality of Life (QOL)
In addition to local control, improved survival and better cosmesis, quality of life is also an important variable in evaluating treatment technique for breast cancer patients; with limited studies evaluating QOL aspects of breast cancer treatment. In a study by Wadasadawala et al , comparing APBI and WBI they found that the scores for social functioning and financial difficulties showed a trend towards a better outcome in the APBI group (p = 0.025 and p = 0.019 respectively). However, body image was significantly better in the APBI group as compared with the WBRT group (p = 0.005). Reports evaluating QOL for the different APBI have not been reported to date; although patients undergoing Mammosite have been reported to be very satisfied with their outcome .
In the age of rapidly increasing health care costs, evaluation of techniques has to include cost effectiveness. Cost comparisons have been reported by Suh et al. [161, 162] and Sher et al.  modeled treatment planning and delivery for different WBI fractionation schemes, Mammosite, MIB, APBI - 3DCRT and APBI-IMRT. They found that the least expensive partial breast-based radiation therapy approaches were the external beam techniques (APBI-3D-CRT and APBI-IMRT); any reduced cost to patients for the HDR brachytherapy-based APBI regimens were overshadowed by substantial increases in cost to payers, resulting in higher total societal costs. The cost of HDR treatment delivery was primarily responsible for the increased direct medical cost. APBI approaches in general were favored over whole-breast techniques when only considering costs to patients. However, If one were to pursue a partial-breast radiation therapy regimen to minimize patient costs, it would be more advantageous from a societal perspective to pursue external beam-based approaches such as APBI-3D-CRT or APBI-IMRT in lieu of the brachytherapy-based regimens . Similarly, Sher et al.  reported that APBI-3DCRT was the most cost-effective strategy for postmenopausal women with early-stage breast cancer. Unless the quality of life after MSB proves to be superior, it is unlikely to be cost-effective .
As eluded in this review, there are still a few unanswered questions including optimal technique, patient selection and target volume definition.
1 Optimal Technique
As reviewed herein, there are quite a variety of techniques available for APBI, but with insufficient clinical and dosimetric data to determine the optimal technique. It is worth noting that none of the current RCT will address this issue since a direct comparison of the technique is not part of any of the current trials. So research is required to determine (a) what is the optimal technique? (b) what technique is best for which patient?. Breast size and location of the lumpectomy cavity might dictate which technique to use. For example, small breasted patients might be best suited for IORT, while larger breasted are best served by balloon based brachytherapy techniques such as the MammoSite.
2 Patient Selection
There is yet to be a consensus in terms of which patients characteristics are suitable for APBI. Different societies have come up with varying patient selection criteria. Current data analysis shows that these recommendations might not be optimal. Therefore there is a need for a definitive clinical and pathological criteria for APBI patient selection.
3. Target Volume Definition
As reviewed herein, the volume of breast tissue irradiated varies with the technique used. Empirical and pathological studies are required to determine the level and degree of spread of micro-calcification. This will give a definitive guidance on how much tissue needs to be irradiated.
4 Optimal Dose and Fractionation Scheme
There is growing evidence that the linear quadratic model (LQM) may not be appropriate for modeling high dose per treatment[164, 165]. It has been suggested that LQM consistently overestimates cell killing at high single doses because it predicts a survival curve that continuously bends downward, whereas the experimental data are consistent with a constant slope (D0) at high doses. Furthermore, high-dose radiotherapy is achieving higher local control than could be explained by our current knowledge of radiation killing of cancer cells in a tumor. Proper radiobiological modeling is required to determine the optimal dose for APBI and fractionation scheme for the different techniques. The impact of the radiation energy used in determining the dosing also has to be investigated. For example, the dose for low energy x-rays will be different from the dose needed for high energy x-rays.
5. Imaging and Pathology
The role of imaging in the management of most diseases is unquestionable. This is also true for breast cancer management. The success of APBI depends highly on the ability to identify patients at low risk of multi-centric disease. Hence, the appropriate imaging technique has to be determined. For example, the value of adding a preoperative breast MRI to conventional mammography remains controversial. Hence, an imaging technique is required to increase the specificity and sensitivity of multi-centric disease diagnosis.
The interest in APBI is evident from the proliferation of approaches and devices. However, studies are required, not only to evaluate the efficacy of APBI, but also to assess the safety and toxicity of the various techniques and dosing schedules. Furthermore, it is hoped that more research will be carried out to determine the strengths and weaknesses of the different techniques; thereby creating a consensus and identifying where each technique may be best applied. Whole Breast Irradiation (WBI) as part of Breast Conservation Therapy has well established results in terms of disease control, good cosmesis, and low toxicity. The acceptance of APBI as a standard of care therefore rides on its ability to match or better WBI in terms of efficacy, quality of life outcomes, and cost-effectiveness.
- Feuer EJ, Wun LM, Boring CC, Flanders WD, Timmel MJ, Tong T: The lifetime risk of developing breast cancer. J Natl Cancer Inst. 1993, 85: 892-897. 10.1093/jnci/85.11.892.PubMedGoogle Scholar
- SEER Cancer Statistics Review, 1975-2006. [http://seer.cancer.gov/csr/1975_2006/]
- Hayat MJ, Howlader N, Reichman ME, Edwards BK: Cancer statistics, trends, and multiple primary cancer analyses from the Surveillance, Epidemiology, and End Results (SEER) Program. Oncologist. 2007, 12: 20-37. 10.1634/theoncologist.12-1-20.PubMedGoogle Scholar
- U.S. Cancer Statistics Working Group: United States Cancer Statistics: 1999-2006 Incidence and Mortality Web-based Report. 2010, Atlanta: U.S. Department of Health and Human Services, Centers for Disease Control and Prevention and National Cancer Institute, [http://www.cdc.gov/uscs]Google Scholar
- anon: Cancer Statistics registrations: Registrations of cancer diagnosed in 2006, England. Book Cancer Statistics registrations: Registrations of cancer diagnosed in 2006, England. (Editor ed.^eds.). 2009, City: National StatisticsGoogle Scholar
- Suzuki T, Toi M, Saji S, Horiguchi K, Aruga T, Suzuki E, Horiguchi S, Funata N, Karasawa K, Kamata N: Early breast cancer. Int J Clin Oncol. 2006, 11: 108-119. 10.1007/s10147-006-0564-7.PubMedGoogle Scholar
- Fisher B, Anderson S, Bryant J, Margolese RG, Deutsch M, Fisher ER, Jeong JH, Wolmark N: Twenty-year follow-up of a randomized trial comparing total mastectomy, lumpectomy, and lumpectomy plus irradiation for the treatment of invasive breast cancer. N Engl J Med. 2002, 347: 1233-1241. 10.1056/NEJMoa022152.PubMedGoogle Scholar
- Poggi MM, Danforth DN, Sciuto LC, Smith SL, Steinberg SM, Liewehr DJ, Menard C, Lippman ME, Lichter AS, Altemus RM: Eighteen-year results in the treatment of early breast carcinoma with mastectomy versus breast conservation therapy: the National Cancer Institute Randomized Trial. Cancer. 2003, 98: 697-702. 10.1002/cncr.11580.PubMedGoogle Scholar
- Veronesi U, Cascinelli N, Mariani L, Greco M, Saccozzi R, Luini A, Aguilar M, Marubini E: Twenty-year follow-up of a randomized study comparing breast-conserving surgery with radical mastectomy for early breast cancer. N Engl J Med. 2002, 347: 1227-1232. 10.1056/NEJMoa020989.PubMedGoogle Scholar
- Veronesi U, Marubini E, Mariani L, Galimberti V, Luini A, Veronesi P, Salvadori B, Zucali R: Radiotherapy after breast-conserving surgery in small breast carcinoma: long-term results of a randomized trial. Ann Oncol. 2001, 12: 997-1003. 10.1023/A:1011136326943.PubMedGoogle Scholar
- Clarke M, Collins R, Darby S, Davies C, Elphinstone P, Evans E, Godwin J, Gray R, Hicks C, James S, et al: Effects of radiotherapy and of differences in the extent of surgery for early breast cancer on local recurrence and 15-year survival: an overview of the randomised trials. Lancet. 2005, 366: 2087-2106.PubMedGoogle Scholar
- Vinh-Hung V, Verschraegen C: Breast-conserving surgery with or without radiotherapy: pooled-analysis for risks of ipsilateral breast tumor recurrence and mortality. J Natl Cancer Inst. 2004, 96: 115-121. 10.1093/jnci/djh013.PubMedGoogle Scholar
- Fisher B, Dignam J, Wolmark N, Mamounas E, Costantino J, Poller W, Fisher ER, Wickerham DL, Deutsch M, Margolese R, et al: Lumpectomy and radiation therapy for the treatment of intraductal breast cancer: findings from National Surgical Adjuvant Breast and Bowel Project B-17. J Clin Oncol. 1998, 16: 441-452.PubMedGoogle Scholar
- Bijker N, Meijnen P, Peterse JL, Bogaerts J, Van Hoorebeeck I, Julien JP, Gennaro M, Rouanet P, Avril A, Fentiman IS, et al: Breast-conserving treatment with or without radiotherapy in ductal carcinoma-in-situ: ten-year results of European Organisation for Research and Treatment of Cancer randomized phase III trial 10853--a study by the EORTC Breast Cancer Cooperative Group and EORTC Radiotherapy Group. J Clin Oncol. 2006, 24: 3381-3387. 10.1200/JCO.2006.06.1366.PubMedGoogle Scholar
- Consensus statement: treatment of early-stage breast cancer. National Institutes of Health Consensus Development Panel. J Natl Cancer Inst Monogr. 1992, 1-5.
- Morrow M, White J, Moughan J, Owen J, Pajack T, Sylvester J, Wilson JF, Winchester D: Factors predicting the use of breast-conserving therapy in stage I and II breast carcinoma. J Clin Oncol. 2001, 19: 2254-2262.PubMedGoogle Scholar
- Hiotis K, Ye W, Sposto R, Skinner KA: Predictors of breast conservation therapy: size is not all that matters. Cancer. 2005, 103: 892-899. 10.1002/cncr.20853.PubMedGoogle Scholar
- Nattinger AB, Gottlieb MS, Veum J, Yahnke D, Goodwin JS: Geographic variation in the use of breast-conserving treatment for breast cancer. N Engl J Med. 1992, 326: 1102-1107. 10.1056/NEJM199204233261702.PubMedGoogle Scholar
- Legorreta AP, Liu X, Parker RG: Examining the use of breast-conserving treatment for women with breast cancer in a managed care environment. Am J Clin Oncol. 2000, 23: 438-441.PubMedGoogle Scholar
- Farrow DC, Hunt WC, Samet JM: Geographic variation in the treatment of localized breast cancer. N Engl J Med. 1992, 326: 1097-1101. 10.1056/NEJM199204233261701.PubMedGoogle Scholar
- Lazovich DA, White E, Thomas DB, Moe RE: Underutilization of breast-conserving surgery and radiation therapy among women with stage I or II breast cancer. JAMA. 1991, 266: 3433-3438. 10.1001/jama.266.24.3433.PubMedGoogle Scholar
- Ballard-Barbash R, Potosky AL, Harlan LC, Nayfield SG, Kessler LG: Factors associated with surgical and radiation therapy for early stage breast cancer in older women. J Natl Cancer Inst. 1996, 88: 716-726. 10.1093/jnci/88.11.716.PubMedGoogle Scholar
- Mitsumori M, Hiraoka M: Current status of accelerated partial breast irradiation. Breast Cancer. 2008, 15: 101-107. 10.1007/s12282-007-0012-1.PubMedGoogle Scholar
- Arthur DW, Vicini FA: Accelerated partial breast irradiation as a part of breast conservation therapy. J Clin Oncol. 2005, 23: 1726-1735. 10.1200/JCO.2005.09.045.PubMedGoogle Scholar
- Kuerer HM, Julian TB, Strom EA, Lyerly HK, Giuliano AE, Mamounas EP, Vicini FA: Accelerated partial breast irradiation after conservative surgery for breast cancer. Ann Surg. 2004, 239: 338-351. 10.1097/01.sla.0000114219.71899.13.PubMed CentralPubMedGoogle Scholar
- Swanson TA, Vicini FA: Overview of accelerated partial breast irradiation. Curr Oncol Rep. 2008, 10: 54-60. 10.1007/s11912-008-0009-8.PubMedGoogle Scholar
- Mannino M, Yarnold J: Accelerated partial breast irradiation trials: diversity in rationale and design. Radiother Oncol. 2009, 91: 16-22. 10.1016/j.radonc.2008.12.011.PubMedGoogle Scholar
- Palacios Eito A, Espinosa Calvo M, Manas Rueda A, de Las Heras M: Radiation oncology: future needs and equipment. Current situation in Spain. Clin Transl Oncol. 2008, 10: 478-485. 10.1007/s12094-008-0236-3.PubMedGoogle Scholar
- Tatsuzaki H, Levin CV: Quantitative status of resources for radiation therapy in Asia and Pacific region. Radiother Oncol. 2001, 60: 81-89. 10.1016/S0167-8140(01)00330-9.PubMedGoogle Scholar
- Zubizarreta EH, Poitevin A, Levin CV: Overview of radiotherapy resources in Latin America: a survey by the International Atomic Energy Agency (IAEA). Radiother Oncol. 2004, 73: 97-100. 10.1016/j.radonc.2004.07.022.PubMedGoogle Scholar
- Levin CV, El Gueddari B, Meghzifene A: Radiation therapy in Africa: distribution and equipment. Radiother Oncol. 1999, 52: 79-84. 10.1016/S0167-8140(99)00069-9.PubMedGoogle Scholar
- Barton MB, Frommer M, Shafiq J: Role of radiotherapy in cancer control in low-income and middle-income countries. Lancet Oncol. 2006, 7: 584-595. 10.1016/S1470-2045(06)70759-8.PubMedGoogle Scholar
- Goyal S, Kearney T, Haffty BG: Current application and research directions for partial-breast irradiation. Oncology (Williston Park). 2007, 21: 449-461; discussion 461-442, 464, 470.Google Scholar
- Sanders ME, Scroggins T, Ampil FL, Li BD: Accelerated partial breast irradiation in early-stage breast cancer. J Clin Oncol. 2007, 25: 996-1002. 10.1200/JCO.2006.09.7436.PubMedGoogle Scholar
- Fisher B, Anderson S: Conservative surgery for the management of invasive and noninvasive carcinoma of the breast: NSABP trials. National Surgical Adjuvant Breast and Bowel Project. World J Surg. 1994, 18: 63-69. 10.1007/BF00348193.PubMedGoogle Scholar
- Holli K, Saaristo R, Isola J, Joensuu H, Hakama M: Lumpectomy with or without postoperative radiotherapy for breast cancer with favourable prognostic features: results of a randomized study. Br J Cancer. 2001, 84: 164-169. 10.1054/bjoc.2000.1571.PubMed CentralPubMedGoogle Scholar
- Malmstrom P, Holmberg L, Anderson H, Mattsson J, Jonsson PE, Tennvall-Nittby L, Balldin G, Loven L, Svensson JH, Ingvar C, et al: Breast conservation surgery, with and without radiotherapy, in women with lymph node-negative breast cancer: a randomised clinical trial in a population with access to public mammography screening. Eur J Cancer. 2003, 39: 1690-1697. 10.1016/S0959-8049(03)00324-1.PubMedGoogle Scholar
- Fisher ER, Anderson S, Tan-Chiu E, Fisher B, Eaton L, Wolmark N: Fifteen-year prognostic discriminants for invasive breast carcinoma: National Surgical Adjuvant Breast and Bowel Project Protocol-06. Cancer. 2001, 91: 1679-1687. 10.1002/1097-0142(20010415)91:8+<1679::AID-CNCR1183>3.0.CO;2-8.PubMedGoogle Scholar
- Vallis KA, Pintilie M, Chong N, Holowaty E, Douglas PS, Kirkbride P, Wielgosz A: Assessment of coronary heart disease morbidity and mortality after radiation therapy for early breast cancer. J Clin Oncol. 2002, 20: 1036-1042. 10.1200/JCO.20.4.1036.PubMedGoogle Scholar
- Kahan Z, Csenki M, Varga Z, Szil E, Cserhati A, Balogh A, Gyulai Z, Mandi Y, Boda K, Thurzo L: The risk of early and late lung sequelae after conformal radiotherapy in breast cancer patients. Int J Radiat Oncol Biol Phys. 2007, 68: 673-681.PubMedGoogle Scholar
- Kwa SL, Lebesque JV, Theuws JC, Marks LB, Munley MT, Bentel G, Oetzel D, Spahn U, Graham MV, Drzymala RE, et al: Radiation pneumonitis as a function of mean lung dose: an analysis of pooled data of 540 patients. Int J Radiat Oncol Biol Phys. 1998, 42: 1-9.PubMedGoogle Scholar
- Darby SC, McGale P, Taylor CW, Peto R: Long-term mortality from heart disease and lung cancer after radiotherapy for early breast cancer: prospective cohort study of about 300,000 women in US SEER cancer registries. Lancet Oncol. 2005, 6: 557-565. 10.1016/S1470-2045(05)70251-5.PubMedGoogle Scholar
- Kirova YM, Gambotti L, De Rycke Y, Vilcoq JR, Asselain B, Fourquet A: Risk of second malignancies after adjuvant radiotherapy for breast cancer: a large-scale, single-institution review. Int J Radiat Oncol Biol Phys. 2007, 68: 359-363.PubMedGoogle Scholar
- Schaapveld M, Visser O, Louwman MJ, de Vries EG, Willemse PH, Otter R, van der Graaf WT, Coebergh JW, van Leeuwen FE: Risk of new primary nonbreast cancers after breast cancer treatment: a Dutch population-based study. J Clin Oncol. 2008, 26: 1239-1246. 10.1200/JCO.2007.11.9081.PubMedGoogle Scholar
- Schaapveld M, Visser O, Louwman WJ, Willemse PH, de Vries EG, van der Graaf WT, Otter R, Coebergh JW, van Leeuwen FE: The impact of adjuvant therapy on contralateral breast cancer risk and the prognostic significance of contralateral breast cancer: a population based study in the Netherlands. Breast Cancer Res Treat. 2008, 110: 189-197. 10.1007/s10549-007-9709-2.PubMed CentralPubMedGoogle Scholar
- Vaidya JS, Vyas JJ, Chinoy RF, Merchant N, Sharma OP, Mittra I: Multicentricity of breast cancer: whole-organ analysis and clinical implications. Br J Cancer. 1996, 74: 820-824.PubMed CentralPubMedGoogle Scholar
- Holland R, Veling SH, Mravunac M, Hendriks JH: Histologic multifocality of Tis, T1-2 breast carcinomas. Implications for clinical trials of breast-conserving surgery. Cancer. 1985, 56: 979-990. 10.1002/1097-0142(19850901)56:5<979::AID-CNCR2820560502>3.0.CO;2-N.PubMedGoogle Scholar
- Arthur DW, Vicini FA, Kuske RR, Wazer DE, Nag S: Accelerated partial breast irradiation: an updated report from the American Brachytherapy Society. Brachytherapy. 2003, 2: 124-130. 10.1016/S1538-4721(03)00107-7.PubMedGoogle Scholar
- Faverly D, Holland R, Burgers L: An original stereomicroscopic analysis of the mammary glandular tree. Virchows Arch A Pathol Anat Histopathol. 1992, 421: 115-119. 10.1007/BF01607043.PubMedGoogle Scholar
- Faverly DR, Burgers L, Bult P, Holland R: Three dimensional imaging of mammary ductal carcinoma in situ: clinical implications. Semin Diagn Pathol. 1994, 11: 193-198.PubMedGoogle Scholar
- Imamura H, Haga S, Shimizu T, Watanabe O, Kinoshita J, Nagumo H, Kajiwara T, Aiba M: Relationship between the morphological and biological characteristics of intraductal components accompanying invasive ductal breast carcinoma and patient age. Breast Cancer Res Treat. 2000, 62: 177-184. 10.1023/A:1006462328544.PubMedGoogle Scholar
- Offersen BV, Overgaard M, Kroman N, Overgaard J: Accelerated partial breast irradiation as part of breast conserving therapy of early breast carcinoma: a systematic review. Radiother Oncol. 2009, 90: 1-13. 10.1016/j.radonc.2008.08.005.PubMedGoogle Scholar
- Zwicker RD, Arthur DW, Kavanagh BD, Mohan R, Schmidt-Ullrich RK: Optimization of planar high-dose-rate implants. Int J Radiat Oncol Biol Phys. 1999, 44: 1171-1177.PubMedGoogle Scholar
- Zwicker RD, Schmidt-Ullrich R: Dose uniformity in a planar interstitial implant system. Int J Radiat Oncol Biol Phys. 1995, 31: 149-155.PubMedGoogle Scholar
- Kuske RR: Breast brachytherapy. Hematol Oncol Clin North Am. 1999, 13: 543-558, vi-vii. 10.1016/S0889-8588(05)70074-5.PubMedGoogle Scholar
- Schmidt-Ullrich PN, Todor DA, Cuttino LW, Arthur DW: Virtual planning of multicatheter brachytherapy implants for accelerated partial breast irradiation. Conf Proc IEEE Eng Med Biol Soc. 2004, 5: 3124-3127.PubMedGoogle Scholar
- Arthur DW, Koo D, Zwicker RD, Tong S, Bear HD, Kaplan BJ, Kavanagh BD, Warwicke LA, Holdford D, Amir C, et al: Partial breast brachytherapy after lumpectomy: low-dose-rate and high-dose-rate experience. Int J Radiat Oncol Biol Phys. 2003, 56: 681-689.PubMedGoogle Scholar
- Polgar C, Major T, Fodor J, Sulyok Z, Somogyi A, Lovey K, Nemeth G, Kasler M: Accelerated partial-breast irradiation using high-dose-rate interstitial brachytherapy: 12-year update of a prospective clinical study. Radiother Oncol. 2010, 94: 274-279. 10.1016/j.radonc.2010.01.019.PubMedGoogle Scholar
- Antonucci JV, Wallace M, Goldstein NS, Kestin L, Chen P, Benitez P, Dekhne N, Martinez A, Vicini F: Differences in patterns of failure in patients treated with accelerated partial breast irradiation versus whole-breast irradiation: a matched-pair analysis with 10-year follow-up. Int J Radiat Oncol Biol Phys. 2009, 74: 447-452.PubMedGoogle Scholar
- Strnad V, Hildebrandt G, Potter R, Hammer J, Hindemith M, Resch A, Spiegl K, Lotter M, Uter W, Bani M, et al: Accelerated Partial Breast Irradiation: 5-Year Results of the German-Austrian Multicenter Phase II Trial Using Interstitial Multicatheter Brachytherapy Alone After Breast-Conserving Surgery. Int J Radiat Oncol Biol Phys. 2010,Google Scholar
- Johansson B, Karlsson L, Liljegren G, Hardell L, Persliden J: Pulsed dose rate brachytherapy as the sole adjuvant radiotherapy after breast-conserving surgery of T1-T2 breast cancer: first long time results from a clinical study. Radiother Oncol. 2009, 90: 30-35. 10.1016/j.radonc.2008.02.022.PubMedGoogle Scholar
- Arthur DW, Winter K, Kuske RR, Bolton J, Rabinovitch R, White J, Hanson WF, Wilenzick RM, McCormick B: A Phase II trial of brachytherapy alone after lumpectomy for select breast cancer: tumor control and survival outcomes of RTOG 95-17. Int J Radiat Oncol Biol Phys. 2008, 72: 467-473.PubMed CentralPubMedGoogle Scholar
- Polgar C, Fodor J, Major T, Nemeth G, Lovey K, Orosz Z, Sulyok Z, Takacsi-Nagy Z, Kasler M: Breast-conserving treatment with partial or whole breast irradiation for low-risk invasive breast carcinoma--5-year results of a randomized trial. Int J Radiat Oncol Biol Phys. 2007, 69: 694-702.PubMedGoogle Scholar
- King TA, Bolton JS, Kuske RR, Fuhrman GM, Scroggins TG, Jiang XZ: Long-term results of wide-field brachytherapy as the sole method of radiation therapy after segmental mastectomy for T(is,1,2) breast cancer. Am J Surg. 2000, 180: 299-304. 10.1016/S0002-9610(00)00454-2.PubMedGoogle Scholar
- Ott OJ, Hildebrandt G, Potter R, Hammer J, Lotter M, Resch A, Sauer R, Strnad V: Accelerated partial breast irradiation with multi-catheter brachytherapy: Local control, side effects and cosmetic outcome for 274 patients. Results of the German-Austrian multi-centre trial. Radiother Oncol. 2007, 82: 281-286. 10.1016/j.radonc.2006.08.028.PubMedGoogle Scholar
- Edmundson GK, Vicini FA, Chen PY, Mitchell C, Martinez AA: Dosimetric characteristics of the MammoSite RTS, a new breast brachytherapy applicator. Int J Radiat Oncol Biol Phys. 2002, 52: 1132-1139.PubMedGoogle Scholar
- Dickler A, Patel RR, Wazer D: Breast brachytherapy devices. Expert Rev Med Devices. 2009, 6: 325-333. 10.1586/erd.09.6.PubMedGoogle Scholar
- Bensaleh S, Bezak E, Borg M: Review of MammoSite brachytherapy: advantages, disadvantages and clinical outcomes. Acta Oncol. 2009, 48: 487-494. 10.1080/02841860802537916.PubMedGoogle Scholar
- Niehoff P, Polgar C, Ostertag H, Major T, Sulyok Z, Kimmig B, Kovacs G: Clinical experience with the MammoSite radiation therapy system for brachytherapy of breast cancer: results from an international phase II trial. Radiother Oncol. 2006, 79: 316-320. 10.1016/j.radonc.2006.05.010.PubMedGoogle Scholar
- Dragun AE, Harper JL, Jenrette JM, Sinha D, Cole DJ: Predictors of cosmetic outcome following MammoSite breast brachytherapy: a single-institution experience of 100 patients with two years of follow-up. Int J Radiat Oncol Biol Phys. 2007, 68: 354-358.PubMedGoogle Scholar
- Vicini F, Beitsch PD, Quiet CA, Keleher AJ, Garcia D, Snider HC Jr, Gittleman MA, Zannis VJ, Kuerer HM, Lyden M: Three-year analysis of treatment efficacy, cosmesis, and toxicity by the American Society of Breast Surgeons MammoSite Breast Brachytherapy Registry Trial in patients treated with accelerated partial breast irradiation (APBI). Cancer. 2008, 112: 758-766. 10.1002/cncr.23227.PubMedGoogle Scholar
- Shah NM, Wazer DE: The MammoSite balloon brachytherapy catheter for accelerated partial breast irradiation. Semin Radiat Oncol. 2005, 15: 100-107. 10.1016/j.semradonc.2004.10.006.PubMedGoogle Scholar
- Benitez PR, Keisch ME, Vicini F, Stolier A, Scroggins T, Walker A, White J, Hedberg P, Hebert M, Arthur D, et al: Five-year results: the initial clinical trial of MammoSite balloon brachytherapy for partial breast irradiation in early-stage breast cancer. Am J Surg. 2007, 194: 456-462. 10.1016/j.amjsurg.2007.06.010.PubMedGoogle Scholar
- Jeruss JS, Kuerer HM, Beitsch PD, Vicini FA, Keisch M: Update on DCIS Outcomes from the American Society of Breast Surgeons Accelerated Partial Breast Irradiation Registry Trial. Ann Surg Oncol.
- Patel RR, Christensen ME, Hodge CW, Adkison JB, Das RK: Clinical outcome analysis in "high-risk" versus "low-risk" patients eligible for national surgical adjuvant breast and bowel B-39/radiation therapy oncology group 0413 trial: five-year results. Int J Radiat Oncol Biol Phys. 2008, 70: 970-973.PubMedGoogle Scholar
- Chen S, Dickler A, Kirk M, Shah A, Jokich P, Solmos G, Strauss J, Dowlatshahi K, Nguyen C, Griem K: Patterns of failure after MammoSite brachytherapy partial breast irradiation: a detailed analysis. Int J Radiat Oncol Biol Phys. 2007, 69: 25-31.PubMedGoogle Scholar
- Belkacemi Y, Chauvet MP, Giard S, Villette S, Lacornerie T, Bonodeau F, Baranzelli MC, Bonneterre J, Lartigau E: Partial breast irradiation as sole therapy for low risk breast carcinoma: early toxicity, cosmesis and quality of life results of a MammoSite brachytherapy phase II study. Radiother Oncol. 2009, 90: 23-29. 10.1016/j.radonc.2008.06.004.PubMedGoogle Scholar
- Voth M, Budway R, Keleher A, Caushaj PF: Local recurrence of breast cancer after MammoSite brachytherapy. Am Surg. 2006, 72: 798-800; discussion 800-791.PubMedGoogle Scholar
- Vicini F, Beitsch P, Quiet C, Gittleman M, Zannis V, Fine R, Whitworth P, Kuerer H, Haffty B, Keisch M, Lyden M: Five-Year Analysis of Treatment Efficacy and Cosmesis by the American Society of Breast Surgeons Mammosite Breast Brachytherapy Registry Trial in Patients Treated with Accelerated Partial Breast Irradiation. Int J Radiat Oncol Biol Phys. 2010,Google Scholar
- Hepel JT, Hiatt JR, Cardarelli GA, Wazer DE: Modeling study for optimization of skin dose for partial breast irradiation using Xoft Axxent electronic brachytherapy applicator. Brachytherapy. 2010, 9: 81-85. 10.1016/j.brachy.2009.08.005.PubMedGoogle Scholar
- Dickler A, Ivanov O, Francescatti D: Intraoperative radiation therapy in the treatment of early-stage breast cancer utilizing xoft axxent electronic brachytherapy. World J Surg Oncol. 2009, 7: 24-10.1186/1477-7819-7-24.PubMed CentralPubMedGoogle Scholar
- Ivanov O, Dickler A, Lum BY, Pellicane JV, Francescatti DS: Twelve-Month Follow-Up Results of a Trial Utilizing Axxent Electronic Brachytherapy to Deliver Intraoperative Radiation Therapy for Early-Stage Breast Cancer. Ann Surg Oncol. 2010,Google Scholar
- Rivard MJ, Davis SD, DeWerd LA, Rusch TW, Axelrod S: Calculated and measured brachytherapy dosimetry parameters in water for the Xoft Axxent X-Ray Source: an electronic brachytherapy source. Med Phys. 2006, 33: 4020-4032. 10.1118/1.2357021.PubMedGoogle Scholar
- Chen SS, Strauss JB, Shah AP, Rao RD, Bernard DA, Griem KL: Radiation recall reaction with docetaxel administration after accelerated partial breast irradiation with electronic brachytherapy. Brachytherapy. 2009, 8: 331-334. 10.1016/j.brachy.2009.01.001.PubMedGoogle Scholar
- Brenner DJ, Leu CS, Beatty JF, Shefer RE: Clinical relative biological effectiveness of low-energy x-rays emitted by miniature x-ray devices. Phys Med Biol. 1999, 44: 323-333. 10.1088/0031-9155/44/2/002.PubMedGoogle Scholar
- Wilder RB, Curcio LD, Khanijou RK, Eisner ME, Kakkis JL, Chittenden L, Agustin J, Lizarde J, Mesa AV, Ravera J, Tokita KM: A Contura catheter offers dosimetric advantages over a MammoSite catheter that increase the applicability of accelerated partial breast irradiation. Brachytherapy. 2009, 8: 373-378. 10.1016/j.brachy.2009.04.002.PubMedGoogle Scholar
- Brown S, McLaughlin M, Pope K, Haile K, Hughes L, Israel PZ: Initial radiation experience evaluating early tolerance and toxicities in patients undergoing accelerated partial breast irradiation using the Contura Multi-Lumen Balloon breast brachytherapy catheter. Brachytherapy. 2009, 8: 227-233. 10.1016/j.brachy.2008.11.013.PubMedGoogle Scholar
- Scanderbeg DJ, Yashar C, White G, Rice R, Pawlicki T: Evaluation of Three APBI Techniques Under NSABP B-39 Guidelines. J Appl Clin Med Phys. 2010, 11: 3021-Google Scholar
- Scanderbeg DJ, Yashar C, Rice R, Pawlicki T: Clinical implementation of a new HDR brachytherapy device for partial breast irradiation. Radiother Oncol. 2009, 90: 36-42. 10.1016/j.radonc.2008.09.024.PubMedGoogle Scholar
- Beriwal S, Coon D, Kim H, Haley M, Patel R, Das R: Multicatheter hybrid breast brachytherapy: a potential alternative for patients with inadequate skin distance. Brachytherapy. 2008, 7: 301-304. 10.1016/j.brachy.2008.07.003.PubMedGoogle Scholar
- Dickler A, Seif N, Kirk MC, Patel MB, Bernard D, Coon A, Dowlatshahi K, Das RK, Patel RR: A dosimetric comparison of MammoSite and ClearPath high-dose-rate breast brachytherapy devices. Brachytherapy. 2009, 8: 14-18. 10.1016/j.brachy.2008.07.006.PubMedGoogle Scholar
- Kozak KR, Doppke KP, Katz A, Taghian AG: Dosimetric comparison of two different three-dimensional conformal external beam accelerated partial breast irradiation techniques. Int J Radiat Oncol Biol Phys. 2006, 65: 340-346.PubMedGoogle Scholar
- Baglan KL, Sharpe MB, Jaffray D, Frazier RC, Fayad J, Kestin LL, Remouchamps V, Martinez AA, Wong J, Vicini FA: Accelerated partial breast irradiation using 3D conformal radiation therapy (3D-CRT). Int J Radiat Oncol Biol Phys. 2003, 55: 302-311.PubMedGoogle Scholar
- Hepel JT, Tokita M, MacAusland SG, Evans SB, Hiatt JR, Price LL, DiPetrillo T, Wazer DE: Toxicity of three-dimensional conformal radiotherapy for accelerated partial breast irradiation. Int J Radiat Oncol Biol Phys. 2009, 75: 1290-1296.PubMedGoogle Scholar
- Formenti SC: External-beam partial-breast irradiation. Semin Radiat Oncol. 2005, 15: 92-99. 10.1016/j.semradonc.2004.10.008.PubMedGoogle Scholar
- Formenti SC, Truong MT, Goldberg JD, Mukhi V, Rosenstein B, Roses D, Shapiro R, Guth A, Dewyngaert JK: Prone accelerated partial breast irradiation after breast-conserving surgery: preliminary clinical results and dose-volume histogram analysis. Int J Radiat Oncol Biol Phys. 2004, 60: 493-504. 10.1016/j.ijrobp.2004.07.269.PubMedGoogle Scholar
- Cox BW, Horst KC, Thornton S, Dirbas FM: Impact of increasing margin around the lumpectomy cavity to define the planning target volume for 3D conformal external beam accelerated partial breast irradiation. Med Dosim. 2007, 32: 254-262. 10.1016/j.meddos.2007.02.003.PubMedGoogle Scholar
- Landis DM, Luo W, Song J, Bellon JR, Punglia RS, Wong JS, Killoran JH, Gelman R, Harris JR: Variability among breast radiation oncologists in delineation of the postsurgical lumpectomy cavity. Int J Radiat Oncol Biol Phys. 2007, 67: 1299-1308.PubMedGoogle Scholar
- Dzhugashvili M, Tournay E, Pichenot C, Dunant A, Pessoa E, Khallel A, Gouy S, Uzan C, Garbay JR, Rimareix F, et al: 3D-conformal accelerated partial breast irradiation treatment planning: the value of surgical clips in the delineation of the lumpectomy cavity. Radiat Oncol. 2009, 4: 70-10.1186/1748-717X-4-70.PubMed CentralPubMedGoogle Scholar
- Rosenstein BS, Lymberis SC, Formenti SC: Biologic comparison of partial breast irradiation protocols. Int J Radiat Oncol Biol Phys. 2004, 60: 1393-1404. 10.1016/j.ijrobp.2004.06.156.PubMedGoogle Scholar
- Taghian AG, Kozak KR, Doppke KP, Katz A, Smith BL, Gadd M, Specht M, Hughes K, Braaten K, Kachnic LA, et al: Initial dosimetric experience using simple three-dimensional conformal external-beam accelerated partial-breast irradiation. Int J Radiat Oncol Biol Phys. 2006, 64: 1092-1099.PubMedGoogle Scholar
- Livi L, Buonamici FB, Simontacchi G, Scotti V, Fambrini M, Compagnucci A, Paiar F, Scoccianti S, Pallotta S, Detti B, et al: Accelerated partial breast irradiation with IMRT: new technical approach and interim analysis of acute toxicity in a phase III randomized clinical trial. Int J Radiat Oncol Biol Phys. 2010, 77: 509-515.PubMedGoogle Scholar
- Cuttino LW, Todor D, Pacyna L, Lin PS, Arthur DW: Three-dimensional conformal external beam radiotherapy (3D-CRT) for accelerated partial breast irradiation (APBI): what is the correct prescription dose?. Am J Clin Oncol. 2006, 29: 474-478. 10.1097/01.coc.0000225409.99284.f2.PubMedGoogle Scholar
- Vicini F, Winter K, Wong J, Pass H, Rabinovitch R, Chafe S, Arthur D, Petersen I, White J, McCormick B: Initial Efficacy Results of RTOG 0319: Three-Dimensional Conformal Radiation Therapy (3D-CRT) Confined to the Region of the Lumpectomy Cavity for Stage I/II Breast Carcinoma. Int J Radiat Oncol Biol Phys. 2010, 77: 1120-1127.PubMed CentralPubMedGoogle Scholar
- Vicini FA, Chen P, Wallace M, Mitchell C, Hasan Y, Grills I, Kestin L, Schell S, Goldstein NS, Kunzman J, et al: Interim cosmetic results and toxicity using 3D conformal external beam radiotherapy to deliver accelerated partial breast irradiation in patients with early-stage breast cancer treated with breast-conserving therapy. Int J Radiat Oncol Biol Phys. 2007, 69: 1124-1130.PubMedGoogle Scholar
- Chen PY, Wallace M, Mitchell C, Grills I, Kestin L, Fowler A, Martinez A, Vicini F: Four-year efficacy, cosmesis, and toxicity using three-dimensional conformal external beam radiation therapy to deliver accelerated partial breast irradiation. Int J Radiat Oncol Biol Phys. 2010, 76: 991-997.PubMedGoogle Scholar
- Taghian AG, El-Din MA, Smith BL, Ancukiewicz M, MacDonald SS, Katz A, Specht M, Hirsch A, Powell SN, Recht A: Interim results of a phase I/II trial of 3D-conformal external beam accelerated partial breast irradiation in patients with early breast cancer. Int J Radiat Oncol Biol Phys. 2008, 72: S4-S4.Google Scholar
- Formenti SC, Rosenstein B, Skinner KA, Jozsef G: T1 stage breast cancer: adjuvant hypofractionated conformal radiation therapy to tumor bed in selected postmenopausal breast cancer patients--pilot feasibility study. Radiology. 2002, 222: 171-178. 10.1148/radiol.2221010769.PubMedGoogle Scholar
- Magee B, Swindell R, Harris M, Banerjee SS: Prognostic factors for breast recurrence after conservative breast surgery and radiotherapy: results from a randomised trial. Radiother Oncol. 1996, 39: 223-227. 10.1016/0167-8140(96)01747-1.PubMedGoogle Scholar
- Leonard CE, Carter D, Howell K, Kaske T, Kercher J, Henkenberns P: A prospective trial of accelerated partial breast intensity modulated radiotherapy. Int J Radiat Oncol Biol Phys. 2008, 72: S152-S152.Google Scholar
- Jagsi R, Ben-David MA, Moran JM, Marsh RB, Griffith KA, Hayman JA, Pierce LJ: Unacceptable cosmesis in a protocol investigating intensity-modulated radiotherapy with active breathing control for accelerated partial-breast irradiation. Int J Radiat Oncol Biol Phys. 2010, 76: 71-78.PubMed CentralPubMedGoogle Scholar
- Reitsamer R, Sedlmayer F, Kopp M, Kametriser G, Menzel C, Glueck S, Nairz O, Deutschmann H, Merz F, Peintinger F: Concepts and techniques of intraoperative radiotherapy (IORT) for breast cancer. Breast Cancer. 2008, 15: 40-46. 10.1007/s12282-007-0001-4.PubMedGoogle Scholar
- Vaidya JS, Tobias JS, Baum M, Keshtgar M, Joseph D, Wenz F, Houghton J, Saunders C, Corica T, D'Souza D, et al: Intraoperative radiotherapy for breast cancer. Lancet Oncol. 2004, 5: 165-173. 10.1016/S1470-2045(04)01412-3.PubMedGoogle Scholar
- Vaidya JS, Tobias JS, Baum M, Wenz F, Kraus-Tiefenbacher U, D'Souza D, Keshtgar M, Massarut S, Hilaris B, Saunders C, Joseph D: TARGeted Intraoperative radiotherapy (TARGIT): an innovative approach to partial-breast irradiation. Semin Radiat Oncol. 2005, 15: 84-91. 10.1016/j.semradonc.2004.10.007.PubMedGoogle Scholar
- Orecchia R, Veronesi U: Intraoperative electrons. Semin Radiat Oncol. 2005, 15: 76-83. 10.1016/j.semradonc.2004.10.009.PubMedGoogle Scholar
- Orecchia R, Luini A, Veronesi P, Ciocca M, Franzetti S, Gatti G, Veronesi U: Electron intraoperative treatment in patients with early-stage breast cancer: data update. Expert Rev Anticancer Ther. 2006, 6: 605-611. 10.1586/14737126.96.36.1995.PubMedGoogle Scholar
- Holmes DR, Baum M, Joseph D: The TARGIT trial: targeted intraoperative radiation therapy versus conventional postoperative whole-breast radiotherapy after breast-conserving surgery for the management of early-stage invasive breast cancer (a trial update). Am J Surg. 2007, 194: 507-510. 10.1016/j.amjsurg.2007.06.018.PubMedGoogle Scholar
- Benda RK, Yasuda G, Sethi A, Gabram SG, Hinerman RW, Mendenhall NP: Breast boost: are we missing the target?. Cancer. 2003, 97: 905-909. 10.1002/cncr.11142.PubMedGoogle Scholar
- Karni T, Pappo I, Sandbank J, Lavon O, Kent V, Spector R, Morgenstern S, Lelcuk S: A device for real-time, intraoperative margin assessment in breast-conservation surgery. Am J Surg. 2007, 194: 467-473. 10.1016/j.amjsurg.2007.06.013.PubMedGoogle Scholar
- Kraus-Tiefenbacher U, Scheda A, Steil V, Hermann B, Kehrer T, Bauer L, Melchert F, Wenz F: Intraoperative radiotherapy (IORT) for breast cancer using the Intrabeam system. Tumori. 2005, 91: 339-345.PubMedGoogle Scholar
- Vaidya JS, Baum M, Tobias JS, D'Souza DP, Naidu SV, Morgan S, Metaxas M, Harte KJ, Sliski AP, Thomson E: Targeted intra-operative radiotherapy (Targit): an innovative method of treatment for early breast cancer. Ann Oncol. 2001, 12: 1075-1080. 10.1023/A:1011609401132.PubMedGoogle Scholar
- Vaidya JS, Baum M, Tobias JS, Morgan S, D'Souza D: The novel technique of delivering targeted intraoperative radiotherapy (Targit) for early breast cancer. Eur J Surg Oncol. 2002, 28: 447-454. 10.1053/ejso.2002.1275.PubMedGoogle Scholar
- Vaidya JS, Joseph DJ, Tobias JS, Bulsara M, Wenz F, Saunders C, Alvarado M, Flyger HL, Massarut S, Eiermann W, et al: Targeted intraoperative radiotherapy versus whole breast radiotherapy for breast cancer (TARGIT-A trial): an international, prospective, randomised, non-inferiority phase 3 trial. Lancet. 2010, 376: 91-102. 10.1016/S0140-6736(10)60837-9.PubMedGoogle Scholar
- Beddar AS, Krishnan S: Intraoperative radiotherapy using a mobile electron LINAC: a retroperitoneal sarcoma case. J Appl Clin Med Phys. 2005, 6: 95-107. 10.1120/jacmp.2025.25349.PubMedGoogle Scholar
- Beddar AS, Kubu ML, Domanovic MA, Ellis RJ, Kinsella TJ, Sibata CH: A new approach to intraoperative radiation therapy. AORN J. 2001, 74: 500-505. 10.1016/S0001-2092(06)61682-7.PubMedGoogle Scholar
- Daves JL, Mills MD: Shielding assessment of a mobile electron accelerator for intraoperative radiotherapy. J Appl Clin Med Phys. 2001, 2: 165-173. 10.1120/1.1385129.PubMedGoogle Scholar
- Veronesi U, Orecchia R, Luini A, Gatti G, Intra M, Zurrida S, Ivaldi G, Tosi G, Ciocca M, Tosoni A, De Lucia F: A preliminary report of intraoperative radiotherapy (IORT) in limited-stage breast cancers that are conservatively treated. Eur J Cancer. 2001, 37: 2178-2183. 10.1016/S0959-8049(01)00285-4.PubMedGoogle Scholar
- Frasson AL, Zerwes FP, Braga AP, Barbosa FS, Koch HA: Intraoperative radiotherapy in the conventional linear accelerator room for early breast cancer treatment: an alternative choice in developing countries. J Exp Clin Cancer Res. 2007, 26: 379-384.PubMedGoogle Scholar
- Cuncins-Hearn A, Saunders C, Walsh D, Borg M, Buckingham J, Frizelle F, Maddern G: A systematic review of intraoperative radiotherapy in early breast cancer. Breast Cancer Res Treat. 2004, 85: 271-280. 10.1023/B:BREA.0000025411.77758.1e.PubMedGoogle Scholar
- Veronesi U, Orecchia R, Luini A, Galimberti V, Gatti G, Intra M, Veronesi P, Leonardi MC, Ciocca M, Lazzari R, et al: Full-dose intraoperative radiotherapy with electrons during breast-conserving surgery: experience with 590 cases. Ann Surg. 2005, 242: 101-106. 10.1097/01.sla.0000167927.82353.bc.PubMed CentralPubMedGoogle Scholar
- Lemanski C, Azria D, Gourgon-Bourgade S, Gutowski M, Rouanet P, Saint-Aubert B, Ailleres N, Fenoglietto P, Dubois JB: Intraoperative radiotherapy in early-stage breast cancer: results of the montpellier phase II trial. Int J Radiat Oncol Biol Phys. 2010, 76: 698-703.PubMedGoogle Scholar
- Mussari S, Sabino Della Sala W, Busana L, Vanoni V, Eccher C, Zani B, Menegotti L, Tomio L: Full-dose intraoperative radiotherapy with electrons in breast cancer. First report on late toxicity and cosmetic results from a single-institution experience. Strahlenther Onkol. 2006, 182: 589-595. 10.1007/s00066-006-1559-z.PubMedGoogle Scholar
- Buchholz TA, Kuerer HM, Strom EA: Is partial breast irradiation a step forward or backward?. Semin Radiat Oncol. 2005, 15: 69-75. 10.1016/j.semradonc.2004.10.003.PubMedGoogle Scholar
- Rose CM, Recht A: Accelerated partial-breast irradiation (APBI): let's give it a good test. Int J Radiat Oncol Biol Phys. 2003, 57: 1217-1218.PubMedGoogle Scholar
- Sarin R, Chopra S: Accelerated partial breast irradiation using multicatheter brachytherapy. Nat Clin Pract Oncol. 2007, 4: 382-383. 10.1038/ncponc0845.PubMedGoogle Scholar
- Vicini F, Arthur D, Polgar C, Kuske R: Defining the efficacy of accelerated partial breast irradiation: the importance of proper patient selection, optimal quality assurance, and common sense. Int J Radiat Oncol Biol Phys. 2003, 57: 1210-1213.PubMedGoogle Scholar
- Polgar C, Van Limbergen E, Potter R, Kovacs G, Polo A, Lyczek J, Hildebrandt G, Niehoff P, Guinot JL, Guedea F, et al: Patient selection for accelerated partial-breast irradiation (APBI) after breast-conserving surgery: recommendations of the Groupe Europeen de Curietherapie-European Society for Therapeutic Radiology and Oncology (GEC-ESTRO) breast cancer working group based on clinical evidence (2009). Radiother Oncol. 2010, 94: 264-273. 10.1016/j.radonc.2010.01.014.PubMedGoogle Scholar
- Smith BD, Arthur DW, Buchholz TA, Haffty BG, Hahn CA, Hardenbergh PH, Julian TB, Marks LB, Todor DA, Vicini FA, et al: Accelerated partial breast irradiation consensus statement from the American Society for Radiation Oncology (ASTRO). Int J Radiat Oncol Biol Phys. 2009, 74: 987-1001.PubMedGoogle Scholar
- Vicini F, Arthur D, Wazer D, Chen P, Mitchell C, Wallace M, Kestin L, Ye H: Limitations of the American Society of Therapeutic Radiology and Oncology Consensus Panel Guidelines on the Use of Accelerated Partial Breast Irradiation. Int J Radiat Oncol Biol Phys. 2010,Google Scholar
- Shaitelman SF, Vicini FA, Beitsch P, Haffty B, Keisch M, Lyden M: Five-year outcome of patients classified using the American Society for Radiation Oncology consensus statement guidelines for the application of accelerated partial breast irradiation: an analysis of patients treated on the American Society of Breast Surgeons MammoSite Registry Trial. Cancer.
- McHaffie DR, Patel RR, Adkison JB, Das RK, Geye HM, Cannon GM: Outcomes After Accelerated Partial Breast Irradiation in Patients with ASTRO Consensus Statement Cautionary Features. Int J Radiat Oncol Biol Phys.
- Njeh CF: Tumor delineation: The weakest link in the search for accuracy in radiotherapy. J Med Phys. 2008, 33: 136-140. 10.4103/0971-6203.44472.PubMed CentralPubMedGoogle Scholar
- Petersen RP, Truong PT, Kader HA, Berthelet E, Lee JC, Hilts ML, Kader AS, Beckham WA, Olivotto IA: Target volume delineation for partial breast radiotherapy planning: Clinical characteristics associated with low interobserver concordance. Int J Radiat Oncol Biol Phys. 2007, 69: 41-48.PubMedGoogle Scholar
- Weed DW, Yan D, Martinez AA, Vicini FA, Wilkinson TJ, Wong J: The validity of surgical clips as a radiographic surrogate for the lumpectomy cavity in image-guided accelerated partial breast irradiation. Int J Radiat Oncol Biol Phys. 2004, 60: 484-492. 10.1016/j.ijrobp.2004.07.410.PubMedGoogle Scholar
- Wong EK, Truong PT, Kader HA, Nichol AM, Salter L, Petersen R, Wai ES, Weir L, Olivotto IA: Consistency in seroma contouring for partial breast radiotherapy: Impact of guidelines. Int J Radiat Oncol Biol Phys. 2006, 66: 372-376.PubMedGoogle Scholar
- Vicini FA, Kestin L, Chen P, Benitez P, Goldstein NS, Martinez A: Limited-field radiation therapy in the management of early-stage breast cancer. J Natl Cancer Inst. 2003, 95: 1205-1210. 10.1093/jnci/djg023.PubMedGoogle Scholar
- Veronesi U, Gatti G, Luini A, Intra M, Ciocca M, Sanchez D, Zurrida S, Navarro S, Orecchia R: Full-dose intraoperative radiotherapy with electrons during breast-conserving surgery. Arch Surg. 2003, 138: 1253-1256. 10.1001/archsurg.138.11.1253.PubMedGoogle Scholar
- Ebell MH, Siwek J, Weiss BD, Woolf SH, Susman J, Ewigman B, Bowman M: Strength of recommendation taxonomy (SORT): a patient-centered approach to grading evidence in the medical literature. Am Fam Physician. 2004, 69: 548-556.PubMedGoogle Scholar
- Atkins D, Best D, Briss PA, Eccles M, Falck-Ytter Y, Flottorp S, Guyatt GH, Harbour RT, Haugh MC, Henry D, et al: Grading quality of evidence and strength of recommendations. BMJ. 2004, 328: 1490-10.1136/bmj.328.7454.1490.PubMedGoogle Scholar
- Ribeiro GG, Magee B, Swindell R, Harris M, Banerjee SS: The Christie Hospital breast conservation trial: an update at 8 years from inception. Clin Oncol (R Coll Radiol). 1993, 5: 278-283.Google Scholar
- Dodwell DJ, Dyker K, Brown J, Hawkins K, Cohen D, Stead M, Ash D: A randomised study of whole-breast vs tumour-bed irradiation after local excision and axillary dissection for early breast cancer. Clin Oncol (R Coll Radiol). 2005, 17: 618-622.Google Scholar
- Lehman M, Hickey B: The less than whole breast radiotherapy approach. Breast. 2010, 19: 180-187. 10.1016/j.breast.2010.03.005.PubMedGoogle Scholar
- Orecchia R, Ciocca M, Tosi G, Franzetti S, Luini A, Gatti G, Veronesi U: Intraoperative electron beam radiotherapy (ELIOT) to the breast: a need for a quality assurance programme. Breast. 2005, 14: 541-546. 10.1016/j.breast.2005.08.038.PubMedGoogle Scholar
- Yau TK, Soong IS, Sze H, Choi CW, Yeung MW, Ng WT, Lee AW: Trends and patterns of breast conservation treatment in Hong Kong: 1994-2007. Int J Radiat Oncol Biol Phys. 2009, 74: 98-103.PubMedGoogle Scholar
- Spilsbury K, Semmens JB, Saunders CM, Hall SE, Holman CD: Subsequent surgery after initial breast conserving surgery: a population based study. ANZ J Surg. 2005, 75: 260-264. 10.1111/j.1445-2197.2005.03352.x.PubMedGoogle Scholar
- Kosaka Y, Mitsumori M, Yamauchi C, Narita Y, Hiraoka M: Feasibility of accelerated partial breast irradiation using three-dimensional conformal radiation therapy for Japanese women: a theoretical plan using six patients' CT data. Breast Cancer. 2008, 15: 108-114. 10.1007/s12282-007-0013-0.PubMedGoogle Scholar
- Sawaki M, Sato S, Kikumori T, Ishihara S, Aoyama Y, Itoh Y, Nakao A, Imai T: A phase I study of intraoperative radiotherapy for early breast cancer in Japan. World J Surg. 2009, 33: 2587-2592. 10.1007/s00268-009-0227-8.PubMedGoogle Scholar
- Weed DW, Edmundson GK, Vicini FA, Chen PY, Martinez AA: Accelerated partial breast irradiation: a dosimetric comparison of three different techniques. Brachytherapy. 2005, 4: 121-129. 10.1016/j.brachy.2004.12.005.PubMedGoogle Scholar
- Wadasadawala T, Budrukkar A, Chopra S, Badwe R, Hawaldar R, Parmar V, Jalali R, Sarin R: Quality of life after accelerated partial breast irradiation in early breast cancer: matched pair analysis with protracted whole breast radiotherapy. Clin Oncol (R Coll Radiol). 2009, 21: 668-675.Google Scholar
- Dragun AE, Harper JL, Taylor CE, Jenrette JM: Patient satisfaction and quality of life after MammoSite breast brachytherapy. Am J Surg. 2008, 196: 545-548. 10.1016/j.amjsurg.2008.06.014.PubMedGoogle Scholar
- Suh WW, Hillner BE, Pierce LJ, Hayman JA: Cost-effectiveness of radiation therapy following conservative surgery for ductal carcinoma in situ of the breast. Int J Radiat Oncol Biol Phys. 2005, 61: 1054-1061.PubMedGoogle Scholar
- Suh WW, Pierce LJ, Vicini FA, Hayman JA: A cost comparison analysis of partial versus whole-breast irradiation after breast-conserving surgery for early-stage breast cancer. Int J Radiat Oncol Biol Phys. 2005, 62: 790-796.PubMedGoogle Scholar
- Sher DJ, Wittenberg E, Suh WW, Taghian AG, Punglia RS: Partial-breast irradiation versus whole-breast irradiation for early-stage breast cancer: a cost-effectiveness analysis. Int J Radiat Oncol Biol Phys. 2009, 74: 440-446.PubMed CentralPubMedGoogle Scholar
- Brown JM, Koong AC: High-dose single-fraction radiotherapy: exploiting a new biology?. Int J Radiat Oncol Biol Phys. 2008, 71: 324-325.PubMedGoogle Scholar
- Kirkpatrick JP, Brenner DJ, Orton CG: Point/Counterpoint. The linear-quadratic model is inappropriate to model high dose per fraction effects in radiosurgery. Med Phys. 2009, 36: 3381-3384. 10.1118/1.3157095.PubMedGoogle Scholar
- Reintgen C, Reintgen D, Solin LJ: Advances in local-regional treatment for patients with early-stage breast cancer: a review of the field. Clin Breast Cancer. 2010, 10: 180-187. 10.3816/CBC.2010.n.025.PubMedGoogle Scholar
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