Hypofractionated radiotherapy for lung tumors with online cone beam CT guidance and active breathing control
© Shen et al; licensee BioMed Central Ltd. 2010
Received: 10 November 2009
Accepted: 27 February 2010
Published: 27 February 2010
To study the set-up errors, PTV margin and toxicity of cone beam CT (CBCT) guided hypofractionated radiotherapy with active breathing control (ABC) for patients with non-small cell lung cancer (NSCLC) or metastatic tumors in lung.
32 tumors in 20 patients were treated. Based on the location of tumor, dose per fraction given to tumor was divided into three groups: 12 Gy, 8 Gy and 6 Gy. ABC is applied for every patient. During each treatment, patients receive CBCT scan for online set-up correction. The pre- and post-correction setup errors between fractions, the interfractional and intrafractional, set-up errors, PTV margin as well as toxicity are analyzed.
The pre-correction systematic and random errors in the left-right (LR), superior-inferior (SI), anterior-posterior (AP) directions were 3.7 mm and 5.3 mm, 3.1 mm and 2.1 mm, 3.7 mm and 2.8 mm, respectively, while the post-correction residual errors were 0.6 mm and 0.8 mm, 0.8 mm and 0.8 mm, 1.2 mm and 1.3 mm, respectively. There was an obvious intrafractional shift of tumor position. The pre-correction PTV margin was 9.5 mm in LR, 14.1 mm in SI and 8.2 mm in AP direction. After CBCT guided online correction, the PTV margin was markedly reduced in all three directions. The post-correction margins ranged 1.5 to 2.1 mm. The treatment was well tolerated by patients, of whom there were 4 (20%) grade1-2 acute pneumonitis, 3 (15%) grade1 acute esophagitis, 2 (10%) grade1 late pneumonitis and 1 (5%) grade 1 late esophagitis.
The positioning errors for lung SBRT using ABC were significant. Online correction with CBCT image guidance should be applied to reduce setup errors and PTV margin, which may reduce radiotherapy toxicity of tissues when ABC was used.
Radiotherapy is the alternative treatment for patients with medically inoperable primary non-small-cell lung cancer (NSCLC) , and also for patients with slow growing metastatic lung tumors  which when managed with high dose localized radiotherapy can prolong patients' symptom-free status.
However, even for inoperable stage I non-small cell lung cancer, the local control rates using standard fractionation schemes (30-76 Gy in 1.8 to 2.0 Gy fractions) have been reported ranging 45-89% [3–5]. Five year actuarial survival of conventional radiotherapy ranged from 6% to 27% [6–9], which was unsatisfactory compared with surgery (with a 5-year survival rate of 60% to 80%) . Dose escalation has been an important issue to improve local tumor control and overall survival [11, 12]. However, dose escalation by conventional fractionated radiotherapy has the risk of increasing normal tissue toxicity and prolonging overall treatment time which will encounter the acceleration of tumor cell proliferation.
The dose escalation within a short treatment time and sparing functional lung tissue is potentially addressed by hypofractionated radiotherapy. It has been shown that the use of hypofractionated lung radiotherapy can achieve excellent local control rates as high as 85-95%, with surprisingly minimal acute or late toxicity [13–15]. The hypofractionation radiotherapy technique employs multiple radiation beams to target a tumor with extreme precision, delivering a high dose of radiation, even in a single fraction. Tumors in the thorax regions are subject to setup errors and respiration motion, which can result in inaccurate assessment of organ shape and locations. Conventionally, these uncertainties are accounted for in treatment planning by using large margins based on motion value , which can limit dose delivered to tumor.
Special immobilization and verification devices have been developed to reduce setup uncertainties. The use of cone-beam CT (CBCT) has provided 3-dimension information of patient position which could be utilized to guide high precision radiotherapy of the lung tumor. The technique of active breathing control (ABC) has been used to reduce the breathing motion. The use of ABC has been reported to have advantages in protection of lung tissues by reducing respiration motion and lung density . However, little has been reported on the combined use of ABC and CBCT in hypofractionated RT of lung tumor.
Given the availability of onboard cone-beam CT (CBCT) imaging and ABC at our institution, we set out to determine how much using image-guided radiotherapy (IGRT) might affect lung tumor targeting accuracy, target volume margin requirements, and normal tissue doses.
Study population and Characterization
Patients with histologically or cytologically confirmed diagnosis of metastatic malignant tumors within the lung or primary NSCLC were eligible for treatment. Patients must have measurable disease and the maximum diameter of tumors is bellow 5 cm. A maximum of 3 lung tumor targets in one patient were allowable. Patients with primary NSCLC either had medically inoperable disease or refused surgery. Patients with metastatic tumors and with life expectancy ≥ 6 months were treated. Patients with a history of prior chest radiotherapy were ineligible. Pretreatment pulmonary function testing was performed, with FEV1 (minimum forced expiration volume at 1 second) ≥ 2.0 L and FEV1/FVC (vital capacity) ≥ 80%. Patients were required to have an ECOG performance status of 2 or less, and not on chemotherapy or hormonal therapy. Informed consent was obtained from all patients before the treatment was initiated.
Patient characteristics are shown in Table 1
Patient and tumor characteristics
≥ 60 yrs
Squamous cell carcinoma
Tumor size (mm)
Immobilization and CT simulation
All patients underwent a virtual radiation simulation using a stereotactic body frame (SBF) (Elekta Crawley, UK) for immobilization. A planning CT scan in 3 mm-cuts of the whole thorax was taken, with the patient in the treatment position and using the Elekta ABC device (Elekta, Crawley, UK). To set the threshold of ABC, the patient was told to take a deep breath and the maximum inspiration volume was measured. The breath-hold threshold was set at 3/4 of the maximum inspiration for each patient. Each patient had accepted the training course with ABC for 2-5 times before irradiation. Oxygen with 5-8 L flow rate was connected to the inhale pipe to help patients enhance breath holding time. Patients can release the control switch when he feels uncomfortable. It is required that the respiration motion of tumor with ABC should be < 3 mm as assessed by fluoroscopy before treatment.
Planning and treatment
Treatment planning was performed using the PrecisePLAN Release 2.1 planning system with considerations made for pulmonary density inhomogeneity. The full area integration dose calculation algorithm was used for dose calculation. Prophylactic nodal irradiation was not performed. Gross tumor volume (GTV) encompassed 1 mm only the radiologically visible tumor as seen by the planning CT with the lung window using a window level of -700 with a width of 1000. Clinical target volume (CTV) was GTV plus a 5 mm margin in all directions. For the planning target volume (PTV), 5 mm security margins in all directions were added to the CTV.
Radiation therapy fractionations protocols according to Abratt model.
Dose (Gy) infraction
Number of fractions
CBCT guidance and adjustment
CBCT was used for verification of tumor position using100 kV, S20 field of view (270 mm), 36.1 mAs, with the kilovoltage source rotating from 260° and ending at 100° for acquisition of 361 frames , which was done in one breath-hold.
Before each fraction, a first CBCT was acquired reconstructed and automatically matched to the planning CT. The positional errors of the target in left-right (LR), superior-inferior (SI) and anterior-posterior (AP) axis were calculated with the XVI software. The errors were corrected online through adjustment of treatment couch. The second CBCT was acquired after online correction. If the residual error is less than 2 mm, radiotherapy was delivered immediately. The third CBCT were acquired after radiotherapy to estimate the residual error. The interfractional errors were defined as the offset between the pre-correction CBCT and the planning CT. The intrafraction error was calculated as the difference between the pre- and post-correction position.
Analysis of positional errors
The inter- and intra-fraction errors are reported as described : for each patient the mean and standard deviation (SD) of all setup errors during treatment were calculated. The group mean error (M) is defined as the average of all individual means. Σ is defined as the variability of the means and calculated as the SD of the individual means. The random uncertainty σ was calculated as the root-mean-square of the individual SD.
PTV margin reduction and impact on normal tissue dose
As ABC was applied to restrict respiration motion (<3 mm), to simplify analysis, the internal margin (IM) due to respiration motion was not included for margin analysis, only positional uncertainty was accounted for, according to van Herk : Msetup(PTV margin) = 2.5 Σ + β√σ2+σ2p - βσp, where σp = 6.4 mm for lung, β = 0.84 for SBRT (80% isodose line) .
To evaluate the benefit of CBCT-guided online setup correction and ABC device on margin reduction for lung hypofractionated RT, the dose reductions to normal tissues with online correction were simulated in three patients with central, peripheral, and inferior lobe tumor locations, respectively.
Acute toxicity was prospectively assessed for lung, esophagus, and skin using the RTOG acute radiation morbidity scoring criteria every week during treatment. Late lung toxicity was evaluated with a modified scoring system considering only the lung symptoms (Common Toxicity Criteria version 2). Our follow up lasts 16 month. The patients got recheck for chest CT every 3 months. The tumor response was evaluated by a senior radiologist and a radiation oncologist using the RECIST criteria.
F-test was applied for error analysis using SPSS software package.
A total of 347 CBCT including 150 pre-correction, 130 post-correction and 67 post-treatment scans were acquired. The CBCT images with ABC yielded good contrast of tumor and structures.
At free breathing, the mean (±SD) of diaphragm displacement was 16.0 (±2.7) mm (range 12-24 mm). With the use of ABC, the mean (±SD) diaphragm displacement was 1.7 (±0.5) mm (range 1.0-2.5 mm). Mean value of the breath-hold time was prolonged from 30 seconds to 57 seconds by means of training course and inhaling oxygen in 20 patients. All patients tolerated ABC well for CBCT scan with a duration ≥ 40 s. To make patients more comfortable, the duration of ABC < 20 s is required during radiation delivery. All patients were tested by the respiratory function 3 months after treatment. The result indicated that none of these parameters (FEV1, FEV1/FVC) was affected by IGRT.
Interfractional errors and intrafracional errors
The systematic and random errors and PTV margins in 20 patients pre- and post-correction, and post-treatment.
(N = 150)
(N = 130)
(N = (67)
After treatment, the tumor positional errors increased compared to post-correction (Table 3). The systematic errors were 1.2 mm for both LR and AP axes, and larger (1.8 mm) in SI direction. The random error was larger in AP (2.8 mm) than in LR and SI (both1.5 mm) direction. The mean errors were all below 0.5 mm. The post-treatment residual errors were larger than the post-correction, with increments ≤ 1 mm, but still much smaller than pre-correction errors.
PTV margin reduction and impact on normal tissue dose
In this study, with ABC device, the respiration motion of tumor was small, only setup uncertainty was included for margin analysis. In Table 3, the pre-correction setup margin was largest (14.1 mm) in SI, intermediate in LR (9.5 mm) and smallest in AP (8.2 mm) directions. The margins decreased markedly after correction to within 3 mm in all directions. After treatment the margins increased to 3.2 - 4.7 mm in three directions.
Reductions in normal tissue dose volume parameters using online CBCT image guidance and ABC for SBRT of three GTV (16 cc) location
Normal tissue parameter
Dose absolute reduction value
Dose reduction %
from PTV2 to PTV3
Mean lung dose(Gy)
inferior lobe of lung
Lung V20 (%)
inferior lobe of lung
Spinal cord Maximum dose(Gy)
inferior lobe of lung
ll patients were followed up for 6 - 16 months, with a median of 10 months. There was one patient dying of brain metastasis. At 6 months post-treatment, 20 (62.5%) out of 32 targets regressed completely after treatment. 9 (28%) targets shrank more than 30% (PR). 2 (6.3%) targets had SD at 6 months post-treatment, 1 target was not assessed. An overall response rate of 90.6% (29/32) was achieved. The CR was higher in patients with BED ≥ 100 Gy (74%) vs. BED < 100 Gy (33%). The maximum dose of the critical organs was well below the tolerance dose for each organ in the whole group. The maximum value of V20 for the whole group was 21%. The maximum point dose of spinal cord, esophagus and mean lung were 15.7 Gy, 32 Gy and 3.0 Gy respectively. Treatment was well tolerated. Majority of patients did not have treatment related symptoms during and after treatment. 3 (15%) patients had grade 1, 1 (5%) patient had grade 2 acute radiation pulmonary toxicity. 3 (15%) had grade 1 acute esophagitis. All these symptoms alleviated after treatment completion without special treatment. There was no pulmonary or esophageal toxicity of grade 3 or above, no acute skin toxicity and no hemotoxicity during treatment. For late effects, only 2 (10%) patients had grade 1 pulmonary toxicity (imaging change but no symptom), 1 patient (5%) had grade 1 dysphasia. No other late toxicities were observed.
In this preliminary study, we evaluated the feasibility of CBCT guided radiotherapy in combination with ABC to restrict tumor positional error. The role of CBCT guidance in improving treatment accuracy and reduction of target margin requirements for stereotactic lung radiotherapy using ABC procedure was studied.
At initial setup, the tumor positional error was significant even with SBF plus ABC. Our results were similar to literature report that utilized SBF immobilization and portal imaging device to evaluate errors  which reported the positioning errors for SBF were 2.3-4.2 mm. Negoro  also reported the positioning accuracy ranged 0-8.5 mm, with the mean of 3.2 mm. Our results demonstrated that the initial errors with SBF plus ABC immobilization were greater than those reported recently which also utilized CBCT online guidance and 4D-CT to detect errors in lung tumor immobilized with SBF alone. In their study, the systematic error ranged 2.5 to 3.4 mm and random errors ranged 1.7 to 2.7 mm . This may be partly due to the poor long-term reproducibility of tumor position when repeat CT scans were performed during ABC . It should be mentioned that the value of using the SBF for improving setup accuracy in SBRT is controversial. In a recent study reported by Sonke et al , 65 patients with small peripheral lung tumors treated with SBRT without a SBF. In their study the positioning accuracy was evaluated using 4DCT and CBCT imaging, and their results were similar to ours. Although online correction markedly reduced the positional error, the tumor position varied during treatment and might affect the dose distribution in stereotactic radiotherapy. The post-treatment residual systematic errors increased, with the greatest increment of 1 mm in SI direction, and 0.4 mm for both LR and AP direction. The increment of intrafractional random error was 1.5 mm in AP, 0.3 mm in SI and 0.8 mm in LR direction. Only few studies have reported on intrafractional tumor position variation, especially in patients applying ABC. Uematsu et al.  used CT scan to measure the intrafraction lung tumor position error and observed that the intrafraction positional variation was small. Guckenberger et al.  has utilized CBCT to determine intrafractional error and postulated that 90% of the intrafractional position errors were within 4.8 mm. A recent literature  reported that the mean (SD) intrafractional errors of -0.1 mm (1.1 mm), 0.2 mm (1.4 mm) and -0.1 mm (1.5 mm) in LR, SI and AP axes respectively, for thoracic tumors at free breathing, which were smaller than this cohort of patients. This implies that using of ABC might increase the intrafractional patient motion. This might be due to the using of ABC which introduces more procedures and variations .
Based on our study, the use of ABC has reduced respiration motion. With ABC, the average diaphragm displacement was significantly reduced from 16.0 mm to 1.7 mm. Hanley et al.  has reported that the diaphragm motion was reduced from 26.4 mm to 2.5 mm (0.5-4.9 mm) with ABC procedure. Sarrut  reported the lung tumor motion of 0.9-5.9 mm with the use of ABC. Our study also showed high reproducibility of 2 ABC procedures, with a diaphragm movement error of 3 mm. However, there is limitation of using diaphragm position as a surrogate for tumor. This is because that the diaphragm is susceptible to imaging artifacts due to large and rapid motion, and the diaphragm motion may also be influenced by nonrespiratory activity .
As ABC was applied to all patients in this study, the tumor respiration motion was small (< 3 mm), the internal target volume (ITV) was considered roughly equal to CTV. Compared to the reliability of tumor motion (average displacement being 1.4 ± 1.0 mm) measured by 4D CT , the reliability of tumor motion measured by fluoroscopy is similar. For simplification, the PTV margin calculation only considered setup errors, other error sources such as delineation uncertainty and breathing pattern variation were not accounted for in this study. The pre-correction PTV margin was 9.5 mm in LR, 14.1 mm in SI and 8.2 mm in AP direction. However, it was recommended a uniform PTV margin of 5 mm axial and 10 mm superior-inferior be added for stereotactic lung radiotherapy when image guidance is not used . Our results showed that the margins in three axes all exceeded the recommended margins for a magnitude about 5 mm if CBCT guidance not applied, indicating the necessity of image guidance for accuracy of lung SBRT with ABC. After CBCT guided online correction, the PTV margin was markedly reduced in all three directions. The post-correction margins ranged 1.5 to 2.1 mm which were similar to the literature which utilized CBCT online correction for lung patients . The PTV margins at the completion of treatment were increased as compared to the post-correction margins. The post-treatment margins were 3.2-4.7 mm in three directions. It was suggested by some investigators that at least 5 mm margin should be added for individualized PTV if image guidance and SBF is used . When intra-and interfractional errors were both accounted for, the PTV margin reduction with online correction ranged about 5 to 10 mm in different axes. In our study the online correction resulted in reduction of lung dose volume endpoints of 47-77.3%, and 55.2-58.5% in spinal cord doses for patients using ABC at different tumor locations. It could be inferred from our study that CBCT and online correction can significantly reduce normal tissue doses. As in our study the tumor respiration motion was not evaluated, the benefit of ABC on ITV reduction could not be discussed. It has been indicated that most lung tumors do not exhibit significant motion  and there remains inter- breath hold variability in peripheral lung tumor position with the use of ABC inspiration breath hold, which prevents significant PTV margin reduction. However, lung volumes can significantly increase, thereby decreasing the mass of lung within a standard PTV . In addition, ABC may result in a mean relative reduction in lung DVH parameters determining risk of pneumonitis by up to 25% with the potential for safe dose escalation as reported in other study . 4DCT scan has become more popular for SBRT, it has been reported that using mid-ventilation CT scans for treatment planning instead of the conventional free-breathing CT scans, margin reduction is possible, which can reduce the treatment volume up to 50% .
Our study found that hypofractionated radiotherapy with BED ranged 72 to 100 Gy could achieve high CR (62.5%), The hypofractionated radiotherapy has radiobiological advantages of counteracting tumor accelerated proliferation. Quite a few researches have been published which showed high local tumor control and surprisingly low toxicities with BED of 100 Gy [35–39]. The response rate in our study seems higher than that reported for NSCLC SBRT, which were assumed to be partly due to the heterogeneity of histopathology in this cohort, since half the cases were metastatic tumors from head and neck, esophagus or breast which were radioresponsive. The small tumor size and small number of cases included in this cohort might be the other contributing factors.
The patients tolerated the treatment well. Only grade 1-2 acute toxicity occurred in 35% of the patients and 15% had grade I late toxicity. Though immobilization device combined with ABC could effectively reduce respiration motion of target, the total margin was not reduced. With the use of online CBCT guided setup correction, PTV margin was substantially reduced, which explained the low toxicity in this patient cohort. Similar results were reported by Fukumoto et al  who treated 22 stage I patients with image guided hypofractionated radiotherapy (48-60 Gy in 8 fractions) and found nearly no impairment of pulmonary functions.
In conclusion, for lung cancer hypofractionated radiotherapy using ABC, CBCT guided online correction effectively reduced setup errors and PTV margins. CBCT guidance markedly improved the precision of lung SBRT which might offer a potential dose escalation and effective reduction of normal tissue toxicity.
Declaration of interests
The authors declare that they have no competing interests.
- Dosoretz DE, Katin MJ, Blitzer PH: Radiation therapy in the management of medically inoperable carcinoma of the lung: Results and implications for future treatment strategies. Int J Radiat Oncol Biol Phys 1992, 24: 3-9.View ArticlePubMedGoogle Scholar
- Kamiyoshihara M, Hirai T, Kawashima O, Morishita Y: Resection of pulmonary metastases in six patients with disease-free interval greater than 10 years. Ann Thorac Surg 1998, 66: 231-33. 10.1016/S0003-4975(98)00347-6View ArticlePubMedGoogle Scholar
- Jeremic B, Classen J, Bamberg M: Radiotherapy alone in technically operable, medically inoperable, early-stage (I/II) non-small cell lung cancer. Int J Radiat Oncol Biol Phys 2002, 54: 119-30.View ArticlePubMedGoogle Scholar
- Sibley G: Radiotherapy for patients with medically inoperable stage I non small cell lung carcinoma: Smaller doses and higher doses--A review. Cancer 1998, 82: 433-38. 10.1002/(SICI)1097-0142(19980201)82:3<433::AID-CNCR2>3.0.CO;2-QView ArticlePubMedGoogle Scholar
- Sibley G, Jamieson T, Marks LB, Anscher MS, Prosnitz LR: Radiotherapy alone for medically inoperable stage I non-small-cell lung cancer: The Duke experience. Int J Radiat Oncol Biol Phys 1998, 40: 149-54. 10.1016/S0360-3016(97)00589-0View ArticlePubMedGoogle Scholar
- Mori Y, Kondziolka D, Flickinger JC, Kirkwood JM, Agarwala S, Lunsford LD: Stereotactic radiosurgery for cerebral metastatic melanoma: factors affecting local disease control and survival. Int J Radiat Oncol Biol Phys 1998, 42: 581-89.View ArticlePubMedGoogle Scholar
- Morita K, Fuwa N, Suzuki Y, Nishio M, Sakai K, Tamaki Y, et al.: Radical radiotherapy for medically inoperable non-small cell lung cancer in clinical stage I: A retrospective analysis of 149 patients. Radiother Oncol 1997, 42: 31-6. 10.1016/S0167-8140(96)01828-2View ArticlePubMedGoogle Scholar
- Cheung PC, Mackillop WJ, Dixon P, Brundage MD, Youssef YM, Zhou S: Involved-field radiotherapy alone for early-stage non-small-cell lung cancer. Int J Radiat Oncol Biol Phys 2000, 48: 703-11.View ArticlePubMedGoogle Scholar
- Gauden S, Ramsay J, Tripcony L: The curative treatment by radiotherapy alone of stage I non-small cell carcinoma of the lung. Chest 1995, 108: 1278-82. 10.1378/chest.108.5.1278View ArticlePubMedGoogle Scholar
- Slotman BJ, Njo KH, Karim AB: Curative radiotherapy for technically operable stage I nonsmall cell lung cancer. Int J Radiat Oncol Biol Phys 1994, 29: 33-7.View ArticlePubMedGoogle Scholar
- Willner J, Baier K, Caragiani E, Tschammler A, Flentje M: Dose, volume, and tumor control prediction in primary radiotherapy of non-small-cell lung cancer. Int J Radiat Oncol Biol Phys 2002, 52: 382-89.View ArticlePubMedGoogle Scholar
- Belderbos J, De Jaeger K, Heemsbergen W, Seppenwoolde Y, Baas P, Boersma LJ, et al.: First results of a phase I/II dose escalation trial in non-small cell lung cancer using three-dimensional conformal radiotherapy. Radiother Oncol 2003, 66: 119-26. 10.1016/S0167-8140(02)00377-8View ArticlePubMedGoogle Scholar
- Uematsu M, Shioda A, Taira J, Wong J, Hama Y, Kusano S: Computed tomography (CT)-guided stereotactic radiation therapy (SRT) for Stage I non-small cell lung cancer (NSCLC): 8-year results of 50 initial patients. Int J Radiat Oncol Biol Phys 2003, 57: S281.View ArticleGoogle Scholar
- Onishi H, Araki T, Shirato H, Nagata Y, Hiraoka M, Gomi K, et al.: Stereotactic hypofractionated high-dose irradiation for Stage I nonsmall cell lung carcinoma: Clinical outcomes in 245 subjects in a Japanese multiinstitutional study. Cancer 2004, 101: 1623-31. 10.1002/cncr.20539View ArticlePubMedGoogle Scholar
- Zimmermann FB, Geinitz H, Schill S, Grosu A, Schratzenstaller U, Molls M, et al.: Stereotactic hypofractionated radiation therapy for Stage I non-small cell lung cancer. Lung Cancer 2005, 48: 107-14. 10.1016/j.lungcan.2004.10.015View ArticlePubMedGoogle Scholar
- Grills IS, Hugo G, Kestin LL, Galerani AP, Chao KK, Wloch J, et al.: Image-guided radiotherapy via daily online cone-beam CT substantially reduces margin requirements for stereotactic lung radiotherapy. Int J Radiat Oncol Biol Phys 2008,70(4):1045-56.View ArticlePubMedGoogle Scholar
- Wong JW, Sharpe MB, Jaffray DA, Kini VR, Robertson JM, Stromberg JS, et al.: The use of active breathing control (ABC) to reduce margin for breathing motion. Int J Radiat Oncol Biol Phys 1999,44(4):911-9.View ArticlePubMedGoogle Scholar
- Xu F, Wang J, Bai S, Li Y, Shen Y, Zhong R, et al.: Detection of intrafractional tumor position error in radiotherapy utilizing cone beam computed tomography. Radiother Oncol 2008, 89: 311-9. 10.1016/j.radonc.2008.08.003View ArticlePubMedGoogle Scholar
- Van Herk M: Errors and margins in radiotherapy. Semin Radiat Oncol 2004,14(1):52-64. 10.1053/j.semradonc.2003.10.003View ArticlePubMedGoogle Scholar
- Sonke JJ, RossiI M, Wolthaus J, et al.: Frameless stereotactic body radiotherapy for lung cancer using four-dimensional cone beam CT guidance. Int J Radiat Oncol Biol Phys 2009, 74: 567-574.View ArticlePubMedGoogle Scholar
- Wulf J, Ulrich H, Ulrich O: Hypofractionated, high-doseradiation under stereotactic conditions in the stereotactic body frame: Accuracy of re-positioning at 11 CT-simulations and 37 applications at the LINAC. Int J Radiat Oncol Biol Phys 1998,42(Suppl 1):215.View ArticleGoogle Scholar
- Negoro Y, Nagata Y, Aoki T, Mizowaki T, Araki N, Takayama K, et al.: The effectiveness of an immobilization device in conformal radiotherapy for lung tumor: Reduction of respiratory tumor movement and evaluation of daily set-up accuracy. Int J Radiat Oncol Biol Phys 2001, 50: 889-98. 10.1016/S0360-3016(01)01516-4View ArticlePubMedGoogle Scholar
- Koshani R, Balter J, Hayman J, Henning G, van Herk M: Short-term and long term reproducibility of lung tumor position using active breathing control (ABC). Int J Radiation Oncology Biol Phys 2006,65(5):1553-1559.View ArticleGoogle Scholar
- Uematsu M, Shioda A, Suda A, Tahara K, Kojima T, Hama Y, et al.: Intrafractional tumor position stability during computed tomography (CT)-guided frameless stereotactic radiation therapy for lung or liver cancers with a fusion of CT and linear accelerator (FOCAL) unit. Int J Radiat Oncol Biol Phys 2000, 48: 443-8.View ArticlePubMedGoogle Scholar
- Guckenberger M, Meyer J, Wilbert J, Richter A, Baier K, Mueller G, et al.: Intra-fractional uncertainties in cone-beam CT based image-guided radiotherapy (IGRT) of pulmonary tumors. Radiotherapy and Oncology 2007, 83: 57-64. 10.1016/j.radonc.2007.01.012View ArticlePubMedGoogle Scholar
- Hanley J, Debois MM, Mah D, Mageras G, Raben A, Rosenzweig K, et al.: Deep inspiration breath-hold technique for lung tumors: the potential value of target immobilization and reduced lung density in dose escalation. [J] Int J Radiat Oncol Biol Phys 1999,45(3):603-11. 10.1016/S0360-3016(99)00154-6View ArticlePubMedGoogle Scholar
- Sarrut D, Blodea V, Ayadi M, Badel JN, Ginestet C, Clippe S, et al.: Nonrigid registration method to assess reproducibility of breath-holding with ABC in lung cancer. [J] Int J Radiat Oncol Biol Phys 2005,61(2):594-607. 10.1016/j.ijrobp.2004.08.007View ArticlePubMedGoogle Scholar
- Spoelstra F, De Koste JR, Vincent A, Cuijpers JP, Slotman BJ, Senan S: An evaluation of two internal surrogates for determining the three-dimensional position of peripheral lung tumors. Int. J. Radiation Oncology Biol. Phys 2009,74(2):623-629.View ArticleGoogle Scholar
- van der Geld Y, Lagerwaard F, van Sörnsen de Koste JR, Cuijpers JP, Slotman BJ, Senan S: Reproducibility of target volumes generated using uncoached 4-dimensional CT scans for peripheral lung cancer. Radiation Oncology 2006, 1: 43. doi: 10.1186/1748-717X-1-43 10.1186/1748-717X-1-43PubMed CentralView ArticlePubMedGoogle Scholar
- Wilson EM, Williams FJ, Lyn EB, Wong JW, Aird EG: Validation of active breathing control in patients with non-small cell lung cancer to be treated with CHARTWEL. Int J Radiat Oncol Biol Phys 2003,57(3):864-84.View ArticlePubMedGoogle Scholar
- Liu HH, Balter P, Tutt T, Choi B, Zhang J, Wang C, et al.: Assessing respiration-induced tumor motion and internal target volume using four-dimensional computed tomography for radiotherapy of lung cancer. Int J Radiation Oncology Biol Phy 2007,68(2):531-540. 10.1016/j.ijrobp.2006.12.066View ArticleGoogle Scholar
- Cheung PC, Sixel KE, Tirona R, Ung YC: Reproducibility of lung tumor position and reduction of lung mass within the planning target volume using active breathing control (ABC). Int J Radiat Oncol Biol Phys 2003, 57: 1437-1442.View ArticlePubMedGoogle Scholar
- Panakis N, McNair HA, Christian JA, Ruheena M, Symonds TJ, Knowles C, et al.: Defining the margins in the radical radiotherapy of non-small cell lung cancer (NSCLC) with active breathing control (ABC) and the effect on physical lung parameters. Radiotherapy and Oncology 2008, 87: 65-73. 10.1016/j.radonc.2007.12.012View ArticlePubMedGoogle Scholar
- Wolthaus JW, Schneider C, Sonke J-J, Van Herk M, Belderbos JS, Rossi M, et al.: Mid-ventilation CT scan construction from four-dimensional respiration-correlated CT scans for radiotherapy planning of lung cancer patients. Int J Radiat Oncol Biol Phys 2006, 65: 1560-1571.View ArticlePubMedGoogle Scholar
- Uematsu M, Shioda A, Tahara K, Fukui T, Yamamoto F, Tsumatori G, et al.: Focal, high dose, and fractionated modified stereotactic radiation therapy for lung carcinoma patients. Cancer 1998, 82: 1062-70. 10.1002/(SICI)1097-0142(19980315)82:6<1062::AID-CNCR8>3.0.CO;2-GView ArticlePubMedGoogle Scholar
- Arimoto T, Usubuchi H, Matsuzawa T, et al.: Small volume multiple non-coplanar arc radiotherapy for tumors of the lung, head and neck and the abdominopelvic region. In CAR'98 computer assisted radiology and surgery. Edited by: Lemke HU. Tokyo; Elsevier; 1998:257-61.Google Scholar
- Nagata Y, Takayama K, Matsuo Y, Norihisa Y, Mizowaki T, Sakamoto T, et al.: Clinical outcome of a phase I/II study of 48 Gy of stereotactic body radiotherapy in 4 fractions for primary lung cancer using a stereotactic body frame. Int J Radiat Oncol Biol Phys 2005, 63: 1427-31. 10.1016/j.ijrobp.2005.05.034View ArticlePubMedGoogle Scholar
- Herfarth KK, Debus J, Lohr F: Stereotactic single dose radiation treatment of tumors in the lung. Radiology 2000,217(Suppl):148.Google Scholar
- Timmerman R, Papiez L, McGarry R, Likes L, DesRosiers C, Frost S, et al.: Extracranial stereotactic radioablation: results of a phase I study in medically inoperable stage I non-small cell lung cancer. Chest 2003,124(5):1946-55. 10.1378/chest.124.5.1946View ArticlePubMedGoogle Scholar
- Fukumoto S, Shirato H, Shimzu S, Ogura S, Onimaru R, Kitamura K, et al.: Small-Volume Image-Guided Radiotherapy Using Hypofractionated, Coplanar, and Noncoplanar Multiple Fields for Patients with Inoperable Stage I Nonsmall Cell Lung Carcinomas. Cancer 2000, 95: 1546-53. 10.1002/cncr.10853View ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.