- Open Access
A Japanese prospective multi-institutional feasibility study on accelerated partial breast irradiation using interstitial brachytherapy: treatment planning and quality assurance
- Yuki Otani1Email author,
- Takayuki Nose2,
- Takushi Dokiya3,
- Toshiaki Saeki4,
- Yu Kumazaki5,
- Shuuji Asahi6,
- Iwao Tsukiyama7,
- Ichirou Fukuda8,
- Hiroshi Sekine9,
- Naoto Shikama5,
- Takao Takahashi4,
- Ken Yoshida10,
- Tadayuki Kotsuma11,
- Norikazu Masuda12,
- Eisaku Yoden13,
- Kazutaka Nakashima14,
- Taisei Matsumura15,
- Shino Nakagawa16,
- Seiji Tachiiri17,
- Yoshio Moriguchi18,
- Jun Itami19 and
- Masahiko Oguchi20
© Otani et al. 2015
- Received: 19 December 2014
- Accepted: 27 May 2015
- Published: 4 June 2015
In Japan, breast-conserving surgery with closed cavity has generally been performed for breast cancer patients, and accelerated partial breast irradiation (APBI) is considered difficult because Asian females generally have smaller breast sizes than Western females. Therefore, common identification of target and treatment plan method in APBI is required. A prospective multicenter study was conducted in Japan to determine institutional compliance with APBI using high-dose-rate interstitial brachytherapy (ISBT) designed for Japanese female patients.
For this study, 46 patients were recruited at eight institutions from January 2009 to December 2011. The reproducibility of the ISBT–APBI plan was evaluated using three criteria: (1) minimum clinical target volume dose with a clip dose ≥ 6 Gy/fraction, (2) irradiated volume constraint of 40-150 cm3, and (3) uniformity of dose distribution, expressed as the dose non-uniformity ratio (DNR, V150/V100) < 0.35. The ISBT–APBI plan for each patient was considered reproducible when all three criteria were met. When the number of non-reproducible patients was ≤ 4 at study completion, APBI at this institution was considered statistically reproducible.
Half of the patients (52 %) had a small bra size (A/B cup). The mean values of the dose-constrained parameters were as follows: Vref, 117 cm3 (range, 40-282), DNR, 0.30 (range, 0.22-0.51), and clip dose, 784 cGy (range, 469-3146). A total of 43/46 treatment plans were judged to be compliant and ISBT–APBI was concluded to be reproducible.
This study showed that multi-institutional ISBT–APBI treatment plan was reproducible for small breast patient with closed cavity.
In Japan, the incidence and mortality rate of breast cancer is growing rapidly, and the annual number of cases is expected to rise above 50,000 by 2020 . Furthermore, the peak age for breast cancer in Japan is 10 years younger than that in Europe and USA, and the disease rate in 45–50-year-old females is high .
Breast-conserving surgery followed by postoperative radiotherapy is the standard of care for early-stage breast carcinoma [3, 4]. Generally, postoperative irradiation by whole-breast irradiation (WBI) reduces the rate of ipsilateral breast recurrence by one-third [4, 5]. However, studies have also reported that WBI prevents recurrence only near the tumor bed [3, 4, 6]. Moreover, WBI raises the mortality rate by increasing the risk of cardiovascular adverse events . Thus, localized irradiation of the tumor bed is preferable for patients at a low risk of recurrence.
Accelerated partial breast irradiation brachytherapy (APBI) delivers radiation near the tumor bed over a short period of time [7–11]. In Europe and the USA, successful phase I/II clinical trials were completed in the 1990s, and large-scale phase III clinical trials are currently underway [8, 10]. In contrast, APBI is rarely used in Japan. One reason for this is the difficulty in target identification, caused by oncoplastic surgery, which is generally adopted in Japan. Moreover, APBI is considered difficult because Asian females generally have smaller breast sizes than Western females.
To promote APBI using interstitial brachytherapy, developing target identification consensus and reproducibility of this treatment among institutions should be first confirmed prospectively. This study presents the creative method of clinical target volume (CTV) and dose limitation for Asian females. Then, the reproducibility of interstitial brachytherapy (ISBT)-APBI is evaluated in breast cancer patients on multi-institutional feasibility clinical trial in Japan.
A multi-institutional clinical trial was conducted from October 2009 to December 2011 at eight institutions in Japan. In total, 46 female patients with breast cancer were recruited prospectively for this study to receive adjuvant radiotherapy by ISBT–APBI alone after breast-conserving surgery.
The Institutional Review Board (IRB) of each institution approved this study. Written informed consent for data acquisition was obtained from each patient.
All patients underwent breast-conserving surgery, defined as resection of the primary tumor with > 0 cm of microscopic free margin. During surgery, the walls of the excision cavity were marked with at least four clips on the superior, inferior, medial, and lateral margins of the tumor bed. The brachytherapy applicators were inserted within 2 months after the breast-conserving surgery. All needles were inserted under image guidance by computed tomography (CT) or ultrasonography (US). More two-plane implants were made. The needles were replaced with flexible catheters and fixed with buttons. If applicator placement was judged insufficient during treatment planning, additional insertions were made.
After applicator implantation, CT data were acquired with the patient in a supine position. CT slice thickness was < 3.0 mm. CT-based treatment planning was performed with the aid of Oncentra or PLATO (Nucletron BV, Veenendaal, The Netherlands). The high-dose-rate (HDR)-ISBT protocol was performed with microSelectron-HDR V2 using 192Ir as the source for monotherapy.
Clip dose: The surgical clips in CTV were irradiated by >100 % of the isodose lines. A clip outside a mammary gland was excluded as an object. No exception was permitted.
Reference volume (Vref): The irradiated volume receiving >100 % of the prescription dose was 40-150 cm3. An exception was made for specific conditions (e.g., larger breast) under the approval of the study office and data center.
Dose non-uniformity ratio (DNR): The ratio was defined as the irradiated volume that received ≥ 1.5 times the reference dose over the volume that received ≥ 1.0 times the reference dose (DNR = V1.5ref/Vref). For all patients, DNR must be < 0.35, with no exception.
Compliance with the treatment plan was acknowledged when all three criteria were within the reference range.
To improve the quality of this study, workshops, rapid review, and Interim analysis were established. Quality assurance was implemented according to Radiation Therapy Oncology Group (RTOG) procedures . Moreover, the data center predicted the total irradiation time from the Vref and source activity.
Three workshops were conducted to homogenize treatments between institutions. A radiation oncologist, a breast surgeon, a medical physicist, and a radiation technologist from each institution participated in all three workshops. The participants discussed the process of applicator insertion and the treatment plan. Moreover, each institution was instructed to submit their calculation of the benchmark treatment plan using uniform sample patient data, and the submitted data were verified at the data center.
Each institution was required to fax a case report form (CRF) to the data center at least 24 h before the onset of treatment. The treatment plan summary contained no patient identifier. If there was any doubt, the data center queried the relevant institution and consulted with the study office. The data center and study office verified the following parameters: applicator length, offset value, clip dose, Vref, DNR, maximum skin dose, total treatment time, and source strength.
Interim and final analyses
The number of patients required for the statistical analysis was determined on the basis of the optimal design of Simon . Interim analysis was performed with data from 19 patients, and this clinical trial was planned to be stopped when non-compliance with the plan was confirmed for >3 patients. Final analysis was performed with data from 46 patients. The ISBT–APBI plan was defined as reproducible if non-compliance with the plan was confirmed for < 5 patients. The electronic data on the treatment plan from each institution was imported to Oncentra at the data center anonymously. The data center and study office reviewed all treatment plans.
Patient demographics and treatment plan index
Mean ± SD (Range)
60 ± 11 (43 – 96)
155 ± 6 (140 – 170)
Body Mass Index
25.0 ± 4.8 (18.4 – 41.6)
Number of catheters (n)
15 ± 3 (8 – 21)
Breast excision weight (g)
82 ± 44 (25 – 234)
Volume of CTV (cm3)
67 ± 29 (26 – 133)
≥ D cup
Index parameters of the treatment plan
Mean ± SD (Range)
117 ± 56 (40 – 282)
0.30 ± 0.05 (0.22 – 0.51)
Clip dose (cGy)
784 ± 224 (469 – 3146)
Max skin dose (cGy)
521 ± 73 (223 – 607)
CTV V1.5ref (cm3)
39 ± 18 (12 – 98)
CTV V2.0ref (cm3)
15 ± 9 (5 – 58)
CTV V100 (cm3)
63 ± 27 (25 –129)
CTV V90 (cm3)
63 ± 28 (26 – 131)
CTV D100 (cGy)
565 ± 125 (146 – 624)
CTV D90 (cGy)
680 ± 97 (225 – 731)
CTV Mean dose (cGy)
927 ± 80 (760 – 1092)
2.07 ± 0.84 (1.07 – 4.45)
Validation of the reference volume
The data center and study office evaluated the adequacy of the Vref values that were outside the 40-150 cm3 range. In total, 14 patients had a Vref above the upper limit, with a median of 191 cm3 (range, 169-287). The patients with a Vref of > 150 cm3 had a median body mass index (BMI) of 28.3 (range, 25.5-41.6) and a median excision weight of 110 g (range, 60-234). In contrast, those with a Vref of ≤ 150 cm3 had a median BMI of 22.5 (range, 18.4-30.8) and a median excision weight of 61 g (range, 25-100). All exceeding Vref values were determined to be appropriate.
Interim and final analyses
The interim analysis identified two non-compliant treatment plans. The analysis report was submitted to the safety monitoring committee, and clinical trial continuation was approved. In the final analysis, one more treatment plan was judged non-compliant with the protocol.
In case #1, the DNR value was 0.51, which was not within the acceptable limit (<0.35). This discrepancy was due to the large size of the patient’s breast (I cup). The target was larger than expected because the cavity was filled with fluid, which required several applicators. However, the patient refused the insertion of additional applicators. In case #2, the CTV creative method was not in accordance with the protocol. Not all 3-cm spheres created around the clips were connected. However, the dose distribution was connected, which was judged to be clinically satisfactory. In case #3, the one clip dose was 469 cGy, less than the reference value and wrong clip dose value was written in CRF. Thus, a total of 43/46 treatment plans were judged to be compliant and ISBT–APBI was concluded to be reproducible.
This study was designed to evaluate the reproducibility of ISBT–APBI for breast cancer patients among Japanese institutions. To our knowledge, this is the first reported ISBT–APBI multi-institutional clinical trial in Asia. In this study, ISBT–APBI was compliant for 43/46 patients. Although ISBT involves multiple manual procedures, standardization of the treatment plan is possible through comprehensive webinars. Two cases (case #2 and #3) deviated from the protocol due to a human error detected in CRF. Thus, careful review of the electronic data on the treatment plan is essential to secure the quality of a multicenter clinical trial.
Most patients with excessive Vref had a pyknic body type and required large-weight excisions. Moreover, six (13 %) patients had a BMI of > 30, corresponding to a 3.2 % deviation (Organization for Economic Co-operation and Development Health data 2009 ) from the general Japanese female population. There is a possibility that the APBI plan deliberately selected large-breast patients, because most Japanese females have small breasts and insertion of the applicator is difficult. This ISBT–APBI plan provided a better coverage of the target area, because a median 98 % of CTV received 100 % of the prescription dose, compared to 96 % of the single-institutional study by Das et al. .
The quality assurance methods of HDR treatment planning have been reported [24–26]. One of a quick, easy way of checking is a method to infer the total irradiation time from the source activity and the Vref. According to our results, there is low correlation among the Vref, the source activity and the total treatment time in the small bra-size treatment plan compared with that in the large bra-size treatment plan (Fig. 3). For small bra size patients, applicator insertion is difficult and the applicator spacing tends to be irregular and narrow. Moreover, each point source stop time in the small bra-size patient treatment plan is short compared with that in the large bra-size patient. The Vref increases exponentially with increasing source stop time because the dose distribution expands concentrically. Therefore, the method of inferring total irradiation time from the source activity and Vref is difficult to adjust to patients with small breasts.
This prospective study defined an ISBT–APBI treatment plan to be clinically feasible for most Asian females with a closed cavity and small breast size. Furthermore, the treatment plan was reproducible between institutions, despite various levels of skills and experience with the technique.
This study was supported in part by a Grant-in-Aid for Cancer Research from the Ministry of Health, Labour and Welfare of the Government of Japan (17–10 and 21-8-2) and MEXT KAKENHI Grant Number 26860401.
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