| Home | E-Submission | Sitemap | Contact Us |  
Radiation Oncology Journal > Volume 40(2); 2022 > Article
Yadav, Gupta, Dahiya, Gupta, and Oinam: Accelerated hypofractionated breast radiotherapy with simultaneous integrated boost: a feasibility study



To assess the feasibility of accelerated hypofractionated radiotherapy with simultaneous integrated boost (SIB) in patients with breast cancer.

Materials and Methods

A total of 27 patients after breast-conserving surgery were included in this study. Patients were planned on a four-dimensional computerized tomogram, and contouring was done using RTOG guidelines. The dose was 34 Gy/10#/2 week to the breast and 40 Gy/10#/2 week to the tumor bed as SIB with volumetric modulated arc technique. The primary endpoint was grade 2 acute skin toxicity. Doses to the organs-at-risk were calculated. Toxicities and cosmesis were assessed using RTOG/LENT/SOMA and HARVARD/NSABP/RTOG grading scales, respectively. Disease-free survival (DFS) and overall survival (OS) were calculated with Kaplan-Meier curves.


The mean age of the patients was 42 years. Left and right breast cancers were seen in 17 (63%) and 10 (37%) patients, respectively. The mean values of ipsilateral lung V16 and contralateral lung V5 were 16.01% and 3.74%, respectively. The mean heart doses from the left and right breast were 7.25 Gy and 4.37 Gy, respectively. The mean doses to the contralateral breast, oesophagus, and Dmax to brachial plexus were 2.64 Gy, 3.69 Gy, and 26.95 Gy, respectively. The mean value of thyroid V25 was 19.69%. Grade 1 and 2 acute skin toxicities were observed in 9 (33%) and 5 (18.5%) patients, respectively. Grade 2 hyperpigmentation, edema, and induration were observed in 1 (3.7%), 2 (7.4%), and 4 (14.8%) patients, respectively. Mild breast pain and arm/shoulder discomfort were reported by 1 (3.4%) patient. The median follow-up was 51 months (range, 12 to 61 months). At four years, breast induration, edema, and fibrosis were observed in 1 (3.7%) patient. Cosmesis was excellent and good in 21 (78%) and 6 (22%) patients, respectively. Local recurrence and distant metastases occurred in 1 (3.7%) and 2 (7.4%) patients, respectively. DFS and OS at four years were 88% and 92%, respectively.


With this radiotherapy schedule, acute and late toxicity rates were acceptable with no adverse cosmesis. Local control, DFS, and OS were good.


Breast cancer is the most common cancer among women globally as well as in our country [1]. Radiotherapy (RT) plays an important role in breast cancer management after breast-conserving surgery (BCS) or mastectomy. In patients with BCS, whole breast irradiation (WBI) can be delivered with many techniques. These techniques include two-dimensional (2D), 3-dimensional conformal RT (3D-CRT) with or without deep inspiration breath hold, field-in-field intensity-modulated radiotherapy (FF IMRT), inverse planning IMRT, tomotherapy, image-guided radiotherapy (IGRT) and proton therapy. RT contributes by sterilizing the microscopic disease. Boost to the primary tumor site further reduces the risk of local recurrence within 2 cm of its location [2,3]. Young patients with ductal carcinoma in situ (DCIS) histology have been reported to benefit from a boost to the primary site [4,5]. There are many techniques and modalities (photons, electrons, and brachytherapy) by which boost can be delivered. The optimal modality, timing, dose fractionation and technique of tumor bed boost have not yet been established, especially with hypofractionated RT. However, for a patient who may benefit from boost, simultaneous integrated boost (SIB) can be one of the methods for its delivery. It achieves dose conformity, homogeneity; lower toxicity rate and completes the treatment fast in one plan only leading to better patient compliance [6-8]. If boost is planned with volumetric-modulated arc therapy (VMAT), the treatment delivery is fast, and planning on four-dimensional computed tomography (4D-CT) can improve its localization and onboard imaging can increase the accuracy of dose delivery [7]. Tumor bed boost has been shown to be associated with increased acute and late toxicity [5,9]. However, it depends on the total dose, dose per fraction, volume of the boost, modality and the technique used for boost delivery. In majority of the studies SIB was delivered in 3–5 weeks and has been shown to be well tolerated [4-11]. SIB with accelerated hypofractionation can further reduce treatment duration from 3 weeks to 2 weeks.
We have published our data with a radiation schedule of 34 Gy in 10 fractions over 2 weeks with 2D technique with acceptable toxicity and local control [12,13]. Breast boost in this study was sequential, 10 Gy/5#/1 week with photons or electrons. We further wanted to reduce this treatment duration to 2 weeks only. So, we planned the current feasibility study. Equivalent doses (EQD2) of this schedule will be 43.52 Gy3 for the WBI and 56 Gy3 for the tumor bed, which is quite similar to the START B trial and our past experience [14]. Here, we report dosimetry, acute and late toxicities and the cosmetic outcomes in patients with breast cancer post-BCS who were treated with accelerated hypofractionated WBI and SIB with VMAT technique over 2 weeks (10 fractions).

Materials and Methods

This prospective phase II study was conducted in the Department of Radiation Oncology, Regional Cancer Centre, PGIMER, Chandigarh from July 2016 to June 2017. Primary objective was to assess grade 2 acute skin toxicity with hypofractionated WBI with SIB completed in 10 fractions. Secondary objectives of the study were to determine dose distribution, target coverage, dose homogeneity dose conformity of the target volume, late toxicity and cosmetic outcomes.

1. Patient selection

Patients with breast cancer who had undergone BCS were included in this study. Institutional Ethics Committee of PGIMER approval was taken (No. INT/IEC/2017/127). Informed consent was taken from all the patients. The trial was registered with clinicaltrials.gov no. NCT04072718. Inclusion criteria were (1) primary cancer of breast of any histology, (2) age >18–70 years, (3) post-BCS with clear margins, healed scar, (4) Karnofsky performance status (KPS) >70, (5) regional nodal radiation when indicated (T3 tumors, positive nodes and T2 tumors with any of the two factors such as age <40 years, grade 3, estrogen receptor/progesterone receptor [ER/PR] negative and with lymphovascular invasion) and (6) no distant metastasis. Indications for the boost were age <40 years, T3 tumors, DCIS >25%, ER/PR negative, and close margins. Close margin was defined as margin <2 mm. Neoadjuvant or adjuvant chemotherapy was allowed. Adjuvant endocrine therapy was given to patients with hormone receptor positive tumors. Exclusion criteria were mastectomy, history of prior primary malignancy, prior irradiation to breast or chest, pregnancy and collagen vascular disease.

2. Radiotherapy planning

All patients were made to lie supine on a carbon fiber breast board or wing board or a T bar with ipsilateral arm abducted to 90º and face turned to the opposite side. Radiopaque markers were placed for defining the superior, inferior, medial, and lateral borders and the surgical scar. Three skin markings were placed along with the fiducials below the breast folds for the purpose of reproducibility and the location of tumor bed with respect to fiducials.
All patients underwent a normal free-breathing scan with virtual CT breast simulation. Axial cuts were taken from the mandible to the upper abdomen with a slice thickness of 3 mm. The 4D-CT images with recording of the respiratory signals were acquired, taking organ motion into account. The delineation of the tumor cavity and contouring of the organs-at-risk (OARs) was done by using RTOG guidelines. Contouring for the target volumes were done on maximum intensity projection (MIP) of the 4D-CT. The OARs contoured were heart, bilateral lungs, contralateral breast, brachial plexus, esophagus, spinal cord, left anterior descending artery (LAD) and thyroid.
The affected breast was contoured as the clinical target volume (CTV) excluding 5 mm from the skin. An additional 5 mm (0.5 cm) margin for setup error and motion was then added to CTV to form the planning target volume (PTV breast), excluding it from lungs and body by 5 mm to spare the skin. The nodal areas, when indicated according to the risk factors, were also contoured following RTOG contouring guidelines.

3. Boost RT planning

In each patient, tumor bed was delineated using clinical, radiological (mammography/CT/ultrasound of breast), surgical (intra-operative notes, external and internal surgical scar location) findings, seroma cavity and surgical clip’s location. Internal target volume (ITV) was generated by contouring tumor bed in all phases of respiratory cycles on 4D-CT based on MIP images. A margin of 5mm was added to the cavity to form PTV boost. A dose of 34 Gy/10#/2 week to the PTV breast and 40 Gy/10#/2 week to the PTV boost was delivered with IGRT using the RapidArc technique. Partial arcs were used for RT planning. Dose distribution and target coverage criteria for PTV breast and PTV boost were 98% of volume should receive >95% of dose and 2% volume should receive <107% of dose. Conformity and homogeneity indices were also calculated for each plan [15-17].
Dose constraints were calculated for this schedule by considering the radiobiological equivalence to conventional fractionation. For example, V20 for the lung, of the conventional fractionation (50 Gy/25#/5 week) will correspond to V16 of the 40 Gy (34 Gy to the breast + 8 Gy to the primary site) dose delivered in this study. Similarly for the heart and LAD Dmax instead of V25 and <20 Gy, V18 and <15 Gy, respectively were used. Dose constraints given were ipsilateral mean lung dose (MLD) ≤9 Gy, V16Gy <20% and contralateral lung V5 <5%. Mean heart dose (MHD) ≤7 Gy, V18 <5% for left side and <1% for the right side. LAD Dmax and Dmean to be <15 Gy and <8 Gy, respectively, from the left breast. Contralateral breast Dmean <3 Gy. Thyroid V25 and V30 should be <50% and <25%, respectively. Dmax and Dmean for oesophagus <20 Gy and <5 Gy, respectively. Dmax for the spinal cord and brachial plexus should be <30 Gy and <40 Gy, respectively.
Cone beam CT was done on the first three consecutive days and then orthogonal images were taken daily for set-up verification. All patients were treated in free breathing.

4. Assessments

1) Toxicities

Baseline assessment was done for all the patients. The physicians examined patients for any toxicity every week during treatment, at the treatment completion and during the follow-up visits. First follow-up was at 2 weeks of completion of radiation and then at 1 month for assessment of acute toxicity. Patients were followed every 3 months in the 1st year, every 4 months in the 2nd year, every 6 months thereafter. Toxicities were scored according to RTOG/LENT/SOMA grading scale. Both physician and patients reported acute toxicities at 1 and 3 months of completion of radiotherapy, which consists of the highest grade/severity observed/reported for the recording purpose. Late effects are reported at 6 months and 4 years follow-up by the patient and the physician.

2) Cosmesis

Cosmetic effects were assessed in the treated breast and compared with the opposite breast and with the baseline photographic evaluation. Both objective (skin reaction, overall grade, edema, induration, subcutaneous fibrosis, tenderness, scar changes and any other skin changes/ulceration) and subjective (hyperpigmentation, change in shape, change in size, nipple changes, heaviness, pain) parameters were used. The Harvard/NSABP/RTOG scale proposed by Harris et al. [18] was used to evaluate the cosmetic parameters. Variability in both objective and subjective assessment was evaluated. Changes in terms of color, shape, size, any swelling, symmetry, texture, and position of nipple were noted in the treated breast. The assessment was done at baseline (before the start of radiation treatment), at the time of completion of treatment, at 1 month, 3 months, 6 months, 1 year and 3 years after completion of treatment. The long-term cosmetic effects were reported at 4 years. For subjective evaluation, a standard scale for assessment of cosmetic effect due to RT after BCS was used. For objective qualification, digital photography of the patient was used, before and after the treatment. Digital photo, in a front view of the patient including the sternal notch and both the breast with a light background with adequate light were taken. Two views with hands by side and hands raised above the head were taken for all the patients. A picture of the scar was also taken by the same person to avoid variability of clicked photos.

3) Clinical outcomes

Disease-free survival (DFS) and overall survival (OS) were summarized by Kaplan-Meier curves. Local recurrence was defined as recurrence in the in the involved breast, axilla, supraclavicular fossa, and internal mammary nodes. Distant metastases were defined as disease occurring in the other sites. Local recurrence and distant metastases were used to calculate DFS. Time was calculated from the date of completion of RT. OS was defined from the date of diagnosis till the last follow-up or death due to breast cancer.

5. Statistical analysis

The purpose of the trial was to reject the experimental treatment from further study if it is too toxic, and to accept it for further study if the toxicity is acceptable. The primary endpoint was grade 2 acute skin toxicity, and other toxicities were considered secondary endpoints. The study was designed as a phase II trial with the following assumptions:
(1) Grade 2 skin toxicity ≥36% was considered unacceptable, and grade 2 skin toxicity ≤11% was considered acceptable. Hence the hypotheses of interest were H0: r≥36% against HA: r≤11%, where r is the proportion of patients with grade 2 skin toxicity.
(2) The type I error rate (a, probability of accepting an overly toxic treatment, a false positive outcome) was set to 5%.
(3) The type II error rate (b, probability of rejecting an acceptably toxic treatment, a false negative outcome) was set to 10%, i.e., the power is equal to 90%.
Under these assumptions, using a one-sided Fisher exact test, the design consists of treating 27 evaluable patients, and
(1) if at most five patients have grade 2 skin toxicity, the treatment was considered acceptable (5/27=19%),
(2) if at least six patients have grade 2 skin toxicity, the treatment was considered too toxic (6/27=22%).


1. Patient characteristics

Between July 2016 to June 2017, 27 patients were treated. Mean age of the patients was 42 years (range, 36 to 67 years). Left and right breast cancer was seen in 17 (63%) and 10 (37%) patients, respectively. Most patients were premenopausal 22 (81%) and had T2 tumors 16 (59%). Nodes were positive in 18 (67%) patients (Table 1). Axillary clearance was till level III in 25 (92.5%) patients and median number of dissected nodes were 19. More than 50% of the patients had grade 3 disease and lymphovascular invasion. None of the patients had oncoplastic reduction. Supraclavicular fossa (SCF) was treated in 20 (74%) patients. Internal mammary nodes were treated in one patient. Chemotherapy was given as neoadjuvant and adjuvant to 4 (14.8%) and 22 (81%) patients, respectively. Hormonal therapy was received by 18 (67%) patients. Trastuzumab was received by 1 (4%) patient only.

2. Dosimetry

Mean PTV and boost volume were 1,099.58 ± 396.81 mL and 76.0 ± 41.89 mL, respectively. The mean conformity index (CI) for the PTV breast was 0.74 ± 12. The mean CI and homogeneity index (HI) for the PTV boost was 0.64 ± 0.15 and 0.09 ± 0.04, respectively. Dmax to PTV boost was 43.2 ± 1.5 Gy. PTV breast and PTV boost V107% and V105% were 4.2 ± 4.6 mL and 11.8 ± 4.3 mL and 2.97 ± 8.81 mL and 8.22 ± 0.74 mL, respectively.
Ipsilateral MLD was 9.86 Gy (range, 7.12 to 13.72 Gy). Ipsilateral lung mean V16 and V10 was 16.01% (2.12%–27.42%) and 39.60% (13.6%–79.8%), respectively. Contralateral lung mean V5 and V2 was 3.74% (0.77%–11.33%) and 52.62% (12.31%–97.90%), respectively. MLD with and without SCF radiotherapy was 10.08 Gy (range, 7.13 to 13.72 Gy) (n = 20) and 9.22 Gy (range, 7.12 to 11.50 Gy) (n = 7), respectively. MHD was 7.25 Gy (range, 4.31 to 10.85 Gy) from the left breast and 4.37 Gy (range, 2.32 to 7.13 Gy) from the right breast. In patients with left breast cancer (n = 17), MHD with and without SCF treatment was 7.25 Gy (n = 12) and 6.6 Gy (n = 5), respectively. Mean V18 and V15 of the heart from the left and right breast was 2.88% (0.05%–8.98%) and 0.30% (0%–1.69%); and 6.20% (0.22%–18.26%) and 1.1% (0%–3.69%), respectively. Dmax to LAD from left breast was 14.24 Gy (8.9–27.86 Gy). Mean LAD dose from the left and right breast was 7.74 Gy (4.42–21.26 Gy) and 3.32 Gy (1.41–6.72 Gy), respectively. Mean dose to the contralateral breast was 2.64 Gy (1.53–4.16 Gy). Thyroid V30 and V25 mean were 11.83% (0%–36.90%) and 19.69% (0%–52.97%), respectively (Table 2). Dmax and Dmean to the oesophagus was 15.65 Gy (4.48–32.8 Gy) and 3.69 Gy (1.55–9.02 Gy), respectively. Dmax and Dmean to spinal cord and was 10.43 Gy (2.32–28.40 Gy) and 3.15 Gy (0.84–18.65 Gy), respectively. Dmax to brachial plexus was 26.95 Gy (6.72–38.42 Gy).
Dose constraints for MLD ≤9 Gy, ipsilateral lung V16 <20% and contralateral lung V5 <5% were achieved in 59.25%, 81.48% and 81.48% of patients, respectively (Table 2). MHD from left breast cancer ≤7 Gy was achieved in 58.82% patients. Heart V18 <5% for left side and <1% for the right side were achieved in 88.24% and 90% of patients, respectively. Heart V15 <10% for left side and <2% for the right side were achieved in 88.24% and 70% of patients, respectively. LAD Dmax (<15 Gy) for left breast was achieved in 82.35% patients. LAD Dmean <8 Gy from left breast and <3 Gy from right breast were achieved in 88.24% and 80% of patients, respectively. Contralateral breast Dmean <3 Gy was achieved in 77.78% of patients. Thyroid V30 and V25, <25% and <50%, were achieved in 70.27% and 88.89% of patients, respectively. Oesophagus Dmax (<20 Gy) and Dmean (<5 Gy) were achieved and 85.19% and 70.03% of patients, respectively. Average of Dmax was higher in patients who received SCF radiation (18.66 Gy) as compared to those who did not (7.0 Gy). Spinal cord Dmean (<5 Gy) and Dmax (<30 Gy) were achieved in 88.89% and 100% patients, respectively.
There was significant dose reduction to the thyroid with head position and whether SCF was treated or not (Table 3). Mean thyroid dose in patients with and without head rotation was 11.00 Gy (95% confidence interval [CI], 6.67–15.32) and 22.68 Gy (95% CI, 20.00–25.36), respectively (p < 0.0001). Similarly, mean thyroid dose with and without SCF treatment was 16.95Gy (95% CI, 13.08–20.82) and 0.67Gy (95% CI, 0.34–0.99), respectively (p < 0.0001).

3. Acute toxicity

Grade 1 and 2 acute skin toxicity was observed in 9 (33%) and 5 (18.5%) patients, respectively (Fig. 1). Acute grade 2 skin toxicity in patients with and without nodal radiotherapy was 4 (20%) and 1 (14.2%), respectively. These were dry desquamations either in axillary fold or in inframammary fold. There was no grade 3 acute skin toxicity. This rate of grade 2 acute skin toxicity met the predefined criteria of ≤5/27 for acceptable toxicity. None of the parameters such as treatment of SCF nodes, V107%, V105%, breast size and boost volume were related with acute toxicity (Table 4).
All the secondary toxicities at 1 month also met the predefined criteria for acceptable toxicity. Grade 2 hyperpigmentation, edema, and induration were observed in 1 (3.7%), 2 (7%), and 4 (14.8%) patients, respectively. At 1 month, patient reported acute toxicities were mild breast swelling, heaviness, and pain in 1 (3.7%), 4 (14.8%), and 8 (29%) patients, respectively. Mild difficulty in swallowing was reported by 1 (3.7%) patient in whom internal mammary nodes were also treated. None of the patients developed acute radiation pneumonitis. Dmax to the oesophagus in this patient was 32.8 Gy. All acute toxicities subsided by 3 months except for the induration (Fig. 1).

4. Late toxicity

Late toxicities were either grade 1 or 2 (Fig. 2). In comparison to the baseline, toxicities increased till 6 months then decreased after that. Late grade 1 and grade 2 breast induration at 4 years was observed in 4 (14.8%) and 1 (3.7%) patient, respectively. These were present at baseline also. Breast edema was seen in 2 (7.4%) patients at baseline, which reduced at 4 years to 1 (3.7%) only. Grade 1 breast fibrosis was observed in 1 (3.7%) patient at 4 years. Grade 1 arm edema was seen in 2 (7.4%) patients at baseline, which persisted in 1 (3.7%) patient till 4th year.
Patient reported outcomes were mild to moderate only. At baseline mild to moderate breast pain was reported by 2 (7.4%) patients, which became mild at 4 years. Breast heaviness was reported by 2 (7.4%) patients at baseline, which persisted till 4th year. Mild breast shrinkage was reported by 1 (3.7%) and 2 (7.4%) patients at baseline and 4 years, respectively. Mild arm/shoulder discomfort was reported by 1 (3.7%) patient only. Arm swelling at 4 years was reported by only 1 (3.7%) patient. There were no grade 3 late toxicities. There was no brachial plexopathy or rib fracture with this schedule. We did not observe any late cardiac or pulmonary toxicity.

5. Cosmesis

Physician/patient observed cosmesis was excellent and good in 21 (78%)/19 (70%) and 6 (22%)/8(30%) patients, respectively (Figs. 3, 4). None of the patients had adverse cosmesis. None of the parameters such as V107%, V105%, breast size and boost volume were related with late effects or cosmesis.

6. Outcomes

At a median follow-up of 51 months (range, 12 to 61 months), local recurrence occurred in 1 (3.7%) patient. Distant metastases were seen in 2 (7.4%) patients. Both patients with distant metastases had triple negative disease. DFS and OS at 4 years was 88% (95% CI, 77%–100%) and 92% (95% CI, 82%–100%), respectively.

Discussion and Conclusion

In this study we reported the doses to the target organ, the OARs, acute and late toxicities and the cosmesis in breast cancer patients post-BCS who were treated with accelerated hypofractionated locoregional RT schedule of 34 Gy/10#/2 week (3.4 Gy/fraction) to the whole breast and 40 Gy (4 Gy/fraction) to the tumor area with SIB with VMAT technique in 12 days. Dose constraints were achieved in most patients with low rates of acute and late toxicities. There was no adverse cosmesis. Local control and survival were good with this schedule. Since grade 2 skin toxicity occurred in 5 (18.5%) patients, this treatment seems to be acceptable according to the assumption in null hypothesis for this study.
WBI dose fractionation has changed over the years. Use of SIB with hypofractionation is investigational. In the present study we integrated boost with accelerated hypofractionation and completed treatment in 2 weeks only. With changes in hypofractionation schedules in breast cancer we have to look for OARs constraints, which can be achieved with a particular dose fractionation schedule. We modified dosimetric constraints for the lung to V16 and heart to V18, which would be biologically equivalent to V20 and V25 that of the conventional schedule, respectively. We achieved dose constraints to the OARs such as lungs, heart (high dose volume), contralateral breast and oesophagus in >80% of patients (Table 2). MLD was slightly higher with SCF treatment (10.08 Gy vs. 9.22 Gy). There was no impact of SCF treatment on the MHD. One of the observations of our study was that dose to the thyroid could be reduced significantly with head rotation (Table 3).
Our results are quite consistent with the studies published in the literature (Table 5) in terms of acute toxicity, cosmetic outcomes, local control, DFS and OS. Acute grade 2 toxicity in the reported studies ranged from 4%–43%, and upper limit of 95% CI of our study 35%, lie well within this range. De Rose et al. [7] reported a phase II trial of hypofractionated RT with VMAT in 787 patients with early breast cancer with a dose of 40.5 Gy to whole breast and 48 Gy to the tumor bed in 15 fractions over 3 weeks with VMAT. Grade 1 and 2 acute toxicity was observed in only 51% and 9.7% patients, respectively. At a median follow-up of 45 months, grade 1 toxicity was 13.5% and 4 patients had distant relapse. Cosmetic outcomes were excellent/good in 100% patients. In our study, grade 1 acute toxicity was less than those reported by De Rose et al. [7], perhaps because of the lower total dose delivered in our study.
We did not observe any late grade 3 toxicities. In the study by Freedman et al. [8], higher grade 2 toxicity could be because of delivery of higher total dose (56 Gy). However, local control was comparable to our study. Bantema-Joppe et al. [19,20] reported cosmetic outcomes with 8.5% grade 2 fibrosis in the boost area, chest wall pain in 6.7% patients, and telangiectasia grade ≥2 in 3.7% patients at a median follow-up of 30 months. All-grade fibrosis outside the tumor bed was observed in 50% of patients. Higher fibrosis, chest wall pain and telangiectasia rate could be because of a high total dose delivered (64.4–67.2 Gy) in their study. We did not observe any telangiectasia or chest wall pain in our study. So, the present schedule may be better in terms of toxicities and cosmetic outcomes with comparable local control, DFS and OS.
MHD dose in the current study was 7.25 Gy, which was because of the partial arcs used for radiation planning. This MHD may not be acceptable currently because of the risk of late-term cardiac complications. In a study by Darby et al. [21], they reported that the rate of major coronary events increased by 7.4% for each 1 Gy increase in MHD. They also demonstrated a threshold MHD of 3 Gy, implying an attributable absolute increased cardiac mortality of 0.5%–0.7% for women <50 years depending on number of cardiac risk factors. As per their observations MHD was a better predictor of coronary events than the mean LAD dose and these events started within 5-years of treatment. However, their study was from 2D era based on average anatomy and lacked individual dosimetric information hence its ramifications remain unresolved. So far, we have not observed any coronary event in our patients. Recently, we published our results at 5-year with this schedule with 2D technique. We did not encounter excess late arm/shoulder and cardiac toxicity, although 5-year may not be adequate to report cardiac toxicities [22]. MHD of 7.25 Gy in the current study was higher so the risk of coronary events in future cannot be ruled out. Earlier studies have also reported that VMAT increases MLD, MHD and dose to the opposite breast [23]. Considering this risk with partial arc VMAT, 3D-CRT with deep inspiration breath hold, inverse planned fixed field IMRT, treatment in prone position, hybrid techniques of combining tangential IMRT with VMAT and proton therapy may be more appropriate in achieving lower MHD and doses to other OARs [24-26]. IMRT has been shown to improve target coverage and reduce dose to the OARs [24]. Taylor et al. [27] in another population-based study calculated the absolute risk of mortality from lung cancer at 5 Gy MLD and ischemic heart disease at 4 Gy MHD after breast RT for smokers and non-smokers to be 4.4% and 0.3%, and 1.2% and 0.3%, respectively. However, all these doses were estimated retrospectively. In a recent study Merzenich et al. [28] reported that average MHD of 4.6 Gy for left-sided breast RT and only pre-exiting cardiac disease was associated with risk of cardiac death. While another study reported V25 and V30 to be detrimental to the heart [29]. So, it is not only the RT dose but co-morbidities and lifestyle also play a significant role in late effects on the heart in patients with breast cancer.
In our previous study with 3D-CRT in patients with left-sided breast cancer postmastectomy; MHD, LAD, proximal LAD, and distal LAD doses were 3.36 Gy, 16.06 Gy, 2.7 Gy, and 27.5 Gy, respectively. Left MLD, V10, and V20 were 5.96 Gy, 14%, and 12.4%, respectively. Mean dose to the right lung and the opposite breast was 0.29 Gy and 0.54 Gy, respectively. V25 for heart was 4.25% [30]. In another study with 3D-CRT in left-sided patients with BCS, MHD in the supine and prone positions was 4.55 Gy and 2.06 Gy (p = 0.02), respectively. MLD in the supine and prone positions was 6.58 Gy and 0.85 Gy (p = 0.001), respectively [31]. All these doses are quite low as compared to the current study. Deep inspiration breath-hold (DIBH) reduces heart volume in the RT field, hence it lead to reduction in all dose parameters (mean, maximum and volume based) of the heart [32,33]. It has been shown to reduce cardiac mortality by 4.7% compared to free breathing, with normal tissue complication probability of 0.1% in patients with left-sided breast cancer [34]. Because of changes in dose fractionation (from conventional to hypofractionation) and techniques of RT for breast cancer (from 2D to 3D-CRT/FIF IMRT); dose constraints to be placed for the heart, LAD and lungs and its impact on the cardiac related morbidity and mortality still remains unclear. Although MHD has been the gold standard for prediction of late cardiac effects in the past but recent studies have suggested that reporting doses to the heart substructures such as apical part of left ventricle and LAD may be more relevant [35,36]. Hypofractionation have been reported to result in lower EQD2 to the heart as compared to conventional fractionation and comparable late effects [37,38]. However, till data comes clear on these aspects, patients with left-sided breast cancer should be offered techniques, which reduce dose to the heart and lungs.
Second cancers after breast radiation are also a possibility with VMAT because of low dose to larger volume of OARs. In the present study 50% volume of the contralateral lung received 2 Gy, so it may put this OAR for second cancer. Hall and Wuu [39] in their study estimated 1% to 1.75% increase in the incidence of second cancers after 3D-CRT and IMRT at 10 years. VMAT technique was also reported to increase this risk in one study [24], where as it was comparable in another study for the contralateral breast and lung, but less risk for the ipsilateral lung because of reduced MLD with VMAT [40]. In a recent review, it was observed that VMAT increases contralateral lung V5 by 25% as compared to other techniques [41]. In our study contralateral lung V5 was lower as compared to other studies. This reduction in V5 is associated with reduction in secondary cancer [40,41]. Since, ipsilateral MLD, contralateral lung V5 and breast mean doses in our study are comparable to those observed by Zhang et al. [42], we may expect similar risk of second cancers in our patients. However, this risk may vary with distance of the organ from the sternum, patient anatomy, dose optimization, set up errors, organ motion [42] and smoking [27]. In our past series we have reported second cancers in the contralateral breast, oesophagus and lung cancers in 3.3%, 0.22% and 0.05% patients, respectively [30].
Many dosimetric studies have explored the potential benefits of integrating boost with WBI, but the majority of them are with conventional fractionation [43-47]. A multicentric study of 151 patients by Dellas et al. [48] from Germany with RT dose of 40 Gy in 16 fractions for WBI and a SIB with 0.5 Gy/fraction to the primary area, reported that SIB was feasible with hypofractionation. A few studies have integrated boost with moderate hypofractionation and treatment completed in 3–4 weeks [6-11,49-51] and 5–6 weeks in others [19,52]. Ours is the first study to report feasibility of accelerated hypofractionation with SIB in 12 days.
There are a few limitations of our study. The number of patients enrolled was less, because of the study design. Median follow-up of 51 months is modest; therefore, late toxicities and long-term clinical outcomes need to be further assessed as accelerated hypofractionation regimen with a dose of 3.4 Gy/fraction to the breast and 4 Gy/fraction to the tumor bed may lead to late radiobiological consequences, although the likely risk is less because the total dose delivered was 40 Gy with one of the optimal techniques of RT. Low doses to lungs and contralateral breast may also not favor VMAT technique but these can be further reduced by using tangential VMAT or hybrid VMAT. Lastly, it is an expensive technique and one of ASTRO Choosing Wisely Campaign initiatives is “Don’t routinely use IMRT to deliver whole breast radiotherapy as part of breast conservation therapy” [53].
With high dose per fraction, we could reduce overall treatment time to 12 days only. It increased treatment compliance because of less acute toxicities. It reduced treatment cost to the patient with increased convenience by reducing the number of hospital visits. It also has potential to reduce risk of local recurrence with acceptable toxicities in the breast because of its low α/β ratio. Therefore, the implication of this study is, reduction of total treatment time from 4 weeks to 2 weeks and reduction in the waiting time for the other patients.
To conclude, this study demonstrated that accelerated hypofractionated RT with SIB boost is feasible and safe in terms of acute and late breast and arm toxicities. Radiation induced heart disease and stochastic effects might be a concern with higher MHD and low dose bath with this technique. VMAT plans may be used when conformal techniques are not able to achieve the desired dosimetric constraints. A phase III randomized controlled trial with same fractionation schedule with 2D/3D-CRT and DIBH techniques (HRBC; NCT04075058) is ongoing and has completed patient accrual.


Statement of Ethics

Institutional Ethics Committee approval was taken. Informed consent was taken from all the patients.


Conflict of Interest

No potential conflict of interest relevant to this article was reported.


Author Contributions

Research Methodology, BSY, SG, DD. Planning and treatment, BSY, SG, AG, AOS. Patient contribution, DD. Analysis, BSY, SG, AG. Manuscript writing, BSY, SG.


Data Availability Statement

Data will be provided on suitable request.

Fig. 1.
Acute toxicity: patient and physician reported (rates along the X-axis)
Fig. 2.
Late toxicity. (A) patient reported (rates along the X-axis). (B) Physician observed (rates along the X-axis).
Fig. 3.
Excellent cosmesis at baseline (A) and at 4 years (B).
Fig. 4.
Good cosmesis at baseline (A) and at 4 years (B).
Table 1.
Patient characteristics
Characteristic n (%)
 Yes 9 (33)
 No 18 (67)
Menopausal status
 Premenopausal 22 (81)
 Postmenopausal 5 (19)
Clinical tumor stage
 T1 9 (33)
 T2 16 (59)
 T3 2 (4)
pTumor stage
 T1 10 (37)
 T2 16 (59)
 T3 1 (4)
pNodal stage
 N0 9 (33)
 N1 11 (41)
 N2 6 (22)
 N3 1 (4)
 1 & 2 13 (48)
 3 14 (52)
Lymphovascular invasion
 Yes 15 (56)
 No 12 (44)
 Present 8 (30)
 Absent 19 (70)
Estrogen receptor
 Positive 15 (56)
 Negative 12 (44)
Progesterone receptor
 Positive 13 (48)
 Negative 14 (52)
 Positive 8 (30)
 Negative 19 (70)
 ≤14 5 (19)
 >14 22 (81)
 Yes 26 (96)
 No 1 (4)
 Yes 18 (67)
 No 9 (33)
 Yes 1 (4)
 No 7 (26)

DCIS, ductal carcinoma in-situ.

Table 2.
Volumes, doses to the organs-at-risk and constraints achieved
Dose constraint n Mean ± SD Constraint achieved, n(%)
Volumes PTV breast (cm3) 1,099.58 ± 396.81
 Conformity index 0.74 ± 0.12
 107% 4.20 ± 10.35
 105% 11.80 ± 19.14
PTV boost (cm3) 76.00 ± 41.89
 Conformity index 0.64 ± 0.15
 Homogeneity index 0.09 ± 0.04
 107% 2.97 ± 5.43
 105% 8.22 ± 16.65
Organ at risk Mean lung dose ≤9 Gy 27 9.86 ± 2.03 16 (59.25)
Ipsilateral lung
 V20Gy ≤10% 27 8.88 ± 4.20 21 (77.78)
 V16Gy <20% 27 16.01 ± 5.60 22 (81.48)
 V10Gy - 27 39.60 ± 15.93 -
Contralateral lung
 V5Gy <5% 27 3.74 ± 3.30 22 (81.48)
 V2Gy - 27 52.62 ± 22.63 -
Heart Dmean
 Left breast ≤7 Gy 17 7.25 ± 2.25 10 (58.82)
 Right breast <3 Gy 10 4.20 ± 2.32 5 (50.00)
Heart V18Gy
 Left breast <5% 17 2.88 ± 2.36 15 (88.24)
 Right breast <1% 10 0.33 ± 0.52 9 (90.00)
Heart V15Gy
 Left breast <10% 6.20 ± 4.67 15 (88.24)
 Right breast 2% 1.10 ± 3.73 7 (70.00)
LAD Dmax
 Left breast <15 Gy 17 14.24 ± 9.78 14 (82.35)
LAD Dmean
 Left breast <8 Gy 17 7.74 ± 3.86 15 (88.24)
 Right breast <3 Gy 10 3.32 ± 2.84 8 (80.00)
Contralateral breast Dmean <3 Gy 27 2.64 ± 0.63 21 (77.78)
 V30 <25% 27 11.82 ± 14.57 19 (70.37)
 V25 <50% 27 19.69 ± 21.23 24 (88.89)
 Dmax <20 Gy 27 15.65 ± 9.47 19 (70.37)
 Dmean <5 Gy 27 3.68 ± 1.58 23 (85.19)
Spinal cord Dmax <30 Gy 27 28.40 Gy 27 (100)
Brachial plexus Dmax <40 Gy 27 38.42 Gy 27 (100)

SD, standard deviation; PTV, planning target volume; LAD, left anterior descending artery.

Table 3.
Thyroid dose with head position and SCF treatment
n Dose 95% CI p-value
Head rotation
 Yes 23 11.00 ± 10.01 6.67–15.32 <0.0001
 No 4 22.68 ± 1.68 20.00–25.36
SCF treatment
 Yes 20 16.95 ± 0.35 13.08–20.82 <0.0001
 No 7 0.67 ± 8.25 0.34–0.99

Values are presented as mean ± standard deviation.

SCF, supraclavicular fossa; CI, confidence interval.

Table 4.
Variables for acute toxicity
Variable Acute toxicity n Mean ± SD p-value (t-test)
Breast volume Grade 0/1 22 1,257.3 ± 471.8 0.50
Grade 2 5 1,106.4 ± 309.7
PTV volume Grade 0/1 22 1,126.3 ± 412.6 0.47
Grade 1 5 982.2 ± 329.4
Boost volume Grade 0/1 22 81.8 ± 39.6 0.14
Grade 2 5 51.2 ± 47.2
V107% Grade 0/1 22 12.4 ± 38.0 0.76
Grade 2 5 7.1 ± 12.0
V105% Grade 0/1 22 29.4 ± 75.8 0.75
Grade 2 5 17.9 ± 29.2

SD, standard deviation; PTV, planning target volume.

Table 5.
Studies with hypofractionated SIB in breast cancer
Study n Dose fractionation (Gy/fx)
Acute skin toxicity, Grade 2 (%) Cosmesis, excellent/good (%) Local control (%)
Whole breast SIB
Franco et al. [6] 82 45/20 50/20 6 91 97
De Rose et al. [7] 787 40.5/15 48/15 9.7 100 99
Freedman et al. [8] 74 45/20 56/20 23 77 97
Chadha et al. [10] 74 40/15 45/15 4 NR 99
Formenti et al. [11] 91 40.5/15 48/15 8.1 96 98
Bantema-Joppe et al. [19,20] 940 50.4/28 64.4–67.2/28 NR 91.5 98.9
Krug et al. [49] 149 40/15 48/15 14.7 91 NR
Cante et al. [50,51] 465 45/20 50/20 NR 95.7 100
McDonald et al. [52] 354 45/25 59.92/28 43 96.5 97
Present study 27 34/10 40/10 18.5 100 96.5

SIB, simultaneous integrated boost; NR, not reported.


1. Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2018;68:394–424.
crossref pmid pdf
2. Freedman GM, Anderson PR, Hanlon AL, Eisenberg DF, Nicolaou N. Pattern of local recurrence after conservative surgery and whole-breast irradiation. Int J Radiat Oncol Biol Phys 2005;61:1328–36.
crossref pmid
3. Polgar C, Janvary L, Major T, et al. The role of high-dose-rate brachytherapy boost in breast-conserving therapy: long-term results of the Hungarian National Institute of Oncology. Rep Pract Oncol Radiother 2010;15:1–7.
crossref pmid pmc
4. Romestaing P, Lehingue Y, Carrie C, et al. Role of a 10-Gy boost in the conservative treatment of early breast cancer: results of a randomized clinical trial in Lyon, France. J Clin Oncol 1997;15:963–8.
crossref pmid
5. Bartelink H, Horiot JC, Poortmans PM, et al. Impact of a higher radiation dose on local control and survival in breast-conserving therapy of early breast cancer: 10-year results of the randomized boost versus no boost EORTC 22881-10882 trial. J Clin Oncol 2007;25:3259–65.
crossref pmid
6. Franco P, Zeverino M, Migliaccio F, et al. Intensity-modulated adjuvant whole breast radiation delivered with static angle tomotherapy (TomoDirect): a prospective case series. J Cancer Res Clin Oncol 2013;139:1927–36.
crossref pmid pdf
7. De Rose F, Fogliata A, Franceschini D, et al. Phase II trial of hypofractionated VMAT-based treatment for early stage breast cancer: 2-year toxicity and clinical results. Radiat Oncol 2016;11:120.
crossref pmid pmc pdf
8. Freedman GM, Anderson PR, Goldstein LJ, et al. Four-week course of radiation for breast cancer using hypofractionated intensity modulated radiation therapy with an incorporated boost. Int J Radiat Oncol Biol Phys 2007;68:347–53.
crossref pmid
9. Yadav BS, Sharma SC, Singh G, Dahiya D. Comparison of two radiation boost schedules in postlumpectomy patients with breast cancer. J Cancer Res Ther 2020;16:1344-9.
10. Chadha M, Woode R, Sillanpaa J, et al. Early-stage breast cancer treated with 3-week accelerated whole-breast radiation therapy and concomitant boost. Int J Radiat Oncol Biol Phys 2013;86:40–4.
crossref pmid
11. Formenti SC, Gidea-Addeo D, Goldberg JD, et al. Phase I-II trial of prone accelerated intensity modulated radiation therapy to the breast to optimally spare normal tissue. J Clin Oncol 2007;25:2236–42.
crossref pmid
12. Yadav BS, Sharma SC. A phase 2 study of 2 weeks of adjuvant whole breast/chest wall and/or regional nodal radiation therapy for patients with breast cancer. Int J Radiat Oncol Biol Phys 2018;100:874-81.
13. Yadav BS, Bansal A, Kuttikat PG, Das D, Gupta A, Dahiya D. Late-term effects of hypofractionated chest wall and regional nodal radiotherapy with two-dimensional technique in patients with breast cancer. Radiat Oncol J 2020;38:109-18.
14. Yadav BS, Loganathan S, Sharma SC, Singh R, Dahiya D. Comparison of toxicity and cosmetic outcomes after accelerated partial breast irradiation or whole breast irradiation using 3-dimensional conformal external beam radiation therapy. Adv Radiat Oncol 2019;5:171-9.
15. Feuvret L, Noel G, Mazeron JJ, Bey P. Conformity index: a review. Int J Radiat Oncol Biol Phys 2006;64:333–42.
crossref pmid
16. Gong Y, Wang J, Bai S, Jiang X, Xu F. Conventionally-fractionated image-guided intensity modulated radiotherapy (IG-IMRT): a safe and effective treatment for cancer spinal metastasis. Radiat Oncol 2008;3:11.
crossref pmid pmc pdf
17. Wu Q, Mohan R, Morris M, Lauve A, Schmidt-Ullrich R. Simultaneous integrated boost intensity-modulated radiotherapy for locally advanced head-and-neck squamous cell carcinomas. I: dosimetric results. Int J Radiat Oncol Biol Phys 2003;56:573–85.
crossref pmid
18. Harris JR, Levene MB, Svensson G, Hellman S. Analysis of cosmetic results following primary radiation therapy for stages I and II carcinoma of the breast. Int J Radiat Oncol Biol Phys 1979;5:257–61.
crossref pmid
19. Bantema-Joppe EJ, Vredeveld EJ, de Bock GH, et al. Five year outcomes of hypofractionated simultaneous integrated boost irradiation in breast conserving therapy; patterns of recurrence. Radiother Oncol 2013;108:269–72.
crossref pmid
20. Bantema-Joppe EJ, Schilstra C, de Bock GH, et al. Simultaneous integrated boost irradiation after breast-conserving surgery: physician-rated toxicity and cosmetic outcome at 30 months’ follow-up. Int J Radiat Oncol Biol Phys 2012;83:e471.
crossref pmid
21. Darby SC, Ewertz M, McGale P, et al. Risk of ischemic heart disease in women after radiotherapy for breast cancer. N Engl J Med 2013;368:987–98.
crossref pmid
22. Yadav BS, Dahiya D, Gupta A, et al. Breast cancer hypofractionated radiotherapy in 2-weeks with 2D technique: 5-year clinical outcomes of a phase 2 trial. Rep Pract Oncol Radiother 2021;26:503-11.
23. Jin GH, Chen LX, Deng XW, Liu XW, Huang Y, Huang XB. A comparative dosimetric study for treating left-sided breast cancer for small breast size using five different radiotherapy techniques: conventional tangential field, filed-in-filed, tangential-IMRT, multi-beam IMRT and VMAT. Radiat Oncol 2013;8:89.
crossref pmid pmc pdf
24. Hurkmans CW, Cho BC, Damen E, Zijp L, Mijnheer BJ. Reduction of cardiac and lung complication probabilities after breast irradiation using conformal radiotherapy with or without intensity modulation. Radiother Oncol 2002;62:163–71.
crossref pmid
25. Krengli M, Masini L, Caltavuturo T, et al. Prone versus supine position for adjuvant breast radiotherapy: a prospective study in patients with pendulous breasts. Radiat Oncol 2013;8:232.
crossref pmid pmc pdf
26. Mast ME, van Kempen-Harteveld L, Heijenbrok MW, et al. Left-sided breast cancer radiotherapy with and without breath-hold: does IMRT reduce the cardiac dose even further? Radiother Oncol 2013;108:248–53.
crossref pmid
27. Taylor C, Correa C, Duane FK, et al. Estimating the risks of breast cancer radiotherapy: evidence from modern radiation doses to the lungs and heart and from previous randomized trials. J Clin Oncol 2017;35:1641–9.
crossref pmid pmc
28. Merzenich H, Baaken D, Schmidt M, et al. Cardiac late effects after modern 3D-conformal radiotherapy in breast cancer patients: a retrospective cohort study in Germany (ESCaRa). Breast Cancer Res Treat 2022;191:147–57.
crossref pmid pmc pdf
29. Gagliardi G, Constine LS, Moiseenko V, et al. Radiation dose-volume effects in the heart. Int J Radiat Oncol Biol Phys 2010;76(3 Suppl):S77–85.
crossref pmid
30. Yadav BS, Das DK, Kumar N, Singhal M, Robert N, Michaelis M. Radiation dose to the heart with hypofractionation in patients with left breast cancer. Exp Results 2021;2:e21.

31. Yadav BS, Dhingra D, Thakur N, Ghoshal S, Sharma R, Singh AO. Dosimetric comparison of supine versus prone radiotherapy techniques in patients with breast cancer. J Radiat Oncol 2020;9:243-8.
32. Nemoto K, Oguchi M, Nakajima M, Kozuka T, Nose T, Yamashita T. Cardiac-sparing radiotherapy for the left breast cancer with deep breath-holding. Jpn J Radiol 2009;27:259–63.
crossref pmid pdf
33. Nissen HD, Appelt AL. Improved heart, lung and target dose with deep inspiration breath hold in a large clinical series of breast cancer patients. Radiother Oncol 2013;106:28–32.
crossref pmid
34. Korreman SS, Pedersen AN, Aarup LR, Nottrup TJ, Specht L, Nystrom H. Reduction of cardiac and pulmonary complication probabilities after breathing adapted radiotherapy for breast cancer. Int J Radiat Oncol Biol Phys 2006;65:1375–80.
crossref pmid
35. Munshi A, Khataniar N, Sarkar B, Bera ML, Mohanti BK. Spatial orientation of coronary arteries and its implication for breast and thoracic radiotherapy-proposing “coronary strip” as a new organ at risk. Strahlenther Onkol 2018;194:711–8.
crossref pmid pdf
36. Piroth MD, Petz D, Pinkawa M, Holy R, Eble MJ. Usefulness of a thermoplastic breast bra for breast cancer radiotherapy : a prospective analysis. Strahlenther Onkol 2016;192:609–16.
crossref pmid pdf
37. Appelt AL, Vogelius IR, Bentzen SM. Modern hypofractionation schedules for tangential whole breast irradiation decrease the fraction size-corrected dose to the heart. Clin Oncol (R Coll Radiol) 2013;25:147–52.
crossref pmid
38. James M, Swadi S, Yi M, Johansson L, Robinson B, Dixit A. Ischaemic heart disease following conventional and hypofractionated radiation treatment in a contemporary breast cancer series. J Med Imaging Radiat Oncol 2018;62:425–31.
crossref pmid pdf
39. Hall EJ, Wuu CS. Radiation-induced second cancers: the impact of 3D-CRT and IMRT. Int J Radiat Oncol Biol Phys 2003;56:83–8.
crossref pmid
40. Abo-Madyan Y, Aziz MH, Aly MM, et al. Second cancer risk after 3D-CRT, IMRT and VMAT for breast cancer. Radiother Oncol 2014;110:471–6.
crossref pmid
41. Ashby O, Bridge P. Late effects arising from volumetric modulated arc therapy to the breast: a systematic review. Radiography (Lond) 2021;27:650–3.
crossref pmid
42. Zhang Q, Liu J, Ao N, et al. Secondary cancer risk after radiation therapy for breast cancer with different radiotherapy techniques. Sci Rep 2020;10:1220.
crossref pmid pmc pdf
43. Rose MA, Olivotto I, Cady B, et al. Conservative surgery and radiation therapy for early breast cancer: long-term cosmetic results. Arch Surg 1989;124:153–7.
crossref pmid
44. Singla R, King S, Albuquerque K, Creech S, Dogan N. Simultaneous-integrated boost intensity-modulated radiation therapy (SIB-IMRT) in the treatment of early-stage left-sided breast carcinoma. Med Dosim 2006;31:190–6.
crossref pmid
45. Hurkmans CW, Meijer GJ, van Vliet-Vroegindeweij C, van der Sangen MJ, Cassee J. High-dose simultaneously integrated breast boost using intensity-modulated radiotherapy and inverse optimization. Int J Radiat Oncol Biol Phys 2006;66:923–30.
crossref pmid
46. van der Laan HP, Dolsma WV, Maduro JH, Korevaar EW, Hollander M, Langendijk JA. Three-dimensional conformal simultaneously integrated boost technique for breast-conserving radiotherapy. Int J Radiat Oncol Biol Phys 2007;68:1018–23.
crossref pmid
47. Hijal T, Fournier-Bidoz N, Castro-Pena P, et al. Simultaneous integrated boost in breast conserving treatment of breast cancer: a dosimetric comparison of helical tomotherapy and three-dimensional conformal radiotherapy. Radiother Oncol 2010;94:300–6.
crossref pmid
48. Dellas K, Vonthein R, Zimmer J, et al. Hypofractionation with simultaneous integrated boost for early breast cancer: results of the German multicenter phase II trial (ARO-2010-01). Strahlenther Onkol 2014;190:646–53.
crossref pmid pdf
49. Krug D, Baumann R, Krockenberger K, et al. Adjuvant hypofractionated radiotherapy with simultaneous integrated boost after breast-conserving surgery: results of a prospective trial. Strahlenther Onkol 2021;197:48–55.
crossref pmid pmc pdf
50. Cante D, Rosa La Porta M, Casanova-Borca V, et al. Accelerated hypofractionated adjuvant whole breast radiotherapy with concomitant photon boost after conserving surgery for early stage breast cancer: a prospective evaluation on 463 patients. Breast J 2011;17:586–93.
crossref pmid
51. Cante D, Franco P, Sciacero P, et al. Five-year results of a prospective case series of accelerated hypofractionated whole breast radiation with concomitant boost to the surgical bed after conserving surgery for early breast cancer. Med Oncol 2013;30:518.
crossref pmid pdf
52. McDonald MW, Godette KD, Whitaker DJ, Davis LW, Johnstone PA. Three-year outcomes of breast intensity-modulated radiation therapy with simultaneous integrated boost. Int J Radiat Oncol Biol Phys 2010;77:523–30.
crossref pmid
53. Choosing Wisely. ASTRO - IMRT for whole breast radiotherapy [Internet]. Philadelphia, PA: Choosing Wisely; 2013 [cited 2022 May 30]. Available from: https://www.choosingwisely.org/clinician-lists/american-society-radiation-oncology-intensity-modulated-radiotherapy/.

Editorial Office
Department of Radiation Oncology, Seoul National University Hospital,
Hamchun Hall, 6F, 95 Daehak-ro, Jongno-gu, Seoul 03082, Republic of Korea
Tel : +82-2-743-6574
E-mail: roj@kosro.or.kr
Copyright © The Korean Society for Radiation Oncology.                      Developed in M2PI
Close layer
prev next