Abstract. Background Post-mastectomy radiation therapy (PMRT) improves local control and survival in patients with breast cancer with a high risk of recurrence (those with advanced tumor and/or multiple lymph node metastases). PMRT reduces locoregional and distant recurrence in patients with axillary dissection and in those with axillary sampling, and radiation dermatitis is its most problematic adverse event (1). Almost all reports have used a bolus to maximize the radiation dose for the chest-wall surface and to decrease the risk of local recurrence, disregarding the radiation dermatitis problem (2). However, the use of a bolus has been reported to increase the frequency of severe radiation dermatitis (3). Few reports have compared the clinical outcomes of PMRT between patients using a bolus and those not using one, and no reports have analyzed the chest-wall dose surface histogram (DSH) parameters for PMRT. Therefore, a retrospective analysis of clinical outcomes in PMRTs without bolus was conducted and the DSH parameters between irradiation plans with and without virtual boluses were compared.
Patients and MethodsPatients. Between October 2011 and December 2016, 55 patients with breast cancer received PMRT at the Gunma University Hospital. Among these patients, three who received boost irradiation with electron beams were excluded because of the difficulty in recreating the precise dose distribution of electron beams using our radiation treatment planning system (RTPS) of the XiO version 4.5 software (ELEKTA, Stockholm, Sweden). Thus, 52 patients with breast cancer who received PMRT were retrospectively analyzed, and all patients were treated with 6 MV X-ray beams without bolus. Patient characteristics are summarized in Table I. Histologically, 46 patients had invasive ductal carcinoma, three had invasive lobular carcinoma, and four had other breast cancer types. Breast cancer subtypes were defined according to the status of estrogen receptor (ER), progesterone receptor (PgR), human epidermal growth factor receptor 2 (HER2), and the Ki-67 index. Twenty-four patients had luminal A (ER-positive and/or PgR-positive, HER2-negative, and Ki-67 <20%), 20 had luminal B (luminal type other than luminal A), four had HER2-enriched (ER-negative, PgR-negative, and HER2-positive), and four had triple-negative (ER-negative, PgRnegative, and HER2-negative) cancer subtypes. Twelve patients had 961