Affiliation:
1. Department of Radiation Oncology, Fujian Medical University Union Hospital, Fujian Key Laboratory of Intelligent Imaging and Precision Radiotherapy for Tumors (Fujian Medical University) Clinical Research Center for Radiology and Radiotherapy of Fujian Province (Digestive, Hematological and Breast Malignancies) Fuzhou Fujian China
2. Department of Follow‐Up Center Fujian Medical University Union Hospital Fuzhou Fujian China
3. Department of Breast Surgery Fujian Medical University Union Hospital Fuzhou Fujian China
Abstract
AbstractObjectiveThis single‐center, prospective, observational study was designed to investigate the toxicities, patient‐reported outcome (PRO), and dosimetric analysis of whole breast ultrafractionation radiotherapy (RT) after breast‐conserving surgery (BCS) in early breast cancer (BC).Patients and methodsPatients diagnosed with BC stage I, II and treated with BCS were enrolled. A dose of 26 Gray (Gy) in five fractions was prescribed to the whole breast and tumor bed. Clinical endpoints included toxicities, PRO, and dosimetric analysis. PRO was measured by the European Organization for Research and Treatment of Cancer general quality of life questionnaire (EORTC QLQ‐C30) and the BC‐specific questionnaire (EORTC QLQ‐BR23) questionnaires.ResultsBetween January 2022 and June 2023, 62 female patients were enrolled. The median age was 45 years. Most patients (83.9%) were diagnosed with pathological stage I disease. The median planning target volume (PTV) was 456.4 mL. The minimum, maximum, and mean doses, and D95 (dose of PTV irradiated volume more than 95%) to PTV were 20.2, 28.8, 27.2, and 26.3 Gy, respectively. The median mean lung dose and percentage lung volume receiving 8 Gy (V8) were 3.6 Gy and 13.4%, respectively. The median mean heart dose, V1.5 (percentage of organ volume irradiated with 1.5 Gy or higher), and V7 (percentage of organ volume irradiated with 7 Gy or higher) were 0.6 Gy, 6.8%, and 0.4%, respectively. Cosmetic effects before RT showed no obvious differences compared to that post RT. No toxicities of grade 3 or higher occurred. Five patients had asymptomatic radiation pneumonia (grade 1), and 12 patients had radiation dermatitis (grade 1). No factor was significantly related to radiation dermatitis or radiation pneumonia. For the EORTC QLQ‐C30 and QLQ‐BR23 questionnaires, all function and symptom scores before RT had no significant differences compared with that after RT, 1−2 months after RT, and 3−4 months after RT. Ultrafractionation RT did not worsen PRO. The 1‐year crude local control was 100%.ConclusionWhole breast ultrafractionation RT after BCS in early BC has no severe toxicities and does not affect PRO. These results need to be further validated with a longer follow‐up and a larger sample size.