Abstract

BackgroundTo evaluate risk of severe breast fibrosis occurrence in patients treated by breast-conserving surgery, adjuvant radiotherapy and hormonotherapy (HT) according to individual radiosensitivity (RILA assay).ResultsHT– and RILAhigh were the two independent factors associated with improved breast-fibrosis free survival (BFFS). BFFS rate at 36 months was lower in patients with RILAlow and HT+ than in patients with RILAhigh and HT– (75.8% and 100%, respectively; p = 0.004, hazard ratio 5.84 [95% confidence interval (CI) 1.8–19.1]). Conversely, BFFS at 36 months was comparable in patients with RILAhigh and HT+ and in patients with RILAlow and HT– (89.8% and 93.5%, respectively; p = 0.39, hazard ratio 1.7 [95% CI 0.51–5.65]), showing that these two parameters influenced independently the occurrence of severe breast fibrosis. BFFS rate was not affected by the HT type (tamoxifen or aromatase inhibitor) and timing (concomitant or sequential with radiotherapy).ConclusionsHT and RILA score independently influenced BFFS rate at 36 months. Patients with RILAhigh and HT– presented an excellent BFFS at 36 months (100%).Materials and methodsBreast Fibrosis-Free Survival (BFFS) rate was assessed relative to RILA categories and to adjuvant HT use (HT+ and HT–, respectively) in a prospective multicentre study (NCT00893035) which enrolled 502 breast cancer patients (456 evaluable patients). Breast fibrosis was recorded according to CTCAE v3.0 grading scale; RILA score was defined according to two categories (<12%: RILAlow; ≥12%: RILAhigh).

Highlights

  • The efficacy of adjuvant breast cancer radiotherapy after breast-conserving surgery is well established

  • HT– and RILAhigh were the two independent factors associated with improved breast-fibrosis free survival (BFFS)

  • BFFS rate at 36 months was lower in patients with RILA low (RILAlow) and HT+ than in patients with RILAhigh and HT– (75.8% and 100%, respectively; p = 0.004, hazard ratio 5.84 [95% confidence interval (CI) 1.8–19.1])

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Summary

Introduction

The efficacy of adjuvant breast cancer radiotherapy after breast-conserving surgery is well established. Late side effects have been reported in long-term survivor patients with better breast cancer outcome. These toxicities, such as radio-induced cardiotoxicity or poor cosmetic outcome, could impair the quality of life and affect the clinical benefit over time [3, 4]. Other risk factors are related to the radiotherapy modalities (high total dose, high dose per fraction, large irradiated volume) and to the treatment combinations (e.g., endocrine therapy, chemotherapy, history of surgery) (reviewed in [6]). To evaluate risk of severe breast fibrosis occurrence in patients treated by breast-conserving surgery, adjuvant radiotherapy and hormonotherapy (HT) according to individual radiosensitivity (RILA assay)

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