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Hypofractionation with no boost after breast conservation in early-stage breast cancer patients
Authors:Francesca Arcadipane  Pierfrancesco Franco  Chiara De Colle  Nadia Rondi  Jacopo Di Muzio  Emanuela Pelle  Stefania Martini  Ada Ala  Mario Airoldi  Michela Donadio  Corrado De Sanctis  Isabella Castellano  Riccardo Ragona  Umberto Ricardi
Institution:1.Department of Oncology, Radiation Oncology,University of Turin School of Medicine,Turin,Italy;2.Department of Oncology, Radiation Oncology,AOU Città della Salute e della Scienza,Turin,Italy;3.Department of General and Specialistic Surgery, Breast Surgery Unit,AOU Città della Salute e della Scienza,Turin,Italy;4.Department of Oncology, Medical Oncology 2,AOU Città della Salute e della Scienza,Turin,Italy;5.Department of Oncology, Breast Oncology Unit,AOU Città della Salute e della Scienza,Turin,Italy;6.Department of Gynecology and Obstetrics, Breast Unit,AOU Città della Salute e della Scienza,Turin,Italy;7.Department of Medical Sciences, Pathology Unit,University of Torino,Turin,Italy
Abstract:The aim of this study was to evaluate local control, survival and toxicity profile of a consecutive cohort of early-stage breast cancer (EBC) patients treated with adjuvant hypofractionated radiotherapy (HF) with no boost delivered to the lumpectomy cavity, after breast-conserving surgery (BCS). Between 2005 and 2015, a total of 493 women affected with EBC were treated with HF (46 Gy/20 fractions or 40.05 Gy/15 fractions) to the whole breast without boost to tumor bed, because of age and/or favorable tumor characteristics. The primary endpoint was 5-year actuarial local control (LC); secondary endpoints included survival, toxicity profile and cosmesis. Median follow-up was 57 months (range 6–124). Actuarial 5-year overall, cancer-specific, disease-free survival and LC were 96.3, 98.9, 97.8 and 98.6 %, respectively. On multivariate analysis, tumor stage (T1 vs. T2) and hormonal status (positive vs. negative estrogen receptors) were significantly correlated with LC. Only 2 % of patients experienced ≥G3 acute skin toxicity. Late toxicity was mild with only 1 case of G3 fibrosis. Most of the patients (95 %) had good–excellent cosmetic results. HF to the whole breast with no boost delivered to the tumor bed is a safe and effective option for a population of low-risk breast cancer patients after BCS, with excellent 5-year LC, mild toxicity profile and promising cosmetic outcome. A subgroup of patients with larger tumors and/or with no estrogen receptor expression may potentially benefit from treatment intensification with a boost dose to the lumpectomy cavity.
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