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接受即刻乳房重建患者的适形调强术后放射治疗:剂量学结果和急性/中期毒性评估。

Hypofractionated postmastectomy radiotherapy with helical tomotherapy in patients with immediate breast reconstruction: dosimetric results and acute/intermediate toxicity evaluation.

机构信息

Department of Medical Imaging and Radiation Sciences, European Institute of Oncology, Milan, Italy.

Department of Oncology and Hemato-oncology, University of Milan, Milan, Italy.

出版信息

Med Oncol. 2018 Feb 13;35(3):39. doi: 10.1007/s12032-018-1095-6.

Abstract

The aim of this study was to evaluate the dosimetry and toxicity of hypofractionation in postmastectomy radiotherapy (PMRT) with intensity-modulated radiotherapy (IMRT) in breast cancer (BC) patients. Stage II-III BC patients with implant-based immediate breast reconstruction received PMRT to the chest wall (CW) and to the infra/supraclavicular nodal region (NR) using a 15-fraction schedule (2.67 Gy/fraction) and helical IMRT (Tomotherapy System, Accuray Incorporated, Sunnyvale, CA). A score was assigned to each treatment plan in terms of planning target volume (PTV) coverage of CW and NR and the sparing of the organs at risk (OARs). The total score for each plan was calculated. Toxicity was prospectively assessed according to validated scales. Data from 120 consecutive patients treated in the period 2012-2015 were analysed with a median follow-up from the end of radiotherapy of 13.2 months (range 0.0-35 months). 70.8% (85/120) of the plans had high total scores as a result of an optimal coverage of both CW and RN and optimal sparing of all OARs. The maximum acute toxicity was of grade 2 in 36.7% of the cases. Early late toxicity was mild in the majority of cases. In the study population, helical tomotherapy-based IMRT produced optimal treatment plans in most cases. Acute and late toxicity was mild/moderate. Hypofractionated helical IMRT appears to be safe and feasible in the moderate term for PMRT.

摘要

本研究旨在评估乳腺癌(BC)患者保乳术后放疗(PMRT)中采用调强放疗(IMRT)的分割剂量和毒性。接受基于植入物的即刻乳房重建的 II-III 期 BC 患者,采用 15 次分割方案(2.67 Gy/次)和螺旋调强放疗(Tomotherapy System,Accuray Incorporated,Sunnyvale,CA)对胸壁(CW)和锁骨下/锁骨上区域(NR)进行 PMRT。根据 CW 和 NR 的计划靶区(PTV)覆盖范围以及危及器官(OAR)的保护情况,为每个治疗计划分配一个分数。计算每个计划的总分数。根据验证量表前瞻性评估毒性。对 2012 年至 2015 年期间治疗的 120 例连续患者的数据进行了分析,中位随访时间为放疗结束后 13.2 个月(范围 0.0-35 个月)。由于 CW 和 RN 的覆盖范围均为最佳,并且所有 OAR 均得到最佳保护,因此 70.8%(85/120)的计划总分数较高。36.7%的病例出现 2 级急性毒性。大多数病例的早期迟发性毒性较轻。在研究人群中,基于螺旋断层放疗的调强放疗在大多数情况下产生了最佳的治疗计划。急性和迟发性毒性为轻度/中度。在中度情况下,短程螺旋调强放疗用于 PMRT 似乎是安全可行的。

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