基于植入物的乳房再造术后的低分次放射治疗与常规分次放射治疗:随机临床试验。

IF 28.4 1区 医学 Q1 Biochemistry, Genetics and Molecular Biology
Julia S Wong, Hajime Uno, Angela C Tramontano, Lauren Fisher, Catherine V Pellegrini, Gregory A Abel, Harold J Burstein, Yoon S Chun, Tari A King, Deborah Schrag, Eric Winer, Jennifer R Bellon, Matthew D Cheney, Patricia Hardenbergh, Alice Ho, Kathleen C Horst, Janice N Kim, Kara-Lynne Leonard, Meena S Moran, Catherine C Park, Abram Recht, Daniel E Soto, Ron Y Shiloh, Susan F Stinson, Kurt M Snyder, Alphonse G Taghian, Laura E Warren, Jean L Wright, Rinaa S Punglia
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引用次数: 0

摘要

重要性:乳房切除术后放射治疗(PMRT)可提高局部区域疾病控制率和患者生存率。与传统分次放疗(CF)相比,低分次放疗(HF)方案的疗效和并发症发生率相当,生活质量也有所改善。然而,对乳房切除术后进行乳房重建的患者使用高频治疗的情况尚未进行前瞻性研究:目的:比较植入式乳房再造术后高频和CF PMRT的疗效:这项随机临床试验评估了 2018 年 3 月 8 日至 2021 年 11 月 3 日期间(中位数[范围]随访 40.4 [15.4-63.0] 个月)在 16 家美国癌症中心或医院接受乳腺癌(Tis、TX 或 T1-3)切除术和即刻扩张器或植入物重建术以及单侧 PMRT 的 18 岁或以上患者。分析在 2023 年 9 月至 12 月间进行:患者按 1:1 随机分配到 HF 或 CF PMRT。HF的胸壁剂量为4256 cGy,16次分割;CF的胸壁剂量为5000 cGy,25次分割。胸壁毒性反应定义为3级或以上不良事件:主要结果是开始PMRT治疗6个月后,乳腺癌治疗功能评估(FACT-B)生活质量评估工具中身体健康(PWB)领域的变化,并控制年龄。次要结果包括毒性反应和癌症复发:在400名女性患者中(CF组201人,HF组199人;年龄中位数[范围]为47[23-79]岁),330名患者在基线和6个月时均有PWB评分。研究臂之间的脉搏波速度变化没有差异(估计值,0.13;95% CI,-0.86 至 1.11;P = .80),但年龄组与研究臂之间存在显著的交互作用(交互作用的 P = .03)。如果采用高频治疗方案而非低频治疗方案,45 岁以下患者的 6 个月绝对脉搏波速度评分更高(23.6 [95% CI, 22.7-24.6] vs 22.0 [95% CI, 20.7-23.3]; P = .047),并称不良反应(高频治疗组平均[标度]为 3.0 [0.9],低频治疗组为 2.6 [1.2];P = .02)或恶心(高频治疗组平均[标度]为 3.8 [0.4],低频治疗组为 3.6 [0.8];P = .04)困扰较少。在治疗组群中,有 23 例远处复发(高频治疗组 11 例,低频治疗组 12 例)和 2 例局部区域复发(高频治疗组 1 例,低频治疗组 1 例)。39例患者(高频治疗组20例,低频治疗组19例)在中位数(IQR)为7.2(1.8-12.9)个月时出现胸壁毒性反应。多变量分析显示,分次治疗与胸壁毒性反应无关(高频治疗组:危险比为 1.02;95% CI 为 0.52-2.00;P = .95)。与 CF 方案相比,接受 HF 方案的患者中途中断治疗(5 [2.7%] vs 15 [7.7%];P = .03)或需要无薪请假(17 [8.5%] vs 34 [16.9%];P = .02)的人数较少:在这项随机临床试验中,与 CF 方案相比,HF 方案并未显著改善脉搏波速度的变化。这些数据丰富了植入式重建患者使用高频 PMRT 的经验:试验注册:ClinicalTrials.gov Identifier:试验注册:ClinicalTrials.gov Identifier:NCT03422003。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hypofractionated vs Conventionally Fractionated Postmastectomy Radiation After Implant-Based Reconstruction: A Randomized Clinical Trial.

Importance: Postmastectomy radiation therapy (PMRT) improves local-regional disease control and patient survival. Hypofractionation (HF) regimens have comparable efficacy and complication rates with improved quality of life compared with conventional fractionation (CF) schedules. However, the use of HF after mastectomy in patients undergoing breast reconstruction has not been prospectively examined.

Objective: To compare HF and CF PMRT outcomes after implant-based reconstruction.

Design, setting, and participants: This randomized clinical trial assessed patients 18 years or older undergoing mastectomy and immediate expander or implant reconstruction for breast cancer (Tis, TX, or T1-3) and unilateral PMRT from March 8, 2018, to November 3, 2021 (median [range] follow-up, 40.4 [15.4-63.0] months), at 16 US cancer centers or hospitals. Analyses were conducted between September and December 2023.

Interventions: Patients were randomized 1:1 to HF or CF PMRT. Chest wall doses were 4256 cGy for 16 fractions for HF and 5000 cGy for 25 fractions for CF. Chest wall toxic effects were defined as a grade 3 or higher adverse event.

Main outcomes and measures: The primary outcome was the change in physical well-being (PWB) domain of the Functional Assessment of Cancer Therapy-Breast (FACT-B) quality-of-life assessment tool at 6 months after starting PMRT, controlling for age. Secondary outcomes included toxic effects and cancer recurrence.

Results: Of 400 women (201 in the CF arm and 199 in the HF arm; median [range] age, 47 [23-79] years), 330 patients had PWB scores at baseline and at 6 months. There was no difference in the change in PWB between the study arms (estimate, 0.13; 95% CI, -0.86 to 1.11; P = .80), but there was a significant interaction between age group and study arm (P = .03 for interaction). Patients younger than 45 years had higher 6-month absolute PWB scores if treated with HF rather than CF regimens (23.6 [95% CI, 22.7-24.6] vs 22.0 [95% CI, 20.7-23.3]; P = .047) and reported being less bothered by adverse effects (mean [SD], 3.0 [0.9] in the HF arm and 2.6 [1.2] in the CF arm; P = .02) or nausea (mean [SD], 3.8 [0.4] in the HF arm and 3.6 [0.8] in the CF arm; P = .04). In the as-treated cohort, there were 23 distant (11 in the HF arm and 12 in the CF arm) and 2 local-regional (1 in the HF arm and 1 in the CF arm) recurrences. Chest wall toxic effects occurred in 39 patients (20 in the HF arm and 19 in the CF arm) at a median (IQR) of 7.2 (1.8-12.9) months. Fractionation was not associated with chest wall toxic effects on multivariate analysis (HF arm: hazard ratio, 1.02; 95% CI, 0.52-2.00; P = .95). Fewer patients undergoing HF vs CF regimens had a treatment break (5 [2.7%] vs 15 [7.7%]; P = .03) or required unpaid time off from work (17 [8.5%] vs 34 [16.9%]; P = .02).

Conclusions and relevance: In this randomized clinical trial, the HF regimen did not significantly improve change in PWB compared with the CF regimen. These data add to the increasing experience with HF PMRT in patients with implant-based reconstruction.

Trial registration: ClinicalTrials.gov Identifier: NCT03422003.

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来源期刊
Jama Oncology
Jama Oncology Medicine-Oncology
CiteScore
37.50
自引率
1.80%
发文量
423
期刊介绍: At JAMA Oncology, our primary goal is to contribute to the advancement of oncology research and enhance patient care. As a leading journal in the field, we strive to publish influential original research, opinions, and reviews that push the boundaries of oncology science. Our mission is to serve as the definitive resource for scientists, clinicians, and trainees in oncology globally. Through our innovative and timely scientific and educational content, we aim to provide a comprehensive understanding of cancer pathogenesis and the latest treatment advancements to our readers. We are dedicated to effectively disseminating the findings of significant clinical research, major scientific breakthroughs, actionable discoveries, and state-of-the-art treatment pathways to the oncology community. Our ultimate objective is to facilitate the translation of new knowledge into tangible clinical benefits for individuals living with and surviving cancer.
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