12基因表达法放射治疗导管原位癌:一项随机临床试验。

IF 20.1 1区 医学 Q1 ONCOLOGY
Seema A Khan,Justin Romanoff,Constantine Gatsonis,Habib Rahbar,Ruth Carlos,Sunil Badve,Jean Wright,Ralph L Corsetti,Constance D Lehman,Derrick W Spell,Linda K Han,John R Bumberry,Ilana Gareen,Bradley S Snyder,Lynne I Wagner,Kathy D Miller,Christopher Comstock,Joseph A Sparano
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引用次数: 0

摘要

重要性乳腺导管原位癌(DCIS)由于其多变的自然病史,需要个性化治疗。该研究报告了12基因分子测定(DCIS评分)指导下放疗决定的第一个前瞻性肿瘤学结果。目的评估DCIS患者术前乳房磁共振成像(MRI)的手术效果,并评估局部切除(WLE)后接受基于ds的术后放疗建议的患者5年和10年同侧乳房事件(IBE)发生率。设计、环境和参与者:2015年3月至2016年4月,入选符合WLE条件的筛查检测到DCIS的女性参加了一项单臂、多中心试验,该试验在东部肿瘤合作组织-美国放射学成像网络学院的75家机构进行,并接受了术前乳房mri引导的手术治疗。对于低DS(<39)的患者建议省略放疗,对于中/高DS(≥39)的患者建议接受放疗。达到WLE作为最终治疗和DS试验成功的患者(n = 171)被纳入预先指定的分析。参与者每6个月随访一次DCIS或浸润性IBE,并分析2023年7月至11月5年IBE发生率。基于干预的术后放疗建议。5年IBE率,ci为95%。结果339名参与者的平均(SD)年龄为59.1(10.1)岁。171名女性(50.4%)接受了无手术切缘的单纯DCIS WLE,并获得了DS数据。共有159例(93.0%)遵循基于放射治疗的建议;82例低DS患者中有7例(8.5%)接受了放疗,89例中高DS患者中有5例(5.6%)拒绝了放疗。在5年(0.5-5.0)的中位(范围)随访中,171名女性中有8名经历了IBEs (4.8%; 95% CI, 2.4%-9.4%)。低DS患者(5.1%,95% CI, 1.9%-12.9%)和中高DS患者(4.5%,95% CI, 1.7%-11.7%)的IBE发生率相似。在159名坚持基于DS的放疗建议的女性中,低DS (5.5%; 95% CI, 2.1%-14.1%)和中/高DS (4.8%; 95% CI, 1.8%-12.3%)的IBE发生率相似。结论和相关性这项预先指定的临床试验分析的结果表明,与先前报道的单纯WLE后的数据相比,WLE后DS引导放射治疗DCIS的中/高DS的5年IBE率(约5%)显着降低。尽管样本量有限,但这些数据可能为中/高退行性椎体滑移患者使用放疗提供了支持,而当退行性椎体滑移较低时则可以忽略,尽管还需要进一步的验证性研究。临床试验注册号:NCT02352883。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Radiotherapy With a 12-Gene Expression Assay for Ductal Carcinoma In Situ: A Randomized Clinical Trial.
Importance Breast ductal carcinoma in situ (DCIS) requires personalized treatment given its variable natural history. This study reports the first prospective oncologic outcomes of radiotherapy decisions as guided by 12-gene molecular assay, the DCIS score (DS). Objective To assess surgical outcomes following preoperative breast magnetic resonance imaging (MRI) in women with DCIS and estimate 5-year and 10-year ipsilateral breast event (IBE) rates in participants given DS-based postoperative radiotherapy recommendations after local excision (WLE). Design, Setting, and Participants Women with screen-detected DCIS who were eligible for WLE were enrolled to a single-arm, multicenter trial conducted at 75 institutions within the Eastern Cooperative Oncology Group-American College of Radiology Imaging Network (March 2015 to April 2016) and received a preoperative breast MRI-guided surgical treatment. Those who underwent successful WLE were advised to omit radiotherapy for low DS (<39) and receive radiotherapy for intermediate/high DS (≥39). Those achieving WLE as final treatment and successful DS assay (n = 171) were included in a prespecified analysis. Participants were followed up every 6 months for DCIS or invasive IBE, and 5-year IBE rates were analyzed from July to November 2023. Intervention DS-based postoperative radiotherapy recommendations. Main Outcomes and Measures Five-year IBE rates, with 95% CIs. Results Among the 339 participants, the mean (SD) age was 59.1 (10.1) years. A total of 171 women (50.4%) received WLE for pure DCIS with free surgical margins and had DS data available. A total of 159 (93.0%) adhered to DS-based radiotherapy recommendations; 7 of 82 patients (8.5%) with a low DS underwent radiotherapy, and 5 of 89 patients (5.6%) with an intermediate/high DS declined radiotherapy. Over median (range) follow-up of 5 (0.5-5.0) years, 8 of 171 women experienced IBEs (4.8%; 95% CI, 2.4%-9.4%). IBE rates were similar for participants with a low DS(5.1%; 95% CI, 1.9%-12.9%) and participants with an intermediate/high DS (4.5%; 95% CI, 1.7%-11.7%). Among the 159 women who had adhered to DS-based radiotherapy recommendations, IBE rates were similar for participants with a low DS (5.5%; 95% CI, 2.1%-14.1%) and intermediate/high DS (4.8%; 95% CI, 1.8%-12.3%). Conclusions and Relevance The findings of this prespecified analysis of a clinical trial suggest that DS-guided radiotherapy post-WLE for DCIS shows markedly lower 5-year IBE rates (approximately 5%) for intermediate/high DS than previously reported data following WLE alone. Despite a limited sample size, these data potentially provide support for radiotherapy use in patients with intermediate/high DS, and omission when DS is low, although confirmatory studies are needed. Trial Registration ClinicalTrials.gov Identifier: NCT02352883.
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来源期刊
JAMA Oncology
JAMA Oncology Medicine-Oncology
自引率
1.80%
发文量
423
期刊介绍: JAMA Oncology is an international peer-reviewed journal that serves as the leading publication for scientists, clinicians, and trainees working in the field of oncology. It is part of the JAMA Network, a collection of peer-reviewed medical and specialty publications.
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