术后放疗±西妥昔单抗治疗中危头颈癌。

IF 42.1 1区 医学 Q1 ONCOLOGY
Journal of Clinical Oncology Pub Date : 2025-04-20 Epub Date: 2025-01-22 DOI:10.1200/JCO-24-01829
Mitchell Machtay, Pedro A Torres-Saavedra, Wade Thorstad, Phuc Felix Nguyen-Tân, Lillian L Siu, F Christopher Holsinger, Adel El-Naggar, Christine Chung, Anthony Cmelak, Barbara Burtness, Greg Bednarz, Harry Quon, Stephen L Breen, Clement K Gwede, Adam P Dicker, Min Yao, Richard C Jordan, Jennifer Dorth, Nancy Lee, Jason W Chan, Neal Dunlap, Voichita Bar-Ad, William A Stokes, Arnab Chakravarti, David Sher, Shyam Rao, Jonathan Harris, Sue S Yom, Quynh-Thu Le
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引用次数: 0

摘要

目的:放疗(RT)/西妥昔单抗(C)治疗局部晚期鳞状头颈癌优于单纯放疗。我们在完全切除的中等风险癌症中进行了测试。方法:口腔、口咽或喉部的头颈部鳞状细胞癌(SCCHN)患者,有一个或多个危险因素需要术后放疗。患者随机按1:1分配到强度调节放疗(60-66 Gy),每周一次C或单独RT。主要假设是RT + C可以提高随机分配/符合条件的患者的总生存期(OS),并有预先指定的次要计划在人乳头瘤病毒(HPV)阴性亚群中进行测试。无病生存期(DFS)和毒性是次要终点。OS和DFS采用分层log-rank检验;通过Fisher的精确试验比较毒性。结果:2009年11月至2018年3月,我们入组了702例患者;577人被随机分配/符合条件。绝大多数(63.6%)为口腔癌,绝大多数(84.6%)表皮生长因子受体高表达。死亡人数(184人)低于预期。OS(中位随访7.2年)无显著改善(风险比[HR], 0.81;单侧P = .0747;5年OS 76.5% v 68.7%),但DFS为(HR, 0.75;单侧P = 0.0168;5年DFS 71.7% vs 63.6%)。RT + C的获益仅见于hpv阴性亚群(试验中80.2%的患者)。3-4级急性毒性率分别为70.3% (RT + C)和39.7% (RT;双侧P < 0.0001),主要是皮肤和/或粘膜作用。晚期≥3级毒性率分别为33.2% (RT + C)和29.0% (RT;双侧P = .3101)。两组均无5级毒性反应。结论:对于切除的中危SCCHN,与单独放疗相比,RT + C显著改善了DFS,但没有改善OS,长期毒性没有增加。对于精心挑选的hpv阴性患者,RT + C是一种合适的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Postoperative Radiotherapy ± Cetuximab for Intermediate-Risk Head and Neck Cancer.

Purpose: Radiotherapy (RT)/cetuximab (C) demonstrated superiority over RT alone for locally advanced squamous head and neck cancer. We tested this in completely resected, intermediate-risk cancer.

Methods: Patients had squamous cell carcinoma of the head and neck (SCCHN) of the oral cavity, oropharynx, or larynx, with one or more risk factors warranting postoperative RT. Patients were randomly assigned 1:1 to intensity-modulated RT (60-66 Gy) with once-per-week C or RT alone. The primary hypothesis was that RT + C would improve overall survival (OS) in randomly assigned/eligible patients, with a prespecified secondary plan to test this in the human papillomavirus (HPV)-negative subpopulation. Disease-free survival (DFS) and toxicity were secondary end points. OS and DFS were tested via stratified log-rank test; toxicity was compared via Fisher's exact test.

Results: We enrolled 702 patients from November 2009 to March 2018; 577 were randomly assigned/eligible. Most (63.6%) had oral cavity cancer and most (84.6%) had high epidermal growth factor receptor expression. There were fewer deaths (184) than expected. OS (median follow up, 7.2 years) was not significantly improved (hazard ratio [HR], 0.81; one-sided P = .0747; 5-year OS 76.5% v 68.7%), but DFS was (HR, 0.75; one-sided P = .0168; 5-year DFS 71.7% v 63.6%). Benefit of RT + C was only seen in the HPV-negative subpopulation (80.2% of patients in the trial). Grade 3-4 acute toxicity rates were 70.3% (RT + C) versus 39.7% (RT; two-sided P < .0001), mostly skin and/or mucosal effects. Late grade ≥3 toxicity rate was 33.2% (RT + C) versus 29.0% (RT; two-sided P = .3101). There were no grade 5 toxicities in either arm.

Conclusion: RT + C significantly improved DFS, but not OS, with no increase in long-term toxicity, compared with RT alone for resected, intermediate-risk SCCHN. RT + C is an appropriate option for carefully selected patients with HPV-negative disease.

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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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