Induction versus Concurrent Chemotherapy for Advanced Nasopharyngeal Carcinoma.

NEJM evidence Pub Date : 2025-05-01 Epub Date: 2025-04-22 DOI:10.1056/EVIDoa2400214
Pei-Yu Huang, Xu-Yin Chen, Xi Ding, Ling Guo, Hao-Yuan Mo, Xiong Zou, Chong-Yang Duan, Li Ling, Rui You, Xin Yang, You-Ping Liu, Yu-Long Xie, Yi-Nuan Zhang, Jing-Yu Cao, Si-Han Liu, Zi-Meng Wang, Qi Yang, Chao Lin, Si-Yuan Chen, Yan-Feng Ouyang, Yong-Long Liu, Kai Wen, Xiao-Tong Duan, Rou Jiang, Rong-Zeng Liu, Tao Yu, Fang Qiu, Yi-Jun Hua, Ka-Jia Cao, Dong-Hua Luo, Ming-Yuan Chen
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引用次数: 0

Abstract

Background: Cisplatin-based concurrent chemoradiotherapy (CCRT) is the mainstay treatment for locoregionally advanced nasopharyngeal carcinoma (LA-NPC), which usually leads to intolerable toxicities. We investigated whether or not induction chemotherapy (IC) plus intensity-modulated radiation therapy (IMRT) could replace CCRT.

Methods: This is an open-label, phase 3, noninferiority trial. Patients with stage T1-4N2-3 or T3-4N0-1 LA-NPC were randomly assigned (1:1) to receive gemcitabine (1000 mg/m2) and cisplatin (80 mg/m2) for two cycles followed by IMRT, or IMRT plus concomitant weekly cisplatin (40 mg/m2) for up to seven cycles. Two-year failure-free survival (FFS) was the primary end point, and noninferiority was confirmed by an upper limit of the 95% confidence interval (CI) for a hazard ratio of less than 2.12 (absolute margin of -10 percentage points). Secondary end points include overall survival, locoregional recurrence-free survival, distant metastasis-free survival, toxicity profile, and quality of life (QoL).

Results: We enrolled 124 patients in the IC group and 125 patients in the CCRT group. The median follow-up was 60 months. Two-year FFS was 90.2% for IC versus 86.3% for CCRT, with a hazard ratio of 0.636 (95% CI, 0.267 to 1.514) and an absolute difference of 3.9 percentage points (95% CI, -5.2 to 13.0). Compared with the CCRT group, fewer grade ≥3 adverse events occurred in the IC group (47.5% vs. 61.5%; P=0.029), including leukopenia, anemia, mucositis, nausea, and dysphagia. IC was associated with better QoL, including global health status, social and cognitive functioning, fatigue, nausea and vomiting, pain, appetite loss, and constipation.

Conclusions: For 2-year FFS for LA-NPC, gemcitabine and cisplatin IC plus IMRT alone was noninferior to CCRT. (Funded by Key-Area Research and Development of Guangdong Province and others.).

晚期鼻咽癌诱导与同步化疗。
背景:以顺铂为基础的同步放化疗(CCRT)是局部晚期鼻咽癌(LA-NPC)的主要治疗方法,通常导致无法忍受的毒性。我们研究了诱导化疗(IC)加调强放疗(IMRT)是否可以取代CCRT。方法:这是一项开放标签、3期、非劣效性试验。T1-4N2-3或T3-4N0-1期LA-NPC患者被随机分配(1:1)接受吉西他滨(1000mg /m2)和顺铂(80mg /m2)两个周期,随后接受IMRT,或IMRT加每周顺铂(40mg /m2)长达7个周期。2年无故障生存(FFS)是主要终点,非劣效性通过95%置信区间(CI)上限确认,风险比小于2.12(绝对差为-10个百分点)。次要终点包括总生存期、局部无复发生存期、远处无转移生存期、毒性概况和生活质量(QoL)。结果:我们纳入了124例IC组患者和125例CCRT组患者。中位随访时间为60个月。IC的两年FFS为90.2%,而CCRT为86.3%,风险比为0.636 (95% CI, 0.267至1.514),绝对差异为3.9个百分点(95% CI, -5.2至13.0)。与CCRT组相比,IC组发生≥3级不良事件较少(47.5% vs 61.5%;P=0.029),包括白细胞减少、贫血、粘膜炎、恶心和吞咽困难。IC与更好的生活质量相关,包括整体健康状况、社会和认知功能、疲劳、恶心和呕吐、疼痛、食欲减退和便秘。结论:对于LA-NPC的2年FFS,吉西他滨和顺铂IC联合IMRT不逊色于CCRT。(广东省重点领域研究与开发等资助项目)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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