Perioperative Durvalumab in Gastric and Gastroesophageal Junction Cancer.

IF 96.2 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
New England Journal of Medicine Pub Date : 2025-07-17 Epub Date: 2025-06-01 DOI:10.1056/NEJMoa2503701
Yelena Y Janjigian, Salah-Eddin Al-Batran, Zev A Wainberg, Kei Muro, Daniela Molena, Eric Van Cutsem, Woo Jin Hyung, Lucjan Wyrwicz, Do-Youn Oh, Takeshi Omori, Markus Moehler, Marcelo Garrido, Sulene C S Oliveira, Moishe Liberman, Victor Castro Oliden, Elizabeth C Smyth, Alexander Stein, Mehmet Bilici, Maria Lorena Alvarenga, Vadim Kozlov, Fernando Rivera, Akihito Kawazoe, Olivier Serrano, Eric Heilbron, Alejandra Negro, John F Kurland, Josep Tabernero
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引用次数: 0

Abstract

Background: Perioperative FLOT (fluorouracil, leucovorin, oxaliplatin, and docetaxel) is a standard therapy for resectable gastric and gastroesophageal junction adenocarcinomas, but recurrence rates remain high. Immunotherapy plus chemotherapy may improve outcomes.

Methods: In a phase 3, multinational, double-blind, randomized trial, we assigned participants with resectable gastric or gastroesophageal junction adenocarcinoma, in a 1:1 ratio, to receive durvalumab at a dose of 1500 mg or placebo every 4 weeks plus FLOT for 4 cycles (2 cycles each of neoadjuvant and adjuvant therapy), followed by durvalumab or placebo every 4 weeks for 10 cycles. The primary end point was event-free survival; secondary end points included overall survival and pathological complete response.

Results: A total of 474 participants were randomly assigned to the durvalumab group, and 474 to the placebo group (median follow-up, 31.5 months; interquartile range, 26.7 to 36.6). Two-year event-free survival (Kaplan-Meier estimate) was 67.4% among the participants in the durvalumab group and 58.5% among those in the placebo group (hazard ratio for event or death, 0.71; 95% confidence interval [CI], 0.58 to 0.86; P<0.001). Two-year overall survival was 75.7% in the durvalumab group and 70.4% in the placebo group (piecewise hazard ratio for death during months 0 to 12, 0.99 [95% CI, 0.70 to 1.39], and during the period from month 12 onward, 0.67 [95% CI, 0.50 to 0.90]; P = 0.03 by a stratified log-rank test [exceeding the significance threshold of P<0.0001]). The percentage of participants with a pathological complete response was 19.2% in the durvalumab group and 7.2% in the placebo group (relative risk, 2.69 [95% CI, 1.86 to 3.90]). Adverse events with a maximum grade of 3 or 4 were reported in 340 participants (71.6%) in the durvalumab group and in 334 (71.2%) in the placebo group. The percentage of participants with delayed surgery was 10.1% and 10.8%, respectively, and the percentage with delayed initiation of adjuvant treatment was 2.3% and 4.6%.

Conclusions: Perioperative durvalumab plus FLOT led to significantly better event-free survival outcomes than FLOT alone among participants with resectable gastric or gastroesophageal junction adenocarcinoma. (Funded by AstraZeneca; MATTERHORN ClinicalTrials.gov number, NCT04592913.).

Durvalumab在胃和胃食管结癌围手术期的应用。
背景:围手术期FLOT(氟尿嘧啶、亚叶酸素、奥沙利铂和多西紫杉醇)是可切除胃和胃食管交界腺癌的标准治疗方法,但复发率仍然很高。免疫治疗加化疗可改善预后。方法:在一项3期、多国、双盲、随机试验中,我们将可切除的胃或胃食管结腺癌患者按1:1的比例分配,每4周接受1500 mg剂量的durvalumab或安慰剂或安慰剂加FLOT治疗4个周期(新辅助治疗和辅助治疗各2个周期),然后每4周接受durvalumab或安慰剂治疗,共10个周期。主要终点为无事件生存期;次要终点包括总生存期和病理完全缓解。结果:共有474名参与者被随机分配到durvalumab组,474名参与者被随机分配到安慰剂组(中位随访,31.5个月;四分位数范围为26.7至36.6)。durvalumab组两年无事件生存率(Kaplan-Meier估计)为67.4%,安慰剂组为58.5%(事件或死亡的风险比,0.71;95%置信区间[CI], 0.58 ~ 0.86;结论:在可切除的胃或胃食管交界区腺癌患者中,围手术期durvalumab联合FLOT的无事件生存结果明显优于FLOT。(阿斯利康资助;MATTERHORN ClinicalTrials.gov号码:NCT04592913)。
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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来源期刊
New England Journal of Medicine
New England Journal of Medicine 医学-医学:内科
CiteScore
145.40
自引率
0.60%
发文量
1839
审稿时长
1 months
期刊介绍: The New England Journal of Medicine (NEJM) stands as the foremost medical journal and website worldwide. With an impressive history spanning over two centuries, NEJM boasts a consistent publication of superb, peer-reviewed research and engaging clinical content. Our primary objective revolves around delivering high-caliber information and findings at the juncture of biomedical science and clinical practice. We strive to present this knowledge in formats that are not only comprehensible but also hold practical value, effectively influencing healthcare practices and ultimately enhancing patient outcomes.
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