Adjuvant nivolumab and relatlimab in stage III/IV melanoma: the randomized phase 3 RELATIVITY-098 trial.

IF 50 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Georgina V Long, Charlie Garnett-Benson, Sonia Dolfi, Paolo A Ascierto, Jun Guo, Ahmad A Tarhini, Sunandana Chandra, Eva Muñoz-Couselo, Michele Del Vecchio, Andreia Cristina de Melo, Margaret Callahan, Helen Gogas, Reinhard Dummer, Dirk Schadendorf, Peter Koelblinger, Gaelle Quereux, Ioannis Thomas, Jia Xin Yu, Andrew Fisher, Bonnie Wang, Patrick Djidel, Armand Chouzy, Mark Semaan, Bohang Chen, Alicia M Y Cheong, Hussein A Tawbi
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引用次数: 0

Abstract

Based on RELATIVITY-047, nivolumab plus relatlimab is approved for advanced melanoma. Here, to address a current unmet need for more efficacious adjuvant regimens for completely resected melanoma, the phase 3, double-blind RELATIVITY-098 trial compared adjuvant nivolumab plus relatlimab to nivolumab after complete resection of stage III/IV melanoma. Patients were randomized 1:1 to receive nivolumab 480 mg plus relatlimab 160 mg (n = 547) or nivolumab 480 mg (n = 546) intravenously every 4 weeks for ≤1 year; safety populations totaled 543 and 545 patients, respectively. The primary endpoint was recurrence-free survival (RFS), and the key secondary was overall survival; translational endpoints were exploratory. There was no difference in RFS for nivolumab plus relatlimab versus nivolumab (hazard ratio = 1.01; 95% confidence interval: 0.83-1.22; P = 0.928); therefore, overall survival was not tested. Translational data across trials showed lower circulating LAG-3+ T cells in the adjuvant setting (RELATIVITY-098) versus advanced melanoma (RELATIVITY-047), where LAG-3+ T cells were enriched in tumor versus blood. The absence of macroscopic tumor and reduced peripheral LAG-3+ T cells may explain the lack of added benefit of nivolumab plus relatlimab over nivolumab in resected versus metastatic melanoma. ClinicalTrials.gov identifier: NCT05002569 .

nivolumab和relatlimumab辅助治疗III/IV期黑色素瘤:随机3期RELATIVITY-098试验
基于RELATIVITY-047, nivolumab + relatlimab被批准用于晚期黑色素瘤。在这里,为了解决目前对完全切除黑色素瘤更有效的辅助方案的未满足需求,3期双盲RELATIVITY-098试验比较了III/IV期黑色素瘤完全切除后辅助nivolumab加relatlimumab和nivolumab。患者按1:1随机分组,接受纳武单抗480 mg加相对单抗160 mg (n = 547)或纳武单抗480 mg (n = 546)静脉注射,每4周一次,持续≤1年;安全人群分别为543例和545例。主要终点是无复发生存期(RFS),次要终点是总生存期;翻译终点是探索性的。纳武单抗联合相对单抗与纳武单抗的RFS无差异(风险比= 1.01;95%可信区间:0.83-1.22;P = 0.928);因此,未检测总生存率。跨试验的转化数据显示,在辅助治疗组(RELATIVITY-098)中,LAG-3+ T细胞循环较低,而在晚期黑色素瘤组(RELATIVITY-047)中,LAG-3+ T细胞在肿瘤中富集,而在血液中富集。宏观肿瘤的缺失和周围LAG-3+ T细胞的减少可能解释了在切除黑色素瘤和转移性黑色素瘤中,纳武单抗加相对单抗缺乏额外的益处。ClinicalTrials.gov识别码:NCT05002569。
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
Nature Medicine
Nature Medicine 医学-生化与分子生物学
CiteScore
100.90
自引率
0.70%
发文量
525
审稿时长
1 months
期刊介绍: Nature Medicine is a monthly journal publishing original peer-reviewed research in all areas of medicine. The publication focuses on originality, timeliness, interdisciplinary interest, and the impact on improving human health. In addition to research articles, Nature Medicine also publishes commissioned content such as News, Reviews, and Perspectives. This content aims to provide context for the latest advances in translational and clinical research, reaching a wide audience of M.D. and Ph.D. readers. All editorial decisions for the journal are made by a team of full-time professional editors. Nature Medicine consider all types of clinical research, including: -Case-reports and small case series -Clinical trials, whether phase 1, 2, 3 or 4 -Observational studies -Meta-analyses -Biomarker studies -Public and global health studies Nature Medicine is also committed to facilitating communication between translational and clinical researchers. As such, we consider “hybrid” studies with preclinical and translational findings reported alongside data from clinical studies.
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