Benzoni Liza, Eberhardt Anaïs, Milley Sarah, Idoudi Safa, Trefcon Camille, Romain-Scelle Nicolas, Thomas Luc, Dalle Stéphane
Service de Dermatologie, Hospices Civils de Lyon, Hôpital Lyon Sud, Lyon, France.
Centre Léon Bérard, Cancer Research Center of Lyon, INSERM 1052, CNRS 5286, Université Claude Bernard Lyon 1, Université de Lyon, Lyon, France.
Cancer Med. 2025 Mar;14(6):e70432. doi: 10.1002/cam4.70432.
Programmed cell death protein-1 (PD1) antibodies are currently the standard treatment for resected high-risk melanoma, yet recurrence rate remains high.
This real-life observational study aimed to describe the outcomes of patients with resected high-risk melanoma following adjuvant anti-PD1 immunotherapy and identify factors associated with recurrence risk.
A total of 235 patients with resected stage III/IV melanoma treated with adjuvant nivolumab or pembrolizumab were included. Imaging scans and cerebral imaging were performed every 12 weeks to detect recurrences. Adverse events were collected. Univariate and multivariate analyses were performed to identify predictive factors of recurrence. Overall survival (OS) and recurrence-free survival (RFS) were estimated.
Among the 235 patients, 103 experienced at least one recurrence (43%); first recurrences were predominantly locoregional (47%). The predictive factor for recurrence identified by multivariate analysis was ulceration (RR 2,03, 95% CI [1,20; 2,86]). RFS was estimated at 75% [70-81] at 12 months and at 64% [58-71] at 24 months. RFS at 12 months was significantly lower in patients with ulcerations (RFS at 83%) compared to those without ulceration (RFS at 66%), p < 0.01. Overall survival (OS) was estimated at 91% [87%-94%] at 12 months and 84% [79%-89%] at 24 months. The OS after a first recurrence was estimated at 69% [60%-80%] at 12 months and decreased to 43% [32%-57%] at 24 months. After a first locoregional recurrence, surgery with a year of adjuvant immunotherapy (40%) was the favoured therapeutic approach. For distant recurrences, clinical trial enrolment was preferred (21%). Double curative immunotherapy was the preferred strategy for cerebral recurrences (30%).
In this cohort, nearly half of the patients underwent recurrences and RFS at 24 months was 64%. The RFS and OS data were comparable o those reported in the pivotal study Ulceration was the only significant predictive factor for recurrence, associated with decreased RFS at 24 months.
程序性细胞死亡蛋白1(PD1)抗体目前是切除的高危黑色素瘤的标准治疗方法,但复发率仍然很高。
这项真实世界观察性研究旨在描述接受辅助抗PD1免疫治疗的切除高危黑色素瘤患者的预后,并确定与复发风险相关的因素。
共纳入235例接受辅助纳武利尤单抗或帕博利珠单抗治疗的III/IV期黑色素瘤切除患者。每12周进行一次影像学扫描和脑部成像以检测复发情况。收集不良事件。进行单因素和多因素分析以确定复发的预测因素。估计总生存期(OS)和无复发生存期(RFS)。
在235例患者中,103例经历了至少一次复发(43%);首次复发主要为局部区域复发(47%)。多因素分析确定的复发预测因素是溃疡(风险比2.03,95%置信区间[1.20;2.86])。12个月时RFS估计为75%[70 - 81],24个月时为64%[58 - 71]。有溃疡的患者12个月时的RFS(83%)显著低于无溃疡的患者(66%),p < 0.01。12个月时总生存期(OS)估计为91%[87% - 94%],24个月时为84%[79% - 89%]。首次复发后的OS在12个月时估计为69%[60% - 80%],24个月时降至43%[32% - 57%]。首次局部区域复发后,采用手术加一年辅助免疫治疗(40%)是首选的治疗方法。对于远处复发,优先考虑参加临床试验(21%)。双重根治性免疫治疗是脑部复发的首选策略(30%)。
在该队列中,近一半的患者出现复发,24个月时的RFS为64%。RFS和OS数据与关键研究中报告的数据相当。溃疡是复发的唯一显著预测因素,与24个月时RFS降低相关。