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辅助抗 PD-1 治疗后黑色素瘤复发的性质和管理。

Nature and management of melanoma recurrences following adjuvant anti-PD-1 based therapy.

机构信息

Melanoma Institute Australia, University of Sydney, 45 Rocklands Road, Wollstonecraft, Sydney, NSW, Australia.

Department of Medical Oncology, Netherlands Cancer Institute (NKI), Plesmanlaan 121, Amsterdam, The Netherlands.

出版信息

Eur J Cancer. 2024 Nov;212:115055. doi: 10.1016/j.ejca.2024.115055. Epub 2024 Sep 29.

Abstract

INTRODUCTION

Approximately 50 % of resected stage II-IV melanoma patients develop recurrent disease by 5 years despite adjuvant anti-PD-1 therapy. Data to define best management of recurrences is lacking.

METHODS

This was a multicentre, international, retrospective cohort study. Patients with resected stage II-IV melanoma who commenced adjuvant anti-PD-1-based therapy before January 2022 and later recurred were identified. Data on demographics, disease characteristics, recurrence patterns, management and outcomes were collected.

RESULTS

711 patients from 17 sites were included. Median age was 60 [range 16-92], 64 % were male, 2 % stage II, 91 % were stage III, 7 % stage IV. Median time to recurrence was 6.2 months (0-68.5) and median follow up time from recurrence was 19.8 months (range 0.2-73.1). 63 % recurred on anti-PD-1 therapy, 36 % off therapy [3 % < 6 months, 33 % > 6 months]. Initial recurrences were locoregional (LR) alone in 44 %, distant alone (DR) in 43 %, and 11 % in both sites. LR recurrences were managed with local therapy, alone (62 %) or with "second adjuvant" anti-PD-1 (14 %) or BRAF/MEK therapy (23 %); 12 m RFS2 was 25 %, 29 % and 69 % respectively (p = 0.0045). Definitive systemic therapy at first recurrence was given in 16 % LR and 86 % DR, with best outcomes for anti-CTLA4 + anti-PD-1 and trial combinations (24 m PFS 63 % and 69 %, respectively). The 24 m OS for the entire cohort was 65 %.

CONCLUSION

Most recurrences following adjuvant anti-PD-1 based therapy occur early and while still on drug. Outcomes are poor, regardless of site, timing of recurrence, and subsequent treatment.

摘要

简介

尽管接受了辅助抗 PD-1 治疗,仍有约 50%的 II-IV 期黑色素瘤患者在 5 年内出现疾病复发。目前尚无关于复发最佳管理的相关数据。

方法

这是一项多中心、国际、回顾性队列研究。纳入了 2022 年 1 月前开始接受辅助抗 PD-1 治疗且随后复发的 II-IV 期黑色素瘤患者。收集了患者的人口统计学、疾病特征、复发模式、治疗和结局数据。

结果

共纳入了 17 个中心的 711 名患者。中位年龄为 60 岁(范围 16-92 岁),64%为男性,2%为 II 期,91%为 III 期,7%为 IV 期。中位复发时间为 6.2 个月(0-68.5 个月),从复发开始的中位随访时间为 19.8 个月(范围 0.2-73.1 个月)。63%的患者在接受抗 PD-1 治疗时复发,36%的患者在停药时复发(3%<6 个月,33%>6 个月)。最初的复发部位为局部(LR)单独复发 44%,远处(DR)单独复发 43%,LR 和 DR 同时复发 11%。LR 复发患者接受局部治疗,单独治疗(62%)或联合“二线辅助”抗 PD-1(14%)或 BRAF/MEK 治疗(23%);12 个月无复发生存率(RFS2)分别为 25%、29%和 69%(p=0.0045)。LR 和 DR 患者在首次复发时均接受了确定性全身治疗,抗 CTLA4+抗 PD-1 和试验联合治疗的最佳结果(24 个月无进展生存期(PFS)分别为 63%和 69%)。整个队列的 24 个月总生存期(OS)为 65%。

结论

辅助抗 PD-1 治疗后大多数复发发生较早,且仍在用药期间。无论复发部位、复发时间和后续治疗如何,结局均较差。

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