梅克尔细胞癌免疫抑制患者的免疫疗法反应:对 183 名患者的分析。

BMJ oncology Pub Date : 2025-03-06 eCollection Date: 2025-01-01 DOI:10.1136/bmjonc-2024-000654
Emily Gong, Lauren Zawacki, Xinyi Fan, Daniel S Hippe, Ankita A Menon, Allison J Remington, Kristina Lachance, Tomoko Akaike, Lisa Tachiki, Song Y Park, Paul Nghiem
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引用次数: 0

摘要

目的:梅克尔细胞癌(MCC)是一种侵袭性皮肤癌,免疫抑制患者的预后较差。免疫检查点抑制剂(ICIs)在免疫功能正常的 MCC 患者中可获得约 60% 的应答率,但由于被排除在试验之外,其在免疫抑制患者中的疗效仍不明确。本研究比较了 ICI 的疗效、安全性以及免疫抑制亚型对这些群体的影响:这项回顾性研究分析了西雅图数据储存库中183名一线使用ICI的晚期MCC患者。其中,147 例免疫功能正常,36 例免疫抑制(慢性淋巴细胞白血病 (CLL) 10 例,自身免疫性疾病 10 例,其他血液恶性肿瘤 9 例,实体器官移植 4 例,艾滋病毒/艾滋病 3 例)。结果包括客观反应率、疾病进展、MCC特异性和总生存概率,并根据开始使用ICI时的年龄、性别和分期进行了调整:结果:免疫抑制患者6个月的初始ICI反应率为50%,免疫功能正常患者为61.5%(HR=0.71,P=0.17)。免疫抑制患者的疾病进展风险更高(2年:53.9% vs 42.1%,HR=1.65,P=0.05),MCC特异性死亡率更高(2年:38.7% vs 24.4%,HR=1.85,P=0.04)。CLL患者(10人)的应答率特别低(应答率:20.0% vs 61.5%,HR=0.18,P=0.02),进展风险高(2年:80.0% vs 42.1%,HR=4.09,P=0.01)。免疫抑制患者面临更高的 ICI 毒性(6 个月风险:51.6% vs 36.6%,HR=1.79,P=0.03):尽管与免疫功能正常的患者相比,免疫抑制MCC患者的应答率较低,病情进展风险较高,但ICIs仍能为他们带来切实的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Immunotherapy response in immunosuppressed patients with Merkel cell carcinoma: analysis of 183 patients.

Immunotherapy response in immunosuppressed patients with Merkel cell carcinoma: analysis of 183 patients.

Immunotherapy response in immunosuppressed patients with Merkel cell carcinoma: analysis of 183 patients.

Immunotherapy response in immunosuppressed patients with Merkel cell carcinoma: analysis of 183 patients.

Objective: Merkel cell carcinoma (MCC) is an aggressive skin cancer with poor outcomes in immunosuppressed patients. While immune checkpoint inhibitors (ICIs) achieve ~60% response rates in immunocompetent MCC patients, their efficacy in immunosuppressed patients remains unclear due to exclusion from trials. This study compares ICI outcomes, safety and the impact of immunosuppression subtypes between these groups.

Methods and analysis: This retrospective study analysed 183 advanced MCC patients on first-line ICIs from a Seattle-based data repository. Of these, 147 were immunocompetent, and 36 were immunosuppressed (chronic lymphocytic leukaemia (CLL) n=10, autoimmune disorders n=10, other haematologic malignancies n=9, solid organ transplants n=4 and HIV/AIDS n=3). Outcomes included objective response rate, disease progression, MCC-specific and overall survival probability, adjusted for age, sex and stage at ICI initiation.

Results: Initial ICI response rates at 6 months were 50% in immunosuppressed and 61.5% in immunocompetent patients (HR=0.71, p=0.17). Immunosuppressed patients had higher risks of disease progression (2 years: 53.9% vs 42.1%, HR=1.65, p=0.05) and MCC-specific mortality (2 years: 38.7% vs 24.4%, HR=1.85, p=0.04). CLL patients (n=10) had a particularly low response rate (response rate: 20.0% vs 61.5%, HR=0.18, p=0.02) and high progression risk (2 years: 80.0% vs 42.1%, HR=4.09, p=0.01). Immunosuppressed patients faced higher rates of ICI toxicity (6-month risk: 51.6% vs 36.6%, HR=1.79, p=0.03).

Conclusions: ICIs provide meaningful benefits to immunosuppressed MCC patients, though their response rates are lower, and progression risk is higher compared with immunocompetent patients.

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