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用于 PD-(L)1 轴抑制的生物标志物开发:SITC 生物标志物委员会的共识观点。

Biomarker development for PD-(L)1 axis inhibition: a consensus view from the SITC Biomarkers Committee.

机构信息

Lady Davis Institute for Medical Research, Montreal, Québec, Canada.

Gilead Sciences, Seattle, Washington, USA.

出版信息

J Immunother Cancer. 2024 Jul 20;12(7):e009427. doi: 10.1136/jitc-2024-009427.

Abstract

Therapies targeting the programmed cell death protein-1/programmed death-ligand 1 (PD-L1) (abbreviated as PD-(L)1) axis are a significant advancement in the treatment of many tumor types. However, many patients receiving these agents fail to respond or have an initial response followed by cancer progression. For these patients, while subsequent immunotherapies that either target a different axis of immune biology or non-immune combination therapies are reasonable treatment options, the lack of predictive biomarkers to follow-on agents is impeding progress in the field. This review summarizes the current knowledge of mechanisms driving resistance to PD-(L)1 therapies, the state of biomarker development along this axis, and inherent challenges in future biomarker development for these immunotherapies. Innovation in the development and application of novel biomarkers and patient selection strategies for PD-(L)1 agents is required to accelerate the delivery of effective treatments to the patients most likely to respond.

摘要

针对程序性死亡蛋白-1/程序性死亡配体 1(PD-L1)(简称 PD-(L)1)轴的治疗方法是治疗多种肿瘤类型的重大进展。然而,许多接受这些药物的患者没有反应或有初始反应后癌症进展。对于这些患者,虽然后续的免疫疗法靶向不同的免疫生物学轴或非免疫联合疗法是合理的治疗选择,但缺乏后续药物的预测生物标志物正在阻碍该领域的进展。这篇综述总结了导致对 PD-(L)1 治疗产生耐药性的机制的现有知识,以及该轴上生物标志物开发的现状,以及这些免疫疗法未来生物标志物开发所固有的挑战。需要创新开发和应用新型生物标志物和 PD-(L)1 药物的患者选择策略,以加快将有效治疗方法提供给最有可能产生反应的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c39/11261685/7d1ec499acea/jitc-12-7-g001.jpg

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