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转移性非小细胞肺癌患者免疫治疗获得性耐药的临床定义。

Clinical definition of acquired resistance to immunotherapy in patients with metastatic non-small-cell lung cancer.

机构信息

Thoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, Memorial Sloan Kettering Cancer Center, Weill Cornell Medical College, New York, USA; Druckenmiller Center for Lung Cancer Research, Memorial Sloan Kettering Cancer Center, New York, USA.

Department of Medical Oncology, Duke Cancer Institute, Duke University Medical Center, Durham, USA.

出版信息

Ann Oncol. 2021 Dec;32(12):1597-1607. doi: 10.1016/j.annonc.2021.08.2151. Epub 2021 Sep 3.

DOI:10.1016/j.annonc.2021.08.2151
PMID:34487855
Abstract

Acquired resistance (AR) to programmed cell death protein 1/programmed death-ligand 1 [PD-(L)1] blockade is frequent in non-small-cell lung cancer (NSCLC), occurring in a majority of initial responders. Patients with AR may have unique properties of persistent antitumor immunity that could be re-harnessed by investigational immunotherapies. The absence of a consistent clinical definition of AR to PD-(L)1 blockade and lack of uniform criteria for ensuing enrollment in clinical trials remains a major barrier to progress; such clinical definitions have advanced biologic and therapeutic discovery. We examine the considerations and potential controversies in developing a patient-level definition of AR in NSCLC treated with PD-(L)1 blockade. Taking into account the specifics of NSCLC biology and corresponding treatment strategies, we propose a practical, clinical definition of AR to PD-(L)1 blockade for use in clinical reports and prospective clinical trials. Patients should meet the following criteria: received treatment that includes PD-(L)1 blockade; experienced objective response on PD-(L)1 blockade (inclusion of a subset of stable disease will require future investigation); have progressive disease occurring within 6 months of last anti-PD-(L)1 antibody treatment or rechallenge with anti-PD-(L)1 antibody in patients not exposed to anti-PD-(L)1 in 6 months.

摘要

获得性抵抗(AR)程序性细胞死亡蛋白 1/程序性死亡配体 1[PD-(L)1]阻断在非小细胞肺癌(NSCLC)中很常见,发生在大多数初始反应者中。具有 AR 的患者可能具有持久的抗肿瘤免疫的独特特性,这些特性可以通过研究性免疫疗法重新利用。缺乏对 PD-(L)1 阻断的 AR 的一致临床定义以及缺乏随后纳入临床试验的统一标准仍然是进展的主要障碍;这种临床定义推动了生物学和治疗学的发现。我们检查了在接受 PD-(L)1 阻断治疗的 NSCLC 中制定 AR 患者水平定义的考虑因素和潜在争议。考虑到 NSCLC 生物学和相应治疗策略的具体情况,我们提出了一种实用的、临床定义的 AR 对 PD-(L)1 阻断,用于临床报告和前瞻性临床试验。患者应符合以下标准:接受包括 PD-(L)1 阻断在内的治疗;在 PD-(L)1 阻断中经历客观反应(包括部分稳定疾病,需要进一步研究);在最后一次抗 PD-(L)1 抗体治疗后 6 个月内或在未接触抗 PD-(L)1 的 6 个月内再次接触抗 PD-(L)1 抗体时出现疾病进展。

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