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小细胞肺癌的免疫治疗方法。

Immunotherapeutic approaches for small-cell lung cancer.

机构信息

Vanderbilt-Ingram Cancer Center, Nashville, TN, USA.

West Cancer Care, Memphis, TN, USA.

出版信息

Nat Rev Clin Oncol. 2020 May;17(5):300-312. doi: 10.1038/s41571-019-0316-z. Epub 2020 Feb 13.

DOI:10.1038/s41571-019-0316-z
PMID:32055013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7212527/
Abstract

Immune-checkpoint inhibitors (ICIs) are approved in the first-line and third-line settings for patients with extensive-stage or relapsed small-cell lung cancer (SCLC), respectively. In the first-line setting, the addition of the anti-programmed cell death 1 ligand 1 (PD-L1) antibody atezolizumab to chemotherapy improves overall survival (OS). In patients with relapsed disease, data from nonrandomized trials have revealed promising responses, although a significant improvement in OS over that obtained with conventional chemotherapy was not achieved in a randomized trial in this setting. Substantial research interest exists in identifying predictive biomarkers that could guide the use of ICIs in patients with SCLC. PD-L1 expression is typically low or absent in SCLC, which has precluded its use as a predictive biomarker. Tumour mutational burden might have some predictive value, although blood-based measures of tumour mutational burden did not have predictive value in patients receiving atezolizumab plus chemotherapy in the first-line setting. After three decades, ICIs have finally enabled an improvement in OS for patients with SCLC; however, a substantial amount of research remains to be done, including identifying the optimal therapeutic strategy and predictive biomarkers. In this Review, we describe the available data on clinical efficacy, the emerging evidence regarding biomarkers and ongoing clinical trials using ICIs and other immunotherapies in patients with SCLC.

摘要

免疫检查点抑制剂(ICI)分别在广泛期或复发性小细胞肺癌(SCLC)的一线和三线治疗中得到批准。在一线治疗中,抗程序性细胞死亡配体 1(PD-L1)抗体阿替利珠单抗联合化疗可改善总生存期(OS)。在复发性疾病患者中,非随机试验的数据显示出有希望的反应,但在该治疗环境中进行的随机试验并未显示 OS 有显著改善。大量研究兴趣在于确定预测生物标志物,以指导 SCLC 患者使用 ICI。PD-L1 在 SCLC 中的表达通常较低或不存在,这使其无法作为预测生物标志物。肿瘤突变负担可能具有一定的预测价值,尽管在一线治疗中接受阿替利珠单抗联合化疗的患者中,基于血液的肿瘤突变负担测量值没有预测价值。三十年后,ICI 终于使 SCLC 患者的 OS 得到改善;然而,仍有大量研究工作要做,包括确定最佳治疗策略和预测生物标志物。在这篇综述中,我们描述了关于临床疗效的现有数据、关于生物标志物的新证据,以及正在使用 ICI 和其他免疫疗法治疗 SCLC 患者的临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dca5/7212527/a81dc25a55c1/nihms-1583851-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dca5/7212527/5adebb92ea54/nihms-1583851-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dca5/7212527/a81dc25a55c1/nihms-1583851-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dca5/7212527/5adebb92ea54/nihms-1583851-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dca5/7212527/a81dc25a55c1/nihms-1583851-f0002.jpg

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