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腔道胃肠道恶性肿瘤中的免疫检查点抑制剂:超越微卫星高度不稳定/错配修复缺陷、肿瘤突变负荷和程序性死亡配体1

Immune checkpoint inhibitors in luminal gastrointestinal malignancies: going beyond MSI-H/dMMR, TMB and PD-L1.

作者信息

Lefler Daniel S, Snook Adam E, Bashir Babar

机构信息

Department of Medical Oncology, Sidney Kimmel Cancer Center, Thomas Jefferson University Hospital, Philadelphia, PA 19107, USA.

Department of Pharmacology & Experimental Therapeutics, Thomas Jefferson University, Philadelphia, PA 19107, USA.

出版信息

Immunotherapy. 2022 Aug;14(11):885-902. doi: 10.2217/imt-2022-0012. Epub 2022 Jun 13.

DOI:10.2217/imt-2022-0012
PMID:35694998
Abstract

In luminal gastrointestinal tumors, immune checkpoint inhibitors (ICIs) targeting PD-1, PD-L1 and CTLA-4 have been investigated in multiple settings. The indications for these drugs are primarily dependent on specific biomarkers that imply immunogenicity: overexpression of PD-L1, tumor mutational burden, loss of mismatch repair proteins (dMMR) and/or high microsatellite instability status. Although these markers can be both predictive and prognostic, there is variability in how they are measured and used to guide therapies. Moreover, the use of ICIs can be further refined with a better understanding of the tumor microenvironment and interactions with other available therapies. The purpose of this review is to characterize luminal gastrointestinal tumors' responses to ICIs considering known predictive biomarkers and discuss emerging therapeutic approaches using ICIs.

摘要

在腔内胃肠道肿瘤中,针对程序性死亡受体1(PD-1)、程序性死亡配体1(PD-L1)和细胞毒性T淋巴细胞相关蛋白4(CTLA-4)的免疫检查点抑制剂(ICIs)已在多种情况下进行了研究。这些药物的适应症主要取决于暗示免疫原性的特定生物标志物:PD-L1的过表达、肿瘤突变负荷、错配修复蛋白缺失(dMMR)和/或高微卫星不稳定状态。尽管这些标志物具有预测性和预后性,但在测量方法和用于指导治疗的方式上存在差异。此外,通过更好地了解肿瘤微环境以及与其他可用疗法的相互作用,ICIs的使用可以进一步优化。本综述的目的是考虑已知的预测性生物标志物来描述腔内胃肠道肿瘤对ICIs的反应,并讨论使用ICIs的新兴治疗方法。

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