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细胞学样本中的程序性死亡受体配体1:综述与实用方法

PD-L1 in Cytological Samples: A Review and a Practical Approach.

作者信息

Tejerina Eva, Garca Tobar Laura, Echeveste Jos I, de Andrea Carlos E, Vigliar Elena, Lozano Mara D

机构信息

Department of Pathology, Hospital Universitario Puerta de Hierro, Madrid, Spain.

Department of Pathology, Clinica University of Navarra, Pamplona, Spain.

出版信息

Front Med (Lausanne). 2021 May 7;8:668612. doi: 10.3389/fmed.2021.668612. eCollection 2021.

DOI:10.3389/fmed.2021.668612
PMID:34026795
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8139418/
Abstract

With a growing number of predictive biomarkers needed to manage patients with non-small cell lung cancer (NSCLC), there has been a paradigm shift in care and handling of diagnostic samples. Among the various testing methods, immunohistochemistry (IHC) is the most cost- effective and widely available. Furthermore, over the past decade immunotherapy has emerged as one of the most promising cancer treatments. In this scenario IHC is the most used testing method available for PDL-1/PD1 immunotherapy. Several monoclonal antibodies targeting programmed death 1 (PD-1)/programmed death ligand-1 (PD-L1) pathways have been integrated into standard-of-care treatments of a wide range of cancer types, once provided evidence of PD-L1 expression in tumor cells by immunohistochemistry (IHC). Since currently available PD-L1 assays have been developed on formalin-fixed paraffin embedded (FFPE) histological specimens, a growing body of research is being dedicated to confirm the feasibility of applying PDL-1 assays also to cytological samples. Albeit promising results have been reported, several important issues still need to be addressed. Among these are the type of cytological samples, pre-analytical issues, cyto-histological correlation, and inter-observer agreement. This review briefly summarizes the knowledge of the role of cytopathology in the analysis of PD-L1 by immunocytochemistry (ICC) and future directions of cytopathology in the immunotherapy setting.

摘要

随着管理非小细胞肺癌(NSCLC)患者所需的预测性生物标志物数量不断增加,诊断样本的处理和管理模式发生了转变。在各种检测方法中,免疫组织化学(IHC)是最具成本效益且应用最广泛的。此外,在过去十年中,免疫疗法已成为最有前景的癌症治疗方法之一。在这种情况下,IHC是可用于PDL-1/PD1免疫疗法的最常用检测方法。一旦通过免疫组织化学(IHC)在肿瘤细胞中证实了PD-L1表达,几种靶向程序性死亡1(PD-1)/程序性死亡配体-1(PD-L1)途径的单克隆抗体已被纳入多种癌症类型的标准治疗方案中。由于目前可用的PD-L1检测方法是基于福尔马林固定石蜡包埋(FFPE)组织学标本开发的,越来越多的研究致力于证实将PD-L1检测方法应用于细胞学样本的可行性。尽管已报道了一些有前景的结果,但仍有几个重要问题需要解决。其中包括细胞学样本的类型、分析前问题、细胞-组织学相关性以及观察者间的一致性。本综述简要总结了细胞病理学在通过免疫细胞化学(ICC)分析PD-L1中的作用的相关知识以及细胞病理学在免疫治疗环境中的未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0735/8139418/d813ab7713ed/fmed-08-668612-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0735/8139418/d813ab7713ed/fmed-08-668612-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0735/8139418/d813ab7713ed/fmed-08-668612-g0001.jpg

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