Department of Pathology and Anatomical Sciences, University of Missouri, Columbia, Missouri, USA.
Department of Surgical Pathology, M.D. Anderson, Houston, Texas, USA.
Diagn Cytopathol. 2023 Jan;51(1):51-58. doi: 10.1002/dc.25043. Epub 2022 Aug 20.
Immunotherapy based on disruption of the PD-1/PD-L1 axis is standard of care for many high stage malignancies including melanomas, non-small cell carcinomas of the lung, triple negative breast carcinomas, and squamous cell carcinomas of the head and neck. Eligibility for immunotherapy requires immunohistochemical assessment of PD-L1 expression. Currently, many high stage malignancies are diagnosed by cytology and cytologic material is the only specimen available for ancillary testing. Formal guidelines do not currently exist defining the optimal specimen type, antibody to be used or the best scoring system for cytologic material. Significant information has been published for PD-L1 testing of pulmonary specimens but much less data exists for the reproducibility, accuracy and best practices for material obtained from other body sites and types of malignancy.
We searched the PubMed data base for manuscripts relating to PD-L1 testing of cytologic specimens. The search period was between 2016 and 2022. The search terms used were PD-L1, cytology, FNA, immunotherapy, immunohistochemistry, immunocytochemistry, cytology-histology correlation. Cross referencing techniques were used to screen for the most relevant manuscripts. The abstracts of these were then reviewed for final data collection and analysis.
A total of 86 studies were identified conforming to study relevancy. These were reviewed in their entirety by two authors (LJL, TZ) for extraction of data. The majority of studies involved pulmonary specimens (79) with three relating to PD-L1 testing of head and neck cytologic specimens and one each for PD-L1 testing of cytology specimens from melanomas, pancreas, pleural fluids, and triple negative breast carcinomas. While smears could be used, most studies found cell blocks optimal for testing.
Currently, four drugs are approved for immunotherapy based on PD-L1 status. These drugs require specific antibody clones as well as scoring systems. Scoring systems and cut points vary with the type of neoplasm being treated. Cytology specimens from the lung, head and neck and melanomas can all be used for PD-L1 testing with good agreement with corresponding histology specimens.
基于 PD-1/PD-L1 轴阻断的免疫疗法是许多晚期恶性肿瘤的标准治疗方法,包括黑色素瘤、非小细胞肺癌、三阴性乳腺癌和头颈部鳞状细胞癌。免疫治疗的资格需要进行 PD-L1 表达的免疫组织化学评估。目前,许多晚期恶性肿瘤是通过细胞学诊断的,而细胞学标本是唯一可用于辅助检测的标本。目前尚无明确的正式指南定义最佳的标本类型、使用的抗体或细胞学标本的最佳评分系统。已经发表了大量关于肺标本 PD-L1 检测的重要信息,但关于从其他部位和类型的恶性肿瘤获得的材料的可重复性、准确性和最佳实践的数据要少得多。
我们在 PubMed 数据库中搜索了与细胞学标本 PD-L1 检测相关的文献。搜索时间为 2016 年至 2022 年。使用的搜索词为 PD-L1、细胞学、细针抽吸术、免疫疗法、免疫组织化学、免疫细胞化学、细胞学-组织学相关性。使用交叉参考技术筛选出最相关的文献。然后对这些文献的摘要进行了回顾,以最终收集和分析数据。
共确定了 86 项符合研究相关性的研究。由两位作者(LJL、TZ)对这些研究进行了全面审查,以提取数据。大多数研究涉及肺标本(79 项),其中 3 项涉及头颈部细胞学标本的 PD-L1 检测,1 项涉及黑色素瘤、胰腺、胸腔积液和三阴性乳腺癌的细胞学标本的 PD-L1 检测。虽然可以使用涂片,但大多数研究发现细胞块更适合检测。
目前,有四种药物基于 PD-L1 状态被批准用于免疫治疗。这些药物需要特定的抗体克隆和评分系统。评分系统和截断值因所治疗的肿瘤类型而异。来自肺、头颈部和黑色素瘤的细胞学标本均可用于 PD-L1 检测,与相应的组织学标本具有良好的一致性。