报告妇科起源癌患者标本的生物标志物检测结果:更新的美国病理学家学会协议。

IF 3.2
Gulisa Turashvili, Anthony N Karnezis, Keren I Hulkower, Colleen Hebert, Lara Harik, Barbara Crothers, Giovanna Giannico, Kristin K Deeb, Krisztina Hanley, Raji Ganesan, Anne Mills, Natalia Buza
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引用次数: 0

摘要

上下文。-:第一版《妇科源性癌患者标本生物标志物检测结果报告模板》(以下简称《妇科生物标志物方案》)由美国病理学家学会(CAP)于2022年发布。较小的更新包括澄清p53状态的内容,以及2023年人类表皮生长因子受体2 (HER2)和错配修复测试的解释性说明。生物标志物检测的最新发展促使该方案进行了重大更新,于2024年12月发布。-:自2023年妇科生物标志物协议发布以来,评估预后和/或治疗标志物,并更新妇科癌的检测建议,本文提供了扩展的解释性说明和说明性示例。-:美国临床肿瘤学会(CAP)癌症委员会组建了一个妇科病理学专家小组,以增加现有的生物标志物,增加新的生物标志物,扩大检测报告,并根据现有证据和临床实践指南(如美国临床肿瘤学会/CAP、国家综合癌症网络和癌症免疫治疗学会的指南)修改解释性说明。-:对妇科生物标志物方案的修改包括更新激素受体和增加错配修复蛋白亚克隆缺失、亚克隆异常p53表达、程序性死亡配体-1 (PD-L1)测试和叶酸受体α测试,以及更新HER2测试和所有解释性说明。-:更新后的CAP妇科生物标志物协议在预后和/或治疗性生物标志物的报告中提供了改进的结构和清晰度,并提供了全面的解释性说明,有助于理解基于当前护理标准的测试理由、解释性指导和常见测试陷阱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reporting Results of Biomarker Testing of Specimens From Patients With Carcinoma of Gynecologic Origin: The Updated College of American Pathologists Protocol.

Context.—: The first version of the Template for Reporting Results of Biomarker Testing of Specimens From Patients With Carcinoma of Gynecologic Origin (hereafter referred to as the Gynecologic Biomarker Protocol) was released by the College of American Pathologists (CAP) in 2022. Minor updates included clarification of the content of p53 status and explanatory notes for human epidermal growth factor receptor 2 (HER2) and mismatch repair testing in 2023. Recent developments in biomarker testing have prompted a major update to this protocol, published in December 2024.

Objective.—: To assess prognostic and/or therapeutic markers since the release of the 2023 Gynecologic Biomarker Protocol and to update testing recommendations in gynecologic carcinomas, with expanded explanatory notes and illustrative examples provided in this article.

Design.—: The CAP Cancer Committee assembled a panel of experts subspecialized in gynecologic pathology to augment the existing biomarkers, add new biomarkers, expand test reporting, and revise explanatory notes based on available evidence and clinical practice guidelines such as those of the American Society of Clinical Oncology/CAP, National Comprehensive Cancer Network, and Society for Immunotherapy of Cancer.

Results.—: The changes to the Gynecologic Biomarker Protocol include updates to hormone receptors and addition of subclonal loss of mismatch repair proteins, subclonal abnormal p53 expression, programmed death ligand-1 (PD-L1) testing, and folate receptor alpha testing, as well as updates to HER2 testing and all explanatory notes.

Conclusions.—: The updated CAP Gynecologic Biomarker Protocol provides improved structure and clarity in the reporting of prognostic and/or therapeutic biomarkers and comprehensive explanatory notes that aid in understanding the rationale for testing, interpretive guidance, and common testing pitfalls, based on the current standard of care.

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