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肺癌细胞学样本的ALK和ROS1检测:观点

ALK and ROS1 testing on lung cancer cytologic samples: Perspectives.

作者信息

Pisapia Pasquale, Lozano Maria D, Vigliar Elena, Bellevicine Claudio, Pepe Francesco, Malapelle Umberto, Troncone Giancarlo

机构信息

Department of Public Health, University of Naples Federico II, Naples, Italy.

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

出版信息

Cancer Cytopathol. 2017 Nov;125(11):817-830. doi: 10.1002/cncy.21899. Epub 2017 Jul 25.

Abstract

Cytologic sampling is the mainstay of diagnosing advanced lung cancer. Moreover, to select patients for personalized first-line or second-line treatment, epidermal growth factor receptor (EGFR) mutations and anaplastic lymphoma kinase (ALK) and c-ros oncogene 1 (ROS1) rearrangements are tested on cytologic preparations. Commercially available fluorescence in situ hybridization (FISH) and immunocytochemistry (ICC) assays have primarily been used for the identification of cells harboring ALK or ROS1 gene fusions on histologic rather than cytologic preparations. However, it is now recognized that FISH and ICC also can be applied on cytologic samples provided the cytopathologist is aware that FISH and ICC results are not always concordant and that the performance of ICC largely depends on antibody clones, signal detection systems, and scoring systems. Notably, the routine clinical use of FISH and ICC may be replaced by emerging next-generation sequencing and digital, color-coded barcode technologies, which have the advantage of simultaneously evaluating ALK, ROS1, and EGFR alterations in a single analysis. Although their use in clinical cytologic practice remains to be fully established, it is conceivable that this technology will replace both FISH and ICC analyses in future diagnostic algorithms. Here, the authors review studies devoted to testing ALK and ROS1 on cytology specimens in an attempt to provide an update for the cytopathologist regarding current and evolving practice. Cancer Cytopathol 2017;125:817-30. © 2017 American Cancer Society.

摘要

细胞学采样是诊断晚期肺癌的主要方法。此外,为了选择适合个性化一线或二线治疗的患者,需要在细胞学标本上检测表皮生长因子受体(EGFR)突变以及间变性淋巴瘤激酶(ALK)和c-ros癌基因1(ROS1)重排。市售的荧光原位杂交(FISH)和免疫细胞化学(ICC)检测主要用于在组织学而非细胞学标本上鉴定携带ALK或ROS1基因融合的细胞。然而,现在人们认识到,如果细胞病理学家意识到FISH和ICC结果并不总是一致,并且ICC的性能很大程度上取决于抗体克隆、信号检测系统和评分系统,那么FISH和ICC也可以应用于细胞学样本。值得注意的是,FISH和ICC的常规临床应用可能会被新兴的下一代测序和数字、彩色编码条形码技术所取代,这些技术具有在单次分析中同时评估ALK、ROS1和EGFR改变的优势。尽管它们在临床细胞学实践中的应用仍有待充分确立,但可以想象,这项技术将在未来的诊断算法中取代FISH和ICC分析。在此,作者回顾了致力于在细胞学标本上检测ALK和ROS1的研究,试图为细胞病理学家提供有关当前和不断发展的实践的最新信息。《癌症细胞病理学》2017年;125:817 - 30。©2017美国癌症协会。

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