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常规诊断中融合基因检测、TRK表达及泛TRK免疫组化的应用:一项基于全国社区队列的研究结果

Detection of Fusions and TRK Expression and Performance of pan-TRK Immunohistochemistry in Routine Diagnostics: Results from a Nationwide Community-Based Cohort.

作者信息

Koopman Bart, Kuijpers Chantal C H J, Groen Harry J M, Timens Wim, Schuuring Ed, Willems Stefan M, van Kempen Léon C

机构信息

Department of Pathology and Medical Biology, University of Groningen, University Medical Center Groningen, P.O. Box 30.001, 9700 RB Groningen, The Netherlands.

Foundation PALGA, De Bouw 123, 3991 SZ Houten, The Netherlands.

出版信息

Diagnostics (Basel). 2022 Mar 9;12(3):668. doi: 10.3390/diagnostics12030668.

Abstract

Gene fusions involving , and are rare drivers of cancer that can be targeted with histology-agnostic inhibitors. This study aimed to determine the nationwide landscape of /TRK testing in the Netherlands and the usage of pan-TRK immunohistochemistry (IHC) as a preselection tool to detect NTRK fusions. All pathology reports in 2017-2020 containing the search term 'TRK' were retrieved from the Dutch Pathology Registry (PALGA). Patient characteristics, tumor histology, /TRK testing methods, and reported results were extracted. /TRK testing was reported for 7457 tumors. Absolute testing rates increased from 815 (2017) to 3380 (2020). Tumors were tested with DNA/RNA-based molecular assay(s) (48%), IHC (47%), or in combination (5%). A total of 69 fusions involving ( = 22), ( = 6) and ( = 41) were identified in tumors from adult ( = 51) and pediatric ( = 18) patients. In patients tested with both IHC and a molecular assay ( = 327, of which 29 fusion-positive), pan-TRK IHC had a sensitivity of 77% (95% confidence interval (CI), 56-91) and a specificity of 84% (95% CI, 78-88%). These results showed that pan-TRK IHC has a low sensitivity in current routine practice and warrants the introduction of quality guidelines regarding the implementation and interpretation of pan-TRK IHC.

摘要

涉及 、 和 的基因融合是罕见的癌症驱动因素,可用组织学无关抑制剂进行靶向治疗。本研究旨在确定荷兰全国范围内 /TRK检测的情况,以及使用泛TRK免疫组织化学(IHC)作为检测NTRK融合的预选工具的情况。从荷兰病理登记处(PALGA)检索了2017 - 2020年所有包含搜索词“TRK”的病理报告。提取了患者特征、肿瘤组织学、/TRK检测方法和报告结果。共报告了7457个肿瘤的/TRK检测情况。绝对检测率从2017年的815例增加到2020年的3380例。肿瘤采用基于DNA/RNA的分子检测方法(48%)、IHC(47%)或联合检测(5%)。在成人( = 51)和儿童( = 18)患者的肿瘤中,共鉴定出69种涉及 ( = 22)、 ( = 6)和 ( = 41)的融合。在同时接受IHC和分子检测的患者中( = 327,其中29例融合阳性),泛TRK IHC的敏感性为77%(95%置信区间(CI),56 - 91),特异性为84%(95% CI,78 - 88%)。这些结果表明,在当前的常规实践中,泛TRK IHC的敏感性较低,因此有必要引入关于泛TRK IHC实施和解释的质量指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccd5/8946871/b20259daeb6f/diagnostics-12-00668-g001.jpg

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