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拓宽 NTRK 重排间叶肿瘤谱及 pan-TRK 免疫组化在鉴定 NTRK 融合中的作用。

Broadening the spectrum of NTRK rearranged mesenchymal tumors and usefulness of pan-TRK immunohistochemistry for identification of NTRK fusions.

机构信息

Diagnostic and Research Institute of Pathology, Comprehensive Cancer Centre Graz, Medical University of Graz, Graz, Austria.

Department of Orthopedics and Trauma, Comprehensive Cancer Centre Graz, Medical University of Graz, Graz, Austria.

出版信息

Mod Pathol. 2021 Feb;34(2):396-407. doi: 10.1038/s41379-020-00657-x. Epub 2020 Aug 28.

Abstract

Fusions involving NTRK1, NTRK2, and NTRK3 are oncogenic drivers occurring in a spectrum of mesenchymal neoplasms ranging from benign to highly malignant tumors. To gain further insights into the staining profile with the pan-TRK assay, we analyzed a large number of soft tissue sarcomas and correlated our findings with molecular testing. Additionally, we expand the spectrum of NTRK-fusion tumors by reporting a mesenchymal lesion in the lung as well as a mesenchymal skin lesion in the spectrum of benign fibrous histiocytoma with NTRK-fusion. We retrospectively reviewed soft tissue sarcomas diagnosed at the Diagnostic and Research Institute of Pathology, Medical University of Graz, between 1999 and 2019, and cases from the consultation files of one of the authors (BLA). In total, 494 cases were analyzed immunohistochemically with pan-TRK antibody (clone EPR17341, RTU, Roche/Ventana) and positive cases (defined as any cytoplasmic/nuclear staining in more than 1% of tumor cells) underwent next-generation sequencing (NGS). Immunohistochemical staining was observed in 16 (3.2%) cases. Eleven cases with focal weak and moderate cytoplasmic/membranous or focal moderate to strong nuclear staining did not harbor an NTRK-fusion (three synovial sarcomas, three leiomyosarcomas, two extraskeletal myxoid chondrosarcomas, and one each: dedifferentiated liposarcoma, pleomorphic liposarcoma, and myxofibrosarcoma). Four cases showed strong diffuse nuclear and/or cytoplasmatic staining, and one case showed diffuse, but weak cytoplasmic staining. All these cases demonstrated an NTRK-fusion (LMNA-NTRK1, IRF2BP2-NTRK1, TMB3-NTRK1, ETV6-NTRK3, RBPMS-NTRK3). Pan-TRK assay (clone EPR17341, RTU, Roche, Ventana) immunohistochemistry serves as a reliable diagnostic marker that can also be expressed in non-NTRK-rearranged mesenchymal neoplasms. It can be used as a surrogate marker for identification of NTRK fusion, nevertheless, an RNA-based NGS for detection of the specific fusion should be performed to confirm the rearrangement, if patients are undergoing targeted therapy. Additionally, we identified NTRK-fusion-positive, primary mesenchymal tumors of the lung and the skin.

摘要

涉及 NTRK1、NTRK2 和 NTRK3 的融合是发生在从良性到高度恶性肿瘤的一系列间充质肿瘤中的致癌驱动因素。为了进一步深入了解泛 TRK 检测的染色特征,我们分析了大量软组织肉瘤,并将我们的发现与分子检测相关联。此外,我们通过报告肺部间叶性病变以及良性纤维组织细胞瘤中具有 NTRK 融合的间叶性皮肤病变,扩展了 NTRK 融合肿瘤的范围。我们回顾性分析了 1999 年至 2019 年在格拉茨医科大学诊断和研究病理学研究所诊断的软组织肉瘤病例,以及一位作者(BLA)的咨询文件中的病例。总共对 494 例病例进行了泛 TRK 抗体(克隆 EPR17341,RTU,罗氏/文塔纳)的免疫组织化学分析,阳性病例(定义为肿瘤细胞中超过 1%的任何细胞质/核染色)进行了下一代测序(NGS)。观察到 16 例(3.2%)病例存在免疫组织化学染色。11 例具有局灶性弱和中等强度的细胞质/膜性或局灶性强至中等强度核染色的病例未携带 NTRK 融合(滑膜肉瘤 3 例,平滑肌肉瘤 3 例,骨外黏液样软骨肉瘤 2 例,以及分化脂肪肉瘤、多形性脂肪肉瘤和黏液纤维肉瘤各 1 例)。4 例显示强弥漫性核和/或细胞质染色,1 例显示弥漫性但弱细胞质染色。所有这些病例均显示 NTRK 融合(LMNA-NTRK1、IRF2BP2-NTRK1、TMB3-NTRK1、ETV6-NTRK3、RBPMS-NTRK3)。泛 TRK 检测(克隆 EPR17341,RTU,罗氏,文塔纳)免疫组织化学作为一种可靠的诊断标志物,也可在非 NTRK 重排的间充质肿瘤中表达。它可用作识别 NTRK 融合的替代标志物,然而,如果患者正在接受靶向治疗,应进行基于 RNA 的 NGS 以检测特定融合以确认重排。此外,我们鉴定了肺和皮肤的 NTRK 融合阳性原发性间叶性肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c8e/7817523/b646b6718317/41379_2020_657_Fig1_HTML.jpg

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