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一种新型的 TMTC2-NTRK3 融合基因存在于未分化高级多形性肉瘤中。

A novel TMTC2-NTRK3 fusion in undifferentiated high-grade pleomorphic sarcoma.

机构信息

Department of Bone and Soft Tissue Tumor, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and Institute, Beijing, 100143, China.

Department of Trauma, The Beijing Water Conservancy Hospital, Beijing, China.

出版信息

J Cancer Res Clin Oncol. 2022 Oct;148(10):2933-2937. doi: 10.1007/s00432-022-04249-x. Epub 2022 Aug 7.

Abstract

Undifferentiated high-grade pleomorphic sarcoma (UHPS) is a rare soft tissue sarcoma (STS) originated from mesenchyme. UHPS is mostly advanced, aggressive and has poor prognosis. Patients with UHPS tend to have a lower 5-year survival rate than patients with other types of STS. NTRK fusions are commonly found in rare histological tumor types. Among sarcomas, 90% of infantile fibrosarcomas have NTRK fusions. Many other types of sarcomas have also been studied for NTRK fusions. Targeted therapy with NTRK inhibitors, such as Larotrectinib and Entrectinib, leads to response in most patients with NTRK1/2/3 gene fusion-positive tumors. Herein, we present a 68-years old man with UHPS by pathological diagnosis. Next-generation sequencing (NGS) revealed a novel TMTC2-NTRK3 fusion, which was also detected by immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH). This report broadens the spectrum of NTRK fusions in UHPS and highlights a new target for treatment.

摘要

未分化高级别多形性肉瘤(UHPS)是一种罕见的起源于间充质的软组织肉瘤(STS)。UHPS 大多为晚期、侵袭性且预后不良。与其他类型的 STS 患者相比,UHPS 患者的 5 年生存率往往较低。NTRK 融合常见于罕见的组织学肿瘤类型。在肉瘤中,90%的婴儿纤维肉瘤存在 NTRK 融合。许多其他类型的肉瘤也已经研究了 NTRK 融合。针对 NTRK 抑制剂(如拉罗替尼和恩曲替尼)的靶向治疗,导致大多数 NTRK1/2/3 基因融合阳性肿瘤患者产生应答。在此,我们通过病理诊断呈现了一名 68 岁的 UHPS 男性患者。下一代测序(NGS)显示了一种新型的 TMTC2-NTRK3 融合,该融合也通过免疫组化(IHC)和荧光原位杂交(FISH)检测到。该报告拓宽了 UHPS 中 NTRK 融合的范围,并强调了一个新的治疗靶点。

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