Brazilian Expert Consensus for NTRK Gene Fusion Testing in Solid Tumors.

IF 1.9 Q3 PATHOLOGY Clinical Pathology Pub Date : 2023-09-15 eCollection Date: 2023-01-01 DOI:10.1177/2632010X231197080
Mariana Petaccia de Macedo, Ellen Caroline Toledo Nascimento, Fernando Augusto Soares, Fernando Costa Santini, Felipe D'Almeida Costa, Isabela Werneck da Cunha, Rodrigo Ramella Munhoz, Pedro De Marchi, Thiago William Carnier Jorge, Kátia Ramos Moreira Leite
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Abstract

Oncogenic neurotrophic tropomyosin receptor kinase gene fusions occur in less than 1% of common cancers. These mutations have emerged as new biomarkers in cancer genomic profiling with the approval of selective drugs against tropomyosin receptor kinase fusion proteins. Nevertheless, the optimal pathways and diagnostic platforms for this biomarker's screening and genomic profiling have not been defined and remain a subject of debate. A panel of national experts in molecular cancer diagnosis and treatment was convened by videoconference and suggested topics to be addressed in the literature review. The authors proposed a testing algorithm for oncogenic neurotrophic tropomyosin receptor kinase gene fusion screening and diagnosis for the Brazilian health system. This review aims to discuss the latest literature evidence and international consensus on neurotrophic tropomyosin receptor kinase gene fusion diagnosis to devise clinical guidelines for testing this biomarker. We propose an algorithm in which testing for this biomarker should be requested to diagnose advanced metastatic tumors without known driver mutations. In this strategy, Immunohistochemistry should be used as a screening test followed by confirmatory next-generation sequencing in immunohistochemistry-positive cases.

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实体瘤NTRK基因融合检测的巴西专家共识。
肿瘤源性神经营养原肌球蛋白受体激酶基因融合发生在不到1%的常见癌症中。随着针对原肌球蛋白受体激酶融合蛋白的选择性药物的批准,这些突变已成为癌症基因组图谱中的新生物标志物。然而,这种生物标志物的筛选和基因组分析的最佳途径和诊断平台尚未确定,仍然是一个争论的主题。通过视频会议召集了癌症分子诊断和治疗国家专家小组,并提出了文献综述中要讨论的主题。作者提出了一种用于巴西卫生系统致癌神经营养原肌球蛋白受体激酶基因融合筛查和诊断的测试算法。本综述旨在讨论神经营养原肌球蛋白受体激酶基因融合诊断的最新文献证据和国际共识,以制定检测该生物标志物的临床指南。我们提出了一种算法,要求对这种生物标志物进行测试,以诊断没有已知驱动突变的晚期转移性肿瘤。在这种策略中,免疫组织化学应被用作筛选测试,然后在免疫组织化学阳性病例中进行下一代验证测序。
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来源期刊
Clinical Pathology
Clinical Pathology PATHOLOGY-
CiteScore
2.20
自引率
7.70%
发文量
66
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