| Literature DB >> 31652375 |
Nicole Pfarr1, Martina Kirchner2, Ulrich Lehmann3, Jonas Leichsenring2, Sabine Merkelbach-Bruse4, Julia Glade2, Michael Hummel5, Fabian Stögbauer1, Annika Lehmann5, Marcel Trautmann6, Jörg Kumbrink7, Andreas Jung7, Wolfgang Dietmaier8, Volker Endris2, Daniel Kazdal2, Matthias Evert8, David Horst5, Hans Kreipe3, Thomas Kirchner7, Eva Wardelmann6, Ulrik Lassen9, Reinhard Büttner4, Wilko Weichert1, Manfred Dietel10, Peter Schirmacher2, Albrecht Stenzinger2.
Abstract
NTRK fusions involving three neurotrophic tyrosine receptor kinase genes NTRK1, NTRK2, and NTRK3 and a variety of fusion partners were identified as oncogenic drivers across many cancer types. Drugs that target the chimeric protein product require the identification of the underlying gene fusion. This advocates the diagnostic use of molecular assays ranging from fluorescence in situ hybridization (FISH) and reverse transcription polymerase chain reaction (RT-PCR)/Sanger approaches to targeted next-generation sequencing (NGS). Immunohistochemistry may be used as a screening tool and adjunct diagnostic assay in this context. Although FISH and RT-PCR/Sanger approaches are widely adopted in routine diagnostics, current experience with targeted RNA-based NGS is limited. Here, we report on the analysis of major assays (TruSight TST170 and TruSight RNA Fusion [Illumina]; Archer FusionPlex Solid Tumor, Archer FusionPlex Lung, and Archer FusionPlex Oncology [Archer]; Oncomine Comprehensive Assay v3 RNA and Oncomine Focus RNA [Thermo Fisher Scientific]) that are commercially available. The data set includes performance results of a multicentric comparative wet-lab study as well as an in silico analysis on the ability to detect the broad range of NTRK fusions reported until now. A test algorithm that reflects assay methodology is provided. This data will support implementation of targeted RNA sequencing in routine diagnostics and inform screening and testing strategies that have been brought forward.Entities:
Keywords: FFPE; NGS; NTRK; RNA sequencing; gene fusion
Year: 2019 PMID: 31652375 DOI: 10.1002/gcc.22819
Source DB: PubMed Journal: Genes Chromosomes Cancer ISSN: 1045-2257 Impact factor: 5.006