Laboratory Medicine Program, University Health Network, Toronto, Ontario, Canada; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada; Advanced Molecular Diagnostics Laboratory, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Department of Pathology and Laboratory Medicine, The Ottawa Hospital, Ottawa, Ontario, Canada.
J Mol Diagn. 2023 Mar;25(3):168-174. doi: 10.1016/j.jmoldx.2022.12.004. Epub 2022 Dec 28.
The Canadian NTRK (CANTRK) study is an interlaboratory comparison ring study to optimize testing for neurotrophic receptor tyrosine kinase (NTRK) fusions in Canadian laboratories. Sixteen diagnostic laboratories used next-generation sequencing (NGS) for NTRK1, NTRK2, or NTRK3 fusions. Each laboratory received 12 formalin-fixed, paraffin-embedded tumor samples with unique NTRK fusions and two control non-NTRK fusion samples (one ALK and one ROS1). Laboratories used validated protocols for NGS fusion detection. Panels included Oncomine Comprehensive Assay v3, Oncomine Focus Assay, Oncomine Precision Assay, AmpliSeq for Illumina Focus, TruSight RNA Pan-Cancer Panel, FusionPlex Lung, and QIAseq Multimodal Lung. One sample was withdrawn from analysis because of sample quality issues. Of the remaining 13 samples, 6 of 11 NTRK fusions and both control fusions were detected by all laboratories. Two fusions, WNK2::NTRK2 and STRN3::NTRK2, were not detected by 10 laboratories using the Oncomine Comprehensive or Focus panels, due to absence of WNK2 and STRN3 in panel designs. Two fusions, TPM3::NTRK1 and LMNA::NTRK1, were challenging to detect on the AmpliSeq for Illumina Focus panel because of bioinformatics issues. One ETV6::NTRK3 fusion at low levels was not detected by two laboratories using the TruSight Pan-Cancer Panel. Panels detecting all fusions included FusionPlex Lung, Oncomine Precision, and QIAseq Multimodal Lung. The CANTRK study showed competency in detection of NTRK fusions by NGS across different panels in 16 Canadian laboratories and identified key test issues as targets for improvements.
加拿大 NTRK(CANTRK)研究是一项旨在优化加拿大实验室神经酪氨酸激酶受体(NTRK)融合检测的实验室间比较环研究。16 家诊断实验室使用下一代测序(NGS)检测 NTRK1、NTRK2 或 NTRK3 融合。每家实验室都收到了 12 份福尔马林固定、石蜡包埋的肿瘤样本,这些样本具有独特的 NTRK 融合,还有两份非 NTRK 融合对照样本(一份 ALK 和一份 ROS1)。实验室使用经过验证的 NGS 融合检测方案。面板包括 Oncomine Comprehensive Assay v3、Oncomine Focus Assay、Oncomine Precision Assay、AmpliSeq for Illumina Focus、TruSight RNA Pan-Cancer Panel、FusionPlex Lung 和 QIAseq Multimodal Lung。由于样本质量问题,一份样本被从分析中剔除。在剩余的 13 份样本中,11 个 NTRK 融合中有 6 个,以及两个对照融合均被所有实验室检测到。由于 WNK2 和 STRN3 不在面板设计中,使用 Oncomine Comprehensive 或 Focus 面板的 10 家实验室未能检测到 WNK2::NTRK2 和 STRN3::NTRK2 这两个融合。由于生物信息学问题,AmpliSeq for Illumina Focus 面板上 TPM3::NTRK1 和 LMNA::NTRK1 这两个融合难以检测。两家实验室使用 TruSight Pan-Cancer Panel 未能检测到低水平的 ETV6::NTRK3 融合。能够检测到所有融合的面板包括 FusionPlex Lung、Oncomine Precision 和 QIAseq Multimodal Lung。CANTRK 研究表明,在 16 家加拿大实验室中,不同的 NGS 面板能够检测到 NTRK 融合,并确定了关键的测试问题,作为改进的目标。