Evaluating Targeted Next-Generation Sequencing Assays and Reference Materials for NTRK Fusion Detection.


Journal

The Journal of molecular diagnostics : JMD
ISSN: 1943-7811
Titre abrégé: J Mol Diagn
Pays: United States
ID NLM: 100893612

Informations de publication

Date de publication:
01 2022
Historique:
received: 28 04 2021
revised: 23 07 2021
accepted: 15 09 2021
pubmed: 18 10 2021
medline: 5 4 2022
entrez: 17 10 2021
Statut: ppublish

Résumé

Neurotrophic tyrosine receptor kinase (NTRK1/2/3) fusions are oncogenic drivers in approximately 0.3% of solid tumors. High-quality testing to identify patients with NTRK fusion-positive tumors who could benefit from tropomyosin receptor kinase inhibitors is recommended, but the current NTRK testing landscape, including next-generation sequencing (NGS), is fragmented and availability of assays varies widely. The analytical and clinical performance of four commonly available RNA-based NGS assays, Archer's FusionPlex Lung panel (AFL), Illumina's TruSight Oncology 500 (TSO500), Thermo Fisher's Oncomine Precision Assay and Oncomine Focus Assay (OFA), were evaluated. Experiments were conducted using contrived samples [formalin-fixed, paraffin-embedded cell lines and SeraSeq formalin-fixed, paraffin-embedded reference material], NTRK fusion-negative clinical samples, and NTRK fusion-positive clinical samples, according to local assays. Estimated limit of detection varied across the four assays: 30 to 620 fusion copies for AFL (cell lines), versus approximately 30 to 290 copies for TSO500 and approximately 1 to 28 copies for OFA and Oncomine Precision Assay. All assays showed 100% specificity for NTRK fusions detection, but quality control pass rate was variable (AFL, 43%; TSO500, 77%; and OFA, 83%). The NTRK fusion detection rate in quality control-validated clinical samples was 100% for all assays. This comparison of the strengths and limitations of four RNA-based NGS assays will inform physicians and pathologists regarding optimal assay selection to identify patients with NTRK fusion-positive tumors.

Identifiants

pubmed: 34656759
pii: S1525-1578(21)00326-3
doi: 10.1016/j.jmoldx.2021.09.008
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
Oncogene Proteins, Fusion 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

18-32

Informations de copyright

Copyright © 2022 Association for Molecular Pathology and American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.

Auteurs

Christina Bormann Chung (C)

Genentech Research and Early Development, Genentech, Inc., South San Francisco, California. Electronic address: bormann-chung.christina@gene.com.

Jeeyun Lee (J)

Division of Hematology/Oncology, Samsung Medical Center Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.

Marc Barritault (M)

Department of Molecular Biopathology, Pathological Anatomy and Cytology, East Group Hospital, Hospices Civils de Lyon, Bron, France.

Pierre-Paul Bringuier (PP)

Department of Molecular Biopathology, Pathological Anatomy and Cytology, East Group Hospital, Hospices Civils de Lyon, Bron, France; Histology Laboratory, Université Claude Bernard Lyon 1, Villeurbanne, France.

Zhaolin Xu (Z)

Department of Pathology, QE II Health Sciences Center, Halifax, Nova Scotia, Canada.

Weei-Yuarn Huang (WY)

Department of Laboratory Medicine and Molecular Diagnostics, Sunnybrook Health Sciences Center, University of Toronto, Toronto, Ontario, Canada.

Andrea Beharry (A)

Department of Laboratory Medicine, William Osler Health System, Brampton, Ontario, Canada.

Joseph Castillo (J)

Genentech Research and Early Development, Genentech, Inc., South San Francisco, California.

Jason Christiansen (J)

Assay Development, Roche Sequencing Solutions, Inc., Pleasanton, California.

Jennifer C Lin (JC)

Genentech Research and Early Development, Genentech, Inc., South San Francisco, California.

Brandon S Sheffield (BS)

Department of Laboratory Medicine, William Osler Health System, Brampton, Ontario, Canada.

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Classifications MeSH