Comparison between next-generation sequencing and multiplex polymerase chain reaction assays for nonsmall-cell lung cancer molecular diagnosis.

AmoyDx pan lung cancer PCR panel Oncomine Dx Target Test nonsmall‐cell lung cancer

Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
Apr 2024
Historique:
revised: 18 03 2024
received: 11 11 2023
accepted: 26 03 2024
medline: 4 4 2024
pubmed: 4 4 2024
entrez: 4 4 2024
Statut: ppublish

Résumé

Genetic mutation detection has become an important step in nonsmall-cell lung cancer (NSCLC) treatment because of the increasing number of drugs that target genomic rearrangements. A multiplex test that can detect multiple gene mutations prior to treatment is thus necessary. Currently, either next-generation sequencing (NGS)-based or polymerase chain reaction (PCR)-based tests are used. We evaluated the performance of the Oncomine Dx Target Test (ODxTT), an NGS-based multiplex biomarker panel test, and the AmoyDx Pan Lung Cancer PCR Panel (AmoyDx PLC panel), a real-time PCR-based multiplex biomarker panel test. Patients with histologically diagnosed NSCLC and a sufficient sample volume to simultaneously perform the AmoyDx PLC panel and ODxTT-M were included in the study. The success and detection rates of both tests were evaluated. Biopsies revealed 116 cases of malignancies, 100 of which were NSCLC. Of these, 59 met the inclusion criteria and were eligible for analysis. The success rates were 100% and 98% for AmoyDx PLC panel and ODxTT-M, respectively. Nine driver mutations were detected in 35.9% and 37.3% of AmoyDx PLC and ODxTT-M panels, respectively. EGFR mutations were detected in 14% and 12% of samples using the AmoyDx PLC panel and ODxTT-M, respectively. Of the 58 cases in which both NGS and AmoyDx PLC panels were successful, discordant results were observed in seven cases. These differences were mainly due to different sensitivities of the detection methods used and the gene variants targeted in each test. The AmoyDx PLC panel, a PCR-based multiplex diagnostic test, exhibits a high success rate. The frequency of the nine genes targeted for treatment detected by the AmoyDx PLC panel was comparable to the frequency of mutations detected by ODxTT-M. Clinicians should understand and use the AmoyDx PLC panel and ODxTT-M with respect to their respective performances and limitations.

Identifiants

pubmed: 38572952
doi: 10.1002/cam4.7162
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e7162

Subventions

Organisme : Riken Genesis Co., Ltd.

Informations de copyright

© 2024 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Shuji Murakami (S)

Department of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Kanagawa, Japan.

Kanako Shinada (K)

Department of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Kanagawa, Japan.

Yuka Otsutsumi (Y)

Department of Pathology, Kanagawa Cancer Center, Yokohama, Kanagawa, Japan.

Fumiko Komine (F)

Riken Genesis Co., Ltd., Shinagawa-ku, Tokyo, Japan.

Yuan Yuan (Y)

Riken Genesis Co., Ltd., Shinagawa-ku, Tokyo, Japan.

Junko Nakamura (J)

Riken Genesis Co., Ltd., Shinagawa-ku, Tokyo, Japan.

Seigo Katakura (S)

Department of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Kanagawa, Japan.

Tetsuro Kondo (T)

Department of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Kanagawa, Japan.

Terufumi Kato (T)

Department of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Kanagawa, Japan.

Tomoyuki Yokose (T)

Department of Pathology, Kanagawa Cancer Center, Yokohama, Kanagawa, Japan.

Haruhiro Saito (H)

Department of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Kanagawa, Japan.

Classifications MeSH