Genomic Characterization of Concurrent Alterations in Non-Small Cell Lung Cancer (NSCLC) Harboring Actionable Mutations.

ALK BRAF EGFR ERBB2 KRAS MET RET co-mutation next generation sequencing predictive biomarker

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
30 Apr 2021
Historique:
received: 16 04 2021
revised: 27 04 2021
accepted: 27 04 2021
entrez: 5 5 2021
pubmed: 6 5 2021
medline: 6 5 2021
Statut: epublish

Résumé

An increasing number of driver genomic alterations with potential targeted treatments have been identified in non-small cell lung cancer (NSCLC). Much less is known about the incidence and different distribution of concurrent alterations, as identified by comprehensive genomic profiling in oncogene-addicted NSCLCs. Genomic data from advanced NSCLC consecutively analyzed using a broad next-generation sequencing panel were retrospectively collected. Tumors harboring at least one main actionable gene alteration were categorized according to the presence/absence of concurrent genomic aberrations, to evaluate different patterns among the main oncogene-addicted NSCLCs. Three-hundred-nine actionable gene alterations were identified in 284 advanced NSCLC patients during the study period. Twenty-five tumor samples (8%) displayed concurrent alterations in actionable genes. Co-occurrences involving any pathogenic variant or copy number variation (CNV) were identified in 82.8% of cases. Overall, statistically significant differences in the number of concurrent alterations, and the distribution of

Identifiants

pubmed: 33946519
pii: cancers13092172
doi: 10.3390/cancers13092172
pmc: PMC8124171
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Antonio Passaro (A)

Division of Thoracic Oncology, IEO, European Institute of Oncology, IRCCS, 20141 Milan, Italy.

Ilaria Attili (I)

Division of Thoracic Oncology, IEO, European Institute of Oncology, IRCCS, 20141 Milan, Italy.

Alessandra Rappa (A)

Division of Pathology and Laboratory Medicine, IEO, European Institute of Oncology, IRCCS, 20141 Milan, Italy.

Davide Vacirca (D)

Division of Pathology and Laboratory Medicine, IEO, European Institute of Oncology, IRCCS, 20141 Milan, Italy.

Alberto Ranghiero (A)

Division of Pathology and Laboratory Medicine, IEO, European Institute of Oncology, IRCCS, 20141 Milan, Italy.

Caterina Fumagalli (C)

Division of Pathology and Laboratory Medicine, IEO, European Institute of Oncology, IRCCS, 20141 Milan, Italy.

Juliana Guarize (J)

Department of Thoracic Surgery, IEO, European Institute of Oncology, IRCCS, 20141 Milan, Italy.

Lorenzo Spaggiari (L)

Department of Thoracic Surgery, IEO, European Institute of Oncology, IRCCS, 20141 Milan, Italy.
Department of Oncology and Hemato-Oncology, University of Milan, 20122 Milan, Italy.

Filippo de Marinis (F)

Division of Thoracic Oncology, IEO, European Institute of Oncology, IRCCS, 20141 Milan, Italy.

Massimo Barberis (M)

Division of Pathology and Laboratory Medicine, IEO, European Institute of Oncology, IRCCS, 20141 Milan, Italy.

Elena Guerini-Rocco (E)

Division of Pathology and Laboratory Medicine, IEO, European Institute of Oncology, IRCCS, 20141 Milan, Italy.
Department of Oncology and Hemato-Oncology, University of Milan, 20122 Milan, Italy.

Classifications MeSH