Epidermal growth factor receptor exon 20 insertion variants in non-small cell lung cancer patients.


Journal

Critical reviews in oncology/hematology
ISSN: 1879-0461
Titre abrégé: Crit Rev Oncol Hematol
Pays: Netherlands
ID NLM: 8916049

Informations de publication

Date de publication:
Jan 2022
Historique:
received: 10 05 2021
revised: 18 10 2021
accepted: 15 11 2021
pubmed: 22 11 2021
medline: 18 1 2022
entrez: 21 11 2021
Statut: ppublish

Résumé

Epidermal growth factor receptor (EGFR) exon 20 insertions occur rarely among different cancer types, with the highest frequency reported among non-small-cell lung cancer (NSCLC) patients, particularly adenocarcinomas (ADCs). Exon 20 insertions fall back in the tyrosine kinase domain, and can be clustered into two principal groups represented by in frame insertions and three to 21 bp (corresponding to 1-7 amino acids) duplications within amino acids 762 and 774. The identification of these alterations is key for an adequate management of NSCLC patients due to the possibility to treat these patients with specific targeted therapies. Next generation sequencing (NGS) technology, able to detect several hotspot gene mutations for different patients simultaneously, is the best detection approach due to its higher sensitivity and specificity compared to other techniques. Here we reviewed the principal biological characteristics, the main detection technologies and treatment options for NSCLC patients harbouring EGFR exon 20 insertions.

Identifiants

pubmed: 34801697
pii: S1040-8428(21)00323-1
doi: 10.1016/j.critrevonc.2021.103536
pii:
doi:

Substances chimiques

Protein Kinase Inhibitors 0
ErbB Receptors EC 2.7.10.1

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

103536

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Umberto Malapelle (U)

Department of Public Health, University of Naples Federico II, Naples, Italy.

Sara Pilotto (S)

U.O.C. of Oncology, Azienda Ospedaliera Universitaria Integrata, University of Verona, Verona, Italy.

Maria Lucia Reale (ML)

Department of Oncology, San Luigi Gonzaga Hospital, University of Turin, Orbassano, Italy.

Francesco Passiglia (F)

Department of Oncology, San Luigi Gonzaga Hospital, University of Turin, Orbassano, Italy.

Pasquale Pisapia (P)

Department of Public Health, University of Naples Federico II, Naples, Italy.

Francesco Pepe (F)

Department of Public Health, University of Naples Federico II, Naples, Italy.

Lorenzo Belluomini (L)

U.O.C. of Oncology, Azienda Ospedaliera Universitaria Integrata, University of Verona, Verona, Italy.

Domenico Galetta (D)

Medical Thoracic Oncology Unit, IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.

Diego Cortinovis (D)

SC Oncologia Medica, SS Lung Unit Asst Ospedale San Gerardo, Monza, Italy.

Marcello Tiseo (M)

Department of Medicine and Surgery, Medical Oncology Unit, University Hospital of Parma, Parma, Italy.

Antonio Passaro (A)

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

Davide Seminati (D)

Department of Medicine and Surgery, Pathology, San Gerardo Hospital, University of Milano-Bicocca, Monza, Italy.

Fabio Pagni (F)

Department of Medicine and Surgery, Pathology, San Gerardo Hospital, University of Milano-Bicocca, Monza, Italy.

Hector Soto Parra (HS)

Department of Oncology, Medical Oncology, University Hospital Policlinico-San Marco, Catania, Italy.

Maria Rita Migliorino (MR)

Pneumo-Oncology Unit, San Camillo Forlanini Hospital, Roma, Italy.

Danilo Rocco (D)

Pneumo-Oncology Unit, Ospedali dei Colli Monaldi Cotugno CTO, Napoli, Italy.

Giancarlo Troncone (G)

Department of Public Health, University of Naples Federico II, Naples, Italy.

Silvia Novello (S)

Department of Oncology, San Luigi Gonzaga Hospital, University of Turin, Orbassano, Italy. Electronic address: silvia.novello@unito.it.

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Classifications MeSH