Clinical Features and Progression Pattern of Acquired T790M-positive Compared With T790M-negative EGFR Mutant Non-small-cell Lung Cancer: Catching Tumor and Clinical Heterogeneity Over Time Through Liquid Biopsy.


Journal

Clinical lung cancer
ISSN: 1938-0690
Titre abrégé: Clin Lung Cancer
Pays: United States
ID NLM: 100893225

Informations de publication

Date de publication:
01 2020
Historique:
received: 02 05 2019
revised: 18 06 2019
accepted: 26 07 2019
pubmed: 12 10 2019
medline: 2 4 2021
entrez: 12 10 2019
Statut: ppublish

Résumé

Clinical-pathologic predictors of acquired T790M epidermal growth factor receptor (EGFR) mutation in Caucasian patients with non-small-cell lung cancer (NSCLC) progressing after first-/second-generation tyrosine kinase inhibitors (TKIs) is an open field for research. Similarly, the best time point for T790M detection by liquid or tissue biopsy after disease progression is currently matter of debate. This is an observational study at 7 Italian centers enrolling patients with EGFR-mutant NSCLC progressing after first-/second-generation EGFR TKIs, between 2014 and 2018, aiming at comparing baseline clinical-pathologic features and progression patterns in acquired T790M-positive compared with T790M-negative cases. A total of 235 patients received first-line treatment with gefitinib (N = 126; 53%), erlotinib (N = 51; 22%), or afatinib (N = 58; 25%). In 120 (51%) cases, T790M was detected in liquid biopsy, tissue biopsy, or both. Age younger than 65 years (P = .037), the presence of common mutations (P = .004), and better response to first-line TKI (P = .023) were correlated with T790M positivity. T790M detection was associated with higher number of new progressing sites (P = .04), liver progression (P = .002), and a lower frequency of lung metastases (P = .027). When serial liquid biopsies were performed (N = 15), an oligoprogressive disease was correlated with a negative test outcome, whereas systemic progression was observed at the time of T790M positivity. This study on a Caucasian population showed that age, type of EGFR mutation at diagnosis, response to first-line treatment, and peculiar progression pattern are associated with T790M status. Serial liquid biopsy might be useful for treatment selection, especially when tissue rebiopsy is not feasible.

Sections du résumé

BACKGROUND
Clinical-pathologic predictors of acquired T790M epidermal growth factor receptor (EGFR) mutation in Caucasian patients with non-small-cell lung cancer (NSCLC) progressing after first-/second-generation tyrosine kinase inhibitors (TKIs) is an open field for research. Similarly, the best time point for T790M detection by liquid or tissue biopsy after disease progression is currently matter of debate.
PATIENTS AND METHODS
This is an observational study at 7 Italian centers enrolling patients with EGFR-mutant NSCLC progressing after first-/second-generation EGFR TKIs, between 2014 and 2018, aiming at comparing baseline clinical-pathologic features and progression patterns in acquired T790M-positive compared with T790M-negative cases.
RESULTS
A total of 235 patients received first-line treatment with gefitinib (N = 126; 53%), erlotinib (N = 51; 22%), or afatinib (N = 58; 25%). In 120 (51%) cases, T790M was detected in liquid biopsy, tissue biopsy, or both. Age younger than 65 years (P = .037), the presence of common mutations (P = .004), and better response to first-line TKI (P = .023) were correlated with T790M positivity. T790M detection was associated with higher number of new progressing sites (P = .04), liver progression (P = .002), and a lower frequency of lung metastases (P = .027). When serial liquid biopsies were performed (N = 15), an oligoprogressive disease was correlated with a negative test outcome, whereas systemic progression was observed at the time of T790M positivity.
CONCLUSION
This study on a Caucasian population showed that age, type of EGFR mutation at diagnosis, response to first-line treatment, and peculiar progression pattern are associated with T790M status. Serial liquid biopsy might be useful for treatment selection, especially when tissue rebiopsy is not feasible.

Identifiants

pubmed: 31601525
pii: S1525-7304(19)30213-X
doi: 10.1016/j.cllc.2019.07.009
pii:
doi:

Substances chimiques

Afatinib 41UD74L59M
Erlotinib Hydrochloride DA87705X9K
EGFR protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1
Gefitinib S65743JHBS

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-14.e3

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Alessandro Dal Maso (A)

Department of Oncology 2, Istituto Oncologico Veneto - IRCCS, Padova, Italy; Department of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.

Martina Lorenzi (M)

Department of Oncology 2, Istituto Oncologico Veneto - IRCCS, Padova, Italy; Department of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.

Elisa Roca (E)

Department of Medical Oncology, ASST - Spedali Civili, Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Brescia, Italy.

Sara Pilotto (S)

Department of Medical Oncology, University of Verona, AOUI Verona, Verona, Italy.

Marianna Macerelli (M)

Department of Medical Oncology - ASUIUD Santa Maria della Misericordia, Udine, Italy.

Valentina Polo (V)

Oncology Unit, AULSS 2 Marca Trevigiana, Ca' Foncello Hospital, Treviso, Italy.

Fabiana Letizia Cecere (FL)

Department of Oncology 1, Regina Elena National Cancer Institute IRCCS Rome, Rome, Italy.

Alessandro Del Conte (A)

Department of Medical Oncology and Immunorelated Tumors, Centro di Riferimento Oncologico (CRO) - IRCCS, Aviano (PN), Italy.

Giorgia Nardo (G)

Immunology and Molecular Oncology Unit, Istituto Oncologico Veneto - IRCCS, Padova, Italy.

Vanessa Buoro (V)

Department of Medical Oncology - ASUIUD Santa Maria della Misericordia, Udine, Italy.

Daniela Scattolin (D)

Department of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.

Sara Monteverdi (S)

Department of Medical Oncology, University of Verona, AOUI Verona, Verona, Italy.

Loredana Urso (L)

Department of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.

Elisabetta Zulato (E)

Immunology and Molecular Oncology Unit, Istituto Oncologico Veneto - IRCCS, Padova, Italy.

Stefano Frega (S)

Department of Oncology 2, Istituto Oncologico Veneto - IRCCS, Padova, Italy.

Laura Bonanno (L)

Department of Oncology 2, Istituto Oncologico Veneto - IRCCS, Padova, Italy.

Stefano Indraccolo (S)

Immunology and Molecular Oncology Unit, Istituto Oncologico Veneto - IRCCS, Padova, Italy.

Fiorella Calabrese (F)

Pathology Unit, Department of Cardio-Thoracic and Vascular Sciences, University of Padova, Padova, Italy.

PierFranco Conte (P)

Department of Oncology 2, Istituto Oncologico Veneto - IRCCS, Padova, Italy; Department of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.

Giulia Pasello (G)

Department of Oncology 2, Istituto Oncologico Veneto - IRCCS, Padova, Italy. Electronic address: giulia.pasello@iov.veneto.it.

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Classifications MeSH