Survival of Patients with Epidermal Growth Factor Receptor-Mutated Metastatic Non-Small Cell Lung Cancer Treated beyond the Second Line in the Tyrosine Kinase Inhibitor Era.

EGFR-genes TKI drug therapy lung cancer metastasis survival analysis

Journal

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

Informations de publication

Date de publication:
02 Aug 2021
Historique:
received: 07 07 2021
revised: 25 07 2021
accepted: 29 07 2021
entrez: 7 8 2021
pubmed: 8 8 2021
medline: 8 8 2021
Statut: epublish

Résumé

The identification of activating mutations in specific genes led to the development of targeted therapies for NSCLC. TKI directed against EGFR-mutations were the first to prove their major efficacy. Medical associations recommend their use as first and second-line metastatic treatments in EGFR-mutated patients. Our objective was to analyze the survival of EGFR-mutated patients treated beyond the second line of treatment. We performed a longitudinal, retrospective and analytical study at APHP (Assistance Publique Hopitaux de Paris) Saint Louis, Paris, France, from 1 January 2010 to 31 December 2020 (11 years), on EGFR-mutated patients with metastatic NSCLC which received TKI or chemotherapy (CT) in third-line. Out of about 107 EGFR-mutated patients, 31 patients who benefited from TKI or CT in the third line of treatment were retained for this study. The mean age was 60.03 ± 11.93 years and the sex ratio male/female was 0.24. Mutations of exon 19, 21 and 20 were found in 21 (67.7%), 7 (22.6%) and 7 (22.6%) patients, respectively. Third-line treatment was CT for 16 patients (51.6%) and TKI for the 15 remaining patients (48.4%). Osimertinib was the most used TKI in third-line ( For patients receiving CT in second-line, TKI appears to be a better alternative in third-line compared to CT. Osimertinib may be used in third line treatment if not used before.

Sections du résumé

BACKGROUND BACKGROUND
The identification of activating mutations in specific genes led to the development of targeted therapies for NSCLC. TKI directed against EGFR-mutations were the first to prove their major efficacy. Medical associations recommend their use as first and second-line metastatic treatments in EGFR-mutated patients. Our objective was to analyze the survival of EGFR-mutated patients treated beyond the second line of treatment.
METHODS METHODS
We performed a longitudinal, retrospective and analytical study at APHP (Assistance Publique Hopitaux de Paris) Saint Louis, Paris, France, from 1 January 2010 to 31 December 2020 (11 years), on EGFR-mutated patients with metastatic NSCLC which received TKI or chemotherapy (CT) in third-line.
RESULTS RESULTS
Out of about 107 EGFR-mutated patients, 31 patients who benefited from TKI or CT in the third line of treatment were retained for this study. The mean age was 60.03 ± 11.93 years and the sex ratio male/female was 0.24. Mutations of exon 19, 21 and 20 were found in 21 (67.7%), 7 (22.6%) and 7 (22.6%) patients, respectively. Third-line treatment was CT for 16 patients (51.6%) and TKI for the 15 remaining patients (48.4%). Osimertinib was the most used TKI in third-line (
CONCLUSIONS CONCLUSIONS
For patients receiving CT in second-line, TKI appears to be a better alternative in third-line compared to CT. Osimertinib may be used in third line treatment if not used before.

Identifiants

pubmed: 34359788
pii: cancers13153887
doi: 10.3390/cancers13153887
pmc: PMC8345514
pii:
doi:

Types de publication

Journal Article

Langues

eng

Références

Ann Oncol. 2018 Jan 1;29(suppl_1):i10-i19
pubmed: 29462254
J Clin Oncol. 2017 Apr 20;35(12):1288-1296
pubmed: 28221867
PLoS One. 2019 Oct 3;14(10):e0223530
pubmed: 31581247
Cancer Chemother Pharmacol. 2018 Jul;82(1):119-127
pubmed: 29737372
Mol Clin Oncol. 2019 Sep;11(3):301-308
pubmed: 31384460
Oncol Lett. 2020 Jul;20(1):391-400
pubmed: 32565965
Lung Cancer. 2019 Jun;132:126-131
pubmed: 31097085
Br J Cancer. 2019 Oct;121(9):725-737
pubmed: 31564718
Future Oncol. 2020 Dec;16(34):2799-2808
pubmed: 32854536
Lung Cancer. 2019 Jan;127:96-102
pubmed: 30642559
Clin Cancer Res. 2011 Sep 1;17(17):5530-7
pubmed: 21775534
Am J Clin Oncol. 2019 May;42(5):432-439
pubmed: 30950859
Cancer Discov. 2017 Jul 20;:
pubmed: 28729406
N Engl J Med. 2018 Jan 11;378(2):113-125
pubmed: 29151359
Anticancer Res. 2019 Jul;39(7):3923-3929
pubmed: 31262922
Mol Cell Oncol. 2018 Oct 9;5(6):e1509488
pubmed: 30525088
J Thorac Oncol. 2017 Mar;12(3):529-538
pubmed: 27908825
J Clin Oncol. 2020 May 10;38(14):1608-1632
pubmed: 31990617
J Thorac Oncol. 2016 Apr;11(4):556-65
pubmed: 26724471
ESMO Open. 2017 May 2;2(2):e000132
pubmed: 28761738
Eur Respir J. 2015 Apr;45(4):1132-41
pubmed: 25700389
Front Med. 2018 Aug;12(4):490-495
pubmed: 30022460
Biomed Rep. 2020 Aug;13(2):2
pubmed: 32509305

Auteurs

Valéry Refeno (V)

Oncology Department, CHU Amiens, Université de Picardie Jules Vernes, 80000 Amiens, France.
Oncology Department, Professeur Zafisaona Gabriel Hospital, Université de Mahajanga, Mahajanga 401, Madagascar.
Faculté de Médecine, Université d'Antananarivo, Antananarivo 101, Madagascar.

Michele Lamuraglia (M)

Oncology Department, CHU Amiens, Université de Picardie Jules Vernes, 80000 Amiens, France.
Sorbonne Universités, UMPC Univ. Paris 06, UMR 7371, UMR S 1146, Laboratoire d'Imagerie Biomédicale, 75005 Paris, France.

Safae Terrisse (S)

AP-HP, Hôpital Saint Louis, Oncology Unit, 1 Avenue Claude Vellefaux, 75010 Paris, France.

Clément Bonnet (C)

AP-HP, Hôpital Saint Louis, Oncology Unit, 1 Avenue Claude Vellefaux, 75010 Paris, France.

Clément Dumont (C)

AP-HP, Hôpital Saint Louis, Oncology Unit, 1 Avenue Claude Vellefaux, 75010 Paris, France.

Ludovic Doucet (L)

Department of Medical Oncology, Institut de Cancérologie de l'Ouest, 44800 Saint-Herblain, France.

Damien Pouessel (D)

Department of Medical Oncology, Institut Claudius Regaud, IUCT-O, 31300 Toulouse, France.

Stephane Culine (S)

AP-HP, Hôpital Saint Louis, Oncology Unit, 1 Avenue Claude Vellefaux, 75010 Paris, France.

Classifications MeSH