Real-Life Efficacy of Osimertinib in Pretreated Octogenarian Patients with T790M-Mutated Advanced Non-small Cell Lung Cancer.


Journal

Targeted oncology
ISSN: 1776-260X
Titre abrégé: Target Oncol
Pays: France
ID NLM: 101270595

Informations de publication

Date de publication:
06 2019
Historique:
pubmed: 24 5 2019
medline: 3 3 2020
entrez: 24 5 2019
Statut: ppublish

Résumé

The resistance mutation T790M is reported in 50-60% of patients pretreated with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs). Osimertinib has been approved in these patients, but data in octogenarians remain rare. The objective of this retrospective analysis was to evaluate in real life the efficacy of osimertinib in a population of octogenarian patients. This retrospective multicentric study included pretreated octogenarian patients with EGFR T790M-mutated advanced non-small cell lung cancer (NSCLC) in the setting of the French early access program for osimertinib. The primary endpoints were progression-free survival (PFS) and overall survival (OS) from osimertinib initiation. In total, 43 patients were included (mean age 84.6 years; women 90.7%: adenocarcinoma 100%; never smokers 90.5%; at osimertinib initiation: performance status ≥ 2, 42.4%; stage 4, 93.0%; brain metastases 16.3%). Patients received a median of two lines of treatment before osimertinib initiation, and all received first- or second-generation EGFR TKIs before osimertinib (first line in 79.1%). Osimertinib was used as a second-line treatment in 41.9% of cases and third line or more in 58.1%. Median PFS was 17.5 (95% confidence interval [CI] 12.2-19.0) months for the entire population: 20.6 (95% CI 18.8-not reached) months in patients with brain metastases and 16.7 (95% CI 10.4-18.9) months in patients without (p = 0.1). There was no significant difference for osimertinib treatment as second or third line or more (17.1 vs. 18.6 months, respectively). OS was 22.8 (95% CI 15.7-not reached) months from osimertinib initiation. The efficacy of osimertinib as second-line treatment or more in octogenarian pretreated patients with EGFR T790M-mutated advanced NSCLC in a real-life setting was similar to that in randomized controlled trials.

Sections du résumé

BACKGROUND
The resistance mutation T790M is reported in 50-60% of patients pretreated with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs). Osimertinib has been approved in these patients, but data in octogenarians remain rare.
OBJECTIVE
The objective of this retrospective analysis was to evaluate in real life the efficacy of osimertinib in a population of octogenarian patients.
METHODS
This retrospective multicentric study included pretreated octogenarian patients with EGFR T790M-mutated advanced non-small cell lung cancer (NSCLC) in the setting of the French early access program for osimertinib. The primary endpoints were progression-free survival (PFS) and overall survival (OS) from osimertinib initiation.
RESULTS
In total, 43 patients were included (mean age 84.6 years; women 90.7%: adenocarcinoma 100%; never smokers 90.5%; at osimertinib initiation: performance status ≥ 2, 42.4%; stage 4, 93.0%; brain metastases 16.3%). Patients received a median of two lines of treatment before osimertinib initiation, and all received first- or second-generation EGFR TKIs before osimertinib (first line in 79.1%). Osimertinib was used as a second-line treatment in 41.9% of cases and third line or more in 58.1%. Median PFS was 17.5 (95% confidence interval [CI] 12.2-19.0) months for the entire population: 20.6 (95% CI 18.8-not reached) months in patients with brain metastases and 16.7 (95% CI 10.4-18.9) months in patients without (p = 0.1). There was no significant difference for osimertinib treatment as second or third line or more (17.1 vs. 18.6 months, respectively). OS was 22.8 (95% CI 15.7-not reached) months from osimertinib initiation.
CONCLUSION
The efficacy of osimertinib as second-line treatment or more in octogenarian pretreated patients with EGFR T790M-mutated advanced NSCLC in a real-life setting was similar to that in randomized controlled trials.

Identifiants

pubmed: 31119481
doi: 10.1007/s11523-019-00646-4
pii: 10.1007/s11523-019-00646-4
doi:

Substances chimiques

Acrylamides 0
Aniline Compounds 0
Antineoplastic Agents 0
Biomarkers, Tumor 0
osimertinib 3C06JJ0Z2O
EGFR protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

307-314

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Auteurs

Jean-Bernard Auliac (JB)

Service de Pneumologie et Oncologie Thoracique, Hôpital F. Quesnay, 2 Boulevard de Sully, 78200, Mantes-la-Jolie, France. j-b.auliac@ch-mantes-la-jolie.fr.

Karima Saboundji (K)

Pneumologie, CH François Quesnay, Mantes-la-Jolie, France.

Michel Andre (M)

Pneumologie, CHU Saint Denis, site Félix Guyon, Réunion, France.

Jeannick Madelaine (J)

Pneumologie, CHU Caen Normandie, Caen, France.

Gilles Quere (G)

Pneumologie, CHRU Brest, site Hôpital Morvan, Brest, France.

Philippe Masson (P)

Pneumologie, CH Cholet, Cholet, France.

Alain Vergnenegre (A)

Pneumologie, CHU Limoges, Limoges, France.

Régine Lamy (R)

Oncologie, CH Bretagne Sud, Lorient, France.

Stéphane Raymond (S)

Pneumologie, Hôpital Robert Schuman, Metz, France.

Anne-Marie Chiappa (AM)

Pneumologie, CH de Cornouaille, Quimper, France.

Pierre-Alexandre Hauss (PA)

Pneumologie, CH Elbeuf, Saint-Aubin-lès-Elbeuf, France.

Pierre Fournel (P)

Oncologie, Institut de Cancérologie de la Loire, Saint-Priest-en-Jarez, France.

Romain Corre (R)

Pneumologie, Hôpital Pontchaillou, Rennes, France.

Christos Chouaid (C)

Service de Pneumologie et Oncologie Thoracique, Hôpital F. Quesnay, 2 Boulevard de Sully, 78200, Mantes-la-Jolie, France.

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Classifications MeSH