Observational Study of Sequential Afatinib and Osimertinib in EGFR Mutation-Positive NSCLC: Patients Treated with a 40-mg Starting Dose of Afatinib.


Journal

Advances in therapy
ISSN: 1865-8652
Titre abrégé: Adv Ther
Pays: United States
ID NLM: 8611864

Informations de publication

Date de publication:
02 2020
Historique:
received: 01 11 2019
pubmed: 22 12 2019
medline: 6 10 2020
entrez: 22 12 2019
Statut: ppublish

Résumé

Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are the standard of care for patients with EGFR mutation-positive non-small cell lung cancer (NSCLC). However, questions remain about the optimal treatment sequence of EGFR TKIs. The global, observational GioTag study demonstrated prolonged time on treatment with sequential afatinib and osimertinib therapy in patients who acquired the T790M mutation. Here, we assessed outcomes in patients who received the approved 40-mg starting dose of afatinib, as used in the clinical trial setting. In the non-interventional, global, multicenter GioTag study, patients had T790M-positive disease following first-line afatinib and started osimertinib treatment ≥ 10 months prior to data entry. Primary outcome was time on treatment. This subanalysis assessed outcomes in patients who received afatinib 40 mg. In 169 patients who received an afatinib starting dose of 40 mg, median time on treatment was 27.6 months (90% confidence interval [CI] 26.3-31.3). Benefit was seen across patient subgroups, particularly those with Del19-positive disease and Asian patients; median time on treatment was 29.9 months (90% CI 27.6-46.7) in patients with Del19-positive disease and 46.7 months (90% CI 28.4-not reached) in Asian patients. The 2-year overall survival rate was 80%. These real-world results support the overall study results and demonstrate prolonged time on treatment with sequential afatinib and osimertinib. The results suggest that sequential afatinib and osimertinib is a feasible therapeutic strategy for patients who acquire the T790M mutation, particularly those with Del19-positive disease or Asian patients. NCT03370770.

Identifiants

pubmed: 31863283
doi: 10.1007/s12325-019-01187-y
pii: 10.1007/s12325-019-01187-y
pmc: PMC7004431
doi:

Substances chimiques

Acrylamides 0
Aniline Compounds 0
Antineoplastic Agents 0
Protein Kinase Inhibitors 0
Afatinib 41UD74L59M
EGFR protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1
Protein-Tyrosine Kinases EC 2.7.10.1

Banques de données

ClinicalTrials.gov
['NCT03370770']
figshare
['10.6084/m9.figshare.11295440']

Types de publication

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

Langues

eng

Pagination

759-769

Références

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Auteurs

Nobuyuki Yamamoto (N)

Division of Pulmonology and Medical Oncology, Wakayama Medical University, Kimiidera, Wakayama City, Wakayama, Japan. nbyamamo@wakayama-med.ac.jp.

Takeshi Mera (T)

Specialty Care Medicine, Medicine Division, Nippon Boehringer Ingelheim Co., Ltd, Tokyo, Japan.

Angela Märten (A)

Medical Affairs Oncology, Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany.

Maximilian J Hochmair (MJ)

Department of Respiratory and Critical Care Medicine, Vienna North Hospital, Karl Landsteiner Institute of Lung Research and Pulmonary Oncology, Vienna, Austria.

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Classifications MeSH