Osimertinib for patients with EGFR T790M mutation-positive non-small-cell lung cancer and a poor performance status.


Journal

Japanese journal of clinical oncology
ISSN: 1465-3621
Titre abrégé: Jpn J Clin Oncol
Pays: England
ID NLM: 0313225

Informations de publication

Date de publication:
01 Jul 2019
Historique:
received: 24 01 2019
revised: 22 02 2019
accepted: 19 03 2019
pubmed: 29 3 2019
medline: 31 10 2019
entrez: 29 3 2019
Statut: ppublish

Résumé

Osimertinib is a third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) that is effective against EGFR T790M mutation-positive non-small-cell lung cancer (NSCLC) in patients who have good performance status (PS). However, the efficacy and safety of osimertinib for patients with poor PS is unknown. We retrospectively evaluated the efficacy and safety of osimertinib in patients with EGFR T790M mutation-positive NSCLC who had Eastern Cooperative Oncology Group PS scores of 2-4 and who were administered 80 mg of osimertinib once daily between March 2016 and February 2017. Thirty patients (8 men and 22 women) with EGFR T790M mutation-positive NSCLC were evaluated; their median age was 66 years (range: 39-89 years). Twenty-four and six patients had PS scores of 2 and 3, respectively; none had a PS score of 4. All patients had previously been treated with first- or second-generation EGFR-TKIs. T790M was detected in the tumor samples of 23 patients, the blood samples of two patients, and both the tumor and blood samples of five patients. The overall response rate was 53% (95% confidence interval: 36-70%), and the PS score improvement rate was 63%. The median progression-free survival was 8.2 months (95% confidence interval: 4.3-13.2 months), while the median overall survival time was not reached. No patient required treatment cessation owing to adverse events, and no treatment-related deaths occurred. Osimertinib therapy demonstrates promising efficacy and acceptable safety in patients with EGFR T790M mutation-positive NSCLC who have poor PS.

Sections du résumé

BACKGROUND BACKGROUND
Osimertinib is a third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) that is effective against EGFR T790M mutation-positive non-small-cell lung cancer (NSCLC) in patients who have good performance status (PS). However, the efficacy and safety of osimertinib for patients with poor PS is unknown.
METHODS METHODS
We retrospectively evaluated the efficacy and safety of osimertinib in patients with EGFR T790M mutation-positive NSCLC who had Eastern Cooperative Oncology Group PS scores of 2-4 and who were administered 80 mg of osimertinib once daily between March 2016 and February 2017.
RESULTS RESULTS
Thirty patients (8 men and 22 women) with EGFR T790M mutation-positive NSCLC were evaluated; their median age was 66 years (range: 39-89 years). Twenty-four and six patients had PS scores of 2 and 3, respectively; none had a PS score of 4. All patients had previously been treated with first- or second-generation EGFR-TKIs. T790M was detected in the tumor samples of 23 patients, the blood samples of two patients, and both the tumor and blood samples of five patients. The overall response rate was 53% (95% confidence interval: 36-70%), and the PS score improvement rate was 63%. The median progression-free survival was 8.2 months (95% confidence interval: 4.3-13.2 months), while the median overall survival time was not reached. No patient required treatment cessation owing to adverse events, and no treatment-related deaths occurred.
CONCLUSIONS CONCLUSIONS
Osimertinib therapy demonstrates promising efficacy and acceptable safety in patients with EGFR T790M mutation-positive NSCLC who have poor PS.

Identifiants

pubmed: 30920616
pii: 5421495
doi: 10.1093/jjco/hyz041
doi:

Substances chimiques

Acrylamides 0
Aniline Compounds 0
Antineoplastic Agents 0
Protein Kinase Inhibitors 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

Langues

eng

Sous-ensembles de citation

IM

Pagination

671-675

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Kazuhisa Nakashima (K)

Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.

Madoka Kimura (M)

Department of Thoracic Oncology, Osaka International Cancer Institute, Osaka, Japan.

Hiroaki Akamatsu (H)

Internal Medicine III, Wakayama Medical University, Wakayama, Japan.

Haruko Daga (H)

Department of Medical Oncology, Osaka City General Hospital, Osaka, Japan.

Hisao Imai (H)

Division of Respiratory Medicine, Gunma Prefectural Cancer Center, Gunma, Japan.

Tetsuhiko Taira (T)

Division of Pulmonary Medicine, Minami Kyushu National Hospital, Kagoshima, Japan.

Ryo Ko (R)

Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.

Yasushi Hisamatsu (Y)

Department of Thoracic Medical Oncology, Oita Prefectural Hospital, Oita, Japan.

Kazumi Nishino (K)

Department of Thoracic Oncology, Osaka International Cancer Institute, Osaka, Japan.

Takeya Sugimoto (T)

Internal Medicine III, Wakayama Medical University, Wakayama, Japan.

Yosuke Miyashita (Y)

Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.

Toshiaki Takahashi (T)

Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan.

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Classifications MeSH