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Real-World Study of Osimertinib in Korean Patients with Epidermal Growth Factor Receptor T790M Mutation-Positive Non-Small Cell Lung CancerReal-World Study of Osimertinib in Korean Patients with Epidermal Growth Factor Receptor T790M Mutation–Positive Non–Small Cell Lung Cancer

Other Titles
Real-World Study of Osimertinib in Korean Patients with Epidermal Growth Factor Receptor T790M Mutation–Positive Non–Small Cell Lung Cancer
Authors
Lee, Jang HoKim, Eun YoungPark, Cheol-KyuLee, Shin YupLee, Min KiYoon, Seong-HoonLee, Jeong EunLee, Sang HoonKim, Seung JoonLee, Sung YongLim, Jun HyeokJang, Tae-WonJang, Seung HunLee, Kye YoungLee, Seung HyeunYang, Sei HoonPark, Dong WonPark, Chan KwonKang, Hye SeonYeo, Chang DongChoi, Chang-MinLee, Jae Cheol
Issue Date
Jan-2023
Publisher
대한암학회
Keywords
Osimertinib; EGFR T790M; Non–small cell lung cancer; Real-world efficacy
Citation
Cancer Research and Treatment, v.55, no.1, pp 112 - 122
Pages
11
Indexed
SCIE
SCOPUS
KCI
Journal Title
Cancer Research and Treatment
Volume
55
Number
1
Start Page
112
End Page
122
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/191645
DOI
10.4143/crt.2022.381
ISSN
1598-2998
2005-9256
Abstract
PURPOSE: Although osimertinib is the standard-of-care treatment of epidermal growth factor receptor (EGFR) T790M mutation-positive non-small cell lung cancer, real-world evidence on the efficacy of osimertinib is not enough to reflect the complexity of the entire course of treatment. Herein, we report on the use of osimertinib in patients with EGFR T790M mutation-positive non-small cell lung cancer who had previously received EGFR tyrosine kinase inhibitor (TKI) treatment in Korea. MATERIALS AND METHODS: Patients with confirmed EGFR T790M after disease progression of prior EGFR-TKI were enrolled and administered osimertinib 80 mg daily. The primary effectiveness outcome was progression-free survival, with time-to-treatment discontinuation, treatment and adverse effects leading to treatment discontinuation, and overall survival being the secondary endpoints. RESULTS: A total of 558 individuals were enrolled, and 55.2% had investigator-assessed responses. The median progression-free survival was 14.2 months (95% confidence interval [CI], 13.0 to 16.4), and the median time-to-treatment discontinuation was 15.0 months (95% CI, 14.1 to 15.9). The median overall survival was 36.7 months (95% CI, 30.9 to not reached). The benefit with osimertinib was consistent regardless of the age, sex, smoking history, and primary EGFR mutation subtype. However, hepatic metastases at the time of diagnosis, the presence of plasma EGFR T790M, and the shorter duration of prior EGFR-TKI treatment were poor predictors of osimertinib treatment. Ten patients (1.8%), including three with pneumonitis, had to discontinue osimertinib due to severe adverse effects. CONCLUSION: Osimertinib demonstrated its clinical effectiveness and survival benefit for EGFR T790M mutation-positive in Korean patients with no new safety signals.
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