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

Authors
 Jang Ho Lee   ;   Eun Young Kim  ;   Cheol-Kyu Park  ;   Shin Yup Lee  ;   Min Ki Lee  ;   Seong-Hoon Yoon  ;   Jeong Eun Lee  ;   Sang Hoon Lee  ;   Seung Joon Kim  ;   Sung Yong Lee  ;   Jun Hyeok Lim  ;   Tae-Won Jang  ;   Seung Hun Jang  ;   Kye Young Lee  ;   Seung Hyeun Lee  ;   Sei Hoon Yang   ;   Dong Won Park  ;   Chan Kwon Park  ;   Hye Seon Kang   ;   Chang Dong Yeo  ;   Chang-Min Choi  ;   Jae Cheol Lee 
Citation
 CANCER RESEARCH AND TREATMENT, Vol.55(1) : 112-122, 2023-01 
Journal Title
CANCER RESEARCH AND TREATMENT
ISSN
 1598-2998 
Issue Date
2023-01
MeSH
Antineoplastic Agents* / adverse effects ; Carcinoma, Non-Small-Cell Lung* / drug therapy ; Carcinoma, Non-Small-Cell Lung* / genetics ; Carcinoma, Non-Small-Cell Lung* / pathology ; ErbB Receptors / genetics ; Humans ; Lung Neoplasms* / drug therapy ; Lung Neoplasms* / genetics ; Lung Neoplasms* / pathology ; Mutation ; Protein Kinase Inhibitors / adverse effects ; Republic of Korea
Keywords
EGFR T790M ; Non–small cell lung cancer ; Osimertinib ; Real-world efficacy
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.
Files in This Item:
T202301273.pdf Download
DOI
10.4143/crt.2022.381
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Eun Young(김은영) ORCID logo https://orcid.org/0000-0002-3281-5744
Lee, Sang Hoon(이상훈) ORCID logo https://orcid.org/0000-0002-7706-5318
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/193643
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