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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

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 repo...

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Autores principales: Lee, Jang Ho, Kim, Eun Young, Park, Cheol-Kyu, Lee, Shin Yup, Lee, Min Ki, Yoon, Seong-Hoon, Lee, Jeong Eun, Lee, Sang Hoon, Kim, Seung Joon, Lee, Sung Yong, Lim, Jun Hyeok, Jang, Tae-Won, Jang, Seung Hun, Lee, Kye Young, Lee, Seung Hyeun, Yang, Sei Hoon, Park, Dong Won, Park, Chan Kwon, Kang, Hye Seon, Yeo, Chang Dong, Choi, Chang-Min, Lee, Jae Cheol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Cancer Association 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873329/
https://www.ncbi.nlm.nih.gov/pubmed/36049499
http://dx.doi.org/10.4143/crt.2022.381
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author Lee, Jang Ho
Kim, Eun Young
Park, Cheol-Kyu
Lee, Shin Yup
Lee, Min Ki
Yoon, Seong-Hoon
Lee, Jeong Eun
Lee, Sang Hoon
Kim, Seung Joon
Lee, Sung Yong
Lim, Jun Hyeok
Jang, Tae-Won
Jang, Seung Hun
Lee, Kye Young
Lee, Seung Hyeun
Yang, Sei Hoon
Park, Dong Won
Park, Chan Kwon
Kang, Hye Seon
Yeo, Chang Dong
Choi, Chang-Min
Lee, Jae Cheol
author_facet Lee, Jang Ho
Kim, Eun Young
Park, Cheol-Kyu
Lee, Shin Yup
Lee, Min Ki
Yoon, Seong-Hoon
Lee, Jeong Eun
Lee, Sang Hoon
Kim, Seung Joon
Lee, Sung Yong
Lim, Jun Hyeok
Jang, Tae-Won
Jang, Seung Hun
Lee, Kye Young
Lee, Seung Hyeun
Yang, Sei Hoon
Park, Dong Won
Park, Chan Kwon
Kang, Hye Seon
Yeo, Chang Dong
Choi, Chang-Min
Lee, Jae Cheol
author_sort Lee, Jang Ho
collection PubMed
description 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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spelling pubmed-98733292023-02-02 Real-World Study of Osimertinib in Korean Patients with Epidermal Growth Factor Receptor T790M Mutation–Positive Non–Small Cell Lung Cancer Lee, Jang Ho Kim, Eun Young Park, Cheol-Kyu Lee, Shin Yup Lee, Min Ki Yoon, Seong-Hoon Lee, Jeong Eun Lee, Sang Hoon Kim, Seung Joon Lee, Sung Yong Lim, Jun Hyeok Jang, Tae-Won Jang, Seung Hun Lee, Kye Young Lee, Seung Hyeun Yang, Sei Hoon Park, Dong Won Park, Chan Kwon Kang, Hye Seon Yeo, Chang Dong Choi, Chang-Min Lee, Jae Cheol Cancer Res Treat Original Article 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. Korean Cancer Association 2023-01 2022-07-19 /pmc/articles/PMC9873329/ /pubmed/36049499 http://dx.doi.org/10.4143/crt.2022.381 Text en Copyright © 2023 by the Korean Cancer Association https://creativecommons.org/licenses/by-nc/4.0/This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Jang Ho
Kim, Eun Young
Park, Cheol-Kyu
Lee, Shin Yup
Lee, Min Ki
Yoon, Seong-Hoon
Lee, Jeong Eun
Lee, Sang Hoon
Kim, Seung Joon
Lee, Sung Yong
Lim, Jun Hyeok
Jang, Tae-Won
Jang, Seung Hun
Lee, Kye Young
Lee, Seung Hyeun
Yang, Sei Hoon
Park, Dong Won
Park, Chan Kwon
Kang, Hye Seon
Yeo, Chang Dong
Choi, Chang-Min
Lee, Jae Cheol
Real-World Study of Osimertinib in Korean Patients with Epidermal Growth Factor Receptor T790M Mutation–Positive Non–Small Cell Lung Cancer
title Real-World Study of Osimertinib in Korean Patients with Epidermal Growth Factor Receptor T790M Mutation–Positive Non–Small Cell Lung Cancer
title_full Real-World Study of Osimertinib in Korean Patients with Epidermal Growth Factor Receptor T790M Mutation–Positive Non–Small Cell Lung Cancer
title_fullStr Real-World Study of Osimertinib in Korean Patients with Epidermal Growth Factor Receptor T790M Mutation–Positive Non–Small Cell Lung Cancer
title_full_unstemmed Real-World Study of Osimertinib in Korean Patients with Epidermal Growth Factor Receptor T790M Mutation–Positive Non–Small Cell Lung Cancer
title_short Real-World Study of Osimertinib in Korean Patients with Epidermal Growth Factor Receptor T790M Mutation–Positive Non–Small Cell Lung Cancer
title_sort real-world study of osimertinib in korean patients with epidermal growth factor receptor t790m mutation–positive non–small cell lung cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873329/
https://www.ncbi.nlm.nih.gov/pubmed/36049499
http://dx.doi.org/10.4143/crt.2022.381
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