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Real‐world outcome of crizotinib for anaplastic lymphoma kinase‐positive lung cancer: Multicenter retrospective analysis in South Korea.

Authors :
Jeon, Da Som
Park, Cheol‐kyu
Kim, Seung Joon
Park, Chan Kwon
Chang, Yoon Soo
Jung, Chi Young
Lee, Sung Yong
Lee, Shin‐Yup
Ryu, Jeong‐Seon
Lee, Jeong Eun
Lee, Kye Young
Jang, Tae Won
Jang, Seung Hun
Yoon, Seong Hoon
Lee, Sang Hoon
Choi, Chang‐min
Kim, Hyeong Ryul
Kim, Yeon Joo
Source :
Thoracic Cancer. Feb2024, Vol. 15 Issue 6, p448-457. 10p.
Publication Year :
2024

Abstract

Background: About 3%–5% of non‐small cell lung cancer (NSCLC) presents positive anaplastic lymphoma kinase (ALK). Recently, several target agents have been approved as a treatment for ALK‐positive NSCLC. This study aimed to analyze the real‐world efficacy and outcome when administered crizotinib, the first approved target agent for ALK‐positive NSCLC, according to first‐ or late‐line treatment. Methods: A total of 290 patients with ALK‐positive advanced NSCLC who were treated with crizotinib in 15 institutions in South Korea from January 2009 to December 2018 were enrolled. Results: The median age of patients was 57.0 years, and 50.3% were male. The median follow‐up duration was 29.3 months. Among them, 113 patients received crizotinib as first‐line therapy. The objective response rate (ORR) was 60.1% (57.0% for first‐line recipients, 61.8% for second−/later‐line). Median (95% CI) progression‐free survival (PFS) was 13.7 (11.6–17.0) months. For first‐line recipients, overall survival (OS) was 26.3 (17.6–35.0) months. No significant difference in ORR, PFS and OS, according to the setting of crizotinib initiation, was observed. In a multivariate Cox regression analysis, old age, male gender, initially metastatic, and number of metastatic organs were associated with poor PFS and OS. The most common adverse events were nausea and vomiting, and severe adverse event leading to dose adjustment was hepatotoxicity. Conclusions: ORR, PFS, OS, and adverse event profiles were comparable to previous clinical trials. Our findings could aid in the efficient management of ALK‐positive lung cancer patients. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17597706
Volume :
15
Issue :
6
Database :
Academic Search Index
Journal :
Thoracic Cancer
Publication Type :
Academic Journal
Accession number :
175605246
Full Text :
https://doi.org/10.1111/1759-7714.15213