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Real-world outcome of crizotinib for anaplastic lymphoma kinase-positive lung cancer: Multicenter retrospective analysis in South Korea.
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.
Affiliation
  • Jeon DS; Department of Pulmonary and Critical Care Medicine, Nowon Eulji Medical Center, University of Eulji, Seoul, South Korea.
  • Park CK; Department of Pulmonary and Critical Care Medicine, Chonnam National University Hwasun hospital, Chonnam National University, Jeollanam-do, Republic of Korea.
  • Kim SJ; Department of Internal Medicine, Postech-Catholic Biomedical Engineering Institute, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
  • Park CK; Department of Pulmonary and Critical Care Medicine, Catholic University of Korean Yeouido Saint Mary's Hospital, Seoul, Korea.
  • Chang YS; Department of Internal Medicine, Yonsei University College of Medicine, 8th Floor Annex Building, Yongdong Severance Hospital, Seoul, Republic of Korea.
  • Jung CY; Department of Internal Medicine, Daegu Catholic University School of Medicine, Daegu, Korea.
  • Lee SY; Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Korea.
  • Lee SY; Division of Pulmonary and Critical Care Medicine, Kyungpook National University Chilgok Hospital, Daegu, Korea.
  • Ryu JS; Department of Pulmonary and Critical Care Medicine, Inha University Hospital, Incheon, Republic of Korea.
  • Lee JE; Department of Internal Medicine, Chungnam National University Hospital, Daejeon, Republic of Korea.
  • Lee KY; Department of Pulmonary Medicine, Konkuk University School of Medicine, Seoul, Republic of Korea.
  • Jang TW; Department of Internal Medicine, Kosin University Medical College, Pusan, Korea.
  • Jang SH; Department of Pulmonary, Allergy and Critical Care Medicine, Hallym University Sacred Heart Hospital, Anyang, Republic of Korea.
  • Yoon SH; Department of Internal Medicine, School of Medicine, Pusan National University, Yangsan, Republic of Korea.
  • Lee SH; Division of Pulmonology, Institute of Chest Disease, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.
  • Choi CM; Department of Pulmonary and Critical Care Medicine, Asan Medical Centre, University of Ulsan College of Medicine, Seoul, Republic of Korea.
  • Kim HR; Department of Oncology, Asan Medical Centre, University of Ulsan College of Medicine, Seoul, Republic of Korea.
  • Kim YJ; Department of Pulmonary and Critical Care Medicine, Asan Medical Centre, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Thorac Cancer ; 15(6): 448-457, 2024 Feb.
Article in En | MEDLINE | ID: mdl-38171544
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Non-Small-Cell Lung / Lung Neoplasms Type of study: Risk_factors_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Thorac Cancer Year: 2024 Document type: Article Affiliation country: Corea del Sur

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Non-Small-Cell Lung / Lung Neoplasms Type of study: Risk_factors_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Thorac Cancer Year: 2024 Document type: Article Affiliation country: Corea del Sur