Wu, Yi-Long; Zhou, Caicun; Hu, Cheng-Ping; Feng, Jifeng; Lu, Shun; Huang, Yunchao; Li, Wei; Hou, Mei; Shi, Jian Hua; Lee, Kye Young; Xu, Chong-Rui; Massey, Dan; Kim, Miyoung; Shi, Yang; Geater, Sarayut L
The Lancet. Oncology
2014Feb ; 15 ( 2 ) :213-22.
PMID : 24439929
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Wu, Yi-Long - Guangdong Lung Cancer Institute, Guangdong General Hospital & Guangdong Academy of Medical Sciences, Guangzhou, China. Electronic address syylwu@live.cn.
Zhou, Caicun - Shanghai Pulmonary Hospital, Yangpu District, Shanghai, China.
Hu, Cheng-Ping - Department of Pulmonary Medicine, Xiangya Hospital, Central South University, Changsha, China.
Feng, Jifeng - Department of Internal Medicine, Jiangsu Provincial Tumor Hospital, Nanjing, Jiangsu, China.
Lu, Shun - Shanghai Lung Tumor Clinical Medical Center, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, China.
Huang, Yunchao - Yunnan Tumor Hospital (The Third Affiliated Hospital of Kunming Medical University), Kunming, Yunnan Province, China.
Li, Wei - Cancer Center, First Hospital of Jilin University, Changchun, China.
Hou, Mei - West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Shi, Jian Hua - Lin Yi Tumor Hospital, Linyi, Shandong Province, China.
Lee, Kye Young - Konkuk University Medical Center, Seoul, South Korea.
Xu, Chong-Rui - Guangdong Lung Cancer Institute, Guangdong General Hospital & Guangdong Academy of Medical Sciences, Guangzhou, China.
Massey, Dan - Boehringer Ingelheim, Bracknell, UK.
Kim, Miyoung - Boehringer Ingelheim Korea, Seoul, South Korea.
Shi, Yang - Boehringer Ingelheim International Trading, Shanghai, China.
Geater, Sarayut L - Division of Respiratory and Respiratory Critical Care Medicine, Department of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand.
ABSTRACT
BACKGROUND: Afatinib-an oral irreversible ErbB family blocker-improves progression-free survival compared with pemetrexed and cisplatin for first-line treatment of patients with EGFR mutation-positive advanced non-small-cell lung cancer (NSCLC). We compared afatinib with gemcitabine and cisplatin-a chemotherapy regimen widely used in Asia-for first-line treatment of Asian patients with EGFR mutation-positive advanced NSCLC.
METHODS: This open-label, randomised phase 3 trial was done at 36 centres in China, Thailand, and South Korea. After central testing for EGFR mutations, treatment-naive patients (stage IIIB or IV cancer [American Joint Committee on Cancer version 6], performance status 0-1) were randomly assigned (2:1) to receive either oral afatinib (40 mg per day) or intravenous gemcitabine 1000 mg/m(2) on day 1 and day 8 plus cisplatin 75 mg/m(2) on day 1 of a 3-week schedule for up to six cycles. Randomisation was done centrally with a random number-generating system and an interactive internet and voice-response system. Randomisation was stratified by EGFR mutation (Leu858Arg, exon 19 deletions, or other; block size three). Clinicians and patients were not masked to treatment assignment, but the independent central imaging review group were. Treatment continued until disease progression, intolerable toxic effects, or withdrawal of consent. The primary endpoint was progression-free survival assessed by independent central review (intention-to-treat population). This study is registered with ClinicalTrials.gov, NCT01121393. FINDINGS: 910 patients were screened and 364 were randomly assigned (242 to afatinib, 122 to gemcitabine and cisplatin). Median progression-free survival was significantly longer in the afatinib group (11·0 months, 95% CI 9·7-13·7) than in the gemcitabine and cisplatin group (5·6 months, 5·1-6·7; hazard ratio 0·28, 95% CI 0·20-0·39; p<0·0001). The most common treatment-related grade 3 or 4 adverse events in the afatinib group were rash or acne (35 [14·6%] of 239 patients), diarrhoea (13 [5·4%]), and stomatitis or mucositis (13 [5·4%]), compared with neutropenia (30 [26·5%] of 113 patients), vomiting (22 [19·5%]), and leucopenia (17 [15·0%]) in the gemcitabine and cisplatin group. Treatment-related serious adverse events occurred in 15 (6·3%) patients in the afatinib group and nine (8·0%) patients in the gemcitabine and cisplatin group. INTERPRETATION: First-line afatinib significantly improves progression-free survival with a tolerable and manageable safety profile in Asian patients with EGFR mutation-positive advanced lung NSCLC. Afatinib should be considered as a first-line treatment option for this patient population. FUNDING: Boehringer Ingelheim. CI - Copyright ??2014 Elsevier Ltd. All rights reserved.
Aged; Antineoplastic Combined Chemotherapy Protocols/adverse effects/*therapeutic use; Asian Continental Ancestry Group/*genetics; Carcinoma, Non-Small-Cell Lung/*drug; China/epidemiology; Cisplatin/administration & dosage; Deoxycytidine/administration & dosage/analogs & derivatives; Disease Progression; Disease-Free Survival; Female; Humans; Intention to Treat Analysis; Kaplan-Meier Estimate; Linear Models; Logistic Models; Lung Neoplasms/*drug therapy/ethnology/genetics/mortality/pathology; Male; Middle Aged; *Mutation; Neoplasm Staging; Odds Ratio; Proportional Hazards Models; Protein Kinase Inhibitors/adverse effects/*therapeutic use; Quinazolines/adverse effects/*therapeutic use; Receptor, Epidermal Growth Factor/antagonists & inhibitors/*genetics; Republic of Korea/epidemiology; Risk Factors; Thailand/epidemiology; Time Factors; Treatment Outcome
MESH
Aged, Antineoplastic Combined Chemotherapy Protocols/adverse effects/*therapeutic use, Asian Continental Ancestry Group/*genetics, Carcinoma, Non-Small-Cell Lung/*drug, China/epidemiology, Cisplatin/administration & dosage, Deoxycytidine/administration & dosage/analogs & derivatives, Disease Progression, Disease-Free Survival, Female, Humans, Intention to Treat Analysis, Kaplan-Meier Estimate, Linear Models, Logistic Models, Lung Neoplasms/*drug therapy/ethnology/genetics/mortality/pathology, Male, Middle Aged, *Mutation, Neoplasm Staging, Odds Ratio, Proportional Hazards Models, Protein Kinase Inhibitors/adverse effects/*therapeutic use, Quinazolines/adverse effects/*therapeutic use, Receptor, Epidermal Growth Factor/antagonists & inhibitors/*genetics, Republic of Korea/epidemiology, Risk Factors, Thailand/epidemiology, Time Factors, Treatment Outcome
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