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Alectinib Versus Crizotinib in Asian Patients With Treatment-Naïve Advanced ALK-Positive NSCLC: Five-Year Update From the Phase 3 ALESIA Study.
Zhou, Caicun; Lu, You; Kim, Sang-We; Reungwetwattana, Thanyanan; Zhou, Jianying; Zhang, Yiping; He, Jianxing; Yang, Jin-Ji; Cheng, Ying; Lee, Se-Hoon; Chang, Jianhua; Fang, Jian; Liu, Zhe; Bu, Lilian; Qian, Li; Xu, Tingting; Archer, Venice; Hilton, Magalie; Zhou, Mingzhu; Zhang, Li.
Afiliación
  • Zhou C; Department of Medical Oncology, Shanghai Pulmonary Hospital, Tongji University, Shanghai, People's Republic of China.
  • Lu Y; Department of Thoracic Oncology, West China Hospital, Sichuan University, Chengdu, People's Republic of China.
  • Kim SW; Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
  • Reungwetwattana T; Division of Medical Oncology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
  • Zhou J; Department of Respiratory Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, People's Republic of China.
  • Zhang Y; Department of Thoracic Oncology, Zhejiang Cancer Hospital, Hangzhou, People's Republic of China.
  • He J; Department of Thoracic Surgery, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, People's Republic of China.
  • Yang JJ; Guangdong Lung Cancer Institute, Guangdong General Hospital, Guangzhou, People's Republic of China.
  • Cheng Y; Department of Oncology, Jilin Cancer Hospital, Changchun, People's Republic of China.
  • Lee SH; Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
  • Chang J; Cancer Hospital and Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, People's Republic of China.
  • Fang J; Department of Thoracic Oncology, Beijing Cancer Hospital, Beijing, People's Republic of China.
  • Liu Z; Department of Oncology, Beijing Chest Hospital, Capital Medical University, Beijing, People's Republic of China.
  • Bu L; Department of Data Science, Roche (China) Holding Ltd., Shanghai, People's Republic of China.
  • Qian L; Department of Clinical Science, Roche (China) Holding Ltd., Shanghai, People's Republic of China.
  • Xu T; Department of Clinical Science, Roche (China) Holding Ltd., Shanghai, People's Republic of China.
  • Archer V; Product Development, Roche Products Ltd., Welwyn Garden City, United Kingdom.
  • Hilton M; Product Development Data Sciences, F. Hoffmann-La Roche Ltd., Basel, Switzerland.
  • Zhou M; Department of Safety, Roche (China) Holding Ltd., Shanghai, People's Republic of China.
  • Zhang L; Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, People's Republic of China.
JTO Clin Res Rep ; 5(9): 100700, 2024 Sep.
Article en En | MEDLINE | ID: mdl-39282663
ABSTRACT

Introduction:

Previous results from the phase 3 ALESIA study (NCT02838420) revealed that alectinib (a central nervous system [CNS]-active, ALK inhibitor) had clinical benefits in treatment-naïve Asian patients with advanced ALK-positive NSCLC, consistent with the global ALEX study. We present updated data after more than or equal to 5 years of follow-up from the "last patient in" date.

Methods:

Adult patients with treatment-naïve, advanced ALK-positive NSCLC from mainland China, South Korea, and Thailand were randomized 21 to receive twice-daily 600 mg alectinib (n = 125) or 250 mg crizotinib (n = 62). The primary endpoint was investigator-assessed progression-free survival. Secondary or exploratory endpoints included overall survival, objective response rate, time to CNS progression, and safety.

Results:

At the data cutoff (May 16, 2022), the median survival follow-up was 61 and 51 months in the alectinib and crizotinib arms, respectively. Median progression-free survival was 41.6 months with alectinib versus 11.1 months with crizotinib (stratified hazard ratio = 0.33, 95% confidence interval 0.23-0.49). Overall survival data remain immature; 5-year overall survival rates were 66.4% (alectinib arm) versus 56.1% (crizotinib arm). Objective response rate was 91.2% versus 77.4% with alectinib and crizotinib, respectively. CNS progression was delayed with alectinib versus crizotinib (cause-specific hazard ratio = 0.16, 95% confidence interval 0.08-0.32). Median treatment duration was longer with alectinib versus crizotinib (42.3 versus 12.6 mo). No new safety signals were observed.

Conclusions:

With four additional years of follow-up, these updated results confirm the clinical benefit and manageable safety of alectinib in Asian patients with advanced ALK-positive NSCLC, and confirm alectinib as a standard-of-care treatment for patients with advanced ALK-positive NSCLC.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: JTO Clin Res Rep Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: JTO Clin Res Rep Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos