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Finotonlimab with chemotherapy in recurrent or metastatic head and neck cancer: a randomized phase 3 trial.
Shi, Yuankai; Guo, Wei; Wang, Wei; Wu, Yunteng; Fang, Meiyu; Huang, Xiaoming; Han, Ping; Zhang, Qingyuan; Dong, Pin; Zhou, Xiaohong; Peng, Hanwei; Hu, Chunhong; Chen, Xiaopin; Zhang, Shurong; Chang, Zhiwei; Li, Xiaojiang; Ding, Yuhai; Qu, Song; Jing, Shanghua; Zhang, Songnan; Gui, Lin; Sun, Yan; Wang, Lin; Liu, Yanyan; Wu, Hui; Li, Guoqing; Fu, Zhichao; Shi, Jianhua; Jiang, Hao; Bai, Yuansong; Cui, Jiuwei; Zheng, Yulong; Cui, Wei; Jia, Xiaojing; Zhai, Limin; Cai, Qingqing; Xiong, Deming; Wu, Yunong; Cao, Junning; Wu, Rong; Hu, Guangyuan; Peng, Liang; Xie, Liangzhi; Gai, Wenlin; Wang, Yan; Su, Yuehua.
Afiliação
  • Shi Y; Department of Medical Oncology, Beijing Key Laboratory of Clinical Study on Anticancer Molecular Targeted Drugs, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China. syuankai@cicam
  • Guo W; Department of Oral and Maxillofacial-Head and Neck Oncology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine; College of Stomatology, National Clinical Research Center for Oral Diseases, Shanghai, China.
  • Wang W; Hunan Cancer Hospital, Changsha, China.
  • Wu Y; Department of Oral and Maxillofacial-Head and Neck Oncology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine; College of Stomatology, National Clinical Research Center for Oral Diseases, Shanghai, China.
  • Fang M; Zhejiang Cancer Hospital, Hangzhou, China.
  • Huang X; Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
  • Han P; Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
  • Zhang Q; Harbin Medical University Cancer Hospital, Harbin, China.
  • Dong P; Shanghai General Hospital, Shanghai, China.
  • Zhou X; Chongqing University Cancer Hospital, Chongqing, China.
  • Peng H; Cancer Hospital of Shantou University Medical College, Shantou, China.
  • Hu C; The Second Xiangya Hospital of Central South University, Changsha, China.
  • Chen X; The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
  • Zhang S; Beijing Tongren Hospital, Capital Medical University, Beijing, China.
  • Chang Z; Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Li X; Yunnan Cancer Hospital, Kunming, China.
  • Ding Y; Ganzhou People's Hospital, Ganzhou, China.
  • Qu S; Guangxi Medical University Cancer Hospital, Nanning, China.
  • Jing S; The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
  • Zhang S; Yanbian University Hospital, Yanji, China.
  • Gui L; Department of Medical Oncology, Beijing Key Laboratory of Clinical Study on Anticancer Molecular Targeted Drugs, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
  • Sun Y; Peking University Cancer Hospital, Beijing, China.
  • Wang L; Hainan General Hospital, Haikou, China.
  • Liu Y; Henan Cancer Hospital, Zhengzhou, China.
  • Wu H; Henan Cancer Hospital, Zhengzhou, China.
  • Li G; Jiangxi Cancer Hospital, Nanchang, China.
  • Fu Z; The 900 Hospital of Joint Logistics Support Force of PLA, Fuzhou, China.
  • Shi J; LinYi Cancer Hospital, Linyi, China.
  • Jiang H; Department of Radiation Oncology, The First Affiliated Hospital of Bengbu Medical University, Bengbu, China.
  • Bai Y; The Third Bethune Hospital of Jilin University, Changchun, China.
  • Cui J; The First Hospital of Jilin University, Changchun, China.
  • Zheng Y; The First Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.
  • Cui W; Affiliated Hospital of Jining Medical University, Jining, China.
  • Jia X; The Second Norman Bethune Hospital of Jilin University, Changchun, China.
  • Zhai L; Shandong First Medical University Affiliated Cancer Hospital, Jinan, China.
  • Cai Q; Sun Yat-sen University Cancer Center, Guangzhou, China.
  • Xiong D; Chongqing University Three Gorges Hospital, Chongqing, China.
  • Wu Y; Stomatological College of Nanjing Medical University, Nanjing, China.
  • Cao J; Fudan University Shanghai Cancer Center, Shanghai, China.
  • Wu R; Shengjing Hospital of China Medical University, Shenyang, China.
  • Hu G; Tongji Medical College of HUST, Wuhan, China.
  • Peng L; Chinese PLA General Hospital, Beijing, China.
  • Xie L; Beijing Engineering Research Center of Protein and Antibody, Sinocelltech Ltd., Beijing, China.
  • Gai W; Beijing Engineering Research Center of Protein and Antibody, Sinocelltech Ltd., Beijing, China.
  • Wang Y; Beijing Engineering Research Center of Protein and Antibody, Sinocelltech Ltd., Beijing, China.
  • Su Y; Beijing Engineering Research Center of Protein and Antibody, Sinocelltech Ltd., Beijing, China.
Nat Med ; 2024 Jun 28.
Article em En | MEDLINE | ID: mdl-38942993
ABSTRACT
Immunotherapy combined with chemotherapy regimen has been shown to be effective in recurrent or metastatic (R/M) head and neck squamous cell carcinoma (HNSCC). However, due to the small number of patients, its efficacy remains controversial in Asian populations, particularly in mainland China. Here a randomized, double-blind phase 3 trial evaluated the efficacy and safety of finotonlimab (SCT-I10A), a programmed cell death 1 (PD-1) monoclonal antibody, combined with cisplatin plus 5-fluorouracil (C5F) for the first-line treatment of R/M HNSCC. Eligible patients (n = 370) were randomly 21 assigned to receive finotonlimab plus C5F (n = 247) or placebo plus C5F (n = 123). The primary endpoint was overall survival (OS). In the finotonlimab plus C5F group, OS was 14.1 months (95% confidence interval (CI) 11.1-16.4), compared with 10.5 months (95% CI 8.1-11.8) in the placebo plus C5F group. The hazard ratio was 0.73 (95% CI 0.57-0.95, P = 0.0165), meeting the predefined superiority criteria for the primary endpoint. Finotonlimab plus C5F showed significant OS superiority compared with C5F alone and acceptable safety profile with R/M HNSCC, supporting its use as a first-line treatment option for R/M HNSCC. These results validate the efficacy and safety of the combination of finotonlimab and C5F in Asian patients with R/M HNSCC. ClinicalTrials.gov identifier NCT04146402 .

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Med Assunto da revista: BIOLOGIA MOLECULAR / MEDICINA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Med Assunto da revista: BIOLOGIA MOLECULAR / MEDICINA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China