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Finotonlimab with chemotherapy in recurrent or metastatic head and neck cancer: a randomized phase 3 trial.

Yuankai ShiWei GuoWei WangYunteng WuMeiyu FangXiaoming HuangPing HanQingyuan ZhangPin DongXiaohong ZhouHanwei PengChunhong HuXiaopin ChenShurong ZhangZhiwei ChangXiaojiang LiYuhai DingSong QuShanghua JingSongnan ZhangLin GuiYan SunLin WangYanyan LiuHui WuGuoqing LiZhichao FuJianhua ShiHao JiangYuansong BaiJiuwei CuiYulong ZhengWei CuiXiaojing JiaLimin ZhaiQing-Qing CaiDeming XiongYunong WuJunning CaoRong WuGuangyuan HuLiang PengLiangzhi XieWenlin GaiYan WangYuehua Su
Published in: Nature medicine (2024)
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 2:1 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 .
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