Nimotuzumab Plus Gemcitabine for K-Ras Wild-Type Locally Advanced or Metastatic Pancreatic Cancer

作者：Qin, Shukui^*; Li, Jin; Bai, Yuxian; Wang, Zishu; Chen, Zhendong; Xu, Ruihua; Xu, Jianming; Zhang, Hongmei; Chen, Jia; Yuan, Ying; Liu, Tianshu; Yang, Lin; Zhong, Haijun; Chen, Donghui; Shen, Lin; Hao, Chunyi; Fu, Deliang; Cheng, Ying; Yang, Jianwei; Wang, Qiong; Qin, Baoli; Pan, Hongming; Zhang, Jun; Bai, Xianhong; Zheng, Qingshan

来源：Journal of Clinical Oncology, 2023, 41(33): 5163-+.

DOI：10.1200/JCO.22.02630

• HAZARD RATIO
• SURVIVAL
• COMBINATION
• MULTICENTER
• BENEFIT
• TRIALS

K-Ras pancreatic cancers benefit overall survival in phase 3 NOTABLE study. @@@ PURPOSEIn a phase IIb trial of nimotuzumab plus gemcitabine, substantial clinical benefits were observed in patients with locally advanced or metastatic pancreatic cancer (PC). Therefore, we conducted a phase III clinical study to verify the efficacy and safety of this combination regimen in patients with K-Ras wild-type tumors (ClinicalTrials.gov identifier: NCT02395016).PATIENTS AND METHODSEligible patients were randomly assigned to receive nimotuzumab (400 mg once per week) or placebo followed by gemcitabine (1,000 mg/m2 on days 1, 8, and 15, once every 4 weeks) until disease progression or unacceptable toxicity. The primary end point was overall survival (OS) and the secondary end points were progression-free survival (PFS), response rates, and safety.RESULTSA total of 480 patients were screened; 92 patients were enrolled and 82 patients with K-Ras wild-type tumors were eligible. In the full analysis set, the median OS was 10.9 versus 8.5 months, while the restricted mean survival time (RMST) was 18.05 versus 11.14 months for the investigational versus control arm (ratio of control v investigation = 0.62 [0.40-0.97]; P = .036). Median PFS was 4.2 versus 3.6 months in the investigational versus control arm (log-rank P = .04; hazard ratio, 0.60 [0.37-0.99]) and the restricted mean PFS time was 8.08 versus 4.76 months (RMST ratio, 0.58 [0.38-0.90]; P = .036). Both OS and PFS were longer in the nimotuzumab group than in the placebo group. The objective response rates and disease control rates were 7% versus 10% and 68% versus 63% for the investigational and control groups, respectively. The incidence of adverse events were comparable between the two groups.CONCLUSIONIn patients with locally advanced or metastatic K-Ras wild-type PC, nimotuzumab plus gemcitabine significantly improved OS and PFS with a good safety profile.

• 单位
  中国科学院研究生院; 上海交通大学; 中山大学; 安徽医科大学; 浙江大学; 中国医学科学院; 中国医学科学院北京协和医院; 哈尔滨医科大学; 复旦大学