首页> 外文期刊>International journal of clinical oncology >Pertuzumab plus trastuzumab and chemotherapy for Japanese patients with HER2-positive metastatic gastric or gastroesophageal junction cancer: a subgroup analysis of the JACOB trial
【24h】

Pertuzumab plus trastuzumab and chemotherapy for Japanese patients with HER2-positive metastatic gastric or gastroesophageal junction cancer: a subgroup analysis of the JACOB trial

机译:Pertuzumab Plus Trastuzumab和日本患者的化疗,Her2阳性转移性胃或胃食管癌症癌症:雅各布试验的亚组分析

获取原文
获取原文并翻译 | 示例
           

摘要

Background The phase III JACOB trial (NCT01774786) compared the efficacy and safety of pertuzumab and trastuzumab plus chemotherapy with placebo and trastuzumab plus chemotherapy in patients with previously untreated human epidermal growth factor receptor 2 (HER2)-positive metastatic gastric or gastroesophageal junction cancer. We conducted a subgroup analysis in Japanese patients. Methods Patients were randomized 1:1 to pertuzumab 840 mg or placebo, plus trastuzumab (loading dose, 8 mg/kg; maintenance dose, 6 mg/kg) and chemotherapy (cisplatin 80 mg/m(2), and capecitabine 1000 mg/m(2) twice daily for 28 doses or 5-fluorouracil 800 mg/m(2) every 24 h for 120 h), every 3 weeks. Continuation of chemotherapy after 6 cycles was at the discretion of the patient and the treating physician. Results A total of 40 Japanese patients were included in each arm. Median overall survival was 22.0 months (95% confidence interval [CI] 13.8-not evaluable) and 15.6 months (95% CI 9.7-19.2) in the pertuzumab and placebo arms, respectively (hazard ratio [HR] 0.64 [95% CI 0.37-1.10]). Median progression-free survival was 12.4 months (95% CI 6.1-14.1) in the pertuzumab arm and 6.3 months (95% CI 4.3-8.1) in the placebo arm (HR 0.50 [95% CI 0.30-0.82]). Grade >= 3 adverse events and serious adverse events were more frequent in the pertuzumab arm than the placebo arm. Conclusions Results from this subgroup analysis of the JACOB trial suggest similar efficacy of pertuzumab in Japanese patients and patients in the overall population, encouraging continued investigation of new agents for gastric cancer in Japanese patients.
机译:背景技术III阶段雅各(NCT01774786)比较了Pertuzumab和Trastuzumab加上化疗与安慰剂和曲妥珠单抗的疗效和安全性在先前未经处理的人表皮生长因子受体2(HER2) - 阳性转移性胃或胃食管接线癌症中的患者的疗效和安全性。我们在日本患者进行了亚组分析。方法将患者随机分配1:1至Pertuzumab 840mg或安慰剂,加上曲妥珠单抗(负载剂量,8mg / kg;维持剂量,6mg / kg)和化疗(顺铂80mg / m(2),和Capecitabine 1000 mg / M(2)每天两次为28剂或5氟尿嘧啶800mg / m(2)每24小时120小时,每3周。 6个循环后的延续化疗是患者和治疗医师的判断。结果每只臂中共有40名日本患者。中位数总生存率为22.0个月(95%置信区间[CI] 13.8-not评估)和15.6个月(95%CI 9.7-19.2)分别在Pertuzumab和安慰剂臂(危险比[HR] 0.64 [95%CI 0.37] -1.10])。中位进展生存期为12.4个月(95%CI 6.1-14.1),在Pertuzumab臂中,安慰剂臂中的6.3个月(95%CI 4.3-8.1)(HR 0.50 [95%CI 0.30-0.82])。等级> = 3不良事件和严重的不良事件在Pertuzumab臂中比安慰剂臂更频繁。结论雅各试验该亚组分析的结果表明,在日本患者和整体人群中患者中Pertuzumab的疗效表明,促进日本患者胃癌新试剂继续调查。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号