Muro Kei, Oh Sang Cheul, Shimada Yasuhiro, Lee Keun-Wook, Yen Chia-Jui, Chao Yee, Cho Jae Yong, Cheng Rebecca, Carlesi Roberto, Chandrawansa Kumari, Orlando Mauro, Ohtsu Atsushi
Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.
Division of Oncology and Hematology, Department of Internal Medicine, College of Medicine, Korea University.
J Gastroenterol Hepatol. 2016 Mar;31(3):581-9. doi: 10.1111/jgh.13153.
East Asia has higher gastric cancer incidence and mortality rates than other regions. We present a subgroup analysis of East Asians in the positive study RAINBOW.
Patients with advanced gastric or gastroesophageal junction adenocarcinoma previously treated with platinum and fluoropyrimidine received ramucirumab 8 mg/kg or placebo on days 1 and 15 plus paclitaxel 80 mg/m(2) on days 1, 8, and 15 of a 28-day cycle.
Of 665 intention-to-treat patients, 223 were East Asian. Median overall survival was 12.1 months for ramucirumab plus paclitaxel and 10.5 months for placebo plus paclitaxel (hazard ratio: 0.986, 95% confidence interval: 0.727-1.337, P = 0.929). Median progression-free survival was 5.5 months for ramucirumab plus paclitaxel and 2.8 months for placebo plus paclitaxel (hazard ratio: 0.628, 95% confidence interval: 0.473-0.834, P = 0.001). Objective response rates were 34% for ramucirumab plus paclitaxel and 20% for placebo plus paclitaxel. Grade ≥ 3 neutropenia (60% vs 28%) and leukopenia (34% vs 13%) were higher for ramucirumab plus paclitaxel. The rate of febrile neutropenia was low (4% vs 4%). Special interest adverse events included any grade bleeding/hemorrhage (55% vs 25%), proteinuria (27% vs 7%), and hypertension (22% vs 2%).
Ramucirumab plus paclitaxel significantly improves progression-free survival and response rate, with prolonged median overall survival and an acceptable safety profile in East Asians with advanced gastric cancer.
东亚地区的胃癌发病率和死亡率高于其他地区。我们在阳性研究RAINBOW中对东亚人群进行了亚组分析。
既往接受过铂类和氟嘧啶治疗的晚期胃或胃食管交界腺癌患者,在28天周期的第1天和第15天接受雷莫西尤单抗8mg/kg或安慰剂治疗,并在第1天、第8天和第15天接受紫杉醇80mg/m²治疗。
在665例意向性治疗患者中,223例为东亚人。雷莫西尤单抗联合紫杉醇组的中位总生存期为12.1个月,安慰剂联合紫杉醇组为10.5个月(风险比:0.986,95%置信区间:0.727-1.337,P = 0.929)。雷莫西尤单抗联合紫杉醇组的中位无进展生存期为5.5个月,安慰剂联合紫杉醇组为2.8个月(风险比:0.628,95%置信区间:0.473-0.834,P = 0.001)。雷莫西尤单抗联合紫杉醇组的客观缓解率为34%,安慰剂联合紫杉醇组为20%。雷莫西尤单抗联合紫杉醇组≥3级中性粒细胞减少(60%对28%)和白细胞减少(34%对13%)的发生率更高。发热性中性粒细胞减少的发生率较低(4%对4%)。特殊关注的不良事件包括任何级别的出血/出血(55%对25%)、蛋白尿(27%对7%)和高血压(22%对2%)。
雷莫西尤单抗联合紫杉醇可显著改善晚期胃癌东亚患者的无进展生存期和缓解率,延长中位总生存期,且安全性可接受。