Subgroup analysis of East Asians in RAINBOW: A phase 3 trial of ramucirumab plus paclitaxel for advanced gastric cancer

被引:29
|
作者
Muro, Kei [1 ]
Oh, Sang Cheul [4 ]
Shimada, Yasuhiro [2 ]
Lee, Keun-Wook [6 ]
Yen, Chia-Jui [7 ,8 ]
Chao, Yee [9 ,10 ]
Cho, Jae Yong [5 ]
Cheng, Rebecca [11 ]
Carlesi, Roberto [12 ]
Chandrawansa, Kumari [13 ]
Orlando, Mauro [14 ]
Ohtsu, Atsushi [3 ]
机构
[1] Aichi Canc Ctr Hosp, Dept Clin Oncol, Nagoya, Aichi 464, Japan
[2] Natl Canc Ctr, 1-1 Tsukiji 5 chome, Tokyo, Japan
[3] Natl Canc Ctr, Exploratory Oncol Res & Clin Trial Ctr EPOC, Kashiwa, Chiba, Japan
[4] Korea Univ, Coll Med, Dept Internal Med, Div Hematol & Oncol, Seoul 136705, South Korea
[5] Yonsei Univ, Coll Med, Gangnam Severance Hosp, Dept Med Oncol, Seoul 120749, South Korea
[6] Seoul Natl Univ, Coll Med, Bundang Hosp, Songnam, South Korea
[7] Natl Cheng Kung Univ, Grad Inst Clin Med, Tainan 701, Taiwan
[8] Natl Cheng Kung Univ Hosp, Dept Internal Med, Div Hematol & Oncol, Tainan 70428, Taiwan
[9] Natl Yang Ming Univ, Fac Med, Taipei 112, Taiwan
[10] Taipei Vet Gen Hosp, Dept Oncol, Taipei, Taiwan
[11] Eli Lilly & Co, Taipei, Taiwan
[12] Eli Lilly & Co, Florence, Italy
[13] Eli Lilly & Co, Bridgewater, NJ USA
[14] Eli Lilly & Co, RA-1430 Buenos Aires, DF, Argentina
关键词
Far East; gastrointestinal neoplasms; paclitaxel; ramucirumab; vascular endothelial growth factor receptor-2; 2ND-LINE CHEMOTHERAPY; DOUBLE-BLIND; ADENOCARCINOMA; MANAGEMENT; ETHNICITY; COMBINATION; SURVIVAL;
D O I
10.1111/jgh.13153
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and AimEast 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. MethodsPatients with advanced gastric or gastroesophageal junction adenocarcinoma previously treated with platinum and fluoropyrimidine received ramucirumab 8mg/kg or placebo on days 1 and 15 plus paclitaxel 80mg/m(2) on days 1, 8, and 15 of a 28-day cycle. ResultsOf 665 intention-to-treat patients, 223 were East Asian. Median overall survival was 12.1months for ramucirumab plus paclitaxel and 10.5months for placebo plus paclitaxel (hazard ratio: 0.986, 95% confidence interval: 0.727-1.337, P=0.929). Median progression-free survival was 5.5months for ramucirumab plus paclitaxel and 2.8months 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%). ConclusionsRamucirumab 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.
引用
收藏
页码:581 / 589
页数:9
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