Network Meta-analysis of Randomized Controlled Trials in Patients with Previously Treated Advanced Gastric or Gastroesophageal Junction Cancer: Comparisons Involving Ramucirumab

被引:0
|
作者
D'yachkova, Yulia [1 ]
Liepa, Astra M. [2 ]
Goel, Rajat [3 ]
Earley-Valovic, Veronika [4 ]
Paine, Abby [5 ]
Gupta, Palvi [6 ]
Taipale, Kaisa [7 ]
机构
[1] Eli Lilly GmbH, Vienna, Austria
[2] Eli Lilly & Co, Indianapolis, IN USA
[3] Eli Lilly & Co India Pvt Ltd, Lilly Capabil Ctr India LCCI, Bangalore, India
[4] Eli Lilly & Co Ltd, Bracknell, England
[5] Zedediah Consulting Clarivate, Wokingham, England
[6] Clarivate, Bangalore, India
[7] Oy Eli Lilly Finland Ab, Helsinki, Finland
关键词
Gastric cancer; Network meta-analysis; Ramucirumab; Randomized controlled trial; Second-line therapy; Systematic literature review; PHASE-III TRIAL; IRINOTECAN PLUS CISPLATIN; 2ND-LINE CHEMOTHERAPY; DOUBLE-BLIND; OPEN-LABEL; COMBINATION CHEMOTHERAPY; SUPPORTIVE CARE; PACLITAXEL; S-1; ADENOCARCINOMA;
D O I
10.1007/s12029-024-01121-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposeWith relatively few direct comparisons among treatment options for previously treated advanced gastric cancer or gastroesophageal junction (GEJ) cancer, network meta-analysis (NMA) may inform evidence-based decision-making. Ramucirumab plus paclitaxel (RAM + PTX) is a preferred regimen in guideline recommendations. NMA of key outcomes may further characterize the relative clinical value of RAM + PTX.MethodsA systematic literature review of randomized controlled trials of adult patients with previously treated advanced gastric/GEJ cancer informed a NMA which compared overall survival, progression-free survival, and discontinuations due to adverse events. Comparisons were reported relative to placebo/best supportive care (BSC) when possible, otherwise relative to RAM + PTX.ResultsThe base-case NMA focused on second-line treatment only, from 19 of 28 studies identified. For overall survival, seven of 16 regimens were favorable relative to placebo/BSC, with RAM + PTX as the most favorable. For progression-free survival, five of 14 regimens were unfavorable relative to RAM + PTX. For discontinuations due to adverse events, two of 13 regimens were similar to placebo/BSC: ramucirumab monotherapy and fluorouracil; relative to RAM-PTX, all regimens were similar except ramucirumab monotherapy which was favorable and irinotecan + cisplatin which was unfavorable.ConclusionThis NMA of trials of previously treated gastric/GEJ cancer suggests that RAM + PTX has one of the more favorable clinical profiles.
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页数:15
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