First-line treatment in the management of advanced renal cell carcinoma: systematic review and network meta-analysis

被引:18
|
作者
Larkin, James [1 ]
Paine, Abby [2 ]
Foley, Grace [3 ]
Mitchell, Stephen [4 ]
Chen, Connie [5 ]
机构
[1] Royal Marsden NHS Fdn Trust, London SW3 6JJ, England
[2] Zedediah Consulting, Wokingham RG41 3AP, Berks, England
[3] Pfizer Ltd, Surrey KT20 7NS, England
[4] Abacus Int, Talisman Business Ctr 6, Systemat Review Dept, Bicester OX26 6HR, Oxon, England
[5] Pfizer Global Pharmaceut, New York, NY 10015 USA
关键词
meta-analysis; progression-free survival; renal cell carcinoma; systematic review; PROGRESSION-FREE SURVIVAL; SURROGATE END-POINT; ISPOR TASK-FORCE; INTERFERON-ALPHA; BEVACIZUMAB; SUNITINIB; TRIAL; SORAFENIB; PAZOPANIB; CANCER;
D O I
10.1517/14656566.2015.1058359
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objectives: To conduct a systematic review and network meta-analysis (NMA) to assess effectiveness of first-line treatments for advanced renal cell carcinoma (RCC). Methods: Database searches were conducted to identify randomized controlled trials (RCTs) reporting results for eligible treatments. A fixed-effect Bayesian NMA was conducted to assess the relative effectiveness of treatments, with progression-free survival (PFS) reported as hazard ratios (HRs) and 95% credible intervals (CrIs). Results: Eleven unique RCTs were suitable for inclusion in the NMA. In the base case, in terms of PFS, sunitinib was superior compared with bevacizumab + IFN-alpha (HR = 0.79, 95% CrI: 0.64 - 0.96), everolimus (HR = 0.70, 95% CrI: 0.56 - 0.87), sorafenib (HR = 0.56, 95% Crl: 0.40 - 0.77) and temsirolimus + bevacizumab (HR = 0.74, 95% Crl: 0.56 - 0.96). Although, the point values for the mean and median HRs were < 1.0, there was no significant difference in PFS between sunitinib and axitinib, pazopanib or tivozanib. Although sensitivity analyses impacted the results of the NMA, no treatment was significantly more efficacious than sunitinib. Conclusion: Results from this analysis suggest that there is no treatment superior to the current benchmark treatment, sunitinib, in the management of advanced RCC in the first-line setting.
引用
收藏
页码:1915 / 1927
页数:13
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