Second-line treatments for the management of advanced renal cell carcinoma: systematic review and meta-analysis

被引:19
作者
Larkin, James [2 ]
Paine, Abby [3 ]
Tumur, Indra [4 ]
Cappelleri, Joseph C. [5 ]
Healey, Paul J., Sr. [6 ]
Foley, Grace [4 ]
Mitchell, Stephen [3 ]
Kroes, Michel [3 ]
Chen, Connie [1 ]
机构
[1] Pfizer Global Pharmaceut, New York, NY 10015 USA
[2] Royal Marsden NHS Fdn Trust, London SW3 6JJ, England
[3] Abacus Int, Systemat Review Dept, Talisman Business Ctr 6, Bicester OX26 6HR, Oxon, England
[4] Pfizer Ltd, Walton Oaks KT20 7NS, Surrey, England
[5] Pfizer Inc, Biostat, Groton, CT 06340 USA
[6] Pfizer Global Pharmaceut, Groton, CT 06340 USA
关键词
disease-free survival; meta-analysis; renal cell carcinoma; systematic review; ISPOR TASK-FORCE; EVEROLIMUS; SUNITINIB; SURVIVAL; SORAFENIB; AXITINIB; INTERLEUKIN-2; BEVACIZUMAB; GUIDELINES; INHIBITOR;
D O I
10.1517/14656566.2013.758713
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objectives: A systematic review/meta-analysis was conducted to assess the effectiveness and safety of second-line treatments for advanced renal cell carcinoma (RCC), which includes the vascular endothelial growth factor inhibitor axitinib. Methods: Database searches were conducted to identify randomised controlled trials (RCTs). Indirect comparisons using a fixed-effect Bayesian model were used to assess the relative effectiveness of treatments and reported as hazard ratio (HR) and 95% credible intervals (CrI). Results: Although 24 RCTs met eligibility criteria, only three studies were included in the fixed-effect Bayesian meta-analysis, due to differences in patient inclusion criteria/reported outcomes in the wider dataset. Robust meta-analysis was restricted to the subgroup pretreated with cytokines. In terms of progression-free survival (PFS), axitinib was superior compared with placebo (HR = 0.25, 95% CrI: 0.17 - 0.38), sorafenib (HR = 0.46, 95% CrI: 0.32 - 0.68) and pazopanib (HR = 0.47, 95% CrI: 0.26 - 0.85). An analysis including all patients, regardless of previous first-line treatment, reported similar results. There was no significant difference in PFS between sorafenib and pazopanib. Conclusion: Results from the present study suggest that axitinib will be an important treatment option to extend PFS in the management of advanced RCC in the second-line setting. Ongoing research will define the optimal treatment algorithm leading to a patient-focused treatment strategy.
引用
收藏
页码:27 / 39
页数:13
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