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Original Research

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

, FRCP PhD (Consultant Medical Oncologist) , , PhD (Senior Statistician) , , MPharm (Senior Oncology Scientific Advisor) , , PhD (Team Leader) & , PharmD
Pages 1915-1927 | Published online: 06 Aug 2015
 

Abstract

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-α (HR = 0.79, 95% CrI: 0.64 – 0.96), everolimus (HR = 0.70, 95% CrI: 0.56 – 0.87), sorafenib (HR = 0.56, 95% CrI: 0.40 – 0.77) and temsirolimus + bevacizumab (HR = 0.74, 95% CrI: 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.

Declaration of interest

This study was sponsored by Pfizer, Inc., A Paine received an honorarium from Pfizer in connection with the development of this manuscript. J Larkin is supported by the Royal Marsden Hospital/Institute of Cancer Research National Institute for Health Research Biomedical Research Centre for Cancer. S Mitchell is an employee of Abacus International and was a paid consultant to Pfizer in connection with the development of this manuscript. C Chen and G Foley are employees of Pfizer Ltd. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.

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