4.5 Review

First-line Treatment of Metastatic Renal Cell Carcinoma: A Systematic Review and Network Meta-analysis

Journal

EUROPEAN UROLOGY ONCOLOGY
Volume 2, Issue 6, Pages 708-715

Publisher

ELSEVIER
DOI: 10.1016/j.euo.2019.09.002

Keywords

Metastatic renal cell carcinoma; Network meta-analysis; International Metastatic Renal Cell Carcinoma Database Consortium; Memorial Sloan Kettering Cancer Center; First line; Pembrolizumab; Avelumab

Funding

  1. Active
  2. Biotech
  3. Astra Zeneca
  4. Bavarian Nordic
  5. BMS
  6. Calithera
  7. Celldex
  8. Eisai
  9. Exelixis
  10. Genetech
  11. GSK (GlaxoSmithKline)
  12. Immunomedics
  13. Janssen
  14. Medivation
  15. Merck
  16. NewLink Genetics
  17. Novartis
  18. Pfizer
  19. Prometheus
  20. Rexahn
  21. Sanofi
  22. Takeda
  23. Tracon

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Context: No head-to-head clinical trials compare contemporary first-line therapies for metastatic renal cell carcinoma (mRCC). A network meta-analysis provides an approach for quantitative analysis. Objective: To indirectly compare the efficacy and safety of first-line treatments for mRCC in the intention-to-treat (ITT) population and by clinical risk group. Evidence acquistion: An updated systematic review from database inception to February 17, 2019 identified all parallel-group randomized controlled trials assessing first-line therapy for mRCC. Clinically relevant studies were selected for a network meta-analysis. Progression-free survival (PFS) was the primary outcome. Overall survival (OS), overall response rate (ORR), and grade 3 and 4 adverse events (AEs) were secondary outcomes. Evidence synthesis: We identified 12 relevant trials: 12 reported outcomes for PFS, nine for OS, 10 for ORR, and nine for AEs. In the ITT population, cabozantinib (surface under the cumulative ranking curves [SUCRA] 84%), avelumab plus axitinib (SUCRA 68%), and pembrolizumab plus axitinib (SUCRA 82%) were superior to the other agents for PFS; pembrolizumab plus axitinib appeared superior for OS (SUCRA 95%); and atezolizumab demonstrated the lowest likelihood of AEs (SUCRA 100%). Findings were similar in the intermediate/poor-risk subgroup. Based on the limited data available, avelumab plus axitinib may be preferred in patients with favorable-risk disease. Conclusions: The optimal first-line treatment for mRCC appears to differ by efficacy endpoint, toxicity, and clinical risk group. Direct comparative studies remain important in guiding treatment choice. Patient summary: Head-to-head comparisons do not exist for the newest treatments of metastatic renal cell carcinoma (mRCC). In an indirect comparison, we found that pembrolizumab plus axitinib and cabozantinib are good options for most patients with mRCC. (C) 2019 Published by Elsevier B.V. on behalf of European Association of Urology.

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