Efficacy of VEGFR-TKIs plus immune checkpoint inhibitors in metastatic renal cell carcinoma patients with favorable IMDC prognosis

Chiara Ciccarese, Roberto Iacovelli, C. Porta, G. Procopio, Emilio Bria, S. Astore, M. A. Cannella, Giampaolo Tortora

Risultato della ricerca: Contributo in rivistaArticolo in rivista

Abstract

Background: Combinations of PD-1/PD-L1 immune checkpoint inhibitors (ICI) with VEGFR-TKIs as first-line therapy significantly improve outcomes of metastatic renal cell carcinoma (mRCC) patients. The benefit of these combinations is well evident in the IMDC intermediate- and poor-risk population, but remains unclear in the subgroup of patients with favorable prognosis. Our meta-analysis aims at evaluating whether the addition of ICIs to VEGFR-TKIs is able to improve the outcome compared to VEGFR-TKIs alone in mRCC patients with favorable prognosis. Methods: This meta-analysis searched MEDLINE/PubMed, the Cochrane Library and ASCO Meeting abstracts for randomized clinical trials (RCTs) testing the combination of VEGFR-TKI + ICI in mRCC. Data extraction was conducted according to the PRISMA statement. Summary hazard ratio (HR) was calculated using random- or fixed-effects models, depending on studies heterogeneity. Results: Four RCTs were selected. VEGFR-TKI + ICI combinations improved PFS compared to sunitinib (fixed-effect, HR = 0.63; p < 0.00001). However, VEGFR-TKI + ICI combinations did not significantly prolong OS (fixed-effect; HR = 0.99; 95% CI 0.74–1.33; p = 0.95). Conclusion: VEGFR-TKI + ICI combinations improved PFS but not OS as first-line therapy for mRCC patients with favorable IMDC prognosis. Longer follow-up and further studies will increase the power of our analysis, suggesting the best first-line therapy for mRCC patients with favorable prognosis.
Lingua originaleEnglish
pagine (da-a)N/A-N/A
RivistaCancer Treatment Reviews
Volume100
DOI
Stato di pubblicazionePubblicato - 2021

Keywords

  • Favourable prognosis
  • First-line
  • Good-risk
  • VEGFR-TKI
  • Immune checkpoint inhibitors
  • Immunotherapy
  • Renal cell carcinoma
  • IMDC

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