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Overall Survival and Updated Results for Sunitinib Compared With Interferon Alfa in Patients With Metastatic Renal Cell Carcinoma

  • Robert J. Motzer
  • , Thomas E. Hutson
  • , Piotr Tomczak
  • , M. Dror Michaelson
  • , Ronald M. Bukowski
  • , Stéphane Oudard
  • , Sylvie Negrier
  • , Cezary Szczylik
  • , Roberto Pili
  • , Georg A. Bjarnason
  • , Xavier Garcia-Del-Muro
  • , Jeffrey A. Sosman
  • , Ewa Solska
  • , George Wilding
  • , John A. Thompson
  • , Sindy T. Kim
  • , Isan Chen
  • , Xin Huang
  • , Robert A. Figlin
  • Memorial Sloan-Kettering Cancer Center
  • Baylor Health Care System
  • Massachusetts General Hospital Cancer Center
  • Cleveland Clinic Foundation
  • Johns Hopkins University
  • Vanderbilt University
  • University of Wisconsin-Madison
  • Seattle Cancer Care Alliance
  • Pfizer
  • City of Hope National Med Center
  • Klinika Onkologii Oddzial Chemioterapii
  • Wojskowy Instytut Medyczny
  • Wojewodzka Przychodnia Onkolog
  • European Georges Pompidou Hospital
  • Centre Léon Bérard
  • University of Toronto
  • Institute Catala Oncologia

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

PurposeA randomized, phase III trial demonstrated superiority of sunitinib over interferon alfa (IFN-α) in progression-free survival (primary end point) as first-line treatment for metastatic renal cell carcinoma (RCC). Final survival analyses and updated results are reported.Patients and MethodsSeven hundred fifty treatment-naïve patients with metastatic clear cell RCC were randomly assigned to sunitinib 50 mg orally once daily on a 4 weeks on, 2 weeks off dosing schedule or to IFN-α 9 MU subcutaneously thrice weekly. Overall survival was compared by two-sided log-rank and Wilcoxon tests. Progression-free survival, response, and safety end points were assessed with updated follow-up.ResultsMedian overall survival was greater in the sunitinib group than in the IFN-α group (26.4 v 21.8 months, respectively; hazard ratio [HR] = 0.821; 95% CI, 0.673 to 1.001; P =.051) per the primary analysis of unstratified log-rank test (P =.013 per unstratified Wilcoxon test). By stratified log-rank test, the HR was 0.818 (95% CI, 0.669 to 0.999; P =.049). Within the IFN-α group, 33% of patients received sunitinib, and 32% received other vascular endothelial growth factor-signaling inhibitors after discontinuation from the trial. Median progression-free survival was 11 months for sunitinib compared with 5 months for IFN-α (P <.001). Objective response rate was 47% for sunitinib compared with 12% for IFN-α (P <.001). The most commonly reported sunitinib-related grade 3 adverse events included hypertension (12%), fatigue (11%), diarrhea (9%), and hand-foot syndrome (9%).ConclusionSunitinib demonstrates longer overall survival compared with IFN-α plus improvement in response and progression-free survival in the first-line treatment of patients with metastatic RCC. The overall survival highlights an improved prognosis in patients with RCC in the era of targeted therapy.

Original languageEnglish
Pages (from-to)1965-1971
Number of pages7
JournalJournal of Clinical Oncology
Volume41
Issue number11
DOIs
StatePublished - Apr 10 2023

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