First-line sunitinib versus pazopanib in metastatic renal cell carcinoma: Results from the International Metastatic Renal Cell Carcinoma Database Consortium

Abstract Background Sunitinib (SU) and pazopanib (PZ) are standards of care for first-line treatment of metastatic renal cell carcinoma (mRCC). However, how the efficacy of these drugs translates into effectiveness on a population-based level is unknown. Patients and methods We used the Internationa...

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Veröffentlicht in:European journal of cancer (1990) 2016-09, Vol.65, p.102-108
Hauptverfasser: Ruiz-Morales, Jose Manuel, Swierkowski, Marcin, Wells, J. Connor, Fraccon, Anna Paola, Pasini, Felice, Donskov, Frede, Bjarnason, Georg A, Lee, Jae-Lyun, Sim, Hao-Wen, Sliwczynsk, Andrzej, Ptak-Chmielewska, Aneta, Teter, Zbigniew, Beuselinck, Benoit, Wood, Lori A, Yuasa, Takeshi, Pezaro, Carmel, Rini, Brian I, Szczylik, Cezary, Choueiri, Toni K, Heng, Daniel Y.C
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Sprache:eng
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Zusammenfassung:Abstract Background Sunitinib (SU) and pazopanib (PZ) are standards of care for first-line treatment of metastatic renal cell carcinoma (mRCC). However, how the efficacy of these drugs translates into effectiveness on a population-based level is unknown. Patients and methods We used the International mRCC Database Consortium (IMDC) to assess overall survival (OS), progression-free survival (PFS), response rate (RR) and performed proportional hazard regression adjusting for IMDC prognostic groups. Second-line OS (OS2) and second-line PFS (PFS2) were also evaluated. Results We obtained data from 7438 patients with mRCC treated with either first-line SU (n = 6519) or PZ (n = 919) with an overall median follow-up of 40.4 months (95% confidence interval [CI] 39.2–42.1). There were no significant differences in IMDC prognostic groups (p = 0.36). There was no OS difference between SU and PZ (22.3 versus 22.6 months, respectively, p = 0.65). When adjusted for IMDC criteria, the hazard ratio (HR) of death for PZ versus SU was 1.03 (95% CI 0.92–1.17, p = 0.58). There was no PFS difference between SU and PZ (8.4 versus 8.3 months, respectively, p = 0.17). When adjusted for IMDC criteria, the HR for PFS for PZ versus SU was 1.08 (95% CI 0.981–1.19, p = 0.12). There was no difference in RR between SU and PZ (30% versus 28%, respectively, p = 0.15). We also found no difference in any second-line treatment between either post-SU or post-PZ groups for OS2 (13.1 versus 11 months, p = 0.27) and PFS2 (3.7 versus 5.0 months, p = 0.07). Conclusions We confirmed in real-world practice that SU and PZ have similar efficacy in the first-line setting for mRCC and do not affect outcomes with subsequent second-line treatment.
ISSN:0959-8049
1879-0852
DOI:10.1016/j.ejca.2016.06.016