TY - JOUR
T1 - First-line sunitinib versus pazopanib in metastatic renal cell carcinoma
T2 - Results from the International Metastatic Renal Cell Carcinoma Database Consortium
AU - Ruiz-Morales, Jose Manuel
AU - Swierkowski, Marcin
AU - Wells, J. Connor
AU - Fraccon, Anna Paola
AU - Pasini, Felice
AU - Donskov, Frede
AU - Bjarnason, Georg A.
AU - Lee, Jae Lyun
AU - Sim, Hao Wen
AU - Sliwczynsk, Andrzej
AU - Ptak-Chmielewska, Aneta
AU - Teter, Zbigniew
AU - Beuselinck, Benoit
AU - Wood, Lori A.
AU - Yuasa, Takeshi
AU - Pezaro, Carmel
AU - Rini, Brian I.
AU - Szczylik, Cezary
AU - Choueiri, Toni K.
AU - Heng, Daniel Y.C.
PY - 2016/9/1
Y1 - 2016/9/1
N2 - 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.
AB - 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.
KW - Carcinoma
KW - Pazopanib
KW - Renal cell
KW - Sunitinib
KW - Vascular endothelial growth factor receptor
UR - http://www.scopus.com/inward/record.url?scp=84979924146&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2016.06.016
DO - 10.1016/j.ejca.2016.06.016
M3 - Article
C2 - 27487293
AN - SCOPUS:84979924146
SN - 0959-8049
VL - 65
SP - 102
EP - 108
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -