TY - JOUR
T1 - Pembrolizumab Plus Axitinib Versus Sunitinib as First-line Treatment of Advanced Renal Cell Carcinoma
T2 - 43-month Follow-up of the Phase 3 KEYNOTE-426 Study
AU - Plimack, Elizabeth R.
AU - Powles, Thomas
AU - Stus, Viktor
AU - Gafanov, Rustem
AU - Nosov, Dmitry
AU - Waddell, Tom
AU - Alekseev, Boris
AU - Pouliot, Frédéric
AU - Melichar, Bohuslav
AU - Soulières, Denis
AU - Borchiellini, Delphine
AU - McDermott, Raymond S.
AU - Vynnychenko, Ihor
AU - Chang, Yen Hwa
AU - Tamada, Satoshi
AU - Atkins, Michael B.
AU - Li, Chenxiang
AU - Perini, Rodolfo
AU - Molife, L. Rhoda
AU - Bedke, Jens
AU - Rini, Brian I.
N1 - Publisher Copyright:
© 2023
PY - 2023/11
Y1 - 2023/11
N2 - Previous analyses of KEYNOTE-426, an open-label, phase 3 randomized study, showed superior efficacy of first-line pembrolizumab plus axitinib to sunitinib in advanced clear cell renal cell carcinoma (ccRCC). We report results of the final protocol-prespecified analysis of KEYNOTE-426. Patients received pembrolizumab 200 mg intravenously every 3 wk plus axitinib 5 mg orally twice daily or sunitinib 50 mg orally once daily (4 wk per 6-wk cycle). The dual primary endpoints were overall survival (OS) and progression-free survival (PFS) as per RECIST v1.1 by a blinded independent central review. The secondary endpoints included objective response rate (ORR) and duration of response (DOR). The median study follow-up was 43 (range, 36–51) mo. Benefit with pembrolizumab plus axitinib versus sunitinib was maintained for OS (hazard ratio [HR], 0.73 [95% confidence interval {CI}, 0.60–0.88]), PFS (HR, 0.68 [95% CI, 0.58–0.80]), and ORR (60% vs 40%). The median DOR was 24 (range, 1.4+ to 43+) versus 15 (range, 2.3–43+) mo in the pembrolizumab plus axitinib versus the sunitinib arm. No new safety signals emerged. These results support pembrolizumab plus axitinib as a standard of care for patients with previously untreated advanced ccRCC. Patient summary: Extended results of KEYNOTE-426 support pembrolizumab plus axitinib as the standard of care for advanced clear cell renal cell carcinoma.
AB - Previous analyses of KEYNOTE-426, an open-label, phase 3 randomized study, showed superior efficacy of first-line pembrolizumab plus axitinib to sunitinib in advanced clear cell renal cell carcinoma (ccRCC). We report results of the final protocol-prespecified analysis of KEYNOTE-426. Patients received pembrolizumab 200 mg intravenously every 3 wk plus axitinib 5 mg orally twice daily or sunitinib 50 mg orally once daily (4 wk per 6-wk cycle). The dual primary endpoints were overall survival (OS) and progression-free survival (PFS) as per RECIST v1.1 by a blinded independent central review. The secondary endpoints included objective response rate (ORR) and duration of response (DOR). The median study follow-up was 43 (range, 36–51) mo. Benefit with pembrolizumab plus axitinib versus sunitinib was maintained for OS (hazard ratio [HR], 0.73 [95% confidence interval {CI}, 0.60–0.88]), PFS (HR, 0.68 [95% CI, 0.58–0.80]), and ORR (60% vs 40%). The median DOR was 24 (range, 1.4+ to 43+) versus 15 (range, 2.3–43+) mo in the pembrolizumab plus axitinib versus the sunitinib arm. No new safety signals emerged. These results support pembrolizumab plus axitinib as a standard of care for patients with previously untreated advanced ccRCC. Patient summary: Extended results of KEYNOTE-426 support pembrolizumab plus axitinib as the standard of care for advanced clear cell renal cell carcinoma.
KW - Axitinib
KW - Immunotherapy
KW - Pembrolizumab
KW - Renal cell carcinoma
KW - Sunitinib
KW - Axitinib/adverse effects
KW - Follow-Up Studies
KW - Carcinoma, Renal Cell/pathology
KW - Humans
KW - Kidney Neoplasms/pathology
KW - Sunitinib/therapeutic use
KW - Antineoplastic Combined Chemotherapy Protocols
UR - http://www.scopus.com/inward/record.url?scp=85165962729&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:001088962600001&DestLinkType=FullRecord&DestApp=WOS
U2 - 10.1016/j.eururo.2023.06.006
DO - 10.1016/j.eururo.2023.06.006
M3 - Article
C2 - 37500340
SN - 0302-2838
VL - 84
SP - 449
EP - 454
JO - European Urology
JF - European Urology
IS - 5
ER -