TY - JOUR
T1 - Nivolumab versus everolimus in patients with advanced renal cell carcinoma
T2 - Updated results with long-term follow-up of the randomized, open-label, phase 3 CheckMate 025 trial
AU - Motzer, Robert J.
AU - Escudier, Bernard
AU - George, Saby
AU - Hammers, Hans J.
AU - Srinivas, Sandhya
AU - Tykodi, Scott S.
AU - Sosman, Jeffrey A.
AU - Plimack, Elizabeth R.
AU - Procopio, Giuseppe
AU - McDermott, David F.
AU - Castellano, Daniel
AU - Choueiri, Toni K.
AU - Donskov, Frede
AU - Gurney, Howard
AU - Oudard, Stéphane
AU - Richardet, Martin
AU - Peltola, Katriina
AU - Alva, Ajjai S.
AU - Carducci, Michael
AU - Wagstaff, John
AU - Chevreau, Christine
AU - Fukasawa, Satoshi
AU - Tomita, Yoshihiko
AU - Gauler, Thomas C.
AU - Kollmannsberger, Christian K.
AU - Schutz, Fabio A.
AU - Larkin, James
AU - Cella, David
AU - McHenry, M. Brent
AU - Saggi, Shruti Shally
AU - Tannir, Nizar M.
N1 - Funding Information:
This study was funded by Bristol‐Myers Squibb Company (BMS) and ONO Pharmaceutical Company, Ltd. The funders contributed to the study design, data analysis, and data interpretation in collaboration with the authors. The funders had no role in data collection. Financial support for editorial and writing assistance was provided by the funders. A data confidentiality agreement was in place between BMS and the investigators. All authors vouch for the completeness and accuracy of the data and analyses and for the adherence of the trial to the protocol. All authors had full access to all of the data included in the study, and all authors contributed to drafting the manuscript and provided final approval to submit the manuscript. The corresponding author had full access to all of the data and the final responsibility to submit the manuscript for publication. Patients treated at Memorial Sloan Kettering Cancer Center were supported in part by the Memorial Sloan Kettering Cancer Center Support Grant/Core Grant (P30 CA008748). The University of Texas MD Anderson Cancer Center is supported by the National Institutes of Health (grant P30 CA016672).
Funding Information:
We thank the patients and their families as well as the investigators and participating clinical study teams for making this study possible. We also thank Elmer Berghorn for his contributions to the study; Dako (an Agilent Technologies, Inc, company) for collaborative development of the PD‐L1 IHC 28‐8 pharmDx assay; and Bristol‐Myers Squibb Company (Princeton, New Jersey) and ONO Pharmaceutical Company, Ltd (Osaka, Japan). Professional medical writing and editorial assistance was provided by Jenny Reinhold, PharmD (Parexel), and was funded by Bristol‐Myers Squibb Company.
Publisher Copyright:
© 2020 American Cancer Society
PY - 2020/9/15
Y1 - 2020/9/15
N2 - Background: CheckMate 025 has shown superior efficacy for nivolumab over everolimus in patients with advanced renal cell carcinoma (aRCC) along with improved safety and tolerability. This analysis assesses the long-term clinical benefits of nivolumab versus everolimus. Methods: The randomized, open-label, phase 3 CheckMate 025 trial (NCT01668784) included patients with clear cell aRCC previously treated with 1 or 2 antiangiogenic regimens. Patients were randomized to nivolumab (3 mg/kg every 2 weeks) or everolimus (10 mg once a day) until progression or unacceptable toxicity. The primary endpoint was overall survival (OS). The secondary endpoints were the confirmed objective response rate (ORR), progression-free survival (PFS), safety, and health-related quality of life (HRQOL). Results: Eight hundred twenty-one patients were randomized to nivolumab (n = 410) or everolimus (n = 411); 803 patients were treated (406 with nivolumab and 397 with everolimus). With a minimum follow-up of 64 months (median, 72 months), nivolumab maintained an OS benefit in comparison with everolimus (median, 25.8 months [95% CI, 22.2-29.8 months] vs 19.7 months [95% CI, 17.6-22.1 months]; hazard ratio [HR], 0.73; 95% CI, 0.62-0.85) with 5-year OS probabilities of 26% and 18%, respectively. ORR was higher with nivolumab (94 of 410 [23%] vs 17 of 411 [4%]; P <.001). PFS also favored nivolumab (HR, 0.84; 95% CI, 0.72-0.99; P =.0331). The most common treatment-related adverse events of any grade were fatigue (34.7%) and pruritus (15.5%) with nivolumab and fatigue (34.5%) and stomatitis (29.5%) with everolimus. HRQOL improved from baseline with nivolumab but remained the same or deteriorated with everolimus. Conclusions: The superior efficacy of nivolumab over everolimus is maintained after extended follow-up with no new safety signals, and this supports the long-term benefits of nivolumab monotherapy in patients with previously treated aRCC. LAY SUMMARY: CheckMate 025 compared the effects of nivolumab (a novel immunotherapy) with those of everolimus (an older standard-of-care therapy) for the treatment of advanced kidney cancer in patients who had progressed on antiangiogenic therapy. After 5 years of study, nivolumab continues to be better than everolimus in extending the lives of patients, providing a long-lasting response to treatment, and improving quality of life with a manageable safety profile. The results demonstrate that the clinical benefits of nivolumab versus everolimus in previously treated patients with advanced kidney cancer continue in the long term.
AB - Background: CheckMate 025 has shown superior efficacy for nivolumab over everolimus in patients with advanced renal cell carcinoma (aRCC) along with improved safety and tolerability. This analysis assesses the long-term clinical benefits of nivolumab versus everolimus. Methods: The randomized, open-label, phase 3 CheckMate 025 trial (NCT01668784) included patients with clear cell aRCC previously treated with 1 or 2 antiangiogenic regimens. Patients were randomized to nivolumab (3 mg/kg every 2 weeks) or everolimus (10 mg once a day) until progression or unacceptable toxicity. The primary endpoint was overall survival (OS). The secondary endpoints were the confirmed objective response rate (ORR), progression-free survival (PFS), safety, and health-related quality of life (HRQOL). Results: Eight hundred twenty-one patients were randomized to nivolumab (n = 410) or everolimus (n = 411); 803 patients were treated (406 with nivolumab and 397 with everolimus). With a minimum follow-up of 64 months (median, 72 months), nivolumab maintained an OS benefit in comparison with everolimus (median, 25.8 months [95% CI, 22.2-29.8 months] vs 19.7 months [95% CI, 17.6-22.1 months]; hazard ratio [HR], 0.73; 95% CI, 0.62-0.85) with 5-year OS probabilities of 26% and 18%, respectively. ORR was higher with nivolumab (94 of 410 [23%] vs 17 of 411 [4%]; P <.001). PFS also favored nivolumab (HR, 0.84; 95% CI, 0.72-0.99; P =.0331). The most common treatment-related adverse events of any grade were fatigue (34.7%) and pruritus (15.5%) with nivolumab and fatigue (34.5%) and stomatitis (29.5%) with everolimus. HRQOL improved from baseline with nivolumab but remained the same or deteriorated with everolimus. Conclusions: The superior efficacy of nivolumab over everolimus is maintained after extended follow-up with no new safety signals, and this supports the long-term benefits of nivolumab monotherapy in patients with previously treated aRCC. LAY SUMMARY: CheckMate 025 compared the effects of nivolumab (a novel immunotherapy) with those of everolimus (an older standard-of-care therapy) for the treatment of advanced kidney cancer in patients who had progressed on antiangiogenic therapy. After 5 years of study, nivolumab continues to be better than everolimus in extending the lives of patients, providing a long-lasting response to treatment, and improving quality of life with a manageable safety profile. The results demonstrate that the clinical benefits of nivolumab versus everolimus in previously treated patients with advanced kidney cancer continue in the long term.
KW - CheckMate 025
KW - advanced renal cell carcinoma (aRCC)
KW - everolimus
KW - immune checkpoint inhibitor
KW - nivolumab
KW - previously treated
UR - http://www.scopus.com/inward/record.url?scp=85088021619&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85088021619&partnerID=8YFLogxK
U2 - 10.1002/cncr.33033
DO - 10.1002/cncr.33033
M3 - Article
C2 - 32673417
AN - SCOPUS:85088021619
SN - 0008-543X
VL - 126
SP - 4156
EP - 4167
JO - Cancer
JF - Cancer
IS - 18
ER -