Nivolumab versus everolimus in patients with advanced renal cell carcinoma: Updated results with long-term follow-up of the randomized, open-label, phase 3 CheckMate 025 trial

被引:230
作者
Motzer, Robert J. [1 ]
Escudier, Bernard [2 ]
George, Saby [3 ]
Hammers, Hans J. [4 ]
Srinivas, Sandhya [5 ]
Tykodi, Scott S. [6 ,7 ]
Sosman, Jeffrey A. [8 ]
Plimack, Elizabeth R. [9 ]
Procopio, Giuseppe [10 ]
McDermott, David F. [11 ]
Castellano, Daniel [12 ]
Choueiri, Toni K. [13 ]
Donskov, Frede [14 ]
Gurney, Howard [15 ,16 ]
Oudard, Stephane [17 ]
Richardet, Martin [18 ]
Peltola, Katriina [19 ]
Alva, Ajjai S. [20 ]
Carducci, Michael [21 ]
Wagstaff, John [22 ,23 ]
Chevreau, Christine [24 ]
Fukasawa, Satoshi [25 ,26 ]
Tomita, Yoshihiko [27 ]
Gauler, Thomas C. [28 ]
Kollmannsberger, Christian K. [29 ]
Schutz, Fabio A. [30 ]
Larkin, James [31 ]
Cella, David [32 ]
McHenry, M. Brent [33 ]
Saggi, Shruti Shally [34 ]
Tannir, Nizar M. [35 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, 1275 York Ave, New York, NY 10021 USA
[2] Gustave Roussy, Dept Med Oncol, Villejuif, France
[3] Roswell Park Canc Inst, Dept Med, Buffalo, NY 14263 USA
[4] UT Southwestern Kidney Canc Program, Div Hematol & Oncol, Dallas, TX USA
[5] Stanford Univ, Med Ctr, Stanford Canc Inst, Stanford, CA 94305 USA
[6] Univ Washington, Dept Med, Seattle, WA USA
[7] Fred Hutchinson Canc Res Ctr, 1124 Columbia St, Seattle, WA 98104 USA
[8] Northwestern Univ, Med Ctr, Dept Hematol Oncol, Chicago, IL 60611 USA
[9] Fox Chase Canc Ctr, Dept Hematol Oncol, 7701 Burholme Ave, Philadelphia, PA 19111 USA
[10] Fdn Ist Nazl Tumori, Milan, Italy
[11] Beth Israel Deaconess Med Ctr, Dana Farber Harvard Canc Ctr, Boston, MA 02215 USA
[12] Hosp Univ 12 Octubre, Oncol Med, Madrid, Spain
[13] Dana Farber Canc Inst, Lank Ctr Genitourinary Oncol, Boston, MA 02115 USA
[14] Aarhus Univ Hosp, Dept Oncol, Aarhus, Denmark
[15] Westmead Hosp, Dept Med Oncol, Westmead, NSW, Australia
[16] Macquarie Univ, Westmead, NSW, Australia
[17] Hop Europeen Georges Pompidou, AP HP, Serv Cancerol Med, Paris, France
[18] Inst Oncol Cordoba, Fdn Richardet Longo, Cordoba, Argentina
[19] Helsinki Univ Hosp, Comprehens Canc Ctr, Helsinki, Finland
[20] Univ Michigan, Div Hematol & Oncol, Ann Arbor, MI 48109 USA
[21] Johns Hopkins Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
[22] South West Wales Canc Inst, Swansea, W Glam, Wales
[23] Swansea Univ, Coll Med, Swansea, W Glam, Wales
[24] Inst Univ Canc Toulouse Oncopole, Inst Claudius Regaud, Toulouse, France
[25] Chiba Canc Ctr, Prostate Ctr, Chiba, Japan
[26] Chiba Canc Ctr, Div Urol, Chiba, Japan
[27] Niigata Univ, Dept Urol, Dept Mol Oncol, Grad Sch Med & Dent Sci, Niigata, Japan
[28] Univ Duisburg Essen, Univ Hosp Essen, Dept Med, Duisburg, Germany
[29] BC Canc Vancouver Canc Ctr, Div Med Oncol, Vancouver, BC, Canada
[30] Beneficencia Portuguesa Sao Paulo, Sao Paulo, Brazil
[31] Royal Marsden Hosp NHS Fdn Trust, London, England
[32] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Feinberg Sch Med, Chicago, IL 60611 USA
[33] Bristol Myers Squibb, Dept Biostat, Princeton, NJ USA
[34] Bristol Myers Squibb, Dept Clin Trials, Princeton, NJ USA
[35] Univ Texas MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX 77030 USA
关键词
advanced renal cell carcinoma (aRCC); CheckMate; 025; everolimus; immune checkpoint inhibitor; nivolumab; previously treated; DOSE RECOMBINANT INTERLEUKIN-2; SURVIVAL; SAFETY; LIFE;
D O I
10.1002/cncr.33033
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:4156 / 4167
页数:12
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