Nivolumab plus Cabozantinib versus Sunitinib for Advanced Renal-Cell Carcinoma

被引:1336
作者
Choueiri, T. K. [1 ,2 ]
Powles, T. [3 ]
Burotto, M. [4 ]
Escudier, B. [5 ]
Bourlon, M. T. [6 ]
Zurawski, B. [9 ]
Juarez, V. M. Oyervides [7 ]
Hsieh, J. J. [11 ]
Basso, U. [12 ]
Shah, A. Y. [13 ,16 ]
Suarez, C. [17 ]
Hamzaj, A. [13 ]
Goh, J. C. [18 ]
Barrios, C. [20 ]
Richardet, M. [21 ]
Porta, C. [14 ,15 ]
Kowalyszyn, R. [22 ]
Feregrino, J. P. [8 ]
Zolnierek, J. [10 ]
Pook, D. [19 ]
Kessler, E. R. [23 ]
Tomita, Y. [24 ,25 ]
Mizuno, R. [26 ]
Bedke, J. [27 ]
Zhang, J. [28 ]
Maurer, M. A. [29 ]
Simsek, B. [30 ]
Ejzykowicz, F. [31 ]
Schwab, G. M. [32 ]
Apolo, A. B. [33 ]
Motzer, R. J. [34 ]
机构
[1] Brigham & Womens Hosp, Dept Med Oncol, Lank Ctr Genitourinary Oncol, Dana Farber Canc Inst, 75 Francis St, Boston, MA 02115 USA
[2] Harvard Med Sch, 450 Brookline Ave, Boston, MA 02215 USA
[3] Queen Mary Univ London, Royal Free Natl Hlth Serv Trust, Canc Res UK Expt Canc Med Ctr, Dept Genitourinary Oncol,Barts Canc Inst, London, England
[4] Bradford Hill Clin Res Ctr, Santiago, Chile
[5] Gustave Roussy, Dept Med Oncol, Villejuif, France
[6] Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Urol Oncol Clin, Dept Hematooncol, Mexico City, DF, Mexico
[7] Univ Autonoma Nuevo Leon, Dept Med Oncol, Ctr Univ Canc, Hosp Univ Dr Jose Eleuterio Gonzalez, San Nicolas De Los Garza, Nuevo Leon, Mexico
[8] Hosp H Queretaro, Dept Med Oncol, Queretaro, Mexico
[9] Franciszek Lukaszczyk Oncol Ctr, Dept Outpatient Chemotherapy, Bydgoszcz, Poland
[10] Reg Specialist Hosp, Dept Clin Oncol & Hematol, Biala Podlaska, Poland
[11] Washington Univ, Sch Med, Dept Med, Siteman Canc Ctr,Div Oncol, St Louis, MO 63110 USA
[12] IRCCS, Ist Oncol Veneto, Dept Oncol, Oncol Unit 1, Padua, Italy
[13] Osped San Donato, Ist Toscano & Arezzo, Dept Med Oncol, Arezzo, Italy
[14] Univ Pavia, Dept Internal Med, Pavia, Italy
[15] Univ Bari A Moro, Bari, Italy
[16] Univ Texas MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX 77030 USA
[17] Hosp Univ Vall Hebron, Vall Hebron Inst Oncol, Dept Med Oncol, Vall Hebron Barcelona Hosp Campus, Barcelona, Spain
[18] Royal Brisbane & Womens Hosp, Dept Med Oncol, Herston, Qld, Australia
[19] Cabrini Monash Univ, Dept Med Oncol, Cabrini Hlth, Malvern, Vic, Australia
[20] Hosp Sao Lucas, Oncol Res Ctr, Porto Alegre, RS, Brazil
[21] Inst Oncol Cordoba, Fdn Richardet Longo, Cordoba, Argentina
[22] Clin Viedma, Inst Multidisciplinario Oncol, Viedma, Argentina
[23] Univ Colorado, Dept Internal Med, Div Med Oncol, Sch Med, Aurora, CO USA
[24] Niigata Univ, Grad Sch Med & Dent Sci, Dept Urol, Niigata, Japan
[25] Niigata Univ, Grad Sch Med & Dent Sci, Dept Mol Oncol, Niigata, Japan
[26] Keio Univ, Sch Med, Dept Urol, Tokyo, Japan
[27] Eberhard Karls Univ Tubingen, Dept Urol, Tubingen, Germany
[28] Bristol Myers Squibb, Dept Clin Res, Princeton, NJ USA
[29] Bristol Myers Squibb, Dept Clin Oncol, Princeton, NJ USA
[30] Bristol Myers Squibb, Dept Biostat, Princeton, NJ USA
[31] Bristol Myers Squibb, Dept Hlth Econ & Outcomes Res, Princeton, NJ USA
[32] Exelixis, Dept Clin Oncol, Alameda, CA USA
[33] NCI, Genitourinary Malignancies Branch, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[34] Mem Sloan Kettering Canc Ctr, Dept Med, 1275 York Ave, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
METASTATIC UROTHELIAL CARCINOMA; FUNCTIONAL ASSESSMENT; OPEN-LABEL; THERAPY; CANCER; IMMUNOTHERAPY; COMBINATION; EVEROLIMUS;
D O I
10.1056/NEJMoa2026982
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
BACKGROUND The efficacy and safety of nivolumab plus cabozantinib as compared with those of sunitinib in the treatment of previously untreated advanced renal-cell carcinoma are not known. METHODS In this phase 3, randomized, open-label trial, we randomly assigned adults with previously untreated clear-cell, advanced renal-cell carcinoma to receive either nivolumab (240 mg every 2 weeks) plus cabozantinib (40 mg once daily) or sunitinib (50 mg once daily for 4 weeks of each 6-week cycle). The primary end point was progression-free survival, as determined by blinded independent central review. Secondary end points included overall survival, objective response as determined by independent review, and safety. Health-related quality of life was an exploratory end point. RESULTS Overall, 651 patients were assigned to receive nivolumab plus cabozantinib (323 patients) or sunitinib (328 patients). At a median follow-up of 18.1 months for overall survival, the median progression-free survival was 16.6 months (95% confidence interval [CI], 12.5 to 24.9) with nivolumab plus cabozantinib and 8.3 months (95% CI, 7.0 to 9.7) with sunitinib (hazard ratio for disease progression or death, 0.51; 95% CI, 0.41 to 0.64; P<0.001). The probability of overall survival at 12 months was 85.7% (95% CI, 81.3 to 89.1) with nivolumab plus cabozantinib and 75.6% (95% CI, 70.5 to 80.0) with sunitinib (hazard ratio for death, 0.60; 98.89% CI, 0.40 to 0.89; P = 0.001). An objective response occurred in 55.7% of the patients receiving nivolumab plus cabozantinib and in 27.1% of those receiving sunitinib (P<0.001). Efficacy benefits with nivolumab plus cabozantinib were consistent across subgroups. Adverse events of any cause of grade 3 or higher occurred in 75.3% of the 320 patients receiving nivolumab plus cabozantinib and in 70.6% of the 320 patients receiving sunitinib. Overall, 19.7% of the patients in the combination group discontinued at least one of the trial drugs owing to adverse events, and 5.6% discontinued both. Patients reported better health-related quality of life with nivolumab plus cabozantinib than with sunitinib. CONCLUSIONS Nivolumab plus cabozantinib had significant benefits over sunitinib with respect to progression-free survival, overall survival, and likelihood of response in patients with previously untreated advanced renal-cell carcinoma. (Funded by Bristol Myers Squibb and others; CheckMate 9ER ClinicalTrials.gov number, NCT03141177.)
引用
收藏
页码:829 / 841
页数:13
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