First-line Nivolumab plus Ipilimumab Versus Sunitinib in Patients Without Nephrectomy and With an Evaluable Primary Renal Tumor in the CheckMate 214 Trial

被引:41
作者
Albiges, Laurence [1 ]
Tannir, Nizar M. [2 ]
Burotto, Mauricio [3 ]
McDermott, David [4 ]
Plimack, Elizabeth R. [5 ]
Barthelemy, Philippe [6 ]
Porta, Camillo [7 ]
Powles, Thomas [8 ]
Donskov, Frede [9 ]
George, Saby [10 ]
Kollmannsberger, Christian K. [11 ]
Gurney, Howard [12 ,13 ]
Grimm, Marc-Oliver [14 ]
Tomita, Yoshihiko [15 ]
Castellano, Daniel [16 ]
Rini, Brian, I [17 ]
Choueiri, Toni K. [18 ,19 ]
Leung, David [20 ]
Saggi, Shruti Shally [21 ]
Lee, Chung-Wei [21 ]
McHenry, M. Brent [22 ]
Motzer, Robert J. [23 ]
机构
[1] Gustave Roussy, Dept Canc Med, Villejuif, France
[2] Univ Texas MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX 77030 USA
[3] Bradford Hill Clin Res Ctr, Santiago, Chile
[4] Beth Israel Deaconess Med Ctr, Dana Farber Harvard Canc Ctr, Div Med Oncol, Boston, MA 02215 USA
[5] Fox Chase Canc Ctr, Dept Hematol & Oncol, 7701 Burholme Ave, Philadelphia, PA 19111 USA
[6] Inst Cancerol Strasbourg Europe, Med Oncol, Strasbourg, France
[7] Univ Pavia, Pavia, Italy
[8] Queen Mary Univ London, Barts Canc Inst, Dept Urol, London, England
[9] Aarhus Univ Hosp, Dept Oncol, Aarhus, Denmark
[10] Roswell Park Canc Inst, Dept Med, Buffalo, NY 14263 USA
[11] British Columbia Canc Agcy, Dept Med, Vancouver, BC, Canada
[12] Westmead Hosp, Dept Med Oncol, Sydney, NSW, Australia
[13] Macquarie Univ, Sydney, NSW, Australia
[14] Jena Univ Hosp, Dept Urol, Jena, Germany
[15] Niigata Univ, Grad Sch Med & Dent Sci, Niigata, Japan
[16] Hosp Univ 12 Octubre, Med Oncol Serv, Madrid, Spain
[17] Vanderbilt Univ, Div Hematol Oncol, Med Ctr, Nashville, TN USA
[18] Brigham & Womens Hosp, Lank Ctr Genitourinary Oncol, Dana Farber Canc Inst, Dept Med Oncol, 75 Francis St, Boston, MA 02115 USA
[19] Harvard Med Sch, Boston, MA 02115 USA
[20] Dept Imaging, Bristol Myers Squibb, Princeton, NJ USA
[21] Bristol Myers Squibb, Dept Clin Trials, Princeton, NJ USA
[22] Bristol Myers Squibb, Dept Biostat, Princeton, NJ USA
[23] 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
Advanced renal cell carcinoma; CheckMate; 214; Cytoreductive nephrectomy; Ipilimumab; Nivolumab;
D O I
10.1016/j.eururo.2021.10.001
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
We present an exploratory post hoc analysis from the phase 3 CheckMate 214 trial of first-line nivolumab plus ipilimumab (NIVO+IPI) versus sunitinib in a subgroup of 108 patients with advanced renal cell carcinoma (aRCC) without prior nephrectomy and with an evaluable primary tumor, a population under-represented in clinical trials. Patients with clear cell aRCC were randomized to NIVO+IPI every 3 wk for four doses followed by NIVO monotherapy, or sunitinib every day for 4 wk (6-wk cycle). Overall survival (OS), progression-free survival (PFS), objective response rate (ORR), and primary tumor shrinkage were assessed. PFS and ORR were assessed per independent radiology review committee using RECIST version 1.1. With minimum study follow-up of 4 yr for intentto-treat patients, OS favored NIVO+IPI (n = 53) over sunitinib (n = 55; hazard ratio 0.63, 95% confidence interval 0.40-1.0) among patients without prior nephrectomy. ORR was higher (34% vs 15%; p = 0.0041) and median duration of response was longer with NIVO +IPI versus sunitinib (20.5 vs 14.1 mo); the best overall response was partial response in either arm. A >= 30% reduction in the diameter of intact target renal tumors was achieved in 35% of patients with NIVO+IPI versus 20% with sunitinib. Safety was consistent with the global study population. In conclusion, in patients with aRCC without prior nephrectomy and with an evaluable primary tumor, NIVO+IPI showed survival benefits and renal tumor reduction versus sunitinib. This trial is registered at ClinicalTrials.gov as NCT02231749. Patient summary: In an exploratory analysis of a large global trial (CheckMate 214), we observed positive outcomes (both survival and tumor response to treatment) with nivolumab plus ipilimumab over sunitinib in a subgroup of patients with advanced kidney cancer who did not undergo removal of their primary kidney tumor. This subset of patients represents a population that has not been studied in clinical trials and for whom outcomes with new immunotherapy combination regimens are not yet known. We conclude that treatment with nivolumab plus ipilimumab offers these patients a survival benefit versus sunitinib, consistent with that observed in the overall study, as well as a notable kidney tumor reduction. (C) 2021 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:266 / 271
页数:6
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