Treatment Beyond Progression in Patients with Advanced Renal Cell Carcinoma Treated with Nivolumab in CheckMate 025

被引:218
作者
Escudier, Bernard [1 ]
Motzer, Robert J. [2 ]
Sharma, Padmanee [3 ]
Wagstaff, John [4 ,5 ]
Plimack, Elizabeth R. [6 ]
Hammers, Hans J. [7 ,22 ]
Donskov, Frede [8 ]
Gurney, Howard [9 ,10 ]
Sosman, Jeffrey A. [11 ,23 ]
Zalewski, Pawel G. [12 ]
Harmenberg, Ulrika [13 ]
McDermott, David F. [14 ,15 ]
Choueiri, Toni K. [16 ]
Richardet, Martin [17 ]
Tomita, Yoshihiko [18 ]
Ravaud, Alain [19 ]
Doan, Justin [20 ]
Zhao, Huanyu [20 ]
Hardy, Helene [20 ]
George, Saby [21 ]
机构
[1] Gustave Roussy, Dept Med Oncol, 114 Rue Edouard Vaillant, F-94800 Villejuif, France
[2] Mem Sloan Kettering Canc Ctr, Dept Med, 1275 York Ave, New York, NY 10021 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Immunol, Dept Genitourinary Med Oncol, Houston, TX 77030 USA
[4] South West Wales Canc Inst, Dept Med Oncol, Swansea, W Glam, Wales
[5] Swansea Univ, Coll Med, Swansea, W Glam, Wales
[6] Fox Chase Canc Ctr, Dept Hematol Oncol, 7701 Burholme Ave, Philadelphia, PA 19111 USA
[7] Johns Hopkins Sidney Kimmel Comprehens Canc Ctr, Dept Med Oncol, Baltimore, MD USA
[8] Aarhus Univ Hosp, Dept Oncol, Aarhus, Denmark
[9] Westmead Hosp, Dept Med Oncol, Sydney, NSW, Australia
[10] Macquarie Univ, Sydney, NSW, Australia
[11] Vanderbilt Univ, Med Ctr, Dept Hematol, Nashville, TN USA
[12] Lakeridge Hlth RS McLaughlin Durham Reg Canc Ctr, Dept Oncol, Oshawa, ON, Canada
[13] Karolinska Univ Hosp, Dept Oncol, Radiumhemmet, Stockholm, Sweden
[14] Dana Farber Harvard Canc Ctr, Beth Israel Deaconess Med Ctr, Biol Therapy Program, Boston, MA USA
[15] Dana Farber Harvard Canc Ctr, Beth Israel Deaconess Med Ctr, Cutaneous Oncol Program, Boston, MA USA
[16] Brigham & Womens Hosp, Dana Farber Canc Inst, Dept Med Oncol, Kidney Canc Ctr, 75 Francis St, Boston, MA 02115 USA
[17] Inst Oncol Cordoba, Dept Med Oncol, Cordoba, Argentina
[18] Niigata Univ, Dept Mol Oncol, Dept Urol, Niigata, Japan
[19] Hop St Andre, Bordeaux Univ Hosp, Dept Med Oncol & Radiotherapy, Bordeaux, France
[20] Bristol Myers Squibb, Princeton, NJ USA
[21] Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
[22] UT Southwestern Kidney Canc Program, Div Hematol & Oncol, Dallas, TX USA
[23] Northwestern Univ, Dept Med Hematol Oncol, Robert Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
关键词
Advanced renal cell carcinoma; Everolimus; Nivolumab; Phase; 3; Treatment beyond progression; IMMUNE-RELATED RESPONSE; DISEASE PROGRESSION; CANCER;
D O I
10.1016/j.eururo.2017.03.037
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
100201 [内科学]; 100221 [泌尿外科学];
摘要
Background: Response patterns to nivolumab differ from those seen with other approved targeted therapies. Objective: To investigate the efficacy of nivolumab in previously treated patients with advanced renal cell carcinoma who were treated beyond (Response Evaluation Criteria In Solid Tumors) RECIST progression. Design, setting, and participants: This was a subgroup analysis of patients treated with nivolumab in the phase 3 CheckMate 025 study. Patients continuing to tolerate therapy and exhibiting investigator-assessed clinical benefit were eligible to be treated beyond RECIST progression (TBP) and received therapy for >= 4 wk after first progression; patients not treated beyond RECIST progression (NTBP) received 0 wk to <4 wk of therapy after progression. Interventions: Nivolumab 3 mg/kg intravenously every 2 wk. Results and limitations: Of 406 nivolumab-treated patients, 316 (78%) progressed by RECIST criteria. Of those who progressed, 48% were TBP, 52% were NTBP. Before being TBP, objective response rate (95% confidence interval) was 20% (14-28) and 14% (9-21) in patients TBP and NTBP, respectively. Differences in clinical characteristics assessed at first progression between patients TBP versus NTBP included better Karnofsky performance status, less deterioration in Karnofsky performance status, shorter time to response, lower incidence of new bone lesions, and improved quality of life. Postprogression, 13% of all patients TBP (20/153) had >= 30% tumor burden reduction including patients with preprogression and postprogression tumor measurements (n = 142) and complete/partial response (28%, 8/29), stable disease (6%, 3/47), and progressive disease (14%, 9/66) as their best response before being TBP. Incidence of treatment-related adverse events in patients TBP was lower after (59%) versus before (71%) progression. Limitations included potential bias from the nonrandomized nature of the analysis. Conclusions: A subset of patients with advanced renal cell carcinoma and RECIST progression experienced tumor reduction postprogression with nivolumab, and had an acceptable safety profile. Clinical judgment remains essential when switching therapy. ClinicalTrials.gov Identifier: NCT01668784. Patient summary: A subset of patients with advanced renal cell carcinoma and disease progression may continue to benefit from nivolumab treatment beyond progression as evidenced by tumor reduction postprogression and an acceptable safety profile. (C) 2017 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:368 / 376
页数:9
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