Phase II trial of second-line everolimus in patients with metastatic renal cell carcinoma (RECORD-4)

被引:37
作者
Motzer, R. J. [1 ]
Alyasova, A. [2 ]
Ye, D. [3 ]
Karpenko, A. [4 ]
Li, H. [5 ]
Alekseev, B. [6 ]
Xie, L. [7 ]
Kurteva, G. [8 ]
Kowalyszyn, R. [9 ]
Karyakin, O. [10 ]
Neron, Y. [11 ]
Cosgriff, T. [12 ]
Collins, L. [13 ]
Brechenmacher, T. [14 ]
Lin, C. [13 ]
Morgan, L. [13 ]
Yang, L. [15 ]
机构
[1] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[2] Prevoljskiy Reg Med Ctr, Novgorod, Russia
[3] Fudan Univ, Shanghai Canc Ctr, Shanghai 200433, Peoples R China
[4] Leningrad Reg Oncol Dispensary, St Petersburg, Russia
[5] Beijing Union Med Coll Hosp, Beijing, Peoples R China
[6] Moscow Hertzen Oncol Inst, Moscow, Russia
[7] Zhejiang Univ, Affiliated Hosp 1, Sch Med, Hangzhou, Zhejiang, Peoples R China
[8] Ctr Oncol, Sofia, Bulgaria
[9] Ctr Invest Clin Clin Viedma, Viedma, Argentina
[10] Med Radiol Res Ctr, Dept Oncol, Obninsk, Russia
[11] Ctr Pesquisas Oncol CEPON, Florianopolis, SC, Brazil
[12] Crescent City Res Consortium, Marrero, LA USA
[13] Novartis Oncol, E Hanover, NJ USA
[14] Novartis Pharma SAS, Rueil Malmaison, France
[15] Chinese Acad Med Sci, Canc Inst & Hosp, Beijing 100730, Peoples R China
关键词
everolimus; metastatic renal cell carcinoma; sequential targeted therapy; second-line; prospective study; THERAPY;
D O I
10.1093/annonc/mdv612
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
RECORD-1 demonstrated clinical benefit of everolimus in patients with metastatic renal cell carcinoma (mRCC) previously treated with sunitinib, sorafenib, or both; prior treatment with cytokines, bevacizumab, and chemotherapy was also permitted. RECORD-4 prospectively assessed everolimus in a purely second-line setting. Patients with clear-cell mRCC were enrolled into one of three cohorts based on first-line therapy with sunitinib, other anti-VEGF agents, or cytokines. Patients were treated with everolimus 10 mg/day until progression (RECIST, v1.0) or intolerance. The primary end point was progression-free survival (PFS) per investigator review. Data cutoff was 1 September 2014, for the primary analysis and 26 June 2015, for the final overall survival (OS) analysis. Enrolled patients (N = 134) previously received sunitinib (n = 58), other anti-VEGF therapy (n = 62; sorafenib, 23; bevacizumab, 16; pazopanib, 13; tivozanib, 5; and axitinib, 3), or cytokines (n = 14). Overall median age was 59 years, and most patients were men (68%) and of favorable/intermediate MSKCC risk (52/37%). Overall median PFS was 7.8 months [95% confidence interval (CI) 5.7-11.0]; in the cohorts, it was 5.7 months (95% CI 3.7-11.3) with previous sunitinib, 7.8 months (95% CI 5.7-11.0) with other previous anti-VEGF therapy, and 12.9 months [95% CI 2.6-not estimable (NE)] with previous cytokines. Overall, 67% of patients achieved stable disease as their best objective response. At final OS analysis, total median OS was 23.8 months (95% CI 17.0-NE) and, in the cohorts, it was 23.8 months (95% CI 13.7-NE) with previous sunitinib, 17.2 months (95% CI 11.9-NE) with other previous anti-VEGF therapy, and NE (95% CI 15.9-NE) with previous cytokine-based therapy. Overall, 56% of patients experienced grade 3 or 4 adverse events (regardless of relationship to study drug). These results confirm the PFS benefit of second-line everolimus after first-line sunitinib or other anti-VEGF therapies. The safety profile of everolimus was consistent with previous experience. Everolimus as Second-line Therapy in Metastatic Renal Cell Carcinoma (RECORD-4), ClinicalTrials.gov identifier, NCT01491672.
引用
收藏
页码:441 / 448
页数:8
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