Efficacy of everolimus in second- and third-line therapy for metastatic renal cell carcinoma: A registry-based analysis

被引:12
作者
Buchler, Tomas [1 ,2 ]
Bortlicek, Zbynek [3 ]
Poprach, Alexandr [4 ]
Kubackova, Katerina [5 ,6 ]
Kiss, Igor [4 ]
Zemanova, Milada [2 ,7 ]
Fiala, Ondrej [8 ]
Dusek, Ladislav [3 ]
Vyzula, Rostislav [4 ]
Melichar, Bohuslav [9 ,10 ]
机构
[1] Thomayer Hosp, Dept Oncol, Prague, Czech Republic
[2] Charles Univ Prague, Fac Med 1, Prague, Czech Republic
[3] Masaryk Univ, Inst Biostat & Anal, Brno, Czech Republic
[4] Masaryk Mem Canc Inst, Dept Comprehens Canc Care, Brno, Czech Republic
[5] Motol Univ Hosp, Dept Oncol, Prague, Czech Republic
[6] Charles Univ Prague, Fac Med 2, Prague, Czech Republic
[7] Gen Univ Hosp, Dept Oncol, Prague, Czech Republic
[8] Univ Hosp, Dept Oncol, Plzen, Czech Republic
[9] Palacky Univ, Dept Oncol, Sch Med, CR-77147 Olomouc, Czech Republic
[10] Teaching Hosp, Olomouc, Czech Republic
关键词
Everolimus; mTOR; Renal cell carcinoma; Tyrosine kinase inhibitors; Therapy;
D O I
10.1016/j.urolonc.2013.12.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: The aim of the present study was to describe the efficacy and safety of everolimus in the treatment of metastatic renal cell carcinoma (mRCC) after administration of 1 vs. 2 prior tyrosine kinase inhibitors (TKIs). Patients and methods: A national renal information system database was used as the data source for the retrospective study. There were 483 patients who received everolimus as the second (n = 350) or the third (n = 112) targeted agent following TKIs. Results: Median progression-free survival (PFS) from the start of everolimus in the second or the third line of targeted therapy was 6.1 months for both subgroups (P = 0.863). Median total PFS from the start of the first targeted agent to progression on the third targeted agent for patients receiving 3 lines of therapy with TKI-TKI-everolimus (n = 112) and TKI-everolimus-TKI (n = 27) sequences was 28.3 months vs. 31.3 months, respectively (P = 0.16), and there was no significant difference in overall survival. PFS on everolimus was associated with PFS on previous TKIs in patients receiving 1 but not 2 previous TKIs. Only 13% of 352 patients starting targeted therapy for mRCC in 2010 had received 3 sequential targeted agents by the data cutoff in March 2013. Conclusion: PFS on everolimus correlated with PFS on TKIs in patients pretreated with 1 but not 2 TKIs. Everolimus can be deferred to the third line without loss of efficacy or increased toxicity. However, only a minority of patients with mRCC starting targeted treatment can be expected to receive third-line therapy. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:569 / 575
页数:7
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