Changes in Renal Function of Patients with Metastatic Renal Cell Carcinoma During Treatment with Molecular-Targeted Agents

被引:6
作者
Miyake, Hideaki [1 ]
Muramaki, Mototsugu [1 ]
Imai, Satoshi [1 ]
Harada, Ken-ichi [1 ]
Fujisawa, Masato [1 ]
机构
[1] Kobe Univ, Div Urol, Grad Sch Med, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan
关键词
MANAGEMENT; THERAPIES;
D O I
10.1007/s11523-015-0395-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Impairment of renal function is a serious issue that should be considered in patients undergoing treatment with molecular-targeted agents for metastatic renal cell carcinoma (mRCC). Aims The objective of this study was to assess the impact of molecular-targeted therapy on changes in renal function among patients with mRCC. Patients and Methods The study included 408mRCC patients treated with sunitinib, sorafenib, axitinib, everolimus and/ or temsirolimus. Among these, 185, 128 and 95 received molecular-targeted agents as first-line (group 1), second-line (group 2) and third-line (group 3) therapy, respectively. Results No significant differences between the estimated glomerular filtration rate (eGFR) at baseline and that at the end of molecular-targeted therapy were noted among the three groups of patients. In addition, there were no significant differences between eGFR prior to the introduction of moleculartargeted therapy and that at the end of therapy across agents and lines of targeted therapy, with the exception of patients treated with axitinib and everolimus in second-line and thirdline therapy, respectively. In group 1, a reduction in eGFR of > 10 % from baseline was independently associated with performance status, hypertension and treatment duration, while in groups 2 and 3, only treatment duration was independently related to a reduction in eGFR of > 10 %. Conclusions It appears that renal function in patients with mRCC is not markedly impaired by molecular-targeted therapies, irrespective of the specific agents introduced; however, it may be necessary to pay special attention to deterioration in renal function when molecular-targeted therapy is continued for longer periods.
引用
收藏
页码:329 / 335
页数:7
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