What is the optimal therapy for patients with metastatic renal cell carcinoma who progress on an initial VEGFr-TKI?

被引:29
作者
Calvo, Emiliano [1 ,2 ]
Ravaud, Alain [3 ]
Bellmunt, Joaquim [4 ]
机构
[1] Ctr Integral Oncol Clara Campal, Madrid, Spain
[2] START Madrid, Madrid, Spain
[3] Bordeaux Univ Hosp CHU, Bordeaux, France
[4] Univ Hosp del Mar IMIM, Med Oncol Serv, Barcelona, Spain
关键词
Anticancer therapy; Axitinib; Everolimus; Kidney cancer; Mechanism of action; Metastatic disease; Resistance; Sequential therapy; TYROSINE KINASE INHIBITORS; INTERFERON-ALPHA; SUBGROUP ANALYSIS; DOUBLE-BLIND; PHASE-II; SUNITINIB; SORAFENIB; EVEROLIMUS; EFFICACY; CANCER;
D O I
10.1016/j.ctrv.2012.06.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sequential treatment with targeted therapies is the current standard of care for patients with metastatic renal cell carcinoma (mRCC). Most patients are initially treated with a first-line vascular endothelial growth factor receptor-tyrosine kinase inhibitor (VEGFr-TKI), but will eventually develop resistance and subsequent disease progression. Patients with mRCC whose disease progresses during initial VEGFr-TKI therapy may continue treatment with a different VEGFr-TKI or they may switch to treatment with a mammalian target of rapamycin (mTOR) inhibitor which has a different mechanism of action. Based on positive results of the phase III RECORD-1 trial, clinical guidelines in the United States and Europe recommend use of everolimus, an mTOR inhibitor, in patients with VEGFr-TKI-refractory mRCC. Positive results of the phase III AXIS trial led to recent approval in the United States of the VEGFr-TKI axitinib for use in patients with mRCC who failed one previous therapy. VEGFr-TKIs and mTOR inhibitors have distinct clinical effects with differing safety profiles, but to date, no head-to-head comparisons in the post-VEGFr-TKI second-line setting are available. This review discusses multiple factors that should be considered when selecting a second-line therapy for patients with VEGFr-TKI-refractory mRCC, including evidence-based guidelines, efficacy, safety, patient profile, and clinician familiarity with available agents. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:366 / 374
页数:9
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