Successes and Limitations of Targeted Therapies in Renal Cell Carcinoma

被引:6
|
作者
Pracht, Marc [1 ]
Berthold, Dominik [1 ]
机构
[1] CHU Vaudois, Dept Oncol, Med Oncol Unit, CH-1011 Lausanne, Switzerland
关键词
POSITRON-EMISSION-TOMOGRAPHY; ENDOTHELIAL GROWTH-FACTOR; BLIND PHASE-III; INTERFERON-ALPHA; CANCER; SORAFENIB; SUNITINIB; SURVIVAL; IMPACT; TEMSIROLIMUS;
D O I
10.1159/000355906
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Until recently, the standard treatment for metastatic renal cell carcinoma (RCC) was nonspecific immunotherapy based on interleukin-2 or interferon-alpha. This was associated with a modest survival benefit and with significant clinical toxicities. The understanding of numerous molecular pathways in RCC, including HIF, VEGF, mTOR, and the consecutive use of targeted therapies since the beginning of 2005 have significantly improved outcomes for patients with metastatic RCC with an overall survival greater than 2 years. At present, at least 7 targeted agents are approved for first and consecutive lines of treatment of clear cell metastatic RCC. Long-term benefit and extended survival may be achieved through the optimal use of targeted therapies: optimal dosing, adverse event management and treatment duration and compliance. Advances in the finding of prognostic factors highlight the potential for personalizing treatment for patients with metastatic RCC. Data regarding the best sequencing of targeted therapies, predictive biomarkers, best timing of surgery, patient risk profiles, understanding of resistance mechanisms and safety of targeted therapies are growing and will provide a further step ahead in the management of advanced RCC. In parallel, a new class of therapeutics is emerging in RCC: immunotherapy; in particular check-point blockade antibodies are showing very promising results. (C) 2014 S. Karger AG, Basel
引用
收藏
页码:98 / 112
页数:15
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