Non-Clear Cell Renal Cancer: Features and Medical Management

被引:33
作者
Heng, Daniel Y. C. [2 ]
Choueiri, Toni K. [1 ]
机构
[1] Harvard Univ, Sch Med, Lank Ctr Genitourinary Oncol, Brigham & Womens Hosp,Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Tom Baker Canc Clin, Calgary, AB, Canada
来源
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK | 2009年 / 7卷 / 06期
关键词
Renal cell cancer; non-clear cell; papillary; chromophobe; collecting duct; sunitinib; sorafenib; temsirolimus; c-MET; COLLECTING DUCT CARCINOMA; EXPANDED ACCESS TRIAL; INTERFERON-ALPHA; SARCOMATOID DIFFERENTIATION; METASTATIC PAPILLARY; HISTOLOGIC SUBTYPES; PROGNOSTIC UTILITY; CLASSIFICATION; SUNITINIB; SURVIVAL;
D O I
10.6004/jnccn.2009.0046
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The treatment of metastatic renal cell carcinoma (RCC) has changed dramatically with the introduction of targeted therapies against vascular endothelial growth factor and the mammalian target of rapamycin. Because patients with clear cell histology account for more than 80% of patients with RCC, little evidence is available on treating patients with non-clear cell histologies. Most clinical trials have excluded them from enrollment, except for a randomized study investigating temsirolimus. Many retrospective studies on the use of sunitinib, sorafenib, and temsirolimus in patients with non-clear cell histology have shown response rates ranging from 3.7% to 16%. Prospective studies in non-clear cell histologies are ongoing. Although response rates may not be as high as those in patients with clear cell histologies, targeted therapy may provide a clinically meaningful response. New investigational therapies are on the horizon for papillary RCC-the most-common non-clear cell RCC histology-targeting pathways specific to this histology, such as the c-MET pathway. (JNCCN 2009;7:659-665)
引用
收藏
页码:659 / 665
页数:7
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