Heng Daniel Y C, Choueiri Toni K
Tom Baker Cancer Center, Calgary, Alberta, Canada.
J Natl Compr Canc Netw. 2009 Jun;7(6):659-65. doi: 10.6004/jnccn.2009.0046.
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.
随着针对血管内皮生长因子和雷帕霉素哺乳动物靶点的靶向治疗药物的引入,转移性肾细胞癌(RCC)的治疗发生了巨大变化。由于透明细胞组织学类型的患者占RCC患者的80%以上,因此关于治疗非透明细胞组织学类型患者的证据很少。除了一项研究替西罗莫司的随机试验外,大多数临床试验都将他们排除在入组之外。许多关于舒尼替尼、索拉非尼和替西罗莫司用于非透明细胞组织学类型患者的回顾性研究显示,缓解率在3.7%至16%之间。针对非透明细胞组织学类型的前瞻性研究正在进行中。虽然缓解率可能不如透明细胞组织学类型的患者高,但靶向治疗可能会提供具有临床意义的缓解。针对乳头状RCC(最常见的非透明细胞RCC组织学类型)的新研究性疗法即将出现,这些疗法靶向该组织学类型特有的通路,如c-MET通路。