Hutson Thomas E, Figlin Robert A
Genitourinary Oncology Program, Texas Oncology, PA, Baylor Sammons Cancer Center, and US Oncology Research Network, Dallas, Texas, USA.
Cancer J. 2007 Sep-Oct;13(5):282-6. doi: 10.1097/PPO.0b013e318156fe69.
Metastatic renal cell cancer has traditionally been treated with interferon and interleukin-2. An improved understanding of the biology of renal cancer has engendered novel targeted therapeutic agents that have altered the natural history of this disease. The vascular endothelial growth factor and its related receptor and the mammalian target of rapamycin signal transduction pathway in particular have been utilized as therapeutic targets. Sunitinib malate, sorafenib tosylate, temsirolimus, and bevacizumab/interferon alfa have improved clinical outcomes in randomized trials. Other antiangiogenic agents have also demonstrated activity in early studies. Given the availability of multiple treatment options, several questions emerge as to how to integrate these new therapies into the management of metastatic renal cell cancer. Recently reported and planned clinical trials will help clarify the role of these agents. The future of therapy for renal cancer appears promising owing to the efficacy of these novel agents.
转移性肾细胞癌传统上采用干扰素和白细胞介素-2进行治疗。对肾癌生物学的深入了解催生了新型靶向治疗药物,这些药物改变了该疾病的自然病程。特别是血管内皮生长因子及其相关受体以及雷帕霉素靶蛋白信号转导通路已被用作治疗靶点。在随机试验中,苹果酸舒尼替尼、甲苯磺酸索拉非尼、替西罗莫司和贝伐单抗/干扰素α改善了临床结局。其他抗血管生成药物在早期研究中也显示出活性。鉴于有多种治疗选择,关于如何将这些新疗法纳入转移性肾细胞癌的治疗管理中出现了几个问题。最近报道的和计划中的临床试验将有助于阐明这些药物的作用。由于这些新型药物的疗效,肾癌治疗的前景似乎很广阔。