Cleveland Clinic Taussig Cancer Center, Cleveland Clinic Foundation, Cleveland, OH, USA.
Cancer Manag Res. 2011;3:273-85. doi: 10.2147/CMR.S15557. Epub 2011 Aug 10.
The management of renal cell carcinoma (RCC) has undergone significant changes during the past 10 years, with the treatment of metastatic RCC undergoing the most radical changes. These developments reflect an enhanced understanding of this tumor's underlying biology, which was then translated into the development of a new treatment paradigm. Current therapeutic approaches for the management of patients with metastatic RCC utilize knowledge of histology, molecular abnormalities, clinical prognostic factors, the natural history of this malignancy, and the treatment efficacy and toxicity of available agents. The treatment options available for patients with metastatic RCC have changed dramatically over the past 6 years. Interferon-α and interleukin-2 were the previous mainstays of therapy, but since December 2005, six new agents have been approved in the US for the treatment of advanced RCC. Three are multi-targeted tyrosine kinase inhibitors (TKI) including sunitinib, sorafenib, and pazopanib, two target the mammalian target of rapamycin (temsirolimus and everolimus), and one is a humanized monoclonal antibody (bevacizumab in combination with interferon-α). The current review focuses on the newest TKI available to treat patients with metastatic RCC, pazopanib. The development of this agent both preclinically and clinically is reviewed. The efficacy and safety data from the pivotal clinical trials are discussed, and the potential role of pazopanib in the treatment of patients with metastatic RCC in comparison to other treatment alternatives is critically appraised. This agent has a favorable overall risk benefit, and the available data demonstrate efficacy in patients with metastatic RCC who are either treatment-naïve or cytokine refractory. It therefore represents another alternative for treatment of metastatic RCC patients.
过去 10 年来,肾细胞癌(RCC)的治疗管理发生了重大变化,转移性 RCC 的治疗变化最大。这些进展反映了对这种肿瘤潜在生物学的认识不断提高,随后转化为新的治疗模式的发展。目前,转移性 RCC 患者的治疗方法利用了组织学、分子异常、临床预后因素、这种恶性肿瘤的自然病史以及现有药物的治疗效果和毒性的知识。过去 6 年来,转移性 RCC 患者的治疗选择发生了巨大变化。干扰素-α和白细胞介素-2曾是以前的主要治疗方法,但自 2005 年 12 月以来,在美国有 6 种新药物被批准用于治疗晚期 RCC。其中三种是多靶点酪氨酸激酶抑制剂(TKI),包括舒尼替尼、索拉非尼和帕唑帕尼,两种靶向哺乳动物雷帕霉素靶蛋白(temsirolimus 和依维莫司),一种是人类单克隆抗体(贝伐单抗联合干扰素-α)。目前的综述重点关注可用于治疗转移性 RCC 患者的最新 TKI 药物帕唑帕尼。本文回顾了该药物的临床前和临床开发。讨论了关键性临床试验的疗效和安全性数据,并批判性地评估了帕唑帕尼在转移性 RCC 患者治疗中的潜在作用与其他治疗方案相比。该药物具有良好的整体风险获益,现有数据表明,它对初治或细胞因子难治的转移性 RCC 患者有效。因此,它代表了转移性 RCC 患者治疗的另一种选择。