Institut Gustave Roussy, 39 Rue Camille Desmoulins, 94805 Villejuif, France.
Expert Rev Anticancer Ther. 2010 Mar;10(3):305-17. doi: 10.1586/era.10.26.
Targeted agents, such as sunitinib (SUTENT((R))) have become central to the management of advanced and/or metastatic renal cell carcinoma (mRCC). Sunitinib is an oral, multitargeted receptor tyrosine kinase inhibitor that has demonstrated efficacy for the treatment of mRCC in multiple clinical trials. In a Phase III trial in previously untreated patients with mRCC, sunitinib was associated with median progression-free survival of 11 months, which was more than double that observed with interferon-alpha (5 months; p < 0.001). As a result, sunitinib is recommended in international treatment guidelines and is considered a reference standard of care in the first-line setting for patients at favorable or intermediate prognostic risk. Sunitinib is generally well tolerated with a predictable adverse-event profile; the majority of adverse events can be managed with standard medical intervention. This paper presents an overview of data supporting the use of sunitinib for mRCC, and considers the optimal management of sunitinib in clinical practice.
靶向药物,如舒尼替尼(SUTENT((R)))已成为晚期和/或转移性肾细胞癌(mRCC)治疗的核心。舒尼替尼是一种口服的、多靶点受体酪氨酸激酶抑制剂,在多项临床试验中已被证明对 mRCC 的治疗有效。在一项未经治疗的 mRCC 患者的 III 期试验中,舒尼替尼的中位无进展生存期为 11 个月,是干扰素-α(5 个月;p<0.001)的两倍多。因此,舒尼替尼在国际治疗指南中被推荐,并被认为是预后良好或中等的患者一线治疗的参考标准。舒尼替尼通常具有良好的耐受性,不良反应可预测;大多数不良反应可通过标准医学干预来管理。本文概述了支持舒尼替尼用于 mRCC 的数据,并考虑了舒尼替尼在临床实践中的最佳管理。