Centre Hospitalier Universitaire Bretonneau, Centre Henry S. Kaplan, Department for Oncology, 2 Boulevard Tonnelle, 37044 Tours Cedex 9, France.
Anticancer Res. 2012 Feb;32(2):697-700.
Six targeted agents [sorafenib, sunitinib, temsirolimus, bevacizumab (plus interferon), everolimus and pazopanib] have been approved for the treatment of patients with metastatic renal cell carcinoma. As disease progression is inevitable, most patients will receive several lines of treatment. However, the choice regarding which sequence of drugs to use remains unclear, particularly concerning the drug class, i.e. those targeting the vascular endothelial growth factor (receptor) [VEGF(R)] pathway versus those acting on the mammalian target of rapamycin pathway. There appears to be no absolute crossresistance between tyrosine kinase inhibitors (TKIs) acting on the VEGF(R) pathway, and there have been numerous reports of two TKIs being successfully used in sequence. We report the case of a 63-year-old woman who responded for 24 months to three successive lines of treatment with different TKIs (sunitinib, axitinib and sorafenib). This suggests that TKIs targeting VEGFR should be considered as individual drugs and not as a single class.
六种靶向药物[索拉非尼、舒尼替尼、替西罗莫司、贝伐珠单抗(联合干扰素)、依维莫司和帕唑帕尼]已被批准用于治疗转移性肾细胞癌患者。由于疾病的进展是不可避免的,大多数患者将接受多线治疗。然而,关于应该使用哪种药物顺序的选择仍然不清楚,特别是关于药物类别,即那些针对血管内皮生长因子(受体)[VEGF(R)]途径的药物与那些作用于哺乳动物雷帕霉素靶蛋白途径的药物。似乎作用于 VEGF(R)途径的酪氨酸激酶抑制剂(TKI)之间没有绝对的交叉耐药性,并且有许多关于两种 TKI 成功序贯使用的报道。我们报告了一例 63 岁女性的病例,她对连续三种不同的 TKI(舒尼替尼、阿昔替尼和索拉非尼)治疗反应持续了 24 个月。这表明,针对 VEGFR 的 TKI 应被视为单独的药物,而不是单一类别。