National Science Foundation, Arlington, VA 22030, USA.
Cell Rep. 2013 Feb 21;3(2):277-81. doi: 10.1016/j.celrep.2013.01.015. Epub 2013 Feb 7.
Preclinical studies have suggested that sunitinib accelerates metastases in animals, ascribing this to inhibition of the vascular endothelial growth factor receptor or the tumor's adaptation. To address whether sunitinib accelerates tumors in humans, we analyzed data from the pivotal randomized phase III trial comparing sunitinib and interferon alfa in patients with metastatic renal cell carcinoma. The evidence clearly shows that sunitinib was not harmful, did not accelerate tumor growth, and did not shorten survival. Specifically, neither longer sunitinib treatment nor a greater effect of sunitinib on tumors reduced survival. Sunitinib did reduce the tumor's growth rate while administered, thereby improving survival, without appearing to alter tumor biology after discontinuation. Concerns arising from animal models do not apply to patients receiving sunitinib and likely will not apply to similar agents.
临床前研究表明,舒尼替尼会加速动物的转移,这归因于对血管内皮生长因子受体或肿瘤的适应性的抑制。为了确定舒尼替尼是否会加速人类肿瘤的生长,我们分析了比较舒尼替尼和干扰素α治疗转移性肾细胞癌的关键性随机 III 期临床试验的数据。证据清楚地表明舒尼替尼没有危害,没有加速肿瘤生长,也没有缩短生存期。具体来说,无论是更长时间的舒尼替尼治疗还是舒尼替尼对肿瘤的更大作用都没有降低生存率。舒尼替尼在给药时确实降低了肿瘤的生长速度,从而提高了生存率,而在停药后似乎并没有改变肿瘤的生物学特性。从动物模型中产生的担忧不适用于接受舒尼替尼治疗的患者,可能也不适用于类似的药物。