Centre Georges François Leclerc, Centre de Recherche INSERM 866, Faculté de Médecine, 7 Boulevard Jeanne d'Arc, 21000 Dijon, France.
Oncologist. 2011;16(1):71-81. doi: 10.1634/theoncologist.2010-0227. Epub 2011 Jan 6.
Purpose. A better identification of patients who are more likely to benefit from vascular endothelial growth factor-targeted therapy is warranted in metastatic renal cell carcinoma (mRCC). As adipose tissue releases angiogenic factors, we determined whether parameters such as visceral fat area (VFA) were associated with outcome in these patients. Experimental Design. In 113 patients with mRCC who received antiangiogenic agents (bevacizumab, sunitinib, or sorafenib) (n = 64) or cytokines (n = 49) as first-line treatment, we used computed tomography to measure VFA and subcutaneous fat area (SFA). We evaluated associations linking body mass index (BMI), SFA, and VFA to time to progression (TTP) and overall survival (OS). Results. High SFA and VFA values were significantly associated with shorter TTP and OS. By multivariate analysis, high VFA was independently associated with shorter TTP and OS. These results were internally validated using bootstrap analysis. By contrast, VFA was not associated with survival in the cytokine group. In the whole population, interaction between VFA and treatment group was significant for TTP and OS, thereby confirming the results. Conclusion. Our study provides the first evidence that high VFA could be a predictive biomarker from shorter survival in patients given first-line antiangiogenic agents for mRCC.
在转移性肾细胞癌(mRCC)中,需要更好地识别更可能从血管内皮生长因子靶向治疗中获益的患者。由于脂肪组织释放血管生成因子,我们确定这些患者的内脏脂肪面积(VFA)等参数是否与预后相关。
在接受抗血管生成药物(贝伐单抗、舒尼替尼或索拉非尼)(n=64)或细胞因子(n=49)作为一线治疗的 113 例 mRCC 患者中,我们使用计算机断层扫描测量 VFA 和皮下脂肪面积(SFA)。我们评估了将体重指数(BMI)、SFA 和 VFA 与无进展生存期(TTP)和总生存期(OS)联系起来的关联。
高 SFA 和 VFA 值与较短的 TTP 和 OS 显著相关。通过多变量分析,高 VFA 与较短的 TTP 和 OS 独立相关。这些结果通过自举分析进行了内部验证。相比之下,VFA 与细胞因子组的生存无关。在整个人群中,VFA 和治疗组之间的相互作用对 TTP 和 OS 有显著影响,从而证实了这一结果。
我们的研究首次提供了证据,表明在接受一线抗血管生成药物治疗的 mRCC 患者中,高 VFA 可能是一个预测生物标志物,与较短的生存时间相关。