Department of Urology and Urologic Oncology, Hannover University Medical School, Hannover, Germany.
Oncologist. 2011;16(11):1565-71. doi: 10.1634/theoncologist.2011-0213. Epub 2011 Oct 21.
Obesity increases the risk for renal cell carcinoma (RCC). However, it has only recently been identified as an independent positive prognostic factor for localized RCC.
To determine whether obesity influences long-term prognosis in metastatic RCC patients receiving vascular endothelial growth factor-targeted therapy.
DESIGN, SETTING, AND PARTICIPANTS: In 116 patients with metastatic RCC who received antiangiogenic agents (sunitinib, sorafenib, axitinib, bevacizumab) in 2005-2010, we evaluated whether body mass index (BMI), a body surface area (BSA) above the European average, the visceral fat area (VFA), or s.c. fat area (SFA) were of predictive relevance.
BMI was categorized based on current World Health Organization definitions. BSA was stratified according to the European average for men (1.98 m(2)) and women (1.74 m(2)). VFA and SFA were dichotomized using the median of the observed distribution as the cutoff. The primary endpoints of this study were time to progression and overall survival time.
The whole population had median progression-free and overall survival times of 8.3 months and 20.5 months, respectively. In contrast to BMI and BSA, higher than average VFA and SFA levels were significant predictors of longer progression-free and overall survival times. The major limitations of this study are its retrospective design and its heterogeneous patient population.
This is the first study to identify high VFA and SFA levels as positive predictive biomarkers for patients who receive first-line antiangiogenic agents for metastatic RCC.
肥胖增加了患肾细胞癌(RCC)的风险。然而,最近才将其确定为局部 RCC 的独立阳性预后因素。
确定肥胖是否会影响接受血管内皮生长因子靶向治疗的转移性 RCC 患者的长期预后。
设计、地点和参与者:在 2005-2010 年间接受抗血管生成药物(舒尼替尼、索拉非尼、阿昔替尼、贝伐珠单抗)治疗的 116 例转移性 RCC 患者中,我们评估了体重指数(BMI)、超过欧洲平均水平的体表面积(BSA)、内脏脂肪面积(VFA)或皮下脂肪面积(SFA)是否具有预测相关性。
BMI 根据当前世界卫生组织的定义进行分类。BSA 根据男性(1.98 m²)和女性(1.74 m²)的欧洲平均值进行分层。VFA 和 SFA 采用观察分布中位数作为截止值进行二分类。本研究的主要终点是无进展生存期和总生存期。
整个人群的中位无进展生存期和总生存期分别为 8.3 个月和 20.5 个月。与 BMI 和 BSA 相反,高于平均水平的 VFA 和 SFA 水平是无进展生存期和总生存期延长的显著预测指标。本研究的主要局限性是其回顾性设计和异质性患者群体。
这是第一项确定高 VFA 和 SFA 水平作为接受转移性 RCC 一线抗血管生成药物治疗的患者的阳性预测生物标志物的研究。