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Loss of expression of von Hippel-Lindau tumor suppressor protein associated with improved survival in patients with early-stage clear cell renal cell carcinoma.

机译:von Hippel-Lindau肿瘤抑制蛋白表达的丧失与早期透明细胞肾细胞癌患者的生存期改善相关。

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OBJECTIVES: To determine whether actual expression of the von Hippel-Lindau (VHL) protein product itself (pVHL) is associated with clear cell renal cell carcinoma (CC-RCC) survival. Recent data have suggested that somatic mutations of the VHL tumor suppressor gene are associated with better cancer-specific survival in patients with CC-RCC. METHODS: Using a large, clinic-based cohort of 273 patients with CC-RCC, we tested the hypothesis that those patients with CC-RCC tumors lacking pVHL expression [pVHL(-)] will experience better cancer-specific survival than those patients with tumors that show pVHL expression [pVHL(+)]. RESULTS: Using a Cox proportional hazard model adjusting for age, patients with pVHL(-) tumors were not at a decreased risk of CC-RCC death compared with patients with pVHL(+) tumors (hazard ratio 1.0, 95% confidence interval 0.7 to 1.5). Adjustment for the Mayo SSIGN score had little effect on the risk estimate (hazard ratio 0.8; 95% confidence interval 0.5 to 1.2). In our stratifiedanalysis, we found evidence of an inverse association with loss of pVHL expression among those patients presenting with early-stage disease (hazard ratio 0.4; 95% confidence interval 0.2 to 0.8), even after adjustment for the Mayo SSIGN score. CONCLUSIONS: Although we report no overall association, the data from this investigation are consistent with earlier findings that suggest somatic VHL alteration is associated with better cancer-specific survival among those patients presenting with early-stage (pT1 and pT2) CC-RCC.
机译:目的:确定von Hippel-Lindau(VHL)蛋白产品本身(pVHL)的实际表达是否与透明细胞肾细胞癌(CC-RCC)存活有关。最近的数据表明,VHL抑癌基因的体细胞突变与CC-RCC患者更好的癌症特异性生存有关。方法:我们采用了一项基于临床的大型队列研究,纳入了273例CC-RCC患者,我们检验了以下假设:那些患有p-VHL表达[pVHL(-)]的CC-RCC肿瘤患者将比那些具有pVHL表达的患者具有更好的癌症特异性生存率显示pVHL表达的肿瘤[pVHL(+)]。结果:使用校正年龄的Cox比例风险模型,与pVHL(+)肿瘤患者相比,pVHL(-)肿瘤患者的CC-RCC死亡风险没有降低(风险比1.0,95%置信区间0.7至1.5)。调整Mayo SSIGN得分对风险估计的影响很小(风险比0.8; 95%置信区间0.5到1.2)。在我们的分层分析中,即使在对Mayo SSIGN评分进行了调整之后,我们也发现了证据,这些证据表明那些患有早期疾病的患者(风险比0.4; 95%置信区间0.2到0.8)与pVHL表达下降呈负相关。结论:尽管我们没有报告总体相关性,但这项研究的数据与早期发现一致,表明在早期(pT1和pT2)CC-RCC患者中,体细胞VHL改变与更好的癌症特异性生存相关。

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