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首页> 外文期刊>Cancer prevention research. >Prognostic Significance of VEGF after Twenty-Year Follow-up in a Randomized Trial of Fenretinide in Non-Muscle-Invasive Bladder Cancer
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Prognostic Significance of VEGF after Twenty-Year Follow-up in a Randomized Trial of Fenretinide in Non-Muscle-Invasive Bladder Cancer

机译:非肌肉浸润性膀胱癌芬尼替尼随机试验二十年随访后VEGF的预后意义

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Non-muscle-invasive bladder cancer (NMIBC) may progress to muscle-invasive disease, but no effective preventive treatments are available. In addition, no reliable prognostic biomarkers have been identified. We assessed the long-term effect of the oral retinoid fenretinide and the prognostic value of circulating VEGF levels. We updated through the Tumor Registry the vital status of 99 patients with resected Ta/T1 bladder tumors who were recruited in a randomized trial of 2 years of fenretinide or no treatment in 1993-1994. Serum VEGF levels measured at baseline and 12 months were available in a subgroup of 62 patients. After a median of 20.5 years, 54 subjects died, 35 of any cancer and 14 of bladder cancer. Neither overall survival (OS), nor cancer survival (CS) or bladder cancer survival (BCS) was affected by fenretinide (log-rank P >= 0.2). DNA aneuploidy in bladder washing was associated with shorter OS (P = 0.02), CS (P = 0.05), and BCS (P = 0.09). Subjects with baseline VEGF levels in the top quintile (>= 350 pg/mL) had a significantly shorter OS (P = 0.01), CS (P = 0.02), and BCS (P = 0.008). The trend across quintiles of VEGF was significant for BCS (P = 0.007). Multivariate analyses showed that, in addition to smoking status, VEGF level in the top quintile was an independent prognostic factor for OS (HR = 2.7; 95% CI, 1.1-6.5), CS (HR = 3.3; 95% CI, 1.1-9.4) and BCS (HR = 8.9; 95% CI, 1.3-61). Fenretinide did not affect the long-term outcome of patients with NMIBC. High serum VEGF level was a significant predictor of overall and cancer death and may help to identify high-risk subjects who may benefit from a preventive therapy. (C) 2016 AACR.
机译:非肌肉浸润性膀胱癌(NMIBC)可能会发展成肌肉浸润性疾病,但尚无有效的预防方法。此外,尚未鉴定出可靠的预后生物标志物。我们评估了口服类维生素A芬维A胺的长期作用以及循环中VEGF水平的预后价值。我们通过肿瘤登记系统更新了99例Ta / T1切除的膀胱肿瘤患者的生命状态,这些患者是在2年的芬维A胺或1993-1994年不进行治疗的随机试验中招募的。 62名患者亚组中有基线和12个月时测得的血清VEGF水平。在中值20.5年之后,有54名受试者死亡,其中35名癌症和14名膀胱癌。 fenretinide既不会影响总生存期(OS),也不会影响癌症生存期(CS)或膀胱癌生存期(BCS)(log-rank P> = 0.2)。膀胱冲洗中的DNA非整倍性与较短的OS(P = 0.02),CS(P = 0.05)和BCS(P = 0.09)相关。基线VEGF在前五分位(> = 350 pg / mL)中的受试者的OS(P = 0.01),CS(P = 0.02)和BCS(P = 0.008)明显较短。对于BCS,VEGF跨五分位数的趋势很明显(P = 0.007)。多因素分析显示,除了吸烟状况外,前五分位的VEGF水平是OS(HR = 2.7; 95%CI,1.1-6.5),CS(HR = 3.3; 95%CI,1.1- 9.4)和BCS(HR = 8.9; 95%CI,1.3-61)。 Fenretinide不会影响NMIBC患者的长期结局。高血清VEGF水平是整体死亡和癌症死亡的重要预测指标,可能有助于确定可能从预防治疗中受益的高风险受试者。 (C)2016 AACR。

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