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Predicting recurrence and progression of noninvasive papillary bladder cancer at initial presentation based on quantitative gene expression profiles.

机译:基于定量的基因表达谱,初步预测非侵入性乳头状膀胱癌的复发和进展。

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BACKGROUND: Currently, tumor grade is the best predictor of outcome at first presentation of noninvasive papillary (Ta) bladder cancer. However, reliable predictors of Ta tumor recurrence and progression for individual patients, which could optimize treatment and follow-up schedules based on specific tumor biology, are yet to be identified. OBJECTIVE: To identify genes predictive for recurrence and progression in Ta bladder cancer at first presentation using a quantitative, pathway-specific approach. DESIGN, SETTING, AND PARTICIPANTS: Retrospective study of patients with Ta G2/3 bladder tumors at initial presentation with three distinct clinical outcomes: absence of recurrence (n=16), recurrence without progression (n=16), and progression to carcinoma in situ or invasive disease (n=16). MEASUREMENTS: Expressions of 24 genes that feature in relevant pathways that are deregulated in bladder cancer were quantified by real-time polymerase chain reaction on tumor biopsies from the patients at initial presentation. RESULTS AND LIMITATIONS: CCND3 (p=0.003) and HRAS (p=0.01) were predictive for recurrence by univariate analysis. In a multivariable model based on CCND3 expression, sensitivity and specificity for recurrence were 97% and 63%, respectively. HRAS (p<0.001), E2F1 (p=0.017), BIRC5/Survivin (p=0.038), and VEGFR2 (p=0.047) were predictive for progression by univariate analysis. Multivariable analysis based on HRAS, VEGFR2, and VEGF identified progression with 81% sensitivity and 94% specificity. Since this is a small retrospective study using medium-throughput profiling, larger confirmatory studies are needed. CONCLUSIONS: Gene expression profiling across relevant cancer pathways appears to be a promising approach for Ta bladder tumor outcome prediction at initial diagnosis. These results could help differentiate between patients who need aggressive versus expectant management.
机译:背景:目前,在无创性乳头状(Ta)膀胱癌首次出现时,肿瘤分级是预后的最佳预测指标。然而,尚未确定可用于个体患者的Ta肿瘤复发和进展的可靠预测因子,该预测因子可根据特定肿瘤生物学优化治疗和随访计划。目的:使用定量的,途径特异性的方法,在首次出现时鉴定出预测膀胱癌复发和进展的基因。设计,地点和参与者:回顾性研究Ta G2 / 3膀胱肿瘤患者最初表现为三种不同的临床结局:无复发(n = 16),无进展复发(n = 16)和癌症进展为癌症。原位或浸润性疾病(n = 16)。测量:在最初出现时,通过对患者肿瘤活检的实时聚合酶链反应对在膀胱癌中失控的相关途径中具有特征的24个基因的表达进行定量。结果与局限性:CCND3(p = 0.003)和HRAS(p = 0.01)通过单因素分析可预测复发。在基于CCND3表达的多变量模型中,复发的敏感性和特异性分别为97%和63%。 HRAS(p <0.001),E2F1(p = 0.017),BIRC5 / Survivin(p = 0.038)和VEGFR2(p = 0.047)可通过单因素分析预测进展。基于HRAS,VEGFR2和VEGF的多变量分析以81%的敏感性和94%的特异性鉴定了进展。由于这是一项使用中通量分析的小型回顾性研究,因此需要更大的验证性研究。结论:跨相关癌症途径的基因表达谱分析似乎是初步诊断Ta膀胱肿瘤预后的有前途的方法。这些结果可以帮助区分需要积极治疗和期望治疗的患者。

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