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Insulin-like growth factor-1 receptor overexpression is associated with outcome in invasive urothelial carcinoma of urinary bladder: A retrospective study of patients treated using radical cystectomy

机译:胰岛素样生长因子-1受体过表达与浸润性膀胱尿路上皮癌的预后相关:根治性膀胱切除术治疗患者的回顾性研究

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Objective To assess the insulin-like growth factor-1 receptor (IGF1R) expression in urothelial carcinoma (UC) and its prognostic role in relation to clinicopathologic parameters. Methods A total of 100 cases of invasive UC were evaluated using tissue microarrays. Membranous IGF1R staining was evaluated using immunohistochemistry. A scoring method analogous to that of HER2 expression in breast carcinoma was used, and the highest score was assigned in each tumor. IGF1R was considered overexpressed in cases with score ≥1. Results We found IGF1R overexpression in 62% of invasive UC. IGF1R overexpression was associated with race (P =.04) and pT category (P =.03). Median follow-up was 29 months (range, 0.5-212). Progression rate was 60%, and overall mortality and cancer-specific mortality rates were 69% and 51%, respectively. In invasive UC, IGF1R overexpression was significantly associated with overall mortality and cancer-specific mortality (Mantel Cox P =.0002 and P =.006, respectively). IGF1R overexpression was associated with increased hazard ratios (HRs) for overall mortality (HR = 2.63, P =.001) and cancer-specific mortality (HR = 2.45, P =.01), independently and after adjusting for clinicopathologic features and treatment modalities. Conclusion We found IGF1R overexpression in 62% of bladder UC. More importantly, IGF1R overexpression was a significant predictor of overall mortality and cancer-specific mortality, suggesting its potential role as a prognosticator in UC of bladder.
机译:目的评估胰岛素样生长因子-1受体(IGF1R)在尿路上皮癌(UC)中的表达及其与临床病理参数的关系。方法采用组织芯片技术对100例浸润性UC患者进行评估。使用免疫组织化学评估膜IGF1R染色。使用类似于HER2在乳腺癌中表达的评分方法,并且在每个肿瘤中分配最高分数。 IGF1R被认为在得分≥1的患者中过表达。结果我们发现62%的浸润性UC中IGF1R过表达。 IGF1R过表达与种族(P = .04)和pT类别(P = .03)有关。中位随访时间为29个月(范围0.5-212)。进展率为60%,总体死亡率和癌症特异性死亡率分别为69%和51%。在浸润性UC中,IGF1R的过表达与总体死亡率和癌症特异性死亡率显着相关(分别为Mantel Cox P = .0002和P = .006)。独立于临床病理特征和治疗方式后,IGF1R的过表达与总体死亡率(HR = 2.63,P = .001)和癌症特异性死亡率(HR = 2.45,P = .01)的危险比(HRs)增加相关。 。结论我们发现62%的膀胱UC中IGF1R过表达。更重要的是,IGF1R的过表达是总体死亡率和癌症特异性死亡率的重要预测指标,表明其作为膀胱UC预后剂的潜在作用。

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    《Urology》 |2014年第6期|共1页
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