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首页> 外文期刊>BMC Cancer >Down-regulation of A-FABP predicts non-muscle invasive bladder cancer progression: investigation with a long term clinical follow-up
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Down-regulation of A-FABP predicts non-muscle invasive bladder cancer progression: investigation with a long term clinical follow-up

机译:A-FABP的下调预测非肌肉侵袭性膀胱癌进展:与长期临床随访进行调查

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摘要

Non-muscle invasive bladder cancers (NMIBC: pTa, pT1) are characterised by a high risk of recurrence and/or progression. Identification of prognostic markers is needed to improve both diagnosis and management of the disease. The aim of this study was to analyse the expression of A-FABP (adipocyte-fatty acid binding protein) and to evaluate its prognostic value in bladder cancer with a long term clinical follow-up. A-FABP expression was investigated by immunohistochemistry in 236 tumours (114 pTa, 61 pT1, 61 pT2-4). Immunostaining was classified as negative (absent or weak immunostaining and moderate or strong staining on ≤10% of cells) or positive (moderate or strong staining on ?10% of cells). Event-free survival (EFS) and overall survival (OS) were determined with a 87.3?months median follow-up in the overall cohort. Recurrence-free survival (RFS) and progression-free survival (PFS) were established in NMIBC. Loss of A-FABP was associated with higher mean age, high stage/grade, and the presence of metastatic lymph nodes. It was correlated with shorter median EFS (17.5 vs 62.5?months; p?=?0.001) and mean OS (76.7 vs 154.2?months; p?=?0.009) and with higher risk of progression in the pTa/pT1 subgroup (HR, 0.36; 95% CI, 0.13-0.96; p?=?0.041) and importantly in the pTa tumours (HR, 0.34; 95% CI, 0.10-0.97; p?=?0.045). These results demonstrated that loss of A-FABP expression following a long follow-up was predictive of pTa and pTa/pT1 progression. Immunohistochemistry on diagnostic biopsy is easy to use and could be of value to help clinicians to propose appropriate treatment for these tumours.
机译:非肌肉侵入性膀胱癌(NMIBC:PTA,PT1)的特征在于复发和/或进展的高风险。需要鉴定预后标志物,以改善疾病的诊断和管理。本研究的目的是分析A-FABP(脂肪细胞 - 脂肪酸结合蛋白)的表达,并评估膀胱癌中的预后价值,长期临床随访。通过免疫组织化学在236颗粒中研究了A-FABP表达(114pta,61pt1,61pt2-4)。免疫染色被归类为阴性(不存在或弱免疫染色,中等或强或强染色≤10%的细胞)或阳性(适度或强染色> 10%的细胞)。无需生存(EFS)和总体生存(OS)以87.3?数月在整体队列中的中间中间后续行动确定。在NMIBC中建立了无复发的存活率(RFS)和无进展的存活率(PFS)。 A-Fabp的丧失与较高的平均年龄,高阶段/等级和转移性淋巴结的存在相关。它与较短的中位数EF(17.5 vs 62.5?月份; p?= 0.001)和均值Os(76.7 vs 154.2?月份; p?= 0.009),并且Pta / pt1子组的进展较高(HR ,0.36; 95%CI,0.13-0.96; p?= 0.041),重要的是在PTA肿瘤中(HR,0.34; 95%CI,0.10-0.97; P?= 0.045)。这些结果证明,长期后续后,损失了PTA和PTA / PT1进展的预测性。免疫组织化学在诊断活检易于使用,可以有价值,以帮助临床医生提出适当治疗这些肿瘤。

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