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首页> 外文期刊>Therapeutic advances in urology. >Fibronectin urothelial gene expression as a new reliable biomarker for early detection of local toxicity secondary to adjuvant intravesical therapy for non-muscle invasive bladder cancer
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Fibronectin urothelial gene expression as a new reliable biomarker for early detection of local toxicity secondary to adjuvant intravesical therapy for non-muscle invasive bladder cancer

机译:纤连蛋白尿路上皮基因表达作为一种新的可靠生物标志物,用于早期检测局部毒性的临床术语术治疗非肌肉侵袭性膀胱癌

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Background: A marker of urothelial damage could be helpful for early detection and monitoring of local toxicity due to intravesical therapy for non-muscle invasive bladder cancer (NMIBC). The aim of the study was to investigate the correlation between fibronectin (FN) gene expression in bladder washings and local toxicity secondary to adjuvant intravesical therapy. Materials and methods: Patients undergoing adjuvant intravesical therapy for NMIBC and age-matched healthy patients were enrolled. Real time polymerase chain reaction was performed to analyze FN expression in bladder washings. Local toxicity was classified as: 0–1 mild (no medical therapy), 2 moderate (medical therapy and/or instillation postponed), 3 severe (discontinuation of therapy). Results: Seventy-two patients and 21 controls entered the study. A useful pellet was obtained in 58 patients and 18 controls. Intravesical Bacillus Calmette–Guerin (BCG), Epirubicin and Mitomycin C was offered to 69%, 13.8% and 17.2% of patients respectively. Compared with healthy controls (FN?=?1.0 fold), overall median FN expression before adjuvant intravesical therapy was 1.73 fold [interquartile range (IQR) 0.8–2.3], while during therapy median FN expression increased to 3.41 (IQR: 1.6–6.1) fold. Considering 40 intermediate and high-risk patients undergoing intravesical BCG, median FN expression before adjuvant treatment was 1.92 [(IQR: 1.0–2.7) fold, increasing up to 4.1 (IQR: 1.9–6.6) during therapy. In more detail, FN increased during BCG therapy, showing a median expression of 4.22 (IQR: 2.2–5.5) and 6.16 (IQR: 2.6–8.7) fold in presence of grade 2 and 3 toxicity respectively, while remaining more or less stable in asymptomatic patients. After receiver operating characteristic curve analysis, FN value of 3.6 fold resulted, corresponding to 75% sensitivity and 69% specificity to predict grade 2–3 toxicity events (area under the curve 0.74, 95% confidence interval 0.63–0.85, p?=?0.001). Conclusion: Our study validated the correlation between FN expression and urothelial damage. BCG seems to induce a urothelial activation with FN overexpression during adjuvant intravesical therapy. Grade of toxicity was related to FN expression.
机译:背景:由于非肌肉侵袭性膀胱癌(NMIBC)的膀胱内治疗,尿路上损伤的标记可能有助于对早期检测和监测局部毒性。该研究的目的是探讨膀胱洗涤中纤连蛋白(FN)基因表达与辅助膀胱内疗法的局部毒性之间的相关性。材料与方法:招收了尼布和年龄匹配的健康患者的辅助介绍介绍的患者。进行实时聚合酶链反应以分析膀胱洗涤中的FN表达。局部毒性被归类为:0-1温和(无医疗疗法),2中等(医疗治疗和/或滴注后滴注),3严重(停止治疗)。结果:七十二名患者和21个对照进入研究。在58名患者和18例对照中获得有用的颗粒。膀胱内芽孢杆菌(BCG),Epirubicin和丝霉素C分别提供69%,13.8%和17.2%的患者。与健康对照(FN?= 1.0倍)相比,佐剂膀胱内治疗前的整体中位数FN表达为1.73折[四分位数范围(IQR)0.8-2.3],而治疗中位数FN表达增加至3.41(IQR:1.6-6.1 ) 折叠。考虑到介绍BCG的40例中间和高风险患者,佐剂治疗前的中位FN表达为1.92 [(IQR:1.0-2.7)折叠,治疗期间增加4.1(IQR:1.9-6.6)。更详细地,FN在BCG疗法期间增加,显示4.22(IQR:2.2-5.5)和6.16(IQR:2.6-8.7)分别在2级和3级毒性的情况下折叠的中值表达,同时仍然或多或少稳定无症状患者。在接收器操作特性曲线分析后,FN值为3.6折,对应于75%的灵敏度和69%的特异性预测2-3级毒性事件(曲线下的面积0.74,95%置信区间0.63-0.85,P?=? 0.001)。结论:我们的研究验证了FN表达与尿路上位损伤之间的相关性。在佐剂膀胱内疗法期间,BCG似乎用FN过度表达诱导尿液激活。毒性等级与FN表达有关。

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