首页> 外文期刊>Journal of Clinical Pathology >Ki-67 MIB1 labelling index and the prognosis of primary TaT1 urothelial cell carcinoma of the bladder.
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Ki-67 MIB1 labelling index and the prognosis of primary TaT1 urothelial cell carcinoma of the bladder.

机译:Ki-67 MIB1标记指数和原发性膀胱TaT1尿路上皮细胞癌的预后。

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AIMS: To evaluate whether ki-67 labelling index (LI) has independent prognostic value for survival of patients with bladder urothelial tumours graded according to the 2004 World Health Organisation classification. METHODS: Ki-67 LI was evaluated in 164 cases using the grid counting method. Non-invasive (stage Ta) tumours were: papilloma (n = 5), papillary urothelial neoplasia of low malignant potential (PUNLMP; n = 26), and low (LG; n = 34) or high grade (HG; n = 15) papillary urothelial carcinoma. Early invasive (stage T1) tumours were: LG (n = 58) and HG (n = 26) carcinoma. Statistical analysis included Fisher and chi2 tests, and mean comparisons by ANOVA and t test. Univariate and multivariate survival analyses were performed according to the Kaplan-Meier method with log rank test and Cox's proportional hazard method. RESULTS: Mean ki-67 LI increased from papilloma to PUNLMP, LG, and HG in stage Ta (p<0.0001) and from LG to HG in stage T1 (p = 0.013) tumours. High tumour proliferation (>13%) was related to greater tumour size (p = 0.036), recurrence (p = 0.036), progression (p = 0.035), survival (p = 0.054), and high p53 accumulation (p = 0.015). Ki-67 LI and tumour size were independent predictors of disease free survival (DFS), but only ki-67 LI was related to progression free survival (PFS). Cancer specific overall survival (OS) was related to ki-67 LI, tumour size, and p27kip1 downregulation. Ki-67 LI was the main independent predictor of DFS (p = 0.0005), PFS (p = 0.0162), and cancer specific OS (p = 00195). CONCLUSION: Tumour proliferation measured by Ki-67 LI is related to tumour recurrence, stage progression, and is an independent predictor of DFS, PFS, and cancer specific OS in TaT1 bladder urothelial cell carcinoma.
机译:目的:评估ki-67标记指数(LI)是否对根据2004年世界卫生组织分类分级的膀胱尿路上皮肿瘤患者的生存具有独立的预后价值。方法:采用网格计数法评估了164例Ki-67 LI。非侵入性(Ta期)肿瘤为:乳头状瘤(n = 5),低恶性潜能(PUNLMP; n = 26),低(LG; n = 34)或高等级(HG; n = 15)的乳头尿路上皮肿瘤)乳头状尿路上皮癌。早期浸润性(T1期)肿瘤为:LG(n = 58)和HG(n = 26)癌。统计分析包括Fisher和chi2检验,以及ANOVA和t检验的均值比较。根据Kaplan-Meier方法,对数秩检验和Cox比例风险法进行单因素和多因素生存分析。结果:在Ta期(p <0.0001),从乳头状瘤至PUNLMP,LG和HG的平均ki-67 LI升高(p <0.0001),在T1期从LG至HG(p = 0.013)。高肿瘤增殖(> 13%)与更大的肿瘤大小(p = 0.036),复发(p = 0.036),进展(p = 0.035),存活率(p = 0.054)和p53积累高(p = 0.015)有关。 Ki-67 LI和肿瘤大小是无病生存期(DFS)的独立预测因子,但只有ki-67 LI与无进展生存期(PFS)相关。癌症特异性总生存期(OS)与ki-67 LI,肿瘤大小和p27kip1下调有关。 Ki-67 LI是DFS(p = 0.0005),PFS(p = 0.0162)和癌症特异性OS(p = 00195)的主要独立预测因子。结论:Ki-67 LI检测的肿瘤增殖与肿瘤复发,分期进展有关,并且是TaT1膀胱尿路上皮细胞癌中DFS,PFS和癌症特异性OS的独立预测因子。

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