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Survivin expression in patients with non-muscle-invasive urothelial cell carcinoma of the bladder.

机译:Survivin在非肌肉浸润性膀胱尿路上皮细胞癌患者中的表达。

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OBJECTIVES: Survivin is a member of the inhibitor of apoptosis gene family that controls mitotic progression and induces tumor cell invasion. Our objectives were to evaluate the association of survivin expression with the presence of urothelial cell carcinoma of the bladder and clinical outcomes in patients with non-muscle-invasive urothelial cell carcinoma of the bladder. METHODS: Immunohistochemical staining for survivin was performed on archival bladder tissue microarray specimens from 9 normal controls and 74 consecutive patients who had Stage Ta, Tis, and/or T1 disease on transurethral resection (TUR). Staining was also performed on cystectomy specimens from 22 of these patients who had undergone radical cystectomy for disease progression. Survivin was considered overexpressed when more than 10% of the cells expressed survivin. RESULTS: Survivin was not expressed in normal bladder urothelium. Survivin was overexpressed in 53% of non-muscle-invasive bladder tumors. Overexpression of survivin was associated with greater tumor grade (P <0.001). On multivariate analyses adjusted for the effects of TUR stage, grade, and intravesical therapy, survivin overexpression was independently associated with cancer recurrence (hazard ratio 2.50, 95% confidence interval 1.09 to 5.69, P = 0.02) and progression (hazard ratio 3.87, 95% confidence interval 1.13 to 13.24, P = 0.03), but not disease-specific survival (hazard ratio 1.88, 95% confidence interval 0.90 to 6.46, P = 0.07). A high concordance rate for survivin expression was found between the 22 matched TUR and cystectomy specimens (86%). CONCLUSIONS: Survivin expression analysis performed on TUR specimens might help identify patients with non-muscle-invasive urothelial cell carcinoma of the bladder at high risk of disease recurrence and progression who would benefit from closer follow-up or more aggressive therapy.
机译:目的:存活蛋白是凋亡基因家族抑制剂的成员,该家族控制有丝分裂进程并诱导肿瘤细胞侵袭。我们的目标是评估survivin表达与膀胱尿路上皮细胞癌的存在和非肌肉浸润性膀胱尿路上皮细胞癌患者的临床结局之间的关系。方法:对9例正常对照和74例经尿道切除术(TUR)患有Ta,Tis和/或T1期疾病的连续患者的档案膀胱组织微阵列标本进行了survivin的免疫组织化学染色。还对其中22位因疾病进展而接受了根治性膀胱切除术的患者的膀胱切除术标本进行了染色。当超过10%的细胞表达Survivin时,则认为Survivin过表达。结果:正常膀胱尿路上皮中未表达survivin。 Survivin在53%的非肌肉浸润性膀胱肿瘤中过表达。 Survivin的过表达与更高的肿瘤分级有关(P <0.001)。在根据TUR分期,分级和膀胱内治疗的影响进行的多因素分析中,survivin过表达与癌症复发(危险比2.50,95%置信区间1.09至5.69,P = 0.02)和进展(危险比3.87、95)独立相关。 %置信区间1.13至13.24,P = 0.03),而不是疾病特异性生存率(危险比1.88,95%置信区间0.90至6.46,P = 0.07)。在22个匹配的TUR和膀胱切除术标本之间,发现survivin表达的一致性很高(86%)。结论:在TUR标本上进行的Survivin表达分析可能有助于鉴定患有疾病复发和进展高风险的非肌肉浸润性膀胱尿路上皮细胞癌的患者,这些患者将从更密切的随访或更积极的治疗中受益。

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