Kim Joo Heon, Park Jinsung
Department of Pathology, Eulji University Hospital, Eulji University College of Medicine, Daejeon, 302-799 Korea.
Department of Urology, Eulji University Hospital, Eulji University College of Medicine, Daejeon, 302-799 Korea.
Hum Pathol. 2014 Sep;45(9):1830-8. doi: 10.1016/j.humpath.2014.04.020. Epub 2014 May 15.
We investigated the prognostic significance of heme oxygenase-1 (HO-1), S100 calcium-binding protein A4 (S100A4), and syndecan-1 (SYND1) expression in patients with primary non-muscle-invasive bladder cancer (NMIBC). Immunohistochemical studies were performed on tissue specimens from 109 patients diagnosed with primary NMIBC following complete transurethral resection, with the expression dichotomized as negative/mild ("low") versus moderate/strong ("high") according to scores based on staining area and intensity. The effect of each biomarker on recurrence-free survival (RFS) and progression-free survival (PFS) was analyzed. The predictive accuracy for RFS and PFS in multivariate Cox regression models with or without (the baseline model) biomarkers was estimated using the Harrell concordance index. High HO-1, S100A4, and SYND1 expressions were observed in 33.0%, 36.7%, and 63.3% cases, respectively. High HO-1 and S100A4 expressions were significantly associated with various adverse pathological characteristics (high T stage and grade); SYND1 expression was inversely correlated with these characteristics (all, P < .05). In the baseline multivariate model, multifocality, intravesical therapy, and T stage were significant predictors for RFS, whereas intravesical therapy and T stage had marginal statistical significance in predicting PFS. In the multivariate model with the biomarkers, the 3 biomarkers were significant predictors for RFS; and HO-1 expression was a significant predictor for PFS. Addition of the 3 biomarkers to the baseline model significantly increased the predictive accuracy for RFS from 0.754 to 0.828 (P = .043). Our findings suggest that HO-1, S100A4, and SYND1 expressions have prognostic value in primary NMIBC; thus, their evaluation might be useful for determining treatment strategies.
我们研究了血红素加氧酶-1(HO-1)、S100钙结合蛋白A4(S100A4)和Syndecan-1(SYND1)表达在原发性非肌层浸润性膀胱癌(NMIBC)患者中的预后意义。对109例经完全经尿道切除术后诊断为原发性NMIBC的患者的组织标本进行免疫组织化学研究,根据染色面积和强度评分将表达分为阴性/轻度(“低”)与中度/重度(“高”)。分析了每种生物标志物对无复发生存期(RFS)和无进展生存期(PFS)的影响。使用Harrell一致性指数估计在有或没有(基线模型)生物标志物的多变量Cox回归模型中RFS和PFS的预测准确性。分别在33.0%、36.7%和63.3%的病例中观察到高HO-1、S100A4和SYND1表达。高HO-1和S100A4表达与各种不良病理特征(高T分期和分级)显著相关;SYND1表达与这些特征呈负相关(均P<0.05)。在基线多变量模型中,多灶性、膀胱内治疗和T分期是RFS的显著预测因素,而膀胱内治疗和T分期在预测PFS方面具有边际统计学意义。在含有生物标志物的多变量模型中,这3种生物标志物是RFS的显著预测因素;HO-1表达是PFS的显著预测因素。将这3种生物标志物添加到基线模型中可使RFS的预测准确性从0.754显著提高到0.828(P=0.043)。我们的研究结果表明,HO-1、S100A4和SYND1表达在原发性NMIBC中具有预后价值;因此,对它们的评估可能有助于确定治疗策略。