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基质变化强度可预测前列腺癌的无生化复发生存率。

Intensity of stromal changes predicts biochemical recurrence-free survival in prostatic carcinoma.

作者信息

Tomas Davor, Spajić Borislav, Milosević Milan, Demirović Alma, Marusić Zlatko, Kruslin Bozo

机构信息

Department of Pathology, Sestre milosrdnice University Hospital, Zagreb, Croatia.

出版信息

Scand J Urol Nephrol. 2010 Nov;44(5):284-90. doi: 10.3109/00365599.2010.485578. Epub 2010 May 12.

Abstract

OBJECTIVE

The reactive stroma of prostate cancer contains a mixture of myofibroblasts and fibroblasts, while fully differentiated smooth-muscle cells are very rare or absent. In experimental prostate cancer models, prostatic stromal cells promote angiogenesis and stimulate prostate tumorigenesis. The aim of this study is to analyse whether the intensity of stromal changes can predict survival in patients with prostatic carcinoma.

MATERIAL AND METHODS

Stromal reaction was quantified histochemically and imunohistochemically in 50 patients treated with radical prostatectomy for clinically localized prostate carcinoma and its relationship with established prognostic factors was assessed.

RESULTS

Kaplan-Meier analysis showed a significant association between the pattern of vimentin and desmin expression and the length of disease-free period; patients with a higher vimentin or lower desmin expression had a shorter disease-free period. On multivariate analysis only vimentin expression (odds ratio 4.06, 95% confidence interval 1.01-16.26, p = 0.049) was a significant predictor of biochemical recurrence. In patients with identical Gleason pattern and Gleason score the level of vimentin expression could identify patients with a higher risk of disease recurrence.

CONCLUSIONS

Intensity of stromal changes could serve as an independent prognostic factor in the assessment of biochemical recurrence-free survival. Among prostate cancer patients with an identical Gleason score, it could identify patients with a higher risk of biochemical recurrence. Thus, stromal changes and their intensity could serve as a novel marker for the recognition of patients with an increased risk of disease recurrence.

摘要

目的

前列腺癌的反应性基质包含肌成纤维细胞和成纤维细胞的混合物,而完全分化的平滑肌细胞非常罕见或不存在。在实验性前列腺癌模型中,前列腺基质细胞促进血管生成并刺激前列腺肿瘤发生。本研究的目的是分析基质变化的强度是否可以预测前列腺癌患者的生存情况。

材料与方法

对50例因临床局限性前列腺癌接受根治性前列腺切除术的患者进行组织化学和免疫组织化学定量分析基质反应,并评估其与既定预后因素的关系。

结果

Kaplan-Meier分析显示波形蛋白和结蛋白表达模式与无病生存期之间存在显著关联;波形蛋白表达较高或结蛋白表达较低的患者无病生存期较短。多因素分析显示,只有波形蛋白表达(优势比4.06,95%置信区间1.01 - 16.26,p = 0.049)是生化复发的显著预测因子。在Gleason模式和Gleason评分相同的患者中,波形蛋白表达水平可以识别疾病复发风险较高的患者。

结论

基质变化强度可作为评估无生化复发生存期的独立预后因素。在Gleason评分相同的前列腺癌患者中,它可以识别生化复发风险较高的患者。因此,基质变化及其强度可作为识别疾病复发风险增加患者的新标志物。

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