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Prognostic significance of PTEN Ki-67 and CD44s expression patterns in gastrointestinal stromal tumors

机译:PTENKi-67和CD44s表达模式在胃肠道间质瘤中的预后意义

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AIM: To develop a prognostic approach for gastrointestinal stromal tumors (GISTs) using a cluster of indicators and follow-up information.METHODS: One hundred and four GISTs that had not been subjected to targeted therapies were collected and classified by NIH risk assessment and anatomic location. By immunohistochemistry, the expressions of PTEN, Ki-67, CD44s matrix metalloproteinase (MMP)-9 and TIMP-1 were detected on tissue microarray. Univariate and multimarker survival analyses were performed and then a COX hazard proportion model was constructed to evaluate a cluster of predictors of GIST.RESULTS: Our data showed small intestinal GIST are more aggressive than gastric GIST. The NIH risk assessment correlated with disease-free survival for either gastric GIST or small intestinal GIST. Immunohistochemical analysis revealed that Ki-67 labeling indexes (LIs) < 5% predicted higher disease-specific survival (DSS) in gastric and small intestinal GIST. CD44s positivity and PTEN LIs ≥ 50% correlated with higher DSS in gastric GIST. MMP-9 and TIMP-1 had no correlation with survival. Multimarker analysis revealed that the expression pattern of PTEN LIs ≥ 50% combined with Ki-67 LIs < 5% and CD44s positivity reliably predicted favorable outcomes for gastric GIST (P = 0.009), as did the combination of PTEN LIs ≥ 50% and Ki-67 LIs < 5% for small intestinal GIST (P = 0.011). Authors also found that high NIH risk grade was correlated with DSS in patients with gastric GIST and disease-free survival in patients with small intestinal GIST.CONCLUSION: PTEN LIs ≥ 50%, Ki-67 LIs < 5% and CD44s positivity provides an accurate, favorable prognosis for gastric GIST. PTEN LIs ≥ 50% and Ki-67 LIs < 5% does the same for small intestinal GIST. Ki-67 LIs enhances the NIH assessment.
机译:目的:利用一系列指标和随访信息,开发一种胃肠道间质瘤(GIST)的预后方法。方法:收集104例未接受靶向治疗的GIST,并通过NIH风险评估和解剖进行分类位置。免疫组织化学法检测组织芯片上PTEN,Ki-67,CD44s基质金属蛋白酶(MMP)-9和TIMP-1的表达。进行了单变量和多标记生存分析,然后构建了COX危险比例模型来评估一组GIST预测因子。结果:我们的数据显示,小肠GIST比胃GIST更具侵略性。 NIH风险评估与胃GIST或小肠GIST的无病生存相关。免疫组织化学分析显示,Ki-67标记指数(LIs)<5%预测胃和小肠GIST的疾病特异性生存率(DSS)更高。 CD44s阳性和PTEN LIs≥50%与胃GIST中较高的DSS相关。 MMP-9和TIMP-1与生存率无关。多标记分析显示,PTEN LIs≥50%结合Ki-67 LIs <5%和CD44s阳性表达模式可靠地预测了胃GIST的良好预后(P = 0.009),PTEN LIs≥50%和Ki小肠GIST的-67 LIs <5%(P = 0.011)。作者还发现,胃GIST患者的高NIH风险等级与DSS相关,小肠GIST患者的无病生存期也得出结论。结论:PTEN LIs≥50%,Ki-67 LIs <5%和CD44s阳性提供了准确的结果,对胃GIST的预后良好。对于小肠GIST,PTEN LIs≥50%,Ki-67 LIs <5%。 Ki-67 LIs增强了NIH评估。

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