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Serum microRNA-210 as a predictive biomarker for treatment response and prognosis in patients with hepatocellular carcinoma undergoing transarterial chemoembolization

机译:血清microRNA-210作为肝动脉癌化疗栓塞患者治疗反应和预后的预测生物标志物

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Purpose To investigate whether serum microRNA-210 (miR-210) level can serve as an indicator of prognosis and a predictor of efficacy of transarterial chemoembolization in patients with hepatocellular carcinoma (HCC). Materials and Methods Serum miR-210 level was measured in 113 patients with HCC before transarterial chemoembolization (t1), 3 days after transarterial chemoembolization (t2), and 4 weeks after transarterial chemoembolization (t3) and compared with 39 healthy control subjects. The correlations between miR-210 levels and clinicopathologic factors, tumor responsiveness, and prognosis were analyzed. The modified Response Evaluation Criteria in Solid Tumors assessment was conducted at t3. Results A higher mean baseline miR-210 level was observed in patients with HCC compared with control subjects (3.69 ± 2.04 vs 1.08 ± 0.45, P <.001). A positive correlation between baseline miR-210 level and tumor size (P <.001), vascular invasion (P =.005), tumor differentiation (P =.037), and Barcelona Clinic Liver Cancer stage (P <.001) was observed. Elevated baseline miR-210 level also served as an independent prognostic factor predicting poor overall survival (risk ratio, 2.082; P =.003). Patients who did not respond to transarterial chemoembolization had higher baseline miR-210 levels than patients who did respond to treatment (4.34 ± 1.67 vs 3.28 ± 2.15, P <.001). In addition, miR-210 levels increased significantly 4 weeks after transarterial chemoembolization in nonresponders (5.79 ± 2.06 at t3 vs 4.34 ± 1.67 at t1, P <.001), whereas no significant change was observed in responders (3.53 ± 2.20 at t3 vs 3.28 ± 2.15 at t1, P =.116). Lastly, an inverse correlation was identified between miR-210 change t1-t3 with the time to radiologic progression (P <.001). Conclusions Serum miR-210 may represent a novel biomarker for predicting efficacy of transarterial chemoembolization and overall survival for patients with HCC.
机译:目的探讨血清microRNA-210(miR-210)水平是否可以作为肝细胞癌(HCC)患者的预后指标和经动脉化学栓塞的疗效预测指标。材料和方法在113例经肝动脉化疗栓塞前(t1),经动脉化疗栓塞后3天(t2)和经动脉化疗栓塞后4周(t3)的HCC患者中测量血清miR-210水平,并与39名健康对照组进行比较。分析了miR-210水平与临床病理因素,肿瘤反应性和预后之间的相关性。在t3进行修改后的实体瘤反应评估标准评估。结果与对照组相比,HCC患者的平均基线miR-210水平更高(3.69±2.04对1.08±0.45,P <.001)。基线miR-210水平与肿瘤大小(P <.001),血管侵犯(P = .005),肿瘤分化(P = .037)和巴塞罗那临床肝癌分期(P <.001)之间呈正相关。观测到的。基线miR-210水平升高也可作为预测整体生存不良的独立预后因素(风险比为2.082; P = .003)。对经动脉化疗栓塞无反应的患者的基线miR-210水平高于对治疗有反应的患者(4.34±1.67对3.28±2.15,P <.001)。此外,在无反应者中,经动脉化学栓塞治疗后4周,miR-210水平显着升高(t3时为5.79±2.06,t1时为4.34±1.67,P <.001),而反应者中未观察到显着变化(t3时为3.53±2.20)。在t1时为3.28±2.15,P = .116)。最后,在miR-210变化t1-t3与放射学进展时间之间发现了负相关(P <.001)。结论血清miR-210可能代表了一种新的生物标志物,可预测HCC患者经动脉栓塞的疗效和总生存期。

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