Department of Surgery, The University of California San Francisco, San Francisco, California, United States of America.
The Helen Diller Family Comprehensive Cancer Center, The University of California San Francisco, San Francisco, California, United States of America.
PLoS One. 2019 Jul 10;14(7):e0219469. doi: 10.1371/journal.pone.0219469. eCollection 2019.
Prognosis after resection of hepatocellular carcinoma (HCC) is highly variable. Compared to clinicopathologic factors, the use of molecular markers to predict outcome has not been well studied. We investigated the prognostic importance of thymidylate synthase (TS) gene expression and polymorphisms in patients after resection of HCC.
Patients who underwent complete resection of HCC for whom tissue was available were identified. TS gene expression level and polymorphisms were determined in HCC specimens. Prognostic factors were evaluated using Kaplan-Meier curves and Cox proportional hazard models.
The study included 67 patients. In univariate analysis, variables that negatively influenced survival included TNM stage, microvascular invasion, and high TS expression. For the high TS expression group, median survival was 54 months and 5-year actuarial survival was 47%. For the low TS expression group, median survival was not reached and the 5-year actuarial survival was 91%. In multivariate analysis, only high TS expression remained an independent predictor of poor survival (HR = 10.77, 95% CI 1.36-84.91; P = 0.02). TS gene polymorphisms were not associated with TS expression or overall survival.
High TS expression predicts poor outcome after resection of HCC. Molecular markers might be robust predictors of patient outcome after resection of HCC.
肝细胞癌(HCC)切除术后的预后差异很大。与临床病理因素相比,分子标志物在预测结局方面的应用尚未得到充分研究。我们研究了胸苷酸合成酶(TS)基因表达和多态性对 HCC 切除术后患者预后的重要性。
确定了接受 HCC 完全切除术且有组织标本的患者。在 HCC 标本中确定 TS 基因表达水平和多态性。使用 Kaplan-Meier 曲线和 Cox 比例风险模型评估预后因素。
该研究共纳入 67 例患者。单因素分析显示,影响生存的变量包括 TNM 分期、微血管侵犯和高 TS 表达。对于高 TS 表达组,中位生存期为 54 个月,5 年生存率为 47%。对于低 TS 表达组,中位生存期未达到,5 年生存率为 91%。多因素分析显示,只有高 TS 表达仍然是不良生存的独立预测因素(HR=10.77,95%CI 1.36-84.91;P=0.02)。TS 基因多态性与 TS 表达或总生存期无关。
高 TS 表达预示着 HCC 切除术后预后不良。分子标志物可能是 HCC 切除术后患者预后的可靠预测指标。