Popat Sanjay, Matakidou Athena, Houlston Richard S
Section of Cancer Genetics, Institute of Cancer Research, Sutton SM2 5NG, UK.
J Clin Oncol. 2004 Feb 1;22(3):529-36. doi: 10.1200/JCO.2004.05.064.
A number of studies have investigated the relationship between thymidylate synthase (TS) expression and survival in colorectal cancer (CRC) patients. Although most have reported poorer overall and progression-free survival with high TS expression, estimates of the hazard ratio (HR) between studies differ wildly. To derive a more precise estimate of the prognostic significance of TS expression, we have reviewed published studies and carried out a meta-analysis.
Twenty studies stratifying overall survival and/or progression-free survival in CRC patients by TS expression status were eligible for analysis. The principal outcome measure was the HR. Data from these studies were pooled using standard meta-analysis techniques.
Thirteen studies investigated outcome in a total of 887 cases with advanced CRC, and seven studies investigated outcome in a total of 2,610 patients with localized CRC. A number of methods were used both to assess TS expression and to assign TS status. Sample sizes varied greatly, small sample sizes being a feature of the advanced disease studies. The combined HR estimate for overall survival (OS) was 1.74 (95% CI, 1.34 to 2.26) and 1.35 (95% CI, 1.07 to 1.80) in the advanced and adjuvant settings, respectively, but there was evidence of heterogeneity and possible publication bias.
Tumors expressing high levels of TS appeared to have a poorer OS compared with tumors expressing low levels. Additional studies with consistent methodology are needed to define the precise prognostic value of TS.
多项研究探讨了胸苷酸合成酶(TS)表达与结直肠癌(CRC)患者生存率之间的关系。尽管大多数研究报告称,TS高表达的患者总生存期和无进展生存期较差,但不同研究对风险比(HR)的估计差异很大。为了更精确地估计TS表达的预后意义,我们回顾了已发表的研究并进行了荟萃分析。
20项根据TS表达状态对CRC患者的总生存期和/或无进展生存期进行分层的研究符合分析条件。主要观察指标为HR。使用标准荟萃分析技术汇总这些研究的数据。
13项研究共调查了887例晚期CRC患者的预后,7项研究共调查了2610例局限性CRC患者的预后。评估TS表达和确定TS状态的方法有多种。样本量差异很大,小样本量是晚期疾病研究的一个特点。晚期和辅助治疗组中,总生存期(OS)的合并HR估计值分别为1.74(95%CI,1.34至2.26)和1.35(95%CI,1.07至1.80),但存在异质性和可能的发表偏倚证据。
与低水平表达的肿瘤相比,高水平表达TS的肿瘤似乎总生存期较差。需要采用一致方法进行更多研究,以确定TS的确切预后价值。