Department of Surgery, Division of Clinical Medical Science, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Ann Surg. 2012 Aug;256(2):288-96. doi: 10.1097/SLA.0b013e3182536a42.
The aim of this study was to evaluate whether intratumoral human equilibrative nucleoside transporter 1 (hENT1) expression can predict the survival of advanced cholangiocarcinoma patients treated with adjuvant gemcitabine-based chemotherapy (AGC) after surgical resection.
There have been no reports concerning a useful predictive biomarker in patients with cholangiocarcinoma treated with adjuvant gemcitabine chemotherapy.
Intratumoral hENT1 expression was investigated immunohistochemically in 105 patients with resected advanced cholangiocarcinoma. Relationships between intratumoral hENT1 expression and clinicopathological factors were evaluated by univariate and multivariate analyses. This study was a retrospective analysis on retrospectively collected tissue and data.
Fifty-one patients received AGC, and 54 did not. High and low intratumoral hENT1 expression was found in 74 (70%) and 31 patients (30%), respectively. There were no significant differences in clinicopathological factors between patients with high hENT1 expression and those with low hENT1 expression. Survival patients with high hENT1 expression were significantly better than those with low hENT1 expression among patients who received AGC (P = 0.008), but not among patients who did not (P = 0.894). Moreover, a significant difference in survival between patients who received AGC and those who did not was observed among patients with high hENT1 expression (P = 0.002), but not among patients with low hENT1 expression (P = 0.525). Intratumoral hENT1 expression was only an independent predictive factor for patients treated with AGC by multivariate analysis (P = 0.027).
Intratumoral hENT1 expression may be a potent predictive marker for advanced cholangiocarcinoma patients treated with AGC.
本研究旨在评估肿瘤内人嘧啶核苷转运蛋白 1(hENT1)表达是否可以预测接受辅助吉西他滨为基础化疗(AGC)的手术切除后晚期胆管癌患者的生存情况。
在接受辅助吉西他滨化疗的胆管癌患者中,尚无有用的预测生物标志物的报道。
通过免疫组织化学方法检测 105 例接受手术切除的晚期胆管癌患者的肿瘤内 hENT1 表达。通过单因素和多因素分析评估肿瘤内 hENT1 表达与临床病理因素的关系。本研究是对回顾性收集的组织和数据进行的回顾性分析。
51 例患者接受 AGC,54 例患者未接受。74 例(70%)和 31 例(30%)患者肿瘤内 hENT1 表达高和低。高 hENT1 表达和低 hENT1 表达患者的临床病理因素无显著差异。接受 AGC 的患者中,高 hENT1 表达患者的生存明显优于低 hENT1 表达患者(P = 0.008),但在未接受 AGC 的患者中无显著差异(P = 0.894)。此外,高 hENT1 表达患者中,接受 AGC 和未接受 AGC 的患者的生存存在显著差异(P = 0.002),但低 hENT1 表达患者中无显著差异(P = 0.525)。多因素分析显示,肿瘤内 hENT1 表达仅为接受 AGC 治疗的患者的独立预测因素(P = 0.027)。
肿瘤内 hENT1 表达可能是接受 AGC 治疗的晚期胆管癌患者的潜在预测标志物。