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胸苷磷酸化酶表达与多西氟尿苷对胃癌的恶性潜能及抗肿瘤作用相关:多西氟尿苷与5-氟尿嘧啶辅助化疗的多因素分析

Thymidine phosphorylase expression correlates with malignant potential and anti-tumor effect of doxifluridine on gastric cancer: multivariate analysis for adjuvant chemotherapy doxifluridine vs. 5-fluorouracil.

作者信息

Takiguchi Nobuhiro, Ishii Rumiko, Koda Keiji, Oda Kenji, Miyazaki Masaru

机构信息

Department of Gastroenterological Surgery, Chiba Cancer Center Hospital, Chiba 260-8677, Japan.

出版信息

Oncol Rep. 2003 Sep-Oct;10(5):1105-11.

Abstract

Doxifluridine (5'-DFUR) is an anticancer drug converted to 5-fluorouracil (5-FU) by thymidine phosphorylase (TP). TP is an angiogenetic and platelet-derived endothelial cell growth factor. We evaluated the relation between TP expression and chemotherapeutic efficacy and prognosis for gastric cancer. Advanced gastric cancer patients given oral adjuvant chemotherapeutics either 5'-DFUR; 163 patients or 5-FU; 162 patients were examined. TP expression was assessed with immunohistochemical staining. Multivariate analysis for influencing survival was done, employing variables such as gender, age, procedure, tumor size, location, Borrmann type, histologic factors [type, depth of invasion, lymph node metastasis (n), lymphatic invasion (ly), and venous invasion (v)], drug administered, and TP expression. In the patients with serosal invasion, 5'-DFUR in TP positive was an independent prognostic factor (risk ratio, 4.450; 95% confidence limit, 2.099-9.436), indicating significantly improved prognosis over the 5-FU group. In TP negative, n and ly were independent prognostic factors, but the survival curves of the two chemotherapeutic groups were not significantly different. TP expression was not prognostic factor in 5'-DFUR group, while, in 5-FU group, TP expression was an independent prognostic factor (2.834, 1.467-5.476). In conclusion, it was suggested that TP positive gastric cancer with serosal invasion increased malignant potential of the tumor and 5'-DFUR efficacy.

摘要

多西氟尿苷(5'-DFUR)是一种抗癌药物,可通过胸苷磷酸化酶(TP)转化为5-氟尿嘧啶(5-FU)。TP是一种血管生成因子和血小板衍生的内皮细胞生长因子。我们评估了TP表达与胃癌化疗疗效及预后之间的关系。对接受口服辅助化疗的晚期胃癌患者进行了检查,其中163例患者使用5'-DFUR,162例患者使用5-FU。通过免疫组织化学染色评估TP表达。采用性别、年龄、手术方式、肿瘤大小、位置、Borrmann分型、组织学因素[类型、浸润深度、淋巴结转移(n)、淋巴管浸润(ly)和静脉浸润(v)]、所用药物和TP表达等变量进行影响生存的多因素分析。在有浆膜侵犯的患者中,TP阳性患者使用5'-DFUR是独立的预后因素(风险比,4.450;95%置信区间,2.099 - 9.436),表明其预后明显优于5-FU组。在TP阴性患者中,n和ly是独立的预后因素,但两个化疗组的生存曲线无显著差异。TP表达在5'-DFUR组不是预后因素,而在5-FU组中,TP表达是独立的预后因素(2.834,1.467 - 5.476)。总之,提示有浆膜侵犯的TP阳性胃癌增加了肿瘤的恶性潜能和5'-DFUR的疗效。

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