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胸苷磷酸化酶和二氢嘧啶脱氢酶在术后氟嘧啶治疗的结直肠癌中的临床作用

Clinical role of thymidine phosphorylase and dihydropyrimidine dehydrogenase in colorectal cancer treated with postoperative fluoropyrimidine.

作者信息

Tokunaga Yukihiko, Takahashi Keichi, Saito Tohru

机构信息

Department of Surgery, Osaka North Japan Post Hospital, Japan.

出版信息

Hepatogastroenterology. 2005 Nov-Dec;52(66):1715-21.

Abstract

BACKGROUND/AIMS: Thymidine phosphorylase (TP) is an essential enzyme for activation of 5-fluorouracil (5-FU) and its derivatives. Dihydropyrimidine dehydrogenase (DPD) is a rate-limiting enzyme for degradation of 5-FU. In colorectal cancer (CRC), several studies have evaluated the relationship between TP, DPD, and clinicopathological features. However, the results may not be definitive since monoclonal antibody sensitive for human TP and DPD has not been established. Now, new monoclonal antibodies for human TP (1C6-203) and human DPD (2H9-1b) are available.

METHODOLOGY

The study included 150 patients whose CRCs were classified into stage II to IV, and resected surgically. TP and DPD expression were evaluated using immunohistochemistry with new antibodies and relationships between their expressions and clinicopathological features. Survival curves were calculated using Kaplan-Meier method, and differences were evaluated with log-rank test. Cox proportional hazards model was also used.

RESULTS

TP and DPD expression showed positive correlations with advances in lymphatic invasion (p=0.049 and 0.032 respectively), venous invasion (p=0.027 and 0.005), and cancer stage (p=0.0003 and 0.006). The patients survival rates were higher in those TP(-) than in those TP(+) (p=0.007), and higher in those DPD(-) than in those DPD(+) (p=0.008). The survival rate was best in the patients negative for TP and DPD, and worst in those positive for both TP and DPD. In regard to the combination of TP and DPD expression, the best survival curve was obtained for the TP(-) DPD(-) group followed by those for the TP(+) DPD(-), TP(-) DPD(+), and TP(+) DPD(+) groups in descending order. The estimated hazard ratio for patients' death with TP and DPD expression were 3.10 and 6.55 (p=0.01 and 0.01) respectively.

CONCLUSIONS

Using new sensitive monoclonal antibodies, the present results indicated that TP and DPD expression were associated with CRC progression, and closely related with poor prognosis in postoperative CRC patients. CRC patients positive for both TP and DPD expression had a poorer prognosis than those negative for one of these expressions in treatment with fluoropyrimidine after surgery. The use of two determinants of response may identify a high percentage of responding patients.

摘要

背景/目的:胸苷磷酸化酶(TP)是激活5-氟尿嘧啶(5-FU)及其衍生物的关键酶。二氢嘧啶脱氢酶(DPD)是5-FU降解的限速酶。在结直肠癌(CRC)中,多项研究评估了TP、DPD与临床病理特征之间的关系。然而,由于尚未建立对人TP和DPD敏感的单克隆抗体,结果可能并不确切。现在,有了针对人TP(1C6-203)和人DPD(2H9-1b)的新型单克隆抗体。

方法

本研究纳入了150例CRC患者,其癌症分期为II至IV期,并接受了手术切除。使用新型抗体通过免疫组织化学评估TP和DPD的表达,以及它们的表达与临床病理特征之间的关系。采用Kaplan-Meier法计算生存曲线,并通过对数秩检验评估差异。还使用了Cox比例风险模型。

结果

TP和DPD的表达与淋巴浸润进展(分别为p=0.049和0.032)、静脉浸润(p=0.027和0.005)以及癌症分期(p=0.0003和0.006)呈正相关。TP(-)患者的生存率高于TP(+)患者(p=0.007),DPD(-)患者的生存率高于DPD(+)患者(p=0.008)。TP和DPD均为阴性的患者生存率最佳,而两者均为阳性的患者生存率最差。就TP和DPD表达的组合而言,TP(-)DPD(-)组的生存曲线最佳,其次依次为TP(+)DPD(-)、TP(-)DPD(+)和TP(+)DPD(+)组。TP和DPD表达的患者死亡估计风险比分别为3.10和6.55(p=0.01和0.01)。

结论

使用新型敏感单克隆抗体,本研究结果表明TP和DPD表达与CRC进展相关,且与CRC术后患者的不良预后密切相关。TP和DPD表达均为阳性的CRC患者在术后接受氟嘧啶治疗时,预后比其中一项表达为阴性的患者更差。使用两个反应决定因素可能会识别出高比例的反应患者。

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