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[胸苷酸合成酶、拓扑异构酶-1和Ki-67在接受伊立替康和氟尿嘧啶治疗的晚期结直肠癌患者中的预后价值]

[Prognostic value of thymidylate synthase, topoisomerase-1 and Ki-67 in advanced colorectal cancer patients on irinotecan and fluorouracil treatment].

作者信息

Xu Jian-ming, Zhu Bu-dong, Mangia Anita, Simone Gianni, Montemurro Severino, Giuliani Francesco, Maiello Evaristo, Colucci Giuseppe, Paradiso Angelo

机构信息

Cancer Center, Beijing 307 Hospital, Beijing 100039, China.

出版信息

Zhonghua Zhong Liu Za Zhi. 2005 May;27(5):312-5.

Abstract

OBJECTIVE

To investigate the prognostic value of thymidylate synthase (TS), topoisomerase-1 (Topo-1), and proliferating index Ki-67 in advanced colorectal cancer patients on irinotecan (CPT-11) in combination with fluorouracil treatment (5-Fu).

METHODS

The biomarker expression of TS, Topo-1 and Ki-67 in 78 patients detected immunohistochemically were correlated with the clinical outcome.

RESULTS

The expressions of those biomarkers were not correlated with clinical therapeutic response, but with time to progression (TTP) and/or overall survival (OS). Patients with low expression of TS had significantly longer TTP (P < 0.05) and in OS (P < 0.05). The low expression of Ki-67 was also significantly predictive of longer survival (P < 0.05). As compared with any biomarker, the combination of any two biomarkers still possessed no predictive value to therapeutic response, but an enhanced predictive value to prognosis. The median time to progression in patients with low expression of TS, or Ki-67, or both were 9, 8 and 17 months, respectively; in patients with low expression of TS, or Topo-1, or both were 9, 9 and 13 months; in patients with low expression of Topo-1, or Ki-67, or both were 8, 9 and 11 months. TTP was significantly longer in patients with low expression of two biomarkers as compared with those with high expression (P = 0.031).

CONCLUSION

TS, Topo-1, and Ki-67 are not predictive for chemotherapy response to CPT-11 combined with 5-Fu, but valuable in predicting prognosis. The combination of any two biomarkers can provide more powerful prognostic information for advanced colorectal cancer patients.

摘要

目的

探讨胸苷酸合成酶(TS)、拓扑异构酶-1(Topo-1)和增殖指数Ki-67在晚期结直肠癌患者接受伊立替康(CPT-11)联合氟尿嘧啶治疗(5-Fu)中的预后价值。

方法

采用免疫组化法检测78例患者的TS、Topo-1和Ki-67生物标志物表达,并与临床结局相关联。

结果

这些生物标志物的表达与临床治疗反应无关,但与疾病进展时间(TTP)和/或总生存期(OS)相关。TS低表达的患者TTP(P < 0.05)和OS(P < 0.05)显著更长。Ki-67低表达也显著预示着更长的生存期(P < 0.05)。与任何单一生物标志物相比,任意两种生物标志物的联合对治疗反应仍无预测价值,但对预后的预测价值增强。TS低表达、或Ki-67低表达、或两者均低表达的患者,其疾病进展的中位时间分别为9、8和17个月;TS低表达、或Topo-1低表达、或两者均低表达的患者,其疾病进展的中位时间分别为9、9和13个月;Topo-1低表达、或Ki-67低表达、或两者均低表达的患者,其疾病进展的中位时间分别为8, 9和11个月。两种生物标志物低表达的患者TTP显著长于高表达患者(P = 0.031)。

结论

TS、Topo-1和Ki-67对CPT-11联合5-Fu化疗反应无预测作用,但对预后有预测价值。任意两种生物标志物的联合可为晚期结直肠癌患者提供更有力的预后信息。

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