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秋水仙碱联合熊去氧胆酸与甲氨蝶呤联合熊去氧胆酸治疗原发性胆汁性肝硬化的随机对照试验:十年结果

A randomized controlled trial of colchicine plus ursodiol versus methotrexate plus ursodiol in primary biliary cirrhosis: ten-year results.

作者信息

Kaplan Marshall M, Cheng Steven, Price Lori Lyn, Bonis Peter A L

机构信息

Division of Gastroenterology, Department of Medicine and the Tupper Research Institute, New England Medical Center and Tufts University School of Medicine, Boston, Massachusetts, USA.

出版信息

Hepatology. 2004 Apr;39(4):915-23. doi: 10.1002/hep.20103.

Abstract

Primary biliary cirrhosis frequently progresses despite treatment with ursodeoxycholic acid (UDCA), the only approved therapy. Previous studies suggested that colchicine and methotrexate may improve biochemical tests of liver function, symptoms, and liver histology. The aim of the present study was to determine if the addition of colchicine or methotrexate to UDCA would improve survival free of liver transplantation. Eighty-five patients with histologically confirmed primary biliary cirrhosis whose serum alkaline phosphatase levels were at least twice the normal level and who were not yet candidates for liver transplantation were randomly assigned to receive colchicine or methotrexate in a double-blind study. UDCA was administered to all patients after 2 years. The primary end point was survival free of liver transplantation. Patients were followed up for a total of up to 10 years or until treatment failure. Data were analyzed on an intention-to-treat basis. Transplant-free survival was similar in both groups: 0.57 for colchicine plus UDCA and 0.44 for methotrexate plus UDCA, results that are similar to those predicted by the Mayo prognostic model. Significant improvement in liver biochemical tests and liver histology was observed in a subset of patients in both treatment groups who remained in the study for all 10 years. In conclusion, neither colchcine plus UDCA nor methotrexate plus UDCA improved survival beyond that predicted by the Mayo prognostic model. However, clinical, histologic, and biochemical improvement observed among those who remained in the study for 10 years suggests a possible benefit of these drugs in a subset of patients.

摘要

尽管使用唯一获批的疗法熊去氧胆酸(UDCA)进行治疗,原发性胆汁性肝硬化仍常常进展。既往研究提示秋水仙碱和甲氨蝶呤可能改善肝功能生化指标、症状及肝脏组织学表现。本研究的目的是确定在UDCA基础上加用秋水仙碱或甲氨蝶呤是否能提高无肝移植生存期。85例经组织学确诊为原发性胆汁性肝硬化、血清碱性磷酸酶水平至少为正常水平两倍且尚未成为肝移植候选者的患者,在一项双盲研究中被随机分配接受秋水仙碱或甲氨蝶呤治疗。2年后所有患者均给予UDCA。主要终点是无肝移植生存期。对患者进行了长达10年的随访或直至治疗失败。数据按意向性分析。两组的无移植生存期相似:秋水仙碱加UDCA组为0.57,甲氨蝶呤加UDCA组为0.44,结果与梅奥预后模型预测的结果相似。在两个治疗组中持续参与研究10年的一部分患者中,观察到肝脏生化指标和肝脏组织学有显著改善。总之,秋水仙碱加UDCA或甲氨蝶呤加UDCA均未使生存期超过梅奥预后模型预测的生存期。然而,在持续参与研究10年的患者中观察到的临床、组织学和生化改善提示这些药物可能对一部分患者有益。

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