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艾曲泊帕用于丙型肝炎相关肝硬化患者的血小板减少症

Eltrombopag for thrombocytopenia in patients with cirrhosis associated with hepatitis C.

作者信息

McHutchison John G, Dusheiko Geoffrey, Shiffman Mitchell L, Rodriguez-Torres Maribel, Sigal Samuel, Bourliere Marc, Berg Thomas, Gordon Stuart C, Campbell Fiona M, Theodore Dickens, Blackman Nicole, Jenkins Julian, Afdhal Nezam H

机构信息

Duke University and Duke Clinical Research Institute, Durham, NC 27705, USA.

出版信息

N Engl J Med. 2007 Nov 29;357(22):2227-36. doi: 10.1056/NEJMoa073255.

Abstract

BACKGROUND

Eltrombopag is a new, orally active thrombopoietin-receptor agonist that stimulates thrombopoiesis. We evaluated its ability to increase platelet counts and facilitate treatment for hepatitis C virus (HCV) infection in patients with thrombocytopenia associated with HCV-related cirrhosis.

METHODS

Seventy-four patients with HCV-related cirrhosis and platelet counts of 20,000 to less than 70,000 per cubic millimeter were randomly assigned to receive eltrombopag (30, 50, or 75 mg daily) or placebo daily for 4 weeks. The primary end point was a platelet count of 100,000 per cubic millimeter or more at week 4. Peginterferon and ribavirin could then be initiated, with continuation of eltrombopag or placebo for 12 additional weeks.

RESULTS

At week 4, platelet counts were increased to 100,000 per cubic millimeter or more in a dose-dependent manner among patients for whom these data were available: in 0 of the 17 patients receiving placebo, in 9 of 12 (75%) receiving 30 mg of eltrombopag, in 15 of 19 (79%) receiving 50 mg of eltrombopag, and in 20 of 21 (95%) receiving 75 mg of eltrombopag (P<0.001). Antiviral therapy was initiated in 49 patients (in 4 of 18 patients receiving placebo, 10 of 14 receiving 30 mg of eltrombopag, 14 of 19 receiving 50 mg of eltrombopag, and 21 of 23 receiving 75 mg of eltrombopag) while the administration of eltrombopag or placebo was continued. Twelve weeks of antiviral therapy, with concurrent receipt of eltrombopag or placebo, were completed by 36%, 53%, and 65% of patients receiving 30 mg, 50 mg, and 75 mg of eltrombopag, respectively, and by 6% of patients in the placebo group. The most common adverse event during the initial 4 weeks was headache; thereafter, the adverse events were those expected with interferon-based therapy.

CONCLUSIONS

Eltrombopag therapy increases platelet counts in patients with thrombocytopenia due to HCV-related cirrhosis, thereby permitting the initiation of antiviral therapy. (ClinicalTrials.gov number, NCT00110799.)

摘要

背景

艾曲泊帕是一种新型口服活性血小板生成素受体激动剂,可刺激血小板生成。我们评估了其在丙型肝炎病毒(HCV)相关肝硬化伴血小板减少症患者中增加血小板计数并促进HCV感染治疗的能力。

方法

74例HCV相关肝硬化且血小板计数为每立方毫米20,000至不足70,000的患者被随机分配,接受艾曲泊帕(每日30、50或75毫克)或安慰剂,为期4周。主要终点是第4周时血小板计数达到每立方毫米100,000或更高。然后可开始使用聚乙二醇干扰素和利巴韦林,并继续使用艾曲泊帕或安慰剂12周。

结果

在第4周时,对于可获得这些数据的患者来说,血小板计数以剂量依赖方式增加至每立方毫米100,000或更高:接受安慰剂的17例患者中0例达到,接受30毫克艾曲泊帕的12例患者中有9例(75%)达到,接受50毫克艾曲泊帕的19例患者中有15例(79%)达到,接受75毫克艾曲泊帕的21例患者中有20例(95%)达到(P<0.001)。49例患者开始抗病毒治疗(接受安慰剂的18例患者中有4例,接受30毫克艾曲泊帕的14例患者中有10例,接受50毫克艾曲泊帕的19例患者中有14例,接受75毫克艾曲泊帕的23例患者中有21例),同时继续给予艾曲泊帕或安慰剂。接受30毫克、50毫克和75毫克艾曲泊帕的患者分别有36%、53%和65%完成了12周的抗病毒治疗并同时接受艾曲泊帕或安慰剂,安慰剂组患者为6%。最初4周内最常见的不良事件是头痛;此后,不良事件为基于干扰素治疗时预期出现的那些。

结论

艾曲泊帕治疗可增加HCV相关肝硬化所致血小板减少症患者的血小板计数,从而使抗病毒治疗得以开始。(临床试验注册号,NCT00110799。)

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