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口服丙酸倍氯米松治疗肠道移植物抗宿主病:一项随机对照试验。

Oral beclomethasone dipropionate for treatment of intestinal graft-versus-host disease: a randomized, controlled trial.

作者信息

McDonald G B, Bouvier M, Hockenbery D M, Stern J M, Gooley T, Farrand A, Murakami C, Levine D S

机构信息

Gastroenterology/Hepatology Section, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.

出版信息

Gastroenterology. 1998 Jul;115(1):28-35. doi: 10.1016/s0016-5085(98)70361-0.

Abstract

BACKGROUND & AIMS: Beclomethasone dipropionate (BDP), a topically active steroid, seemed to be an effective treatment for intestinal graft-versus-host disease (GVHD) in a phase I study. The aim of this study was to compare the effectiveness of oral BDP to that of placebo capsules in treatment of intestinal GVHD.

METHODS

Sixty patients with anorexia and poor oral intake because of intestinal GVHD were randomized to receive prednisone (1 mg.kg-1.day-1) plus either oral BDP (8 mg/day) or placebo capsules. Initial responders who were eating at least 70% of caloric needs at evaluation on day 10 continued to take study capsules for an additional 20 days while the prednisone dose was rapidly tapered. The primary end point was the frequency of a durable treatment response at day 30 of treatment.

RESULTS

The initial treatment response at day 10 was 22 of 31 (71%) in the BDP/prednisone group vs. 16 of 29 (55%) for the placebo/prednisone group. The durable treatment response at day 30 was 22 of 31 (71%) vs. 12 of 29 (41%), respectively (P = 0.02).

CONCLUSIONS

The combination of oral BDP capsules and prednisone was more effective than prednisone alone in treating intestinal GVHD. Oral BDP allowed prednisone doses to be rapidly tapered without recurrent intestinal symptoms.

摘要

背景与目的

在一项I期研究中,局部活性类固醇二丙酸倍氯米松(BDP)似乎是治疗肠道移植物抗宿主病(GVHD)的有效药物。本研究旨在比较口服BDP与安慰剂胶囊治疗肠道GVHD的有效性。

方法

60例因肠道GVHD导致厌食和口服摄入量低的患者被随机分组,分别接受泼尼松(1mg·kg⁻¹·d⁻¹)加口服BDP(8mg/天)或安慰剂胶囊治疗。在第10天评估时,进食量至少达到热量需求70%的初始反应者继续服用研究胶囊20天,同时泼尼松剂量迅速递减。主要终点是治疗第30天时持久治疗反应的频率。

结果

BDP/泼尼松组第10天的初始治疗反应为31例中的22例(71%),而安慰剂/泼尼松组为29例中的16例(55%)。第30天的持久治疗反应分别为31例中的22例(71%)和29例中的12例(41%)(P = 0.02)。

结论

口服BDP胶囊与泼尼松联合治疗肠道GVHD比单用泼尼松更有效。口服BDP可使泼尼松剂量迅速递减,且不会出现肠道症状复发。

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