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口服二丙酸倍氯米松治疗人类肠道移植物抗宿主病。

Oral beclomethasone dipropionate for treatment of human intestinal graft-versus-host disease.

作者信息

Baehr P H, Levine D S, Bouvier M E, Hockenbery D M, Gooley T A, Stern J G, Martin P J, McDonald G B

机构信息

Fred Hutchinson Cancer Research Center, University of Washington, Seattle, USA.

出版信息

Transplantation. 1995 Dec 15;60(11):1231-8.

PMID:8525516
Abstract

Intestinal graft-versus-host disease (GVHD) causes anorexia, vomiting, abdominal pain, and diarrhea. We investigated oral beclomethasone dipropionate (BDP), a potent, topically active corticosteroid, as therapy for this disease. Forty-two allogeneic marrow-graft recipients with biopsy-proven intestinal graft-versus-host disease of mild-to-moderate severity received BDP (8 mg daily) for up to 28 days. Weekly symptom scores, oral intake, and surveillance throat and stool cultures were compared with baseline values. Adrenal testing was performed serially in patients not receiving concurrent prednisone. Improvement was seen in appetite (P < 0.001), oral intake (P < 0.001), nausea (P = 0.013), and diarrhea (P = 0.02) over the course of therapy, and an overall beneficial response was observed in 72% of 40 evaluable patients. Surveillance cultures of throat and stool showed no increase in bacterial or fungal colonization over time. The adrenal axis became suppressed in 11 of 20 evaluable patients (55%) but suppression was not a prerequisite for clinical response, as 6 of 9 patients who retained normal adrenal function improved clinically. We conclude that oral BDP is a safe and effective treatment for mild-to-moderate intestinal graft-versus-host disease. Systemic absorption probably occurs, but adrenal suppression is not a prerequisite for clinical efficacy, suggesting that the biological effect is primarily topical. BDP should be further investigated as a topical therapy for intestinal GVHD.

摘要

肠道移植物抗宿主病(GVHD)会导致厌食、呕吐、腹痛和腹泻。我们研究了强效局部活性皮质类固醇丙酸倍氯米松(BDP)作为该病的治疗方法。42名经活检证实为轻至中度肠道移植物抗宿主病的异基因骨髓移植受者接受了BDP(每日8毫克)治疗,最长治疗28天。将每周的症状评分、口服摄入量以及监测咽喉和粪便培养结果与基线值进行比较。对未同时接受泼尼松治疗的患者进行连续的肾上腺功能测试。在治疗过程中,食欲(P < 0.001)、口服摄入量(P < 0.001)、恶心(P = 0.013)和腹泻(P = 0.02)均有改善,40名可评估患者中有72%观察到总体有益反应。咽喉和粪便的监测培养显示,随着时间推移,细菌或真菌定植没有增加。20名可评估患者中有11名(55%)肾上腺轴受到抑制,但抑制并非临床反应的先决条件,因为9名肾上腺功能正常的患者中有6名临床症状改善。我们得出结论,口服BDP是治疗轻至中度肠道移植物抗宿主病的一种安全有效的方法。可能发生全身吸收,但肾上腺抑制并非临床疗效的先决条件,这表明其生物学效应主要是局部性的。BDP作为肠道GVHD的局部治疗方法应进一步研究。

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