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布地奈德作为急性肠道移植物抗宿主病局部皮质类固醇治疗的可行性及反应

Feasibility and response to budesonide as topical corticosteroid therapy for acute intestinal GVHD.

作者信息

Bertz H, Afting M, Kreisel W, Duffner U, Greinwald R, Finke J

机构信息

Department of Hematology/Oncology, University Medical Hospital, Freiburg, Germany.

出版信息

Bone Marrow Transplant. 1999 Dec;24(11):1185-9. doi: 10.1038/sj.bmt.1702055.

Abstract

Therapy of acute intestinal GVHD is still one of the main challenges after allogeneic transplantation. Increasing systemic immunosuppression (IS) is the first choice and includes corticosteroids and lymphocyte antibodies, often associated with severe side-effects. In inflammatory bowel diseases such as Crohn's disease and ulcerative colitis, topical steroid therapy is used very successfully. Because of the similarity between these and acute intestinal GVHD we conducted a trial with oral budesonide (Budenofalk), a new topically active glucocorticoid, to treat patients with acute GVHD > or = grade II. After a diagnosis of aGVHD > or = grade II, 22 patients received increased IS, mainly systemic corticosteroids, and additionally budesonide 9 mg/day divided into three doses. Improvement in aGVHD, infectious side-effects, reduction of systemic IS and outcome were documented. Results were compared with the results of 19 control patients, who were treated only by increasing IS dose. In 17/22 patients (70%), treated with budesonide, the acute intestinal GVHD resolved and no relapse occurred after decreasing the systemic IS, while continuing budesonide. In only 8/19 patients in the control group did the acute intestinal GVHD resolve and 2/8 patients had a relapse of intestinal GVHD after decreasing IS, with an overall response of 33%. No severe intestinal infections occurred. We conclude that budesonide may be effective in acute intestinal GVHD as a topical corticosteroid and prospective, randomized studies should demonstrate its efficacy in allowing reduction of systemic immunosuppressive therapy, and its side-effects.

摘要

急性肠道移植物抗宿主病(GVHD)的治疗仍是异基因移植后的主要挑战之一。增加全身免疫抑制(IS)是首选治疗方法,包括使用皮质类固醇和淋巴细胞抗体,但这些治疗常伴有严重的副作用。在克罗恩病和溃疡性结肠炎等炎症性肠病中,局部使用类固醇疗法取得了很好的疗效。鉴于这些疾病与急性肠道GVHD的相似性,我们开展了一项试验,使用新型局部活性糖皮质激素布地奈德(Budenofalk)口服治疗II级及以上的急性GVHD患者。确诊为II级及以上的急性GVHD后,22例患者接受了强化IS治疗,主要是全身使用皮质类固醇,另外还服用9毫克/天的布地奈德,分三次服用。记录了急性GVHD的改善情况、感染性副作用、全身IS的减少情况及治疗结果。将结果与19例仅通过增加IS剂量进行治疗的对照患者的结果进行了比较。在接受布地奈德治疗的22例患者中,有17例(70%)的急性肠道GVHD得到缓解,在减少全身IS并继续使用布地奈德后未出现复发。而在对照组的19例患者中,只有8例的急性肠道GVHD得到缓解,8例中有2例在减少IS后出现肠道GVHD复发,总体缓解率为33%。未发生严重的肠道感染。我们得出结论,布地奈德作为局部皮质类固醇在急性肠道GVHD中可能有效,前瞻性随机研究应证实其在减少全身免疫抑制治疗及其副作用方面的疗效。

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