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氟替卡松、阿奇霉素和孟鲁司特治疗降低异基因造血干细胞移植后闭塞性细支气管炎综合征患者的皮质激素暴露:八例患者的病例系列研究。

Fluticasone, azithromycin and montelukast therapy in reducing corticosteroid exposure in bronchiolitis obliterans syndrome after allogeneic hematopoietic SCT: a case series of eight patients.

机构信息

Department of Medicine, University of Washington Affiliated Hospitals, Seattle, WA, USA.

出版信息

Bone Marrow Transplant. 2011 Oct;46(10):1369-73. doi: 10.1038/bmt.2010.311. Epub 2010 Dec 6.

Abstract

Bronchiolitis obliterans syndrome (BOS) is a devastating pulmonary complication affecting long-term survivors of allogeneic hematopoietic cell transplantation. Treatment of BOS with prolonged courses of high dose corticosteroids is often associated with significant morbidity. Reducing the exposure to corticosteroids may reduce treatment-related morbidity. Our institution has recently begun to treat patients with emerging therapies in an effort to diminish corticosteroid exposure. We retrospectively reviewed the 6-month corticosteroid exposure, lung function and failure rates in eight patients with newly diagnosed BOS who were treated with a combination of fluticasone, azithromycin and montelukast (FAM) and a rapid corticosteroid taper. These patients were compared with 14 matched historical patients who received high-dose corticosteroids, followed by a standard taper. The median 6-month prednisone exposure in FAM-treated patients was 1819 mg (0-4036 mg) compared with 7163 mg (6551-7829 mg) in the control group (P=0.002). The median forced expiratory volume in 1 s (FEV(1)) change in FAM-treated patients was 2% (-3 to 4%] compared with 1% (-4 to 5%) in the control group (P=1.0). Prednisone exposure in FAM patients was one quarter that of a retrospective-matched group of patients, with minimal change in median FEV(1), suggesting that BOS may be spared of the morbidities associated with long-term corticosteroid use by using alternative agents with less side effects.

摘要

闭塞性细支气管炎综合征(BOS)是一种严重的肺部并发症,影响所有异基因造血细胞移植的长期幸存者。长期大剂量皮质类固醇治疗 BOS 常伴有显著的发病率。减少皮质类固醇的暴露可能会降低治疗相关的发病率。我们机构最近开始使用新的治疗方法治疗新诊断为 BOS 的患者,以减少皮质类固醇的暴露。我们回顾性地分析了 8 例新诊断为 BOS 的患者,他们接受了氟替卡松、阿奇霉素和孟鲁司特(FAM)联合治疗,并进行了快速皮质类固醇减量,以及 14 例接受大剂量皮质类固醇治疗、随后进行标准减量的匹配历史患者的 6 个月皮质类固醇暴露、肺功能和失败率。与对照组相比,FAM 治疗组患者的中位 6 个月泼尼松暴露量为 1819mg(0-4036mg),而对照组为 7163mg(6551-7829mg)(P=0.002)。FAM 治疗组患者的用力呼气量(FEV1)中位数变化为 2%(-3 至 4%),而对照组为 1%(-4 至 5%)(P=1.0)。FAM 患者的泼尼松暴露量为回顾性匹配组患者的四分之一,中位 FEV1 变化极小,这表明通过使用副作用较小的替代药物,BOS 可能不会出现与长期使用皮质类固醇相关的发病率。

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