Steroid myopathy in patients with acute graft-versus-host disease treated with high-dose steroid therapy

Steroid myopathy in patients with acute graft-versus-host disease treated with high-dose steroid therapy
复制标题

DOI:
10.1038/sj.bmt.1705435
复制
发表时间:
2006-08-01
影响因子:
4.8
通讯作者:
Giralt, S.
Giralt, S.
中科院分区:
医学3区
文献类型:
--
作者:
Lee, H. J.;Oran, B.;Giralt, S.

文献摘要

被引文献

相似文献

高剂量类固醇是治疗急性移植物抗宿主病(aGVHD)的第一线。类固醇肌病是一种使人衰弱的类固醇引起的并发症,显著损害患者的体力状态。为了确定异基因造血干细胞移植(HSCT)后发生≥ 2级aGVHD的急性髓性白血病(AML)/骨髓增生异常综合征(MDS)患者类固醇肌病和其他类固醇相关并发症的频率和严重程度,我们进行了一项回顾性分析。如果患者被诊断为AML/MDS,在1996年1月至2001年12月期间接受了同种异体HSCT,并发生了>= 2级aGVHD,用2 mg/kg甲泼尼龙治疗,并在移植后存活至少100天,则将其纳入分析。共有70名患者符合我们的入选标准。29例(41%)患者发现类固醇肌病。类固醇肌病的严重程度一般为中度,仅3%的患者出现重度衰弱性类固醇肌病。我们的结论是类固醇肌病是AML/MDS患者异基因HSCT后大剂量类固醇治疗的常见并发症。旨在预防和治疗这种并发症的干预措施是必要的,需要在前瞻性临床试验中进行探索。
High-dose steroids are the first line of treatment for acute graft-versus-host disease (aGVHD). Steroid myopathy is a debilitating steroid-induced complication that significantly impairs a patient's performance status. To determine the frequency and severity of steroid myopathy and other steroid related complications in patients with acute myeloid leukemia (AML)/myelodysplastic syndrome (MDS) who developed grade >= 2 aGVHD after allogeneic hematopoietic stem cell transplantation (HSCT), we performed a retrospective analysis. Patients were included in the analysis if they had a diagnosis of AML/MDS, underwent an allogeneic HSCT between January 1996 and December 2001 and developed grade >= 2 aGVHD that was treated with 2 mg/kg of methylprednisolone and survived at least 100 days post transplant. A total of 70 patients fulfilled our inclusion criteria. Steroid myopathy was identified in 29 (41%) patients. Steroid myopathy was generally of moderate severity with severe debilitating steroid myopathy seen in only 3% of patients. We concluded that steroid myopathy is a common complication of high-dose steroid therapy after allogeneic HSCT in AML/MDS. Interventions aimed at preventing and treating this complication are warranted and need to be explored in prospective clinical trials.