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Hematopoietic SCT in patients with a history of invasive fungal infection.

机译:有浸润性真菌感染史的患者的造血SCT。

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Earlier invasive fungal infections (IFI) put recipients of hematopoietic SCT (HSCT) at a high risk of IFI-related mortality. We retrospectively assessed the feasibility of HSCT for patients with a history of IFI and the efficacy of secondary prophylaxis. From January 2001 to December 2007, 49 patients with a history of IFI underwent HSCT and most of them received broad-spectrum antifungal agents as secondary prophylaxis. After a median follow-up of 355 days (15-967), nine patients experienced failure of IFI prophylaxis, including three cases of IFI-related death, leading to a 2-year cumulative incidence of 18.4 and 6.1%, respectively. Four risk factors for the failure of prophylaxis were found, namely time interval from the diagnosis of IFI to transplantation, residual diseases before transplantation, infection with CMV and use of corticosteroid for the treatment of GVHD. A similar outcome can be achieved in recipients of Auto- and Auto-HSCT. Despite a higher risk of post-transplant progression, residual features of IFI did not affect the overall outcome of HSCT. In conclusion, a history of IFI and residual features are not contraindications to HSCT and secondary prophylaxis by broad-spectrum antifungal agents can protect patients from relapse or progression of an earlier infection.
机译:较早的侵袭性真菌感染(IFI)使造血SCT(HSCT)的接受者面临与IFI相关的死亡的高风险。我们回顾性地评估了具有IFI病史的患者进行HSCT的可行性以及二次预防的有效性。从2001年1月至2007年12月,对49名具有IFI病史的患者进行了HSCT,其中大多数接受了广谱抗真菌药的二次预防。在中位随访355天(15-967天)后,有9名患者发生了IFI预防失败,包括3例IFI相关死亡,导致2年累积发生率分别为18.4和6.1%。发现了预防失败的四个危险因素,即从诊断IFI到移植的时间间隔,移植前残留的疾病,CMV感染以及使用皮质类固醇治疗GVHD。在Auto-HSCT和Auto-HSCT的接受者中也可以达到类似的结果。尽管移植后进展的风险较高,但IFI的残留特征并未影响HSCT的总体结果。总之,IFI的病史和残留特征不是HSCT的禁忌症,而广谱抗真菌剂的二级预防可以保护患者免受复发或早期感染的发展。

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