Döring M, Blume O, Haufe S, Hartmann U, Kimmig A, Schwarze C-P, Lang P, Handgretinger R, Müller I
Department of Pediatric Hematology and Oncology, University Children's Hospital Tübingen, Hoppe-Seyler-St. 1, 72076, Tübingen, Germany,
Eur J Clin Microbiol Infect Dis. 2014 Apr;33(4):629-38. doi: 10.1007/s10096-013-1998-2. Epub 2013 Oct 31.
Oral antifungal prophylaxis with extended-spectra azoles is widely used in pediatric patients after allogeneic hematopoietic stem cell transplantation (HSCT), while controlled studies for oral antifungal prophylaxis after bone marrow transplantation in children are not available. This survey analyzed patients who had received either itraconazole, voriconazole, or posaconazole. We focused on the safety, feasibility, and initial data of efficacy in a cohort of pediatric patients and adolescents after high-dose chemotherapy and HSCT. Fifty consecutive pediatric patients received itraconazole, 50 received voriconazole, and 50 pediatric patients received posaconazole after HSCT as oral antifungal prophylaxis. The observation period lasted from the start of oral prophylactic treatment with itraconazole, voriconazole, or posaconazole until two weeks after terminating the oral antifungal prophylaxis. No incidences of proven or probable invasive mycosis were observed during itraconazole, voriconazole, or posaconazole treatment. A total of five possible invasive fungal infections occurred, two in the itraconazole group (4%) and three in the voriconazole group (6%). The percentage of patients with adverse events potentially related to clinical drugs were 14% in the voriconazole group, 12% in the itraconazole group, and 8% in the posaconazole group. Itraconazole, voriconazole, and posaconazole showed comparable efficacy as antifungal prophylaxis in pediatric patients after allogeneic HSCT.
广谱唑类口服抗真菌预防用药在异基因造血干细胞移植(HSCT)后的儿科患者中广泛使用,而关于儿童骨髓移植后口服抗真菌预防用药的对照研究尚不可得。本调查分析了接受伊曲康唑、伏立康唑或泊沙康唑治疗的患者。我们关注了大剂量化疗和HSCT后的一组儿科患者及青少年的安全性、可行性和疗效初步数据。50例连续的儿科患者在HSCT后接受伊曲康唑作为口服抗真菌预防用药,50例接受伏立康唑,50例儿科患者接受泊沙康唑。观察期从使用伊曲康唑、伏立康唑或泊沙康唑开始口服预防性治疗起,至口服抗真菌预防用药结束后两周。在伊曲康唑、伏立康唑或泊沙康唑治疗期间,未观察到确诊或疑似侵袭性真菌病的发生。共发生5例可能的侵袭性真菌感染,伊曲康唑组2例(4%),伏立康唑组3例(6%)。伏立康唑组、伊曲康唑组和泊沙康唑组中可能与临床药物相关的不良事件患者百分比分别为14%、12%和8%。在异基因HSCT后的儿科患者中,伊曲康唑、伏立康唑和泊沙康唑作为抗真菌预防用药显示出相当的疗效。