Goscicki Breana K, Yan Shirley Q, Mathew Sherry, Mauguen Audrey, Cohen Nina
Department of Pharmacy (BKG), UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA.
Department of Pharmacy (SQY, NC), Memorial Sloan Kettering Cancer Center, New York, NY.
J Pediatr Pharmacol Ther. 2024 Aug;29(4):379-384. doi: 10.5863/1551-6776-29.4.379. Epub 2024 Aug 13.
Literature is limited regarding ideal micafungin dosing in pediatric patients with hematologic malignancies receiving chemotherapy or hematopoietic stem cell transplantation. Micafungin is an intravenous echinocandin with activity against and species and has a favorable safety profile compared with other antifungal classes. Our objective was to evaluate the breakthrough invasive fungal infection (IFI) rate in pediatric patients who received a prophylactic micafungin course at our institution.
A single-center, retrospective study was conducted between January 1, 2011, and July 31, 2017, to determine the IFI rate in patients receiving micafungin prophylaxis. Patients with suspected IFI were evaluated for probable or proven infection based on European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Cooperative Group and the National Institute of Allergy and Infectious Diseases Mycoses Study Group Consensus Group invasive fungal disease definitions. Statistical analyses were descriptive.
A total of 170 prophylactic micafungin courses from 129 unique patients ages <12 years at a median dose of 3 mg/kg daily were identified. The rate of probable or proven breakthrough IFIs was 2.4% as determined by clinical, radiologic, microbiologic, and histopathologic criteria.
A low rate of breakthrough IFI was seen with micafungin prophylaxis that is consistent with prior published adult hematopoietic stem cell transplantation studies. Micafungin was well tolerated, with liver function test elevations being transient in most cases and thought to be related to alternative factors.
关于接受化疗或造血干细胞移植的血液系统恶性肿瘤儿科患者的米卡芬净理想给药剂量,相关文献有限。米卡芬净是一种静脉用棘白菌素,对[具体菌种1]和[具体菌种2]有活性,与其他抗真菌类别相比具有良好的安全性。我们的目的是评估在我们机构接受预防性米卡芬净疗程的儿科患者中突破性侵袭性真菌感染(IFI)的发生率。
于2011年1月1日至2017年7月31日进行了一项单中心回顾性研究,以确定接受米卡芬净预防的患者中的IFI发生率。根据欧洲癌症研究与治疗组织/侵袭性真菌感染合作组以及美国国立过敏与传染病研究所真菌病研究组共识组的侵袭性真菌病定义,对疑似IFI的患者进行可能或确诊感染的评估。统计分析为描述性分析。
共确定了129例年龄<12岁的独特患者的170个预防性米卡芬净疗程,中位剂量为每日3mg/kg。根据临床、放射学、微生物学和组织病理学标准确定,可能或确诊的突破性IFI发生率为2.4%。
米卡芬净预防治疗的突破性IFI发生率较低,这与先前发表的成人造血干细胞移植研究一致。米卡芬净耐受性良好,大多数情况下肝功能检查升高是短暂的,且认为与其他因素有关。