Infectious Diseases Unit, Internal Medicine Department, Hospital Universitario Puerta de Hierro-Majadahonda, Instituto de Investigación Sanitaria Puerta de Hierro-Segovia de Arana, Madrid, Spain.
Clinic of Infectious Diseases, Department of Medical and Surgical Sciences, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Clin Infect Dis. 2020 Jul 27;71(3):685-692. doi: 10.1093/cid/ciz1195.
Treatment duration for invasive mold disease (IMD) in patients with hematological malignancy is not standardized and is a challenging subject in antifungal stewardship. Concerns for IMD relapse during subsequent reinduction or consolidation chemotherapy or graft versus host disease treatment in hematopoietic stem cell transplant recipients often results in prolonged or indefinite antifungal treatment. There are no validated criteria that predict when it is safe to stop antifungals. Decisions are individualized and depend on the offending fungus, site and extent of IMD, comorbidities, hematologic disease prognosis, and future plans for chemotherapy or transplantation. Recent studies suggest that FDG-PET/CT could help discriminate between active and residual fungal lesions to support decisions for safely stopping antifungals. Validation of noninvasive biomarkers for monitoring treatment response, tests for quantifying the "net state of immunosuppression," and genetic polymorphisms associated with poor fungal immunity could lead to a personalized assessment for the continued need for antifungal therapy.
治疗侵袭性霉菌病(IMD)的时间在血液病患者中没有标准化,这是抗真菌药物管理中的一个具有挑战性的课题。造血干细胞移植受者在随后的再诱导或巩固化疗或移植物抗宿主病治疗期间,对 IMD 复发的担忧常常导致抗真菌治疗延长或无限期进行。目前还没有验证的标准可以预测何时停止使用抗真菌药物是安全的。决策是个体化的,取决于致病真菌、IMD 的部位和范围、合并症、血液疾病的预后,以及未来化疗或移植的计划。最近的研究表明,FDG-PET/CT 有助于区分活跃和残留的真菌病变,以支持安全停止抗真菌药物的决策。监测治疗反应的非侵入性生物标志物的验证、用于量化“免疫抑制的净状态”的检测以及与真菌免疫不良相关的遗传多态性,可能导致对继续进行抗真菌治疗的个性化评估。