Escalation Antifungal Prophylaxis for Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation
Fungal Infection
About this trial
This is an interventional prevention trial for Fungal Infection focused on measuring fungal infection, stem cell transplantation, prophylaxis
Eligibility Criteria
Inclusion Criteria:
- patients undergo allogeneic HSCT
- Conditioning regimens: myelo-ablative, reduced toxicity
- No proven or probable IFD before HSCT
- No allergy to fluconazole, voriconazle and posaconazole
- Inform consent given
Exclusion Criteria:
- Imparied liver function with (AST or ALT>3ULN, TBil >2ULN)
Sites / Locations
- Blood & Marrow Transplantation Center, RuiJin HospitalRecruiting
Arms of the Study
Arm 1
Experimental
Escalating prophylaxis
For all patients without documented proven or probable invasive fungal disease (IFD), patients will receive fluconazole during the treatment in the laminar air flow units (LAF). After discharged from LAF units, patients will receive anti-mold prophylaxis in case of haplo-identical or HLA-matched unrelated donor transplantation to d+100 without active acute GVHD (aGVHD). In case of active aGVHD, the prophylaxis treatment will be extended until recovery of aGVHD and tapering of immunosuppression. In case of HLA-matched sibling donor, fluconazole will be continued to d+100 and anti-mold prophylaxis will be given in case of active aGVHD.