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Escalation Antifungal Prophylaxis for Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation

Primary Purpose

Fungal Infection

Status
Recruiting
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Escalating prophylaxis
Sponsored by
Shanghai Jiao Tong University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Fungal Infection focused on measuring fungal infection, stem cell transplantation, prophylaxis

Eligibility Criteria

16 Years - 65 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Arm Label

Escalating prophylaxis

Arm Description

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.

Outcomes

Primary Outcome Measures

Incidence of IFD
Proven and probable diagnosis of IFD

Secondary Outcome Measures

Incidence of IFD2
Proven, probable and possible IFD
Incidence of IFD associated mortality
Documentation of death due to proven, probable and possible IFD
Incidence of nor-relapse mortality (NRM)
Documentation of death not due to disease relapse or progression

Full Information

First Posted
February 14, 2020
Last Updated
November 23, 2021
Sponsor
Shanghai Jiao Tong University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT04273178
Brief Title
Escalation Antifungal Prophylaxis for Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation
Official Title
Feasibility and Outcome of Anti-fungal Prophylaxis With an Escalation Pattern for Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Recruiting
Study Start Date
January 15, 2020 (Actual)
Primary Completion Date
January 15, 2022 (Anticipated)
Study Completion Date
June 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai Jiao Tong University School of Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is single arm study to evaluate an escalation anti-fungal prophylaxis protocol for patients undergoing allogeneic stem cell transplantation. 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.
Detailed Description
Based on CAESAR study, the IFD incidence increased significantly in patients with unrelated donor or hallo-donor HSCT after patients being discharged from LAF units. The overall incidence of IFD in patients with HLA-matched sibling donor remain low unless in patients with active aGVHD. In this single-arm prospective study, we plan to evaluate the feasibility and effect of an escalation anti-fungal prophylaxis protocol for patients undergoing allogeneic stem cell transplantation. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fungal Infection
Keywords
fungal infection, stem cell transplantation, prophylaxis

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
175 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Escalating prophylaxis
Arm Type
Experimental
Arm Description
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.
Intervention Type
Drug
Intervention Name(s)
Escalating prophylaxis
Intervention Description
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.
Primary Outcome Measure Information:
Title
Incidence of IFD
Description
Proven and probable diagnosis of IFD
Time Frame
day 180 after transplantation
Secondary Outcome Measure Information:
Title
Incidence of IFD2
Description
Proven, probable and possible IFD
Time Frame
day 180 after transplantation
Title
Incidence of IFD associated mortality
Description
Documentation of death due to proven, probable and possible IFD
Time Frame
day 180 after transplantation
Title
Incidence of nor-relapse mortality (NRM)
Description
Documentation of death not due to disease relapse or progression
Time Frame
day 180 after transplantation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
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)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jiong Hu
Phone
86-21-64370045
Ext
601878
Email
hj10709@rjh.com.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jiong Hu
Organizational Affiliation
Ruijin Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Blood & Marrow Transplantation Center, RuiJin Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200025
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jiong HU, M.D.,
Phone
86-21-64370045
Email
hujiong@medmail.com.cn
First Name & Middle Initial & Last Name & Degree
Ling Wang, M.D.,
Phone
86-21-64370045
Email
cclingjar@163.com

12. IPD Sharing Statement

Learn more about this trial

Escalation Antifungal Prophylaxis for Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation

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