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The Use of N-acetylcysteine for Thrombotic Events After Allogenic Hematopoietic Stem Cell Transplantation

Primary Purpose

Thrombotic Disorder

Status
Not yet recruiting
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
N-acetyl-cysteine
Busulfan
Cytarabine
Cyclophosphamide
Sponsored by
The First Affiliated Hospital of Soochow University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Thrombotic Disorder focused on measuring Thrombotic disorder, Hematopoietic stem cell transplantation

Eligibility Criteria

16 Years - 70 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Aged 16-70 years old Diagnosed as myeloid malignancies, and about to undergo allo-HSCT; ECOG: 0-2; Expected survival longer than 1 month Exclusion Criteria: Allergic to any components of NAC; Severe dysfunction of heart, liver, lung and kidney; Relapse before HSCT; A history of bronchial asthma, bronchospasm or moderate / severe gastrohelcosis.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Arm A

    Arm B

    Arm Description

    Modified BUCY conditioning regimen: busulfan (3.2mg/kg, day-7 to day -5), cytarabine (2g/m2, day -8), cyclophosphamide (1.8g/m2, day -4 to day -3), followed by stem cells infusion; N-acetyl-cysteine (Zambon Pharma, Hainan, China) : 8g/d (>=45kg); 200mg/kg.d (<45kg), intravenously for at least 4 hours, day -9 to day +45.

    Modified BUCY conditioning regimen: busulfan (3.2mg/kg, day-7 to day -5), cytarabine (2g/m2, day -8), cyclophosphamide (1.8g/m2, day -4 to day -3), followed by stem cells infusion.

    Outcomes

    Primary Outcome Measures

    The incidence of thrombotic disorders
    The incidence of thrombotic disorders (TA-TMA, SOS, DVT, PTE, CRT, SVT) after allogenic hematopoietic stem cell transplantation
    Overall survival
    The rate of overall survival after allogenic hematopoietic stem cell transplantation

    Secondary Outcome Measures

    The incidence of relapse
    The incidence of relapse after allogenic hematopoietic stem cell transplantation
    The incidence of GVHD
    The incidence of GVHD after allogenic hematopoietic stem cell transplantation
    The incidence of hematopoietic reconstitution
    The incidence of hematopoietic reconstitution after allogenic hematopoietic stem cell transplantation

    Full Information

    First Posted
    June 8, 2023
    Last Updated
    June 8, 2023
    Sponsor
    The First Affiliated Hospital of Soochow University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05907486
    Brief Title
    The Use of N-acetylcysteine for Thrombotic Events After Allogenic Hematopoietic Stem Cell Transplantation
    Official Title
    The Efficiency and Safety of N-acetylcysteine for Prevention of Thrombotic Events After Allogenic Hematopoietic Stem Cell Transplantation
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    August 1, 2023 (Anticipated)
    Primary Completion Date
    August 1, 2025 (Anticipated)
    Study Completion Date
    December 1, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    The First Affiliated Hospital of Soochow University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    We aim to assess the the efficiency and safety of N-acetylcysteine for prevention of thrombotic events after allogenic hematopoietic stem cell transplantation.
    Detailed Description
    The thrombotic events are increasingly recognized complications of hematopoietic cell transplantation (HCT) associated with significant morbidity and mortality, which include transplantation-associated thrombotic microangiopathy (TA-TMA), sinusoidal obstructive syndrome (SOS), deep vein thrombosis (DVT), pulmonary thromboembolism (PTE), catheter-related thrombosis (CRT), superficial vein thrombosis (SVT), etc. There is a complex interplay on balancing the risk for thrombosis and bleeding in these patients, making treatment decisions particularly challenging. Emerging studies revealed that endothelial injury is the common underlying mechanism among different thrombotic disorders. There is increasing data that N-acetyl-cysteine (NAC) may prevent or improve endothelial dysfunction by inhibiting ROS production and preventing endothelial apoptosis. Our previous study showed low dose NAC could decrease the incidence of TA-TMA. In this study, we aim to assess the the efficiency and safety of N-acetylcysteine for prevention of thrombotic events after allogenic hematopoietic stem cell transplantation.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Thrombotic Disorder
    Keywords
    Thrombotic disorder, Hematopoietic stem cell transplantation

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    260 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Arm A
    Arm Type
    Experimental
    Arm Description
    Modified BUCY conditioning regimen: busulfan (3.2mg/kg, day-7 to day -5), cytarabine (2g/m2, day -8), cyclophosphamide (1.8g/m2, day -4 to day -3), followed by stem cells infusion; N-acetyl-cysteine (Zambon Pharma, Hainan, China) : 8g/d (>=45kg); 200mg/kg.d (<45kg), intravenously for at least 4 hours, day -9 to day +45.
    Arm Title
    Arm B
    Arm Type
    Active Comparator
    Arm Description
    Modified BUCY conditioning regimen: busulfan (3.2mg/kg, day-7 to day -5), cytarabine (2g/m2, day -8), cyclophosphamide (1.8g/m2, day -4 to day -3), followed by stem cells infusion.
    Intervention Type
    Drug
    Intervention Name(s)
    N-acetyl-cysteine
    Other Intervention Name(s)
    NAC
    Intervention Description
    8g/d (>=45kg); 200mg/kg.d (<45kg), intravenously for at least 4 hours, day -9 to day +45
    Intervention Type
    Drug
    Intervention Name(s)
    Busulfan
    Other Intervention Name(s)
    BU
    Intervention Description
    3.2mg/kg, day-7 to day -5, intravenously
    Intervention Type
    Drug
    Intervention Name(s)
    Cytarabine
    Other Intervention Name(s)
    Ara-C
    Intervention Description
    2g/m2, day -8, intravenously
    Intervention Type
    Drug
    Intervention Name(s)
    Cyclophosphamide
    Other Intervention Name(s)
    CTX
    Intervention Description
    1.8g/m2, day -4 to day -3, intravenously
    Primary Outcome Measure Information:
    Title
    The incidence of thrombotic disorders
    Description
    The incidence of thrombotic disorders (TA-TMA, SOS, DVT, PTE, CRT, SVT) after allogenic hematopoietic stem cell transplantation
    Time Frame
    1 year
    Title
    Overall survival
    Description
    The rate of overall survival after allogenic hematopoietic stem cell transplantation
    Time Frame
    1 year
    Secondary Outcome Measure Information:
    Title
    The incidence of relapse
    Description
    The incidence of relapse after allogenic hematopoietic stem cell transplantation
    Time Frame
    1 year
    Title
    The incidence of GVHD
    Description
    The incidence of GVHD after allogenic hematopoietic stem cell transplantation
    Time Frame
    1 year
    Title
    The incidence of hematopoietic reconstitution
    Description
    The incidence of hematopoietic reconstitution after allogenic hematopoietic stem cell transplantation
    Time Frame
    1 year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    16 Years
    Maximum Age & Unit of Time
    70 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Aged 16-70 years old Diagnosed as myeloid malignancies, and about to undergo allo-HSCT; ECOG: 0-2; Expected survival longer than 1 month Exclusion Criteria: Allergic to any components of NAC; Severe dysfunction of heart, liver, lung and kidney; Relapse before HSCT; A history of bronchial asthma, bronchospasm or moderate / severe gastrohelcosis.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Yaqiong Tang, Doctor
    Phone
    18896588075
    Email
    tangyaqiong@suda.edu.cn
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Yue Han, Professor
    Organizational Affiliation
    The First Affiliated Hospital of Soochow University
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
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    22899581
    Citation
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    Results Reference
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    PubMed Identifier
    21596850
    Citation
    Laskin BL, Goebel J, Davies SM, Jodele S. Small vessels, big trouble in the kidneys and beyond: hematopoietic stem cell transplantation-associated thrombotic microangiopathy. Blood. 2011 Aug 11;118(6):1452-62. doi: 10.1182/blood-2011-02-321315. Epub 2011 May 19.
    Results Reference
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    PubMed Identifier
    14962323
    Citation
    George JN, Li X, McMinn JR, Terrell DR, Vesely SK, Selby GB. Thrombotic thrombocytopenic purpura-hemolytic uremic syndrome following allogeneic HPC transplantation: a diagnostic dilemma. Transfusion. 2004 Feb;44(2):294-304. doi: 10.1111/j.1537-2995.2004.00700.x.
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    19766729
    Citation
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    PubMed Identifier
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    Citation
    Tsirigotis PD, Resnick IB, Avni B, Grisariu S, Stepensky P, Or R, Shapira MY. Incidence and risk factors for moderate-to-severe veno-occlusive disease of the liver after allogeneic stem cell transplantation using a reduced intensity conditioning regimen. Bone Marrow Transplant. 2014 Nov;49(11):1389-92. doi: 10.1038/bmt.2014.168. Epub 2014 Jul 28.
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    Citation
    Carreras E, Diaz-Beya M, Rosinol L, Martinez C, Fernandez-Aviles F, Rovira M. The incidence of veno-occlusive disease following allogeneic hematopoietic stem cell transplantation has diminished and the outcome improved over the last decade. Biol Blood Marrow Transplant. 2011 Nov;17(11):1713-20. doi: 10.1016/j.bbmt.2011.06.006. Epub 2011 Jun 25.
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    Citation
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    The Use of N-acetylcysteine for Thrombotic Events After Allogenic Hematopoietic Stem Cell Transplantation

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