NMA Haplo or MUD BMT for Newly Diagnosed Severe Aplastic Anemia
Primary Purpose
Severe Aplastic Anemia, Aplastic Anemia, Bone Marrow Failure
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Thymoglobulin
Fludarabine
Cyclophosphamide
Total body irradiation
Tacrolimus
Mycophenolate mofetil
Sponsored by
About this trial
This is an interventional treatment trial for Severe Aplastic Anemia focused on measuring immunosuppression, nonmyeloablative, non-myeloablative, allogeneic, tacrolimus, bone marrow, bone marrow transplant, cyclophosphamide, thymoglobulin, ATG, fludarabine
Eligibility Criteria
Inclusion Criteria:
- Confirmed diagnosis of inherited or acquired severe aplastic anemia (SAA)
One of the following available donors:
- HLA-haploidentical relative
- If recipient is >= 40 years old, may use HLA-matched related donor
- For recipients with inherited bone marrow failure syndromes (IBMFS) with clear evidence of same disorder in potential related donors, may use 10/10 matched unrelated donor
- Recipient and/or legal guardian must sign protocol informed consent
- Donor must be willing to donate bone marrow
- Left ventricular ejection fraction (LVEF) >= 40%. For recipients < 13 years old, shortening fraction >= 26% may be used instead.
- Bilirubin < 3 x upper limit of normal (ULN) for age, unless patient has Gilbert's disease
- aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 5 x ULN for age
- For patients >= 13 years old: estimated creatinine clearance > 50 mL/min using Cockcroft-Gault formula and actual body weight
- For patients >= 1 but < 13 years old: glomerular filtration rate (GFR) estimated by updated Schwartz formula >= 90 mL/min/1.73 m^2. If estimated GFR is < 90 mL/min/1.73 m^2, 24-hour measured creatinine clearance must be > 50 mL/min/1.73 m^2.
- For patients >= 8 years old, diffusing capacity of the lung for carbon monoxide (DLCO) (corrected for hemoglobin) > 40%; forced expiratory volume at one second (FEV1) > 50%; forced vital capacity (FVC) > 50%
- For patients < 8 years old or unable to undergo pulmonary function testing: no evidence of dyspnea at rest; no need for supplemental oxygen; oxygen saturation > 92% on room air
- Karnofsky/Lansky status (depending on age) >= 70%
- Females and males of childbearing potential must agree to practice 2 effective methods of contraception at the same time. If unwilling, they must agree to complete abstinence.
Exclusion Criteria:
- Previous administration of immunosuppressive therapy for SAA.
- Fanconi anemia. At minimum, this diagnosis must be excluded by diepoxybutane (DEB) or equivalent testing on peripheral blood or marrow in patients < 30 years old.
- Clonal cytogenetic abnormalities consistent with pre-myelodysplastic syndrome (pre-MDS) or MDS on bone marrow examination
- Presence of anti-donor antibodies
- Prior allogeneic stem cell transplant
- Prior solid organ transplant
- Uncontrolled bacterial, viral, or fungal infection
- HIV seropositivity
- Active hepatitis B or C infection determined by serology and/or nucleic acid testing (NAT)
- Pregnancy or active breastfeeding
- Prior malignancies except: resected basal carcinoma or treated cervical carcinoma in situ; cancer treated with curative intent > 5 years previously. Other prior cancers will not be allowed unless approved by the PI.
Sites / Locations
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Bone marrow transplant
Arm Description
Non-myeloablative bone marrow transplant with a Thymoglobulin (ATG), fludarabine (Flu), cyclophosphamide (Cy), total body irradiation (TBI) preparative regimen and post-transplant Cy, mycophenolate mofetil (MMF), and tacrolimus as GVHD prophylaxis.
Outcomes
Primary Outcome Measures
Overall Survival and Engraftment at One Year
Number of enrolled participants who receive BMT, achieve engraftment, and are alive at one year post bone marrow transplant (BMT).
Secondary Outcome Measures
Overall Survival at One Year
Number of participants alive at one year after BMT.
Probability of Neutrophil Recovery as Assessed by the Number of Participants Who Have Recovered Neutrophil Counts
Probability of neutrophil recovery will be assessed by the number of participants who have recovered neutrophil counts at 1 year (>500 ANC).
Probability of Platelet Recovery as Assessed by Number of Participants Who Have Recovered Platelet Counts
Probability of platelet recovery will be assessed by the number of participants who have recovered platelet counts at 1 year.
Number of Participants Who Experience Primary Graft Failure
Number of participants who experience primary graft failure by one year after BMT.
Number of Participants Who Experience Secondary Graft Failure
Number of participants who experience secondary graft failure by one year after BMT.
Number of Participants Who Experience Grades II-IV Acute GVHD
Number of participants who experience grade II, III, or IV acute GVHD by Day 100.
Number of Participants Who Experience Grades III-IV Acute GVHD
Number of participants who experience grade III or IV acute GVHD by Day 100.
Number of Participants Who Experience Chronic GVHD
Number of participants who experience chronic GVHD by two years after BMT.
Number of Participants With Full Donor Chimerism
Number of participants with full donor chimerism at Day 60.
GVHD-free Relapse-free Survival (GRFS)
Number of participants alive, without relapse, and without GVHD at 1 year.
Transplant-related Mortality
Number of participants deceased for reasons related to BMT at 1 year.
Full Information
NCT ID
NCT02833805
First Posted
July 12, 2016
Last Updated
June 16, 2022
Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
1. Study Identification
Unique Protocol Identification Number
NCT02833805
Brief Title
NMA Haplo or MUD BMT for Newly Diagnosed Severe Aplastic Anemia
Official Title
A Phase II Trial of Non-Myeloablative (NMA) Conditioning and Transplantation of Partially HLA-Mismatched/Haploidentical Related or Matched Unrelated Donor (MUD) Bone Marrow for Newly Diagnosed Patients With Severe Aplastic Anemia
Study Type
Interventional
2. Study Status
Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
September 2016 (Actual)
Primary Completion Date
July 2021 (Actual)
Study Completion Date
July 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Our primary objective is to determine if it is feasible for previously untreated severe aplastic anemia (SAA) patients to be transplanted using non-myeloablative conditioning and post transplantation cyclophosphamide.
Detailed Description
This is a clinical trial of upfront bone marrow transplantation for patients with SAA who do not have a fully human leukocyte antigen (HLA) matched donor. The trial uses a conditioning regimen which has been successful in the refractory and relapsed setting to maximize engraftment and post transplant therapy to minimize graft versus host disease (GVHD). This would be used here in patients who have not yet undergone immunosuppressive therapy for their SAA or are thought to be unlikely to respond to immunosuppressive therapy for SAA.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Aplastic Anemia, Aplastic Anemia, Bone Marrow Failure, Immunosuppression
Keywords
immunosuppression, nonmyeloablative, non-myeloablative, allogeneic, tacrolimus, bone marrow, bone marrow transplant, cyclophosphamide, thymoglobulin, ATG, fludarabine
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
21 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Bone marrow transplant
Arm Type
Experimental
Arm Description
Non-myeloablative bone marrow transplant with a Thymoglobulin (ATG), fludarabine (Flu), cyclophosphamide (Cy), total body irradiation (TBI) preparative regimen and post-transplant Cy, mycophenolate mofetil (MMF), and tacrolimus as GVHD prophylaxis.
Intervention Type
Drug
Intervention Name(s)
Thymoglobulin
Other Intervention Name(s)
Anti-thymocyte globulin, ATG
Intervention Description
Day -9: 0.5 mg/kg Days -8 and -7: 2 mg/kg daily
Intervention Type
Drug
Intervention Name(s)
Fludarabine
Other Intervention Name(s)
Fludara
Intervention Description
Days -6 through -2: 30 mg/m^2 IV daily
Intervention Type
Drug
Intervention Name(s)
Cyclophosphamide
Other Intervention Name(s)
Cytoxan, Cy, CTX
Intervention Description
Days -6 and -5: 14.5 mg/kg IV daily Days 3 and 4: 50 mg/kg IV daily
Intervention Type
Radiation
Intervention Name(s)
Total body irradiation
Other Intervention Name(s)
TBI
Intervention Description
Day -1: 200 centigray (cGy) in a single fraction
Intervention Type
Drug
Intervention Name(s)
Tacrolimus
Other Intervention Name(s)
FK-506, FK506, Prograf
Intervention Description
Start on Day 5 through Day 365
Intervention Type
Drug
Intervention Name(s)
Mycophenolate mofetil
Other Intervention Name(s)
MMF, CellCept
Intervention Description
Days 5 through 35: 15 mg/kg PO three times daily (max 3 g/day)
Primary Outcome Measure Information:
Title
Overall Survival and Engraftment at One Year
Description
Number of enrolled participants who receive BMT, achieve engraftment, and are alive at one year post bone marrow transplant (BMT).
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Overall Survival at One Year
Description
Number of participants alive at one year after BMT.
Time Frame
1 year
Title
Probability of Neutrophil Recovery as Assessed by the Number of Participants Who Have Recovered Neutrophil Counts
Description
Probability of neutrophil recovery will be assessed by the number of participants who have recovered neutrophil counts at 1 year (>500 ANC).
Time Frame
1 year
Title
Probability of Platelet Recovery as Assessed by Number of Participants Who Have Recovered Platelet Counts
Description
Probability of platelet recovery will be assessed by the number of participants who have recovered platelet counts at 1 year.
Time Frame
1 year
Title
Number of Participants Who Experience Primary Graft Failure
Description
Number of participants who experience primary graft failure by one year after BMT.
Time Frame
1 year
Title
Number of Participants Who Experience Secondary Graft Failure
Description
Number of participants who experience secondary graft failure by one year after BMT.
Time Frame
1 year
Title
Number of Participants Who Experience Grades II-IV Acute GVHD
Description
Number of participants who experience grade II, III, or IV acute GVHD by Day 100.
Time Frame
Day 100
Title
Number of Participants Who Experience Grades III-IV Acute GVHD
Description
Number of participants who experience grade III or IV acute GVHD by Day 100.
Time Frame
Day 100
Title
Number of Participants Who Experience Chronic GVHD
Description
Number of participants who experience chronic GVHD by two years after BMT.
Time Frame
2 years
Title
Number of Participants With Full Donor Chimerism
Description
Number of participants with full donor chimerism at Day 60.
Time Frame
Day 60
Title
GVHD-free Relapse-free Survival (GRFS)
Description
Number of participants alive, without relapse, and without GVHD at 1 year.
Time Frame
1 year
Title
Transplant-related Mortality
Description
Number of participants deceased for reasons related to BMT at 1 year.
Time Frame
1 year
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Confirmed diagnosis of inherited or acquired severe aplastic anemia (SAA)
One of the following available donors:
HLA-haploidentical relative
If recipient is >= 40 years old, may use HLA-matched related donor
For recipients with inherited bone marrow failure syndromes (IBMFS) with clear evidence of same disorder in potential related donors, may use 10/10 matched unrelated donor
Recipient and/or legal guardian must sign protocol informed consent
Donor must be willing to donate bone marrow
Left ventricular ejection fraction (LVEF) >= 40%. For recipients < 13 years old, shortening fraction >= 26% may be used instead.
Bilirubin < 3 x upper limit of normal (ULN) for age, unless patient has Gilbert's disease
aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 5 x ULN for age
For patients >= 13 years old: estimated creatinine clearance > 50 mL/min using Cockcroft-Gault formula and actual body weight
For patients >= 1 but < 13 years old: glomerular filtration rate (GFR) estimated by updated Schwartz formula >= 90 mL/min/1.73 m^2. If estimated GFR is < 90 mL/min/1.73 m^2, 24-hour measured creatinine clearance must be > 50 mL/min/1.73 m^2.
For patients >= 8 years old, diffusing capacity of the lung for carbon monoxide (DLCO) (corrected for hemoglobin) > 40%; forced expiratory volume at one second (FEV1) > 50%; forced vital capacity (FVC) > 50%
For patients < 8 years old or unable to undergo pulmonary function testing: no evidence of dyspnea at rest; no need for supplemental oxygen; oxygen saturation > 92% on room air
Karnofsky/Lansky status (depending on age) >= 70%
Females and males of childbearing potential must agree to practice 2 effective methods of contraception at the same time. If unwilling, they must agree to complete abstinence.
Exclusion Criteria:
Previous administration of immunosuppressive therapy for SAA.
Fanconi anemia. At minimum, this diagnosis must be excluded by diepoxybutane (DEB) or equivalent testing on peripheral blood or marrow in patients < 30 years old.
Clonal cytogenetic abnormalities consistent with pre-myelodysplastic syndrome (pre-MDS) or MDS on bone marrow examination
Presence of anti-donor antibodies
Prior allogeneic stem cell transplant
Prior solid organ transplant
Uncontrolled bacterial, viral, or fungal infection
HIV seropositivity
Active hepatitis B or C infection determined by serology and/or nucleic acid testing (NAT)
Pregnancy or active breastfeeding
Prior malignancies except: resected basal carcinoma or treated cervical carcinoma in situ; cancer treated with curative intent > 5 years previously. Other prior cancers will not be allowed unless approved by the PI.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amy E DeZern, MD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
32343796
Citation
DeZern AE, Zahurak ML, Symons HJ, Cooke KR, Rosner GL, Gladstone DE, Huff CA, Swinnen LJ, Imus P, Borrello I, Wagner-Johnston N, Ambinder RF, Luznik L, Bolanos-Meade J, Fuchs EJ, Jones RJ, Brodsky RA. Haploidentical BMT for severe aplastic anemia with intensive GVHD prophylaxis including posttransplant cyclophosphamide. Blood Adv. 2020 Apr 28;4(8):1770-1779. doi: 10.1182/bloodadvances.2020001729.
Results Reference
derived
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NMA Haplo or MUD BMT for Newly Diagnosed Severe Aplastic Anemia
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