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Trial record 8 of 40 for:    Recruiting, Not yet recruiting, Available Studies | "Unrelated Donors"

HLA-Mismatched Unrelated Donor Bone Marrow Transplantation With Post-Transplantation Cyclophosphamide

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ClinicalTrials.gov Identifier: NCT02793544
Recruitment Status : Recruiting
First Posted : June 8, 2016
Last Update Posted : June 18, 2018
Sponsor:
Collaborators:
National Marrow Donor Program
Resource for Clinical Investigation in Blood and Marrow Transplantation
Information provided by (Responsible Party):
Center for International Blood and Marrow Transplant Research

Brief Summary:
This is a multi-center, single arm Phase II study of hematopoietic cell transplantation (HCT) using human leukocyte antigen (HLA)-mismatched unrelated bone marrow transplantation donors and post-transplantation cyclophosphamide (PTCy), sirolimus and mycophenolate mofetil (MMF) for graft versus host disease (GVHD) prophylaxis in patients with hematologic malignancies.

Condition or disease Intervention/treatment Phase
Myelodysplastic Syndrome (MDS) Chronic Lymphocytic Leukemia (CLL) Chemotherapy-sensitive Lymphoma Acute Lymphoblastic Leukemia (ALL)/T Lymphoblastic Lymphoma Acute Myelogenous Leukemia (AML) Acute Biphenotypic Leukemia (ABL) Acute Undifferentiated Leukemia (AUL) Drug: Fludarabine Drug: Cyclophosphamide 14.5 mg/kg/day IV on Days -6, -5 Radiation: Total Body Irradiation (TBI) 200cGy on Day -1 Procedure: Infusion of non-T-cell depleted bone marrow on Day 0 Drug: Busulfan Drug: Cyclophosphamide 50mg/kg/day IV on Days -2,-1 Drug: Cyclophosphamide 50mg/kg/day IV on Days -5,-4 Radiation: Total Body Irradiation (TBI) 200cGy twice a day on Days -3, -2, -1 Drug: Post-HCT Cyclophosphamide 50mg/kg IV on Day+3, +4 Drug: Sirolimus Drug: Mycophenolate mofetil Drug: G-CSF Drug: Pre-HCT Mesna on Days -6 and -5 Drug: Pre-HCT Mesna on Days -2 and -1 Drug: Pre-HCT Mesna on Days -5 and -4 Drug: Post-HCT Mesna Phase 2

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 80 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Multi-Center, Phase II Trial of HLA-Mismatched Unrelated Donor Bone Marrow Transplantation With Post-Transplantation Cyclophosphamide for Patients With Hematologic Malignancies
Actual Study Start Date : December 2016
Estimated Primary Completion Date : December 2019
Estimated Study Completion Date : December 2019


Arm Intervention/treatment
Active Comparator: Regimen A (RIC: Flu/Cy/TBI)
  1. Fludarabine 30 mg/m2/day IV on Days -6, -5, -4, -3, -2
  2. Cyclophosphamide 14.5 mg/kg/day IV on Days -6, -5
  3. Total Body Irradiation (TBI) 200cGy on Day -1
  4. Infusion of non-T-cell depleted bone marrow on Day 0

Although a schedule is proposed above, the regimen can be given according to institutional standards as long as the prescribed doses are the same as in the recommended regimen above.

Drug: Fludarabine
  • Fludarabine 30 mg/m2/day (adjusted for renal function) is administered over a 30-60 minute IV infusion on Days -6 through -2 (maximum cumulative dose, 150 mg/m2).
  • The body surface area (BSA) for fludarabine dosing is based on adjusted ideal body weight (IBW) (Appendix K).
  • creatinine clearance may change during the days fludarabine is given. Adjustment in fludarabine dose due to creatinine changes during conditioning is permitted.
Other Name: Fludara®

Drug: Cyclophosphamide 14.5 mg/kg/day IV on Days -6, -5
  • Cy 14.5 mg/kg/day is administered as a 1-2 hour IV infusion on Days -6 and -5 after hydration.
  • Use of Mesna and dosing will be done according to institutional standards. A recommended approach is as follows: Mesna IV dose of ≥ 80% of the total daily dose of Cy and given in divided doses 30 minutes before and at 3, 6, and 8-9 hours after completion of Cy.
  • Hydration prior to Cy may be given according to institutional guideline.
  • Cy and mesna are dosed according to adjusted IBW (Appendix K), unless the subject weighs less than IBW, in which case these drugs will be dosed according to actual weight.
Other Name: Cytoxan®

Radiation: Total Body Irradiation (TBI) 200cGy on Day -1
  • 200 cGy TBI is administered in a single fraction on Day -1.
  • Radiation sources, dose rates, and shielding follow institutional practice.

Procedure: Infusion of non-T-cell depleted bone marrow on Day 0
  • On Day 0, the harvested bone marrow is infused.
  • Donor bone marrow will be harvested with a target yield of 4 x 108 nucleated cells/kg recipient weight.
  • The lowest acceptable nucleated cells yield is 1.5 x 108 cells/kg recipient weight.

Drug: Post-HCT Cyclophosphamide 50mg/kg IV on Day+3, +4
  • Cy 50mg/kg IV, over 1-2 hours (depending on volume), is given on Day+3 (ideally between 60 and 72 hours after bone marrow infusion) and on Day+4 (approximately 24 hours after Day+3 Cy).
  • Hydration with Cy, management of volume status, and monitoring for hemorrhagic cystitis will follow institutional standards.
  • Mesna is required. Mesna IV dose must be ≥ 80% of the total daily dose of Cy and given in divided doses 30 minutes before and at 3, 6, and 8-9 hours after completion of Cy.
  • Cy is dosed according to IBW, unless the subject weighs less than IBW, in which case these drugs will be dosed according to actual body weight.

Drug: Sirolimus
  • Sirolimus dosing is based on adjusted IBW (Appendix K).
  • Sirolimus prophylaxis is discontinued after the last dose on Day+180, or may be continued if there is GVHD.

For subjects ≥ 18 years old:

  • A one-time sirolimus loading dose, 6 mg PO, is given on Day+5, at least 24 hours after Cy completion.
  • Sirolimus is then continued at a maintenance dose (starting dose 2 mg PO QD), with dose adjustments to maintain a trough of 5 - 15 ng/mL as measured by high performance liquid chromatography (HPLC) or immunoassay.

For subjects < 18 years old:

  • A one-time sirolimus loading dose, 3 mg/m2 PO with the dose not to exceed 6 mg, is given on Day+5, at least 24 hours after Cy completion.
  • Sirolimus is then continued at a maintenance dose (starting dose 1 mg/m2 PO QD, maximum 2 mg PO QD), with dose adjustments to maintain a trough of 5 - 15 ng/mL as measured by HPLC or immunoassay.
Other Names:
  • rapamycin
  • Rapamune®

Drug: Mycophenolate mofetil

MMF begins on Day+5, at least 24 hours after completion of PTCy. MMF dose is 15 mg/kg PO TID (adjusted IBW (Appendix K)) with total daily dose not to exceed 3 grams (i.e. maximum 1 g PO TID).

An equivalent IV dose (1:1 conversion) may instead be given. MMF prophylaxis is discontinued after the last dose on Day+35, or may be continued if there is GVHD.

Other Names:
  • MMF
  • Cellcept®

Drug: G-CSF

Granulocyte-colony stimulating factor (G-CSF): filgrastim or a biosimilar begins on Day+5 at a dose of 5 mcg/kg/day (actual body weight) IV or subcutaneously (SC) (rounding to the nearest vial dose is allowed), until the absolute neutrophil count (ANC) is ≥ 1,000/mm3 over the course of 3 consecutive days.

Additional G-CSF may be administered as warranted.

Other Name: filgrastim

Drug: Pre-HCT Mesna on Days -6 and -5

Use of Mesna and dosing will be done according to institutional standards. A recommended approach is as follows: Mesna IV dose of ≥ 80% of the total daily dose of Cy and given in divided doses 30 minutes before and at 3, 6, and 8-9 hours after completion of Cy.

Mesna is dosed according to adjusted IBW (Appendix K), unless the subject weighs less than IBW, in which case Mesna will be dosed according to actual weight.


Drug: Post-HCT Mesna

Mesna is required. Mesna IV dose must be ≥ 80% of the total daily dose of Cy and given in divided doses 30 minutes before and at 3, 6, and 8-9 hours after completion of Cy on Day+3 and Day+4.

Mesna is dosed according to IBW, unless the subject weighs less than IBW, in which case Mesna will be dosed according to actual body weight.


Active Comparator: Regimen B 2a (FIC: Bu/Cy)
  1. Busulfan ≥ 9mg/kg total dose on Days -6, -5, -4, -3 (IV or PO)
  2. Cyclophosphamide 50mg/kg/day IV on Days -2,-1
  3. Infusion of non-T-cell depleted bone marrow on Day 0

Although a schedule is proposed above, the regimen can be given according to institutional standards as long as the prescribed doses are the same as in the recommended regimen above.

Procedure: Infusion of non-T-cell depleted bone marrow on Day 0
  • On Day 0, the harvested bone marrow is infused.
  • Donor bone marrow will be harvested with a target yield of 4 x 108 nucleated cells/kg recipient weight.
  • The lowest acceptable nucleated cells yield is 1.5 x 108 cells/kg recipient weight.

Drug: Busulfan
  • Busulfan ≥ 9mg/kg total dose (IV or PO) on Days -6, -5, -4, -3 (PK monitoring required to achieve a daily area under the curve (AUC) target of 4800-5300 μM*min (Perkins et al., 2012))
  • Busulfan dosing is based on adjusted IBW (Appendix K)
Other Name: Busulfex®

Drug: Cyclophosphamide 50mg/kg/day IV on Days -2,-1
  • Cy 50mg/kg/day is administered as a 1-2 hour IV infusion on Days -2 and -1 after hydration.
  • Use of Mesna and dosing will be done according to institutional standards. A recommended approach is as follows: Mesna IV dose of ≥ 80% of the total daily dose of Cy and given in divided doses 30 minutes before and at 3, 6, and 8-9 hours after completion of Cy.
  • Hydration prior to Cy may be given according to institutional guideline.
  • Cy and mesna are dosed according to adjusted IBW (Appendix K), unless the subject weighs less than IBW, in which case these drugs will be dosed according to actual weight.
Other Name: Cytoxan®

Drug: Post-HCT Cyclophosphamide 50mg/kg IV on Day+3, +4
  • Cy 50mg/kg IV, over 1-2 hours (depending on volume), is given on Day+3 (ideally between 60 and 72 hours after bone marrow infusion) and on Day+4 (approximately 24 hours after Day+3 Cy).
  • Hydration with Cy, management of volume status, and monitoring for hemorrhagic cystitis will follow institutional standards.
  • Mesna is required. Mesna IV dose must be ≥ 80% of the total daily dose of Cy and given in divided doses 30 minutes before and at 3, 6, and 8-9 hours after completion of Cy.
  • Cy is dosed according to IBW, unless the subject weighs less than IBW, in which case these drugs will be dosed according to actual body weight.

Drug: Sirolimus
  • Sirolimus dosing is based on adjusted IBW (Appendix K).
  • Sirolimus prophylaxis is discontinued after the last dose on Day+180, or may be continued if there is GVHD.

For subjects ≥ 18 years old:

  • A one-time sirolimus loading dose, 6 mg PO, is given on Day+5, at least 24 hours after Cy completion.
  • Sirolimus is then continued at a maintenance dose (starting dose 2 mg PO QD), with dose adjustments to maintain a trough of 5 - 15 ng/mL as measured by high performance liquid chromatography (HPLC) or immunoassay.

For subjects < 18 years old:

  • A one-time sirolimus loading dose, 3 mg/m2 PO with the dose not to exceed 6 mg, is given on Day+5, at least 24 hours after Cy completion.
  • Sirolimus is then continued at a maintenance dose (starting dose 1 mg/m2 PO QD, maximum 2 mg PO QD), with dose adjustments to maintain a trough of 5 - 15 ng/mL as measured by HPLC or immunoassay.
Other Names:
  • rapamycin
  • Rapamune®

Drug: Mycophenolate mofetil

MMF begins on Day+5, at least 24 hours after completion of PTCy. MMF dose is 15 mg/kg PO TID (adjusted IBW (Appendix K)) with total daily dose not to exceed 3 grams (i.e. maximum 1 g PO TID).

An equivalent IV dose (1:1 conversion) may instead be given. MMF prophylaxis is discontinued after the last dose on Day+35, or may be continued if there is GVHD.

Other Names:
  • MMF
  • Cellcept®

Drug: G-CSF

Granulocyte-colony stimulating factor (G-CSF): filgrastim or a biosimilar begins on Day+5 at a dose of 5 mcg/kg/day (actual body weight) IV or subcutaneously (SC) (rounding to the nearest vial dose is allowed), until the absolute neutrophil count (ANC) is ≥ 1,000/mm3 over the course of 3 consecutive days.

Additional G-CSF may be administered as warranted.

Other Name: filgrastim

Drug: Pre-HCT Mesna on Days -2 and -1

Use of Mesna and dosing will be done according to institutional standards. A recommended approach is as follows: Mesna IV dose of ≥ 80% of the total daily dose of Cy and given in divided doses 30 minutes before and at 3, 6, and 8-9 hours after completion of Cy.

Mesna is dosed according to adjusted IBW (Appendix K), unless the subject weighs less than IBW, in which case Mesna will be dosed according to actual weight.


Drug: Post-HCT Mesna

Mesna is required. Mesna IV dose must be ≥ 80% of the total daily dose of Cy and given in divided doses 30 minutes before and at 3, 6, and 8-9 hours after completion of Cy on Day+3 and Day+4.

Mesna is dosed according to IBW, unless the subject weighs less than IBW, in which case Mesna will be dosed according to actual body weight.


Active Comparator: Regimen B 2b (FIC: Bu/Flu)
  1. Busulfan ≥ 9mg/kg total dose on Days -6, -5, -4, -3 (IV or PO)
  2. Fludarabine 30 mg/m2/day IV on Days -6, -5, -4, -3, -2
  3. Infusion of non-T-cell depleted bone marrow on Day 0

Although a schedule is proposed above, the regimen can be given according to institutional standards as long as the prescribed doses are the same as in the recommended regimen above.

Drug: Fludarabine
  • Fludarabine 30 mg/m2/day (adjusted for renal function) is administered over a 30-60 minute IV infusion on Days -6 through -2 (maximum cumulative dose, 150 mg/m2).
  • The body surface area (BSA) for fludarabine dosing is based on adjusted ideal body weight (IBW) (Appendix K).
  • creatinine clearance may change during the days fludarabine is given. Adjustment in fludarabine dose due to creatinine changes during conditioning is permitted.
Other Name: Fludara®

Procedure: Infusion of non-T-cell depleted bone marrow on Day 0
  • On Day 0, the harvested bone marrow is infused.
  • Donor bone marrow will be harvested with a target yield of 4 x 108 nucleated cells/kg recipient weight.
  • The lowest acceptable nucleated cells yield is 1.5 x 108 cells/kg recipient weight.

Drug: Busulfan
  • Busulfan ≥ 9mg/kg total dose (IV or PO) on Days -6, -5, -4, -3 (PK monitoring required to achieve a daily area under the curve (AUC) target of 4800-5300 μM*min (Perkins et al., 2012))
  • Busulfan dosing is based on adjusted IBW (Appendix K)
Other Name: Busulfex®

Drug: Post-HCT Cyclophosphamide 50mg/kg IV on Day+3, +4
  • Cy 50mg/kg IV, over 1-2 hours (depending on volume), is given on Day+3 (ideally between 60 and 72 hours after bone marrow infusion) and on Day+4 (approximately 24 hours after Day+3 Cy).
  • Hydration with Cy, management of volume status, and monitoring for hemorrhagic cystitis will follow institutional standards.
  • Mesna is required. Mesna IV dose must be ≥ 80% of the total daily dose of Cy and given in divided doses 30 minutes before and at 3, 6, and 8-9 hours after completion of Cy.
  • Cy is dosed according to IBW, unless the subject weighs less than IBW, in which case these drugs will be dosed according to actual body weight.

Drug: Sirolimus
  • Sirolimus dosing is based on adjusted IBW (Appendix K).
  • Sirolimus prophylaxis is discontinued after the last dose on Day+180, or may be continued if there is GVHD.

For subjects ≥ 18 years old:

  • A one-time sirolimus loading dose, 6 mg PO, is given on Day+5, at least 24 hours after Cy completion.
  • Sirolimus is then continued at a maintenance dose (starting dose 2 mg PO QD), with dose adjustments to maintain a trough of 5 - 15 ng/mL as measured by high performance liquid chromatography (HPLC) or immunoassay.

For subjects < 18 years old:

  • A one-time sirolimus loading dose, 3 mg/m2 PO with the dose not to exceed 6 mg, is given on Day+5, at least 24 hours after Cy completion.
  • Sirolimus is then continued at a maintenance dose (starting dose 1 mg/m2 PO QD, maximum 2 mg PO QD), with dose adjustments to maintain a trough of 5 - 15 ng/mL as measured by HPLC or immunoassay.
Other Names:
  • rapamycin
  • Rapamune®

Drug: Mycophenolate mofetil

MMF begins on Day+5, at least 24 hours after completion of PTCy. MMF dose is 15 mg/kg PO TID (adjusted IBW (Appendix K)) with total daily dose not to exceed 3 grams (i.e. maximum 1 g PO TID).

An equivalent IV dose (1:1 conversion) may instead be given. MMF prophylaxis is discontinued after the last dose on Day+35, or may be continued if there is GVHD.

Other Names:
  • MMF
  • Cellcept®

Drug: G-CSF

Granulocyte-colony stimulating factor (G-CSF): filgrastim or a biosimilar begins on Day+5 at a dose of 5 mcg/kg/day (actual body weight) IV or subcutaneously (SC) (rounding to the nearest vial dose is allowed), until the absolute neutrophil count (ANC) is ≥ 1,000/mm3 over the course of 3 consecutive days.

Additional G-CSF may be administered as warranted.

Other Name: filgrastim

Drug: Post-HCT Mesna

Mesna is required. Mesna IV dose must be ≥ 80% of the total daily dose of Cy and given in divided doses 30 minutes before and at 3, 6, and 8-9 hours after completion of Cy on Day+3 and Day+4.

Mesna is dosed according to IBW, unless the subject weighs less than IBW, in which case Mesna will be dosed according to actual body weight.


Active Comparator: Regimen C (FIC: Cy/TBI)
  1. Cyclophosphamide 50mg/kg/day IV on Days -5,-4
  2. Total Body Irradiation (TBI) 200cGy twice a day on Days -3, -2, -1
  3. Infusion of non-T-cell depleted bone marrow on Day 0

Although a schedule is proposed above, the regimen can be given according to institutional standards as long as the prescribed doses are the same as in the recommended regimen above.

Procedure: Infusion of non-T-cell depleted bone marrow on Day 0
  • On Day 0, the harvested bone marrow is infused.
  • Donor bone marrow will be harvested with a target yield of 4 x 108 nucleated cells/kg recipient weight.
  • The lowest acceptable nucleated cells yield is 1.5 x 108 cells/kg recipient weight.

Drug: Cyclophosphamide 50mg/kg/day IV on Days -5,-4
  • Cy 50mg/kg/day is administered as a 1-2 hour IV infusion on Days -5 and -4 after hydration.
  • Use of Mesna and dosing will be done according to institutional standards. A recommended approach is as follows: Mesna IV dose of ≥ 80% of the total daily dose of Cy and given in divided doses 30 minutes before and at 3, 6, and 8-9 hours after completion of Cy.
  • Hydration prior to Cy may be given according to institutional guideline.
  • Cy and mesna are dosed according to adjusted IBW (Appendix K), unless the subject weighs less than IBW, in which case these drugs will be dosed according to actual weight.
Other Name: Cytoxan®

Radiation: Total Body Irradiation (TBI) 200cGy twice a day on Days -3, -2, -1
  • 200cGy TBI is administered in twice daily on Days -3, -2, and -1.
  • Radiation sources, dose rates, and shielding follow institutional practice.

Drug: Post-HCT Cyclophosphamide 50mg/kg IV on Day+3, +4
  • Cy 50mg/kg IV, over 1-2 hours (depending on volume), is given on Day+3 (ideally between 60 and 72 hours after bone marrow infusion) and on Day+4 (approximately 24 hours after Day+3 Cy).
  • Hydration with Cy, management of volume status, and monitoring for hemorrhagic cystitis will follow institutional standards.
  • Mesna is required. Mesna IV dose must be ≥ 80% of the total daily dose of Cy and given in divided doses 30 minutes before and at 3, 6, and 8-9 hours after completion of Cy.
  • Cy is dosed according to IBW, unless the subject weighs less than IBW, in which case these drugs will be dosed according to actual body weight.

Drug: Sirolimus
  • Sirolimus dosing is based on adjusted IBW (Appendix K).
  • Sirolimus prophylaxis is discontinued after the last dose on Day+180, or may be continued if there is GVHD.

For subjects ≥ 18 years old:

  • A one-time sirolimus loading dose, 6 mg PO, is given on Day+5, at least 24 hours after Cy completion.
  • Sirolimus is then continued at a maintenance dose (starting dose 2 mg PO QD), with dose adjustments to maintain a trough of 5 - 15 ng/mL as measured by high performance liquid chromatography (HPLC) or immunoassay.

For subjects < 18 years old:

  • A one-time sirolimus loading dose, 3 mg/m2 PO with the dose not to exceed 6 mg, is given on Day+5, at least 24 hours after Cy completion.
  • Sirolimus is then continued at a maintenance dose (starting dose 1 mg/m2 PO QD, maximum 2 mg PO QD), with dose adjustments to maintain a trough of 5 - 15 ng/mL as measured by HPLC or immunoassay.
Other Names:
  • rapamycin
  • Rapamune®

Drug: Mycophenolate mofetil

MMF begins on Day+5, at least 24 hours after completion of PTCy. MMF dose is 15 mg/kg PO TID (adjusted IBW (Appendix K)) with total daily dose not to exceed 3 grams (i.e. maximum 1 g PO TID).

An equivalent IV dose (1:1 conversion) may instead be given. MMF prophylaxis is discontinued after the last dose on Day+35, or may be continued if there is GVHD.

Other Names:
  • MMF
  • Cellcept®

Drug: G-CSF

Granulocyte-colony stimulating factor (G-CSF): filgrastim or a biosimilar begins on Day+5 at a dose of 5 mcg/kg/day (actual body weight) IV or subcutaneously (SC) (rounding to the nearest vial dose is allowed), until the absolute neutrophil count (ANC) is ≥ 1,000/mm3 over the course of 3 consecutive days.

Additional G-CSF may be administered as warranted.

Other Name: filgrastim

Drug: Pre-HCT Mesna on Days -5 and -4

Use of Mesna and dosing will be done according to institutional standards. A recommended approach is as follows: Mesna IV dose of ≥ 80% of the total daily dose of Cy and given in divided doses 30 minutes before and at 3, 6, and 8-9 hours after completion of Cy.

Mesna is dosed according to adjusted IBW (Appendix K), unless the subject weighs less than IBW, in which case Mesna will be dosed according to actual weight.


Drug: Post-HCT Mesna

Mesna is required. Mesna IV dose must be ≥ 80% of the total daily dose of Cy and given in divided doses 30 minutes before and at 3, 6, and 8-9 hours after completion of Cy on Day+3 and Day+4.

Mesna is dosed according to IBW, unless the subject weighs less than IBW, in which case Mesna will be dosed according to actual body weight.





Primary Outcome Measures :
  1. Overall Survival [ Time Frame: 1 year post transplant ]

Secondary Outcome Measures :
  1. Progression-free survival [ Time Frame: 180 days and 365 days post-transplant ]
  2. Transplant-related mortality [ Time Frame: 100 days, 180 days, and 365 days post-transplant ]
  3. Cumulative incidence of neutrophil recovery [ Time Frame: 1 year post transplant ]
  4. Cumulative incidence of platelet recovery [ Time Frame: 1 year post transplant ]
  5. Cumulative incidence of primary graft failure [ Time Frame: 56 days post-transplant ]
  6. Donor Chimerism [ Time Frame: 28 days, 56 days, 100 days, 180 days, and 365 days post-transplant ]
    Peripheral blood chimerism (% of donor chimerism) in whole blood (unsorted)

  7. Peripheral blood chimerism [ Time Frame: 56 days post-transplant ]
    The percentage of subjects with peripheral blood (unsorted) chimerism>95%

  8. Cumulative incidence of acute GVHD [ Time Frame: 100 days post-transplant ]
  9. Cumulative incidence of chronic GVHD [ Time Frame: 180 days and 365 days post-transplant ]
  10. Cumulative incidences of viral reactivations and infections [ Time Frame: 100 days, 180 days and 365 days post-transplant ]
  11. Cumulative incidence of relapse/progression [ Time Frame: 180 days and 365 days post-transplant ]
  12. Cumulative incidences of thrombotic microangiopathy (TMA) and hepatic veno-occlusive disease (VOD)/sinusoidal obstruction syndrome (SOS) [ Time Frame: 1 year post transplant ]
  13. Proportion of subjects proceeding to transplant [ Time Frame: 1 year post transplant ]
  14. Donor Selection Characteristics [ Time Frame: 1 year post transplant ]
    number of mismatches at HLA-A, -B, -C, -DRB1, -DQB1, -DPB1, donor age, donor-recipient CMV serostatus match, donor weight, donor-recipient sex match and donor-recipient ABO group match

  15. Time from search to donor identification [ Time Frame: 1 year post transplant ]
  16. Subgroup analysis of HIV-positive subjects [ Time Frame: 1 year post transplant ]
    If CCR5delta32 homozygous donors are successfully found and used for one or more HIV-positive subjects, a descriptive analysis of baseline characteristics and outcomes for those HIV-positive subjects will be conducted, including the viral load detected over time obtained from collected samples.

  17. Donor clonal hematopoiesis [ Time Frame: 100 days and 365 days post-transplant ]
    The proportion of subjects developing donor clonal hematopoiesis



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   15 Years to 70 Years   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Age ≥ 15 years and < 71 years at the time of signing the informed consent form
  2. Partially HLA-mismatched unrelated donor: HLA typing will be performed at high resolution (allele level) for the HLA-A, -B, -C, and -DRB1 loci; a minimum match of 4/8 at HLA-A, -B, -C, and -DRB1 is required
  3. Product planned for infusion is bone marrow
  4. Disease and disease status:

    1. Acute Leukemias or T lymphoblastic lymphoma in 1st or subsequent complete remission (CR): Acute lymphoblastic leukemia (ALL)/T lymphoblastic lymphoma; acute myelogenous leukemia (AML); acute biphenotypic leukemia (ABL); acute undifferentiated leukemia (AUL)
    2. Myelodysplastic Syndrome (MDS), fulfilling the following criteria: Subjects with de novo MDS who have or have previously had Intermediate-2 or High risk disease as determined by the International Prognostic Scoring System (IPSS). Current Intermediate-2 or High risk disease is not a requirement; Subjects must have < 20% bone marrow blasts, assessed within 60 days of informed consent; Subjects may have received prior therapy for the treatment of MDS prior to enrollment
    3. Chronic Lymphocytic Leukemia (CLL) in CR if RIC is to be used; in CR or partial response (PR) if FIC is to be used
    4. Chronic myeloid leukemia (CML) in 1st or subsequent chronic phase characterized by <10% blasts in the blood or bone marrow.
    5. Chemotherapy-sensitive lymphoma in status other than 1st CR
  5. Performance status: Karnofsky or Lansky score ≥ 60% (Appendix A)
  6. Adequate organ function defined as:

    1. Cardiac: left ventricular ejection fraction (LVEF) at rest ≥ 35% (RIC cohort) or LVEF at rest ≥ 40% (FIC cohort), or left ventricular shortening fraction (LVFS) ≥ 25%
    2. Pulmonary: diffusing capacity of the lungs for carbon monoxide (DLCO), forced expiratory volume (FEV1), forced vital capacity (FVC) ≥ 50% predicted by pulmonary function tests (PFTs)
    3. Hepatic: total bilirubin ≤ 2.5 mg/dL, and alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) < 5 x upper limit of (ULN) (unless disease related)
    4. Renal: serum creatinine (SCr) within normal range for age (see table 2.3). If SCr is outside normal range for age, creatinine clearance (CrCl) > 40 mL/min/1.73m2 must be obtained (measured by 24-hour (hr) urine specimen or nuclear glomerular filtration rate (GFR), or calculated GFR (by Cockcroft-Gault formula for those aged ≥ 18 years; by Original Schwartz estimate for those < 18 years))
  7. Subjects ≥ 18 years of age must have the ability to give informed consent according to applicable regulatory and local institutional requirements. Legal guardian permission must be obtained for subjects < 18 years of age. Pediatric subjects will be included in age appropriate discussion in order to obtain assent.
  8. Subjects with documentation of confirmed HIV-1 infection (i.e. HIV-positive), and a hematologic malignancy who meets all other eligibility requirements must:

    1. Receive only RIC regimen (i.e. Regimen A)
    2. Be willing to comply with effective antiretroviral therapy (ARV)
    3. Have achieved a sustained virologic response for 12 weeks after cessation of hepatitis C antiviral treatment (in HIV-positive subjects with hepatitis C)

Exclusion Criteria:

  1. HLA-matched related or 8/8 allele matched (HLA-A, -B, -C, -DRB1) unrelated donor available. This exclusion does not apply to HIV-positive subjects who have a CCR5delta32 homozygous donor.
  2. Autologous HCT < 3 months prior to the time of signing the informed consent form
  3. Females who are breast-feeding or pregnant
  4. HIV-positive subjects:

    1. Acquired immunodeficiency syndrome (AIDS) related syndromes or symptoms that may pose an excessive risk for transplantation-related morbidity as determined by the Treatment Review Committee (see Appendix D).
    2. Untreatable HIV infection due to multidrug ARV resistance. Subjects with a detectable or standard viral load > 750 copies/mL should be evaluated with an HIV drug resistance test (HIV-1 genotype). The results should be included as part of the ARV review (described in Appendix D).
    3. May not be currently prescribed ritonavir, cobacistat and/or zidovudine
  5. Current uncontrolled bacterial, viral or fungal infection (currently taking medication with evidence of progression of clinical symptoms or radiologic findings)
  6. Prior allogeneic HCT
  7. History of primary idiopathic myelofibrosis
  8. MDS subjects may not receive RIC and must be < 50 years of age at the time of signing the informed consent form

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02793544


Contacts
Contact: Erin Leckrone 763-406-5124 eleckron@NMDP.ORG
Contact: Mike Tierney 763-406-8245 mtierney@nmdp.org

Locations
United States, Florida
Shands HealthCare & University of Florida Recruiting
Gainesville, Florida, United States, 32610
Contact: Maxim Norkin, MD       Maxim.Norkin@medicine.ufl.edu   
Contact: Meghan Vazquez       meghan.vazquez@medicine.ufl.edu   
Principal Investigator: Maxim Norkin, MD         
University of Miami Recruiting
Miami, Florida, United States, 33136
Contact: Antonio Jimenez, MD       amjimenez@miami.edu   
Contact: Kirenia Correa       k.correa@med.miami.edu   
Principal Investigator: Antonio Jimenez, MD         
H. Lee Moffitt Cancer Center and Research Institute Recruiting
Tampa, Florida, United States, 33612
Contact: Farhad Khimani, MD       Farhad.Khimani@moffitt.org   
Contact: Carmen Patton       Carmen.Patton@moffitt.org   
Principal Investigator: Farhad Khimani, MD         
United States, Maryland
University of Maryland Greenebaum Cancer Center Recruiting
Baltimore, Maryland, United States, 21201
Contact: Nancy Hardy, MD       nhardy1@umm.edu   
Contact: Sherri Bauman       sphilip1@umm.edu   
Principal Investigator: Nancy Hardy, MD         
The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Recruiting
Baltimore, Maryland, United States, 21287
Contact: Javier Bolanos Meade, MD       fbolano2@jhmi.edu   
Contact: Leo Luznik, MD       luznile@jhmi.edu   
Principal Investigator: Javier Bolanos Meade, MD         
Principal Investigator: Leo Luznik, MD         
United States, Michigan
Karmanos Cancer Institute Recruiting
Detroit, Michigan, United States, 48201
Contact: Asif Alavi, MD       alavia@karmanos.org   
Contact: Charlotte Brown       brownc@karmanos.org   
Principal Investigator: Asif Alavi, MD         
United States, New York
Memorial Sloan Kettering Cancer Center - Adults Recruiting
New York, New York, United States, 10065
Contact: Brian Shaffer, MD       shaffeb1@mskcc.org   
Contact: Stephanie Chinapen       chinapes@mskcc.org   
Principal Investigator: Brian Shaffer, MD         
United States, North Carolina
University of North Carolina Hospitals Recruiting
Chapel Hill, North Carolina, United States, 27599
Contact: Katarzyna Jamieson, MD       katarzyna_jamieson@med.unc.edu   
Contact: Mary Owen       mary_owen@med.unc.edu   
Principal Investigator: Katarzyna Jamieson, MD         
United States, Ohio
Ohio State Medical Center, James Cancer Center Recruiting
Columbus, Ohio, United States, 43210
Contact: Hannah Choe, MD         
Contact: Nicole Szuminski       Nicole.Szuminski@osumc.edu   
Principal Investigator: Hannah Choe, MD         
United States, Virginia
Virginia Commonwealth University Massey Cancer Center Bone Marrow Transplant Program Recruiting
Richmond, Virginia, United States, 23298
Contact: John McCarty, MD       john.mccarty@vcuhealth.org   
Contact: Kathy Candler       kcandler@mcvh-vcu.edu   
Principal Investigator: John McCarty, MD         
United States, Wisconsin
Froedtert Memorial Lutheran Hospital Recruiting
Milwaukee, Wisconsin, United States, 53226
Contact: Bronwen Shaw, MD, PhD       beshaw@mcw.edu   
Contact: Sharon Yim       syim@mcw.edu   
Principal Investigator: Bronwen Shaw, MD, PhD         
Sponsors and Collaborators
Center for International Blood and Marrow Transplant Research
National Marrow Donor Program
Resource for Clinical Investigation in Blood and Marrow Transplantation
Investigators
Study Chair: Javier Bolaños Meade, MD Sidney Kimmel Comprehensive Cancer Centre at Johns Hopkins
Study Chair: Bronwen E. Shaw, MD, PhD CIBMTR/Medical College of Wisconsin

Responsible Party: Center for International Blood and Marrow Transplant Research
ClinicalTrials.gov Identifier: NCT02793544     History of Changes
Other Study ID Numbers: 15-MMUD
First Posted: June 8, 2016    Key Record Dates
Last Update Posted: June 18, 2018
Last Verified: June 2018

Additional relevant MeSH terms:
Lymphoma
Leukemia
Myelodysplastic Syndromes
Preleukemia
Leukemia, Lymphoid
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Leukemia, Lymphocytic, Chronic, B-Cell
Leukemia, Myeloid
Leukemia, Myeloid, Acute
Leukemia, Biphenotypic, Acute
Neoplasms by Histologic Type
Neoplasms
Lymphoproliferative Disorders
Lymphatic Diseases
Immunoproliferative Disorders
Immune System Diseases
Bone Marrow Diseases
Hematologic Diseases
Precancerous Conditions
Leukemia, B-Cell
Cyclophosphamide
Fludarabine phosphate
Sirolimus
Everolimus
Busulfan
Fludarabine
Mycophenolic Acid
Vidarabine
Mesna
Immunosuppressive Agents