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Tacrolimus and Mycophenolate Mofetil as Post-Grafting Immunosuppression

Primary Purpose

Graft Versus Host Disease

Status
Unknown status
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Tacrolimus and MMF.
Sponsored by
Colorado Blood Cancer Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Graft Versus Host Disease focused on measuring TACROLIMUS, MYCOPHENOLATE MOFETIL, FLUDARABINE, HLA-MATCHED, MIS-MATCHED

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with AML, ALL, CML, CLL, myelodysplastic syndrome (MDS), NHL, Hodgkin's disease (HD), paroxysmal nocturnal hemoglobinuria (PNH), hypoproliferative dysplasia with or without increased blasts, or myeloma, who are at significantly higher than usual risk for mortality from conventional myeloablative allogeneic SCT due to age or comorbidities:
  • Age ≥ to 50 years with AML or ALL in complete remission or with <18% blasts in bone marrow
  • Age ≥ to 50 years with MDS or CML.
  • Age 16 to 75 years with lymphomas or myeloma, who have failed chemotherapy and are not candidates for an autologous transplant, or who have failed a prior autologous SCT.
  • Patients of any age with CLL or low-grade NHL. Patients with CLL and low-grade NHL need to have failed at least first-line treatment, with an alkylating agent, fludarabine or 2-chlorodeoxyadenosine (2-CDA), or anti-CD20 monoclonal antibody rituximab.
  • Patients of any age with marrow failure
  • Patients ≥60 years old will first be considered for an allogeneic stem cell transplant from a family member and will be offered an unrelated donor transplant only if no suitable family member, preferably an HLA-matched sibling, is available.
  • Patients with hematological malignancy relapsed after prior auto transplantation.
  • Patients at high-risk (>60%) of relapsing after autologous transplantation for hematological malignancies may receive allogeneic transplant as "consolidative immunotherapy". Diagnoses include MM, non-HL, HL, AML, ALL and MDS. Minimal duration between auto and allo transplants is 4 weeks.
  • Patients of any age with hematologic malignancies treatable by allo SCT, who, because of pre-existing medical conditions or the disease itself (Fanconi anemia or PNH), are considered to be at significantly increased risk for transplant toxicity using high-dose transplantation regimens.
  • Patients with metastatic renal cell carcinoma. Must have include good performance status (Karnofsky score ≥ 60%), no active brain metastases, life expectancy of at least 6 months, absence of bulky liver metastases. Patients will be treated on other active disease-specific protocols when available.
  • Patients with other malignant diseases treatable with allogeneic SCT may be eligible for this protocol on a case by case basis, if approved by the principal investigator and the BMT attending physicians group.
  • Available HLA-identical, a one-antigen mis-matched sibling donor, a phenotypically HLA-matched family member, a phenotypically matched unrelated donor, or a 9/10 matched unrelated donor.
  • Age ≤ 75 years.

Exclusion Criteria:

  • Patients with hematological malignancies eligible for a curative autologous SCT: intermediate- or high-grade NHL with chemo-sensitive first relapse.
  • HD with chemo-sensitive first relapse.
  • Otherwise healthy patients who are eligible for a conventional myeloablative allogeneic SCT.
  • Patients with rapidly progressive intermediate or high-grade NHL, unless in minimal disease state after the last treatment.
  • Patients with active uncontrolled CNS involvement with malignancy.
  • Fertile men or women unwilling to use contraceptive techniques during and for 12 months following treatment.
  • Females who are pregnant.
  • Patients who are HIV positive
  • Organ dysfunction

    • Left ventricle ejection fraction < 35%.
    • DLCO <35% of predicted, or receiving continuous supplementary oxygen.
    • Liver function tests: total bilirubin >2x the upper limit of normal, and/or transaminases >4x the upper limit of normal.
    • Karnofsky score <50 for patients < 60 years, or <70 for patients aged 60 - 69 years
    • Creatinine clearance < 60 ml/min.
    • Patients with hypertension that is poorly controlled on antihypertensive therapy.
    • Patients with a positive PRA or anti-donor T or B cell (+) will be considered for this treatment protocol only if no other option is available.

Sites / Locations

  • Colorado Blood Cancer InstituteRecruiting

Arms of the Study

Arm 1

Arm Type

No Intervention

Arm Label

Tacrolimus and Mycophenolate Mofetil

Arm Description

Non-myeloablative allogeneic SCT from an HLA-Identical or non-identical family onor or unrelated donors, with fludarabine and low-dose TBI, with immunosuppression utilizing tacrolimus and MMF.

Outcomes

Primary Outcome Measures

Engraftment
To measure safe, stable engraftment using Tacrolimus and Mycophenolate Mofetil as post-grafting immunosuppression in patients following conditioning with fludarabine and total-body irradiation for allogeneic stem cell transplant.

Secondary Outcome Measures

Graft Versus Host Disease
To measure the incidence of grade II-IV GVHD associated with Tacrolimus and Mycophenolate Mofetil as post-grafting immunosuppression.

Full Information

First Posted
May 16, 2014
Last Updated
June 27, 2014
Sponsor
Colorado Blood Cancer Institute
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1. Study Identification

Unique Protocol Identification Number
NCT02178683
Brief Title
Tacrolimus and Mycophenolate Mofetil as Post-Grafting Immunosuppression
Official Title
Tacrolimus and Mycophenolate Mofetil as Post-Grafting Immunosuppression After Conditioning With Fludarabine and Low-Dose Total Body Irradiation for Recipients of HLA-Matched or Mis-Matched Family or Unrelated Donor HCT
Study Type
Interventional

2. Study Status

Record Verification Date
June 2014
Overall Recruitment Status
Unknown status
Study Start Date
November 2010 (undefined)
Primary Completion Date
December 2016 (Anticipated)
Study Completion Date
December 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Colorado Blood Cancer Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This protocol will evaluate Tacrolimus and MMF after conditioning with fludarabine and low-dose TBI in patients who are not candidates for conventional allografting. A novel approach to immunosuppression will be tested incorporating an early but extended taper of Tacrolimus starting on day +80 or in the case of relapse. The goal is to induce early immunity and GVT effects without compromising GVHD control. The anti-metabolite MMF will be re-introduced on day +100 to try and induce tolerance and block chronic GVHD during the taper of the Tacrolimus. DLI may be given in the presence of disease progression but not for mixed chimerism as in previous protocols.
Detailed Description
OBJECTIVES Major Objectives A. To determine whether stable allogeneic hematopoietic engraftment can be safely established in patients receiving a non-myeloablative allogeneic SCT from an HLA-Identical or non-identical family donor or unrelated donors, with fludarabine and low-dose TBI, with immunosuppression utilizing tacrolimus and MMF. B. To evaluate the incidence of grade II-IV GVHD associated with this treatment. C. To evaluate the engraftment when donors who are not HLA-identical family members are utilized for allogeneic stem cell transplantation. D. To evaluate the incidence of GVHD using three times per day MMF after unrelated donor stem cell transplants or two times per day MMF after family donor stem cell transplant. Minor Objectives A. To evaluate the incidence of chronic GVHD utilizing Tac/MMF with peripheral blood stem cells from matched or mis-matched allogeneic donors. B. To evaluate disease responses and survival after Flu/TBI allogeneic SCT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Graft Versus Host Disease
Keywords
TACROLIMUS, MYCOPHENOLATE MOFETIL, FLUDARABINE, HLA-MATCHED, MIS-MATCHED

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Tacrolimus and Mycophenolate Mofetil
Arm Type
No Intervention
Arm Description
Non-myeloablative allogeneic SCT from an HLA-Identical or non-identical family onor or unrelated donors, with fludarabine and low-dose TBI, with immunosuppression utilizing tacrolimus and MMF.
Intervention Type
Drug
Intervention Name(s)
Tacrolimus and MMF.
Other Intervention Name(s)
Cellcept, MYCOPHENOLATE MOFETIL
Intervention Description
First dose of Tacrolimus is given day -4, this continues through day +365. First dose of MMF is given within 4 hours of stem cell infusion, this continues through day +365.
Primary Outcome Measure Information:
Title
Engraftment
Description
To measure safe, stable engraftment using Tacrolimus and Mycophenolate Mofetil as post-grafting immunosuppression in patients following conditioning with fludarabine and total-body irradiation for allogeneic stem cell transplant.
Time Frame
Post 100 days
Secondary Outcome Measure Information:
Title
Graft Versus Host Disease
Description
To measure the incidence of grade II-IV GVHD associated with Tacrolimus and Mycophenolate Mofetil as post-grafting immunosuppression.
Time Frame
Post 100 days
Other Pre-specified Outcome Measures:
Title
Survival
Description
Overall survival will be followed
Time Frame
Post 100 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with AML, ALL, CML, CLL, myelodysplastic syndrome (MDS), NHL, Hodgkin's disease (HD), paroxysmal nocturnal hemoglobinuria (PNH), hypoproliferative dysplasia with or without increased blasts, or myeloma, who are at significantly higher than usual risk for mortality from conventional myeloablative allogeneic SCT due to age or comorbidities: Age ≥ to 50 years with AML or ALL in complete remission or with <18% blasts in bone marrow Age ≥ to 50 years with MDS or CML. Age 16 to 75 years with lymphomas or myeloma, who have failed chemotherapy and are not candidates for an autologous transplant, or who have failed a prior autologous SCT. Patients of any age with CLL or low-grade NHL. Patients with CLL and low-grade NHL need to have failed at least first-line treatment, with an alkylating agent, fludarabine or 2-chlorodeoxyadenosine (2-CDA), or anti-CD20 monoclonal antibody rituximab. Patients of any age with marrow failure Patients ≥60 years old will first be considered for an allogeneic stem cell transplant from a family member and will be offered an unrelated donor transplant only if no suitable family member, preferably an HLA-matched sibling, is available. Patients with hematological malignancy relapsed after prior auto transplantation. Patients at high-risk (>60%) of relapsing after autologous transplantation for hematological malignancies may receive allogeneic transplant as "consolidative immunotherapy". Diagnoses include MM, non-HL, HL, AML, ALL and MDS. Minimal duration between auto and allo transplants is 4 weeks. Patients of any age with hematologic malignancies treatable by allo SCT, who, because of pre-existing medical conditions or the disease itself (Fanconi anemia or PNH), are considered to be at significantly increased risk for transplant toxicity using high-dose transplantation regimens. Patients with metastatic renal cell carcinoma. Must have include good performance status (Karnofsky score ≥ 60%), no active brain metastases, life expectancy of at least 6 months, absence of bulky liver metastases. Patients will be treated on other active disease-specific protocols when available. Patients with other malignant diseases treatable with allogeneic SCT may be eligible for this protocol on a case by case basis, if approved by the principal investigator and the BMT attending physicians group. Available HLA-identical, a one-antigen mis-matched sibling donor, a phenotypically HLA-matched family member, a phenotypically matched unrelated donor, or a 9/10 matched unrelated donor. Age ≤ 75 years. Exclusion Criteria: Patients with hematological malignancies eligible for a curative autologous SCT: intermediate- or high-grade NHL with chemo-sensitive first relapse. HD with chemo-sensitive first relapse. Otherwise healthy patients who are eligible for a conventional myeloablative allogeneic SCT. Patients with rapidly progressive intermediate or high-grade NHL, unless in minimal disease state after the last treatment. Patients with active uncontrolled CNS involvement with malignancy. Fertile men or women unwilling to use contraceptive techniques during and for 12 months following treatment. Females who are pregnant. Patients who are HIV positive Organ dysfunction Left ventricle ejection fraction < 35%. DLCO <35% of predicted, or receiving continuous supplementary oxygen. Liver function tests: total bilirubin >2x the upper limit of normal, and/or transaminases >4x the upper limit of normal. Karnofsky score <50 for patients < 60 years, or <70 for patients aged 60 - 69 years Creatinine clearance < 60 ml/min. Patients with hypertension that is poorly controlled on antihypertensive therapy. Patients with a positive PRA or anti-donor T or B cell (+) will be considered for this treatment protocol only if no other option is available.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Juli Murphy
Phone
720-754-4890
Email
Juli.Murphy@healthonecares.com
First Name & Middle Initial & Last Name or Official Title & Degree
Nicole Stephens, RN
Phone
720-754-4891
Email
Nicole.Stephens@healthonecares.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark W Brunvand, MD
Organizational Affiliation
Colorado Blood Cancer Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Colorado Blood Cancer Institute
City
Denver
State/Province
Colorado
ZIP/Postal Code
80218
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Juli B Murphy
Phone
720-754-4890
Email
Juli.Murphy@healthonecares.com
First Name & Middle Initial & Last Name & Degree
Mark Brunvand, MD
Phone
720-754-4800
Email
Mark.Brunvand@healthonecares.com
First Name & Middle Initial & Last Name & Degree
Mark Brunvand, MD
First Name & Middle Initial & Last Name & Degree
Peter McSweeney, MD
First Name & Middle Initial & Last Name & Degree
Michael Maris, MD
First Name & Middle Initial & Last Name & Degree
Jeff Matous, MD
First Name & Middle Initial & Last Name & Degree
Scott Bearman, MD
First Name & Middle Initial & Last Name & Degree
Tara Gregory, MD
First Name & Middle Initial & Last Name & Degree
Richard Nash, MD

12. IPD Sharing Statement

Learn more about this trial

Tacrolimus and Mycophenolate Mofetil as Post-Grafting Immunosuppression

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