search
Back to results

T-Cell Depletion and Stem Cell Transplant for Immune Deficiencies and Histiocytic Disorders

Primary Purpose

Hemophagocytic Lymphohistiocytosis, X-Linked Lymphoproliferative Disorders, Chediak-Higashi Syndrome

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Stem Cell Transplant
Myeloablative conditioning regimen
Sponsored by
Masonic Cancer Center, University of Minnesota
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hemophagocytic Lymphohistiocytosis focused on measuring Stem Cell Transplant, T-cell depletion, immune deficiencies, Busulfan pharmacokinetics, Non-Malignant Hematological Disorders

Eligibility Criteria

undefined - 55 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Any patient from birth to < 55 years of age fulfilling the following criteria will be eligible for this study. Patients meeting clinical diagnostic criteria for Hemophagocytic Lymphohistiocytosis (HLH) Patients meeting clinical diagnostic criteria or genetic diagnosis of X-linked lymphoproliferative disorder (XLP) and whose disease is ACTIVE but STABLE, or NON-ACTIVE/QUIESCENT. Patients with Chediak-Higashi Syndrome who meet the following diagnostic criteria and whose disease is ACTIVE but STABLE, or NON-ACTIVE/QUIESCENT as defined in Appendix V of the study protocol. Patients with Viral Associated Hemophagocytic Syndrome (VAHS) - if relapsed after other therapy or supportive care. Diagnostic criteria as above for HLH. Disease status must be ACTIVE but STABLE, or NON-ACTIVE/QUIESCENT as defined in Appendix V. It is cautioned that many patients with HLH or familial hemophagocytic lymphohistiocytosis (FHL) will have a viral infection at time of initial presentation and may therefore be misdiagnosed as having VAHS. Griscelli Syndrome Primary immune deficiencies with non-genotypic identical donors only. Progressive Langerhans cell histiocytosis unresponsive to standard therapy. Other non-malignant hematological disorders in which stem cell transplant with a myeloablative regimen is indicated. Diamond Blackfan Anemia if transfusion dependent Schwachman Diamond Syndrome: with cytopenias or transformation to myelodysplastic syndrome (MDS) Kostman's Syndrome (if ANC <500 without GCSF support, or transformation to MDS) Congenital dyserythropoietic anemia if transfusion dependent Amegakaryocytic thrombocytopenia if baseline platelet counts <20,000 or requiring transfusions. Cardiac, hepatic, renal and pulmonary function deemed adequate for high dose chemotherapy with stem cell rescue as per institutional standards. General guidelines are as follows: Cardiac: Asymptomatic or, if symptomatic, then left ventricular ejection fraction at rest must be > 40% and must improve with exercise, or shortening fraction by echocardiogram must be within institutional normals Hepatic: < 3 x normal SGOT and < 2.5 mg/dL serum bilirubin Renal: Serum creatinine within normal range, or if serum creatinine outside normal range then creatinine clearance or glomerular filtration study should be > 50% of normal. Pulmonary: Asymptomatic or, if symptomatic, diffusing capacity of the lung for carbon monoxide (DLCO) > 45% of predicted (corrected for hemoglobin). For children unable to perform pulmonary function testing, then oxygen saturation should be >95%. Availability of a suitable allogeneic bone marrow donor as per current institutional guidelines for non-T cell depleted hematopoietic stem cell transplant (HSCT). Patients who have undergone previous stem cell transplant (SCT) and failed engraftment or who had relapse of their disease are considered eligible if they meet other eligibility criteria and if the second SCT would occur 6 months or more after the first. If the first SCT preparative regimen was of a non-myeloablative intensity then the second SCT could be performed earlier when the acute toxicity from that procedure was resolved. Exclusion Criteria: Patients who are moribund or whose life expectancy is severely limited by disease other than their underlying disorder. Karnofsky performance status < 70% or Lansky < 50% for patients < 16 years. Patients with hemophagocytic disorders secondary to underlying malignancy. Patients who have ACTIVE/UNSTABLE disease as defined in Appendix V. Significant active infections, including Human Immunodeficiency Virus (HIV). Age > 55 years. Not providing informed consent.

Sites / Locations

  • Masonic Cancer Center, University of Minnesota

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intent-To-Treat

Arm Description

Patients who were treated with chemotherapies (myeloablative conditioning regimen) and stem cell transplant. Busulfan intravenously for 4 days followed by cyclophosphamide intravenously for 4 days. Rabbit ATG is given intravenously for 4 doses pre-transplant.

Outcomes

Primary Outcome Measures

Time to Transplant Engraftment

Secondary Outcome Measures

Number of Patients With Treatment Related Mortality.
Number of Patients Surviving (Disease-free)
Number of Patients With Grade II-IV Graft-Versus-Host Disease (GVHD)
Number of Patients With Graft Failure
Number of Patients With III-IV Graft-Versus-Host Disease (GVHD)
Number of Patients Surviving (Disease-free)

Full Information

First Posted
September 12, 2005
Last Updated
December 29, 2017
Sponsor
Masonic Cancer Center, University of Minnesota
search

1. Study Identification

Unique Protocol Identification Number
NCT00176826
Brief Title
T-Cell Depletion and Stem Cell Transplant for Immune Deficiencies and Histiocytic Disorders
Official Title
In-vivo T-cell Depletion and Hematopoietic Stem Cell Transplantation for Life-Threatening Immune Deficiencies and Histiocytic Disorders
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Terminated
Why Stopped
Replaced by another protocol
Study Start Date
September 2000 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
August 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Masonic Cancer Center, University of Minnesota

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The hypothesis is to determine if a preparative regimen of busulfan, cyclophosphamide, and antithymocyte globulin (ATG) plus allogeneic stem cell transplantation will be effective in the treatment of immune deficiencies and histiocytic disorders.
Detailed Description
Subjects will begin chemotherapy as a preparative regimen, which is intended to completely eliminate their defective immune system and bone marrow. The preparative regimen consists of the chemotherapy drugs (busulfan, cyclophosphamide, and antithymocyte globulin (ATG)). Transplantation: subjects will then have a source of blood stem cells (bone marrow) from their donor administered into their catheter. Medication will be given to help prevent Graft-Versus Host Disease (GVHD). The ATG will help to deplete the donor stem cells of the type of cells that can cause GVHD and will also help to promote engraftment of the new stem cells. Recovery Phase: The second phase of treatment consists of a period after transplantation during which we wait for the return of bone marrow function. This usually takes two to four weeks. Subjects will be given a blood cell growth factor, G-CSF, to help speed recovery of the white blood cells and potentially decrease the risk of infection and decrease the time until the bone marrow recovers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemophagocytic Lymphohistiocytosis, X-Linked Lymphoproliferative Disorders, Chediak-Higashi Syndrome, Griscelli Syndrome, Immunologic Diseases, Langerhans-Cell Histiocytosis, Hematologic Diseases
Keywords
Stem Cell Transplant, T-cell depletion, immune deficiencies, Busulfan pharmacokinetics, Non-Malignant Hematological Disorders

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
22 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intent-To-Treat
Arm Type
Experimental
Arm Description
Patients who were treated with chemotherapies (myeloablative conditioning regimen) and stem cell transplant. Busulfan intravenously for 4 days followed by cyclophosphamide intravenously for 4 days. Rabbit ATG is given intravenously for 4 doses pre-transplant.
Intervention Type
Procedure
Intervention Name(s)
Stem Cell Transplant
Other Intervention Name(s)
HSCT
Intervention Description
Infusion of hematopoietic stem cells (bone marrow, cord blood, peripheral blood stem cells) following myeloablative conditioning regimen.
Intervention Type
Drug
Intervention Name(s)
Myeloablative conditioning regimen
Other Intervention Name(s)
Busulfex, Cytoxan, ATG
Intervention Description
Busulfan intravenously for 4 days followed by cyclophosphamide intravenously for 4 days. Rabbit ATG is given intravenously for 4 doses pre-transplant.
Primary Outcome Measure Information:
Title
Time to Transplant Engraftment
Time Frame
Day 100 Post Transplant
Secondary Outcome Measure Information:
Title
Number of Patients With Treatment Related Mortality.
Time Frame
Day 100 Post Transplant
Title
Number of Patients Surviving (Disease-free)
Time Frame
1 year
Title
Number of Patients With Grade II-IV Graft-Versus-Host Disease (GVHD)
Time Frame
Day 100 Post Transplant
Title
Number of Patients With Graft Failure
Time Frame
Day 100 Post transplant
Title
Number of Patients With III-IV Graft-Versus-Host Disease (GVHD)
Time Frame
Day 100 Post Transplant
Title
Number of Patients Surviving (Disease-free)
Time Frame
3 years

10. Eligibility

Sex
All
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Any patient from birth to < 55 years of age fulfilling the following criteria will be eligible for this study. Patients meeting clinical diagnostic criteria for Hemophagocytic Lymphohistiocytosis (HLH) Patients meeting clinical diagnostic criteria or genetic diagnosis of X-linked lymphoproliferative disorder (XLP) and whose disease is ACTIVE but STABLE, or NON-ACTIVE/QUIESCENT. Patients with Chediak-Higashi Syndrome who meet the following diagnostic criteria and whose disease is ACTIVE but STABLE, or NON-ACTIVE/QUIESCENT as defined in Appendix V of the study protocol. Patients with Viral Associated Hemophagocytic Syndrome (VAHS) - if relapsed after other therapy or supportive care. Diagnostic criteria as above for HLH. Disease status must be ACTIVE but STABLE, or NON-ACTIVE/QUIESCENT as defined in Appendix V. It is cautioned that many patients with HLH or familial hemophagocytic lymphohistiocytosis (FHL) will have a viral infection at time of initial presentation and may therefore be misdiagnosed as having VAHS. Griscelli Syndrome Primary immune deficiencies with non-genotypic identical donors only. Progressive Langerhans cell histiocytosis unresponsive to standard therapy. Other non-malignant hematological disorders in which stem cell transplant with a myeloablative regimen is indicated. Diamond Blackfan Anemia if transfusion dependent Schwachman Diamond Syndrome: with cytopenias or transformation to myelodysplastic syndrome (MDS) Kostman's Syndrome (if ANC <500 without GCSF support, or transformation to MDS) Congenital dyserythropoietic anemia if transfusion dependent Amegakaryocytic thrombocytopenia if baseline platelet counts <20,000 or requiring transfusions. Cardiac, hepatic, renal and pulmonary function deemed adequate for high dose chemotherapy with stem cell rescue as per institutional standards. General guidelines are as follows: Cardiac: Asymptomatic or, if symptomatic, then left ventricular ejection fraction at rest must be > 40% and must improve with exercise, or shortening fraction by echocardiogram must be within institutional normals Hepatic: < 3 x normal SGOT and < 2.5 mg/dL serum bilirubin Renal: Serum creatinine within normal range, or if serum creatinine outside normal range then creatinine clearance or glomerular filtration study should be > 50% of normal. Pulmonary: Asymptomatic or, if symptomatic, diffusing capacity of the lung for carbon monoxide (DLCO) > 45% of predicted (corrected for hemoglobin). For children unable to perform pulmonary function testing, then oxygen saturation should be >95%. Availability of a suitable allogeneic bone marrow donor as per current institutional guidelines for non-T cell depleted hematopoietic stem cell transplant (HSCT). Patients who have undergone previous stem cell transplant (SCT) and failed engraftment or who had relapse of their disease are considered eligible if they meet other eligibility criteria and if the second SCT would occur 6 months or more after the first. If the first SCT preparative regimen was of a non-myeloablative intensity then the second SCT could be performed earlier when the acute toxicity from that procedure was resolved. Exclusion Criteria: Patients who are moribund or whose life expectancy is severely limited by disease other than their underlying disorder. Karnofsky performance status < 70% or Lansky < 50% for patients < 16 years. Patients with hemophagocytic disorders secondary to underlying malignancy. Patients who have ACTIVE/UNSTABLE disease as defined in Appendix V. Significant active infections, including Human Immunodeficiency Virus (HIV). Age > 55 years. Not providing informed consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Angela Smith, MD
Organizational Affiliation
University of Minnesota Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Masonic Cancer Center, University of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55455
Country
United States

12. IPD Sharing Statement

Learn more about this trial

T-Cell Depletion and Stem Cell Transplant for Immune Deficiencies and Histiocytic Disorders

We'll reach out to this number within 24 hrs