Planned Donor Lymphocyte Infusion (DLI) After Allogeneic Stem Cell Transplantation (SCT)

Sponsor
M.D. Anderson Cancer Center (Other)
Overall Status
Terminated
CT.gov ID
NCT01518153
Collaborator
(none)
16
1
2
30
0.5

Study Details

Study Description

Brief Summary

The goal of this clinical research study is to learn what dose of a kind of immune cell called T-lymphocytes (T-cells) given as a donor infusion about 8-9 weeks after a stem cell transplant has the best results. The safety of this treatment will also be studied. This will be tested in patients with leukemia, MDS, lymphoma, Hodgkin disease, and multiple myeloma. These results are measured as helping to control the disease without severe graft-versus-host disease (GvHD). GvHD is when transplanted donor tissue attacks the tissues of the recipient's body.

Fludarabine, melphalan, and alemtuzumab are commonly given before stem cell transplants:
  • Fludarabine is designed to interfere with the DNA (genetic material) of cancer cells, which may cause the cancer cells to die.

  • Melphalan is designed to bind to the DNA of cells, which may cause cancer cells to die.

  • Alemtuzumab is designed to weaken the immune system and reduce the risk of rejection of the transplant and graft-vs-host disease (GvHD).

The donor infusion of T-cells is designed to help restore the immune system after the transplant, cause an immune reaction against the cancer, and reduce the risk of the cancer coming back.

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

Study Groups:

If you agree to take part in this study, you will be randomly assigned (as in the flip of a coin) to 1 of 2 study groups involving the dose of T-cells in the donor lymphocyte infusion.

  • Group 1 will receive a low dose of donor T-cells.

  • Group 2 will receive a higher dose of donor T-cells than Group 1.

Both you and your study doctor will know which group you are in. Both groups will have a stem cell transplant. The stem cells will be given by vein. The cells will travel to your bone marrow where they are designed to make healthy, new blood cells after several weeks.

Study Drug Administration:

Patients receive fludarabine, melphalan and alemtuzumab to kill malignant cells and suppress immunity to prevent rejection of the stem cell transplant. The day you receive the stem cells is called Day 0. The days before you receive your stem cells are called minus days. The days after you receive the stem cells are called plus days.

On Day -7, you will be admitted to the hospital and given fluids by vein to hydrate you.

On Days -6 through -3, you will receive fludarabine by vein over 1 hour each day.

On Day -2, you will receive melphalan by vein over 30 minutes.

On Day -1, you will receive alemtuzumab by vein over 2 hours.

On Day 0, you will receive the stem cell transplant as a cell infusion by vein.

After the transplant, you will receive tacrolimus and methotrexate. At first, you will receive tacrolimus as a continuous (nonstop) infusion until you are able to take it by mouth. You will then take tacrolimus by mouth 2 times a day for about 5 weeks and then your doctor will tell you how to taper it off (gradually stop taking it). On Days 1, 3, and 6 after the transplant, you will receive methotrexate by vein over 30 minutes.

You will receive filgrastim as an injection under the skin 1 time a day, starting 1 week after the transplant, until your blood cell levels return to normal. Filgrastim is designed to help with the growth of white blood cells.

Between Day +56 and +64, if you are in stable medical condition and have not developed GvHD, you will receive a donor lymphocyte infusion containing T-cells by vein over 10-30 minutes. You will receive Benadryl (diphenhydramine) by vein over 15 minutes before the infusion to lower the risk of an allergic reaction.

Study Visits:
Before the T-cell infusion:
  • You will have a physical exam, including measurement of your vital signs (blood pressure, heart rate, temperature, and breathing rate).

  • You will be asked about how you are feeling and about any side effects you may be having.

  • Blood (about 2 teaspoons) will be drawn to see how well the transplant has "taken".

  • You will have a bone marrow aspiration and biopsy to check the status of the disease, if your doctor thinks it is needed. To collect a bone marrow aspiration/biopsy, an area of the hip or other site is numbed with anesthetic, and a small amount of bone marrow and bone is withdrawn through a large needle.

After the T-cell infusion, you will have a physical exam every week for at least 6 weeks.

About 3, 6, and 12 months after the transplant:
  • You will have a physical exam, including measurement of your vital signs.

  • You will be asked about how you are feeling and about any side effects you may be having.

  • Blood (about 4 tablespoons) will be drawn for routine tests and to check the level of the infused T-cells, for immune function tests, and to check the status of the disease.

  • You will have a bone marrow aspiration, blood tests and CT scans as medically necessary to check the status of the disease, if your doctor thinks it is needed.

During the study, you will have blood draws (about 2 teaspoons) and urine will be collected for routine tests, to check your blood counts, kidney and liver function, and/or to check for infections as often as the doctor thinks is needed during this time.

Length of Treatment:

You will be off study after your 12-month follow-up visit. You will be taken off study early if you have graft failure (the donor cells did not "take") or if the cancer comes back and needs another treatment.

This is an investigational study. Melphalan, fludarabine, and alemtuzumab are FDA approved and commercially available for the treatment of blood cancers. Donor T-cell infusions are commonly used to treat blood cancers that come back after a stem cell transplant. The investigational part of this study is to find the best dose of T-cells that are given with the goal of helping to prevent the cancer from coming back.

Up to 56 patients will take part in this study. All will be enrolled at MD Anderson.

Study Design

Study Type:
Interventional
Actual Enrollment :
16 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Phase 2 Study of Planned Donor Lymphocyte Infusion After Reduced Intensity Allogeneic Stem Cell Transplantation
Study Start Date :
Feb 1, 2012
Actual Primary Completion Date :
Aug 1, 2014
Actual Study Completion Date :
Aug 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: Low Dose Donor T-Cells

Fludarabine 40 mg/m^2 by vein on Day -6 to -3. Melphalan 140 mg/m^2 by vein on Day -2. Alemtuzumab 50 mg by vein on Day -1. Reduced intensity stem cell transplant on Day 0. Planned Donor Lymphocyte Infusion CD3+ cells: 3 * 106 CD3+ cells/kg between Day +56 and +64. Tacrolimus 0.015 mg/kg by vein as a 24 hour continuous infusion daily adjusted to achieve a therapeutic level of 5-15 ng/ml (target is 10 ng/ml). Tacrolimus is changed to oral dosing when tolerated. Tapering should start on approximately Day +24 with intention to be completely off drug by approximately Day +35. Methotrexate 5 mg/m2 dosed based on actual body surface area and administered intravenously on days +1, +3, +6. G-CSF 5 mcg/kg/day subcutaneously beginning on Day +7, and continuing until absolute neutrophil count (ANC) is > 500 * 10/L for 3 consecutive days.

Drug: Fludarabine
40 mg/m^2 by vein on Day -6 to -3.
Other Names:
  • Fludarabine Phosphate
  • Fludara
  • Drug: Melphalan
    140 mg/m^2 by vein on Day -2.
    Other Names:
  • Alkeran
  • Drug: Alemtuzumab
    50 mg by vein on Day -1.
    Other Names:
  • CAMPATH-1H
  • Campath
  • Procedure: Stem Cell Infusion
    Reduced intensity stem cell transplant on Day 0.

    Drug: Tacrolimus
    0.015 mg/kg by vein as a 24 hour continuous infusion daily adjusted to achieve a therapeutic level of 5-15 ng/ml (target is 10 ng/ml). Tacrolimus is changed to oral dosing when tolerated. Tapering should start on approximately Day +24 with intention to be completely off drug by approximately Day +35.
    Other Names:
  • Prograf
  • Drug: Methotrexate
    5 mg/m2 dosed based on actual body surface area and administered intravenously on days +1, +3, +6.

    Drug: G-CSF
    5 mcg/kg/day subcutaneously beginning on Day +7, and continuing until absolute neutrophil count (ANC) is > 500 * 10/L for 3 consecutive days.
    Other Names:
  • Filgrastim
  • NeupogenTM
  • Procedure: Low Dose Donor T-Cells
    Planned Donor Lymphocyte Infusion CD3+ cells: 3 * 106 CD3+ cells/kg between Day +56 and +64.

    Experimental: High Dose Donor T-Cells

    Fludarabine 40 mg/m^2 by vein on Day -6 to -3. Melphalan 140 mg/m^2 by vein on Day -2. Alemtuzumab 50 mg by vein on Day -1. Reduced intensity stem cell transplant on Day 0. High Dose Donor T-Cells Planned Donor Lymphocyte Infusion CD3+ cells: 1 * 107 CD3+ cells/kg between Day +56 and +64. Tacrolimus 0.015 mg/kg by vein as a 24 hour continuous infusion daily adjusted to achieve a therapeutic level of 5-15 ng/ml (target is 10 ng/ml). Tacrolimus is changed to oral dosing when tolerated. Tapering should start on approximately Day +24 with intention to be completely off drug by approximately Day +35. Methotrexate 5 mg/m2 dosed based on actual body surface area and administered intravenously on days +1, +3, +6. G-CSF 5 mcg/kg/day subcutaneously beginning on Day +7, and continuing until absolute neutrophil count (ANC) is > 500 * 10/L for 3 consecutive days.

    Drug: Fludarabine
    40 mg/m^2 by vein on Day -6 to -3.
    Other Names:
  • Fludarabine Phosphate
  • Fludara
  • Drug: Melphalan
    140 mg/m^2 by vein on Day -2.
    Other Names:
  • Alkeran
  • Drug: Alemtuzumab
    50 mg by vein on Day -1.
    Other Names:
  • CAMPATH-1H
  • Campath
  • Procedure: Stem Cell Infusion
    Reduced intensity stem cell transplant on Day 0.

    Drug: Tacrolimus
    0.015 mg/kg by vein as a 24 hour continuous infusion daily adjusted to achieve a therapeutic level of 5-15 ng/ml (target is 10 ng/ml). Tacrolimus is changed to oral dosing when tolerated. Tapering should start on approximately Day +24 with intention to be completely off drug by approximately Day +35.
    Other Names:
  • Prograf
  • Drug: Methotrexate
    5 mg/m2 dosed based on actual body surface area and administered intravenously on days +1, +3, +6.

    Drug: G-CSF
    5 mcg/kg/day subcutaneously beginning on Day +7, and continuing until absolute neutrophil count (ANC) is > 500 * 10/L for 3 consecutive days.
    Other Names:
  • Filgrastim
  • NeupogenTM
  • Procedure: High Dose Donor T-Cells
    Planned Donor Lymphocyte Infusion CD3+ cells: 1 * 107 CD3+ cells/kg between Day +56 and +64.

    Outcome Measures

    Primary Outcome Measures

    1. Success Rate [100 days]

      Success rate defined as alive, engrafted without grade 3 or 4 GvHD or relapse at day 100 post allogeneic stem cell transplantation followed by donor lymphocyte infusion (DLI).

    Secondary Outcome Measures

    1. Overall Survival (OS) [Every 3 months until day of death]

      Overall Survival is defined as the interval between day of transplant and day of death.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Age >/= 18 years and </= 65 years with one of the following: a. Acute leukemia past first remission, in first or subsequent relapse, in second or greater remission. Patients in first remission should have intermediate or high cytogenetic risk factors or flt3 mutation. Patients with primary induction failure or relapse are eligible if they have <10% bone marrow blasts, and no circulating blasts. b. Myelodysplastic syndrome with intermediate or high risk IPSS score, or treatment related MDS. c. CML resistant to tyrosine kinase inhibitor treatment in a first or subsequent chronic phase, or in accelerated phase. d. CLL, Lymphoma or Hodgkin's disease which has failed to achieve remission or recurred following initial chemotherapy. Patients must have at least a PR to salvage therapy, or low bulk untreated relapse (<2 cm largest mass). e. Multiple myeloma which has relapsed or progressed and has achieved a partial response to salvage chemotherapy.

    2. Patients must have one of the following donor types identified and willing to donate:

    1. Related donor, HLA-matched for HLA-A, -B, C and DR matched or, b. Matched Unrelated Donor (MUD), HLA-matched for HLA A, B, C and DRB1 using allele level typing.
    1. Performance score of at least 80% by Karnofsky or performance score 0 to 2 (ECOG).

    2. Estimated creatinine clearance >40 ml/min (based on serum creatinine)

    3. Bilirubin <1.5 mg/dl except for Gilbert's disease.

    4. ALT < 300 IU/ml d.

    5. Left ventricular ejection fraction equal or greater than 40%.

    6. Pulmonary function test (PFT) demonstrating a diffusion capacity (corrected for hemoglobin) of least 50% predicted.

    7. Patient or patient's legal representative able to sign informed consent.

    Exclusion Criteria:
    1. Patients who have had prior autologous transplants or prior allogeneic transplants are not eligible.

    2. Uncontrolled active infection.

    3. Positive Beta HCG test in a woman with child bearing potential, defined as not post-menopausal for 12 months or no previous surgical sterilization.

    4. Women of child bearing potential not willing to use an effective contraceptive measure while on study.

    5. Subject has known sensitivity to any of the products that will be administered during the study.

    6. Patients who are HIV seropositive.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Texas MD Anderson Cancer Center Houston Texas United States 77030

    Sponsors and Collaborators

    • M.D. Anderson Cancer Center

    Investigators

    • Principal Investigator: Richard E. Champlin, MD,BS, M.D. Anderson Cancer Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    M.D. Anderson Cancer Center
    ClinicalTrials.gov Identifier:
    NCT01518153
    Other Study ID Numbers:
    • 2011-1104
    • NCI-2012-00131
    First Posted:
    Jan 25, 2012
    Last Update Posted:
    Mar 17, 2016
    Last Verified:
    Feb 1, 2016

    Study Results

    Participant Flow

    Recruitment Details Recruitment Period: February 6, 2012 to February 27, 2014. All recruitment done at The University of Texas (UT) MD Anderson Cancer Center.
    Pre-assignment Detail Sixteen participants have been treated on study and were evaluable for treatment response. Out of 16, 7 participants met the criteria to receive planned Donor Lymphocyte Infusion (DLI). 9 participants did not meet the criteria to receive randomized planned DLI.
    Arm/Group Title Stem Cell Infusion Low Dose Donor T-Cells High Dose Donor T-Cells
    Arm/Group Description Fludarabine 40 mg/m^2 intravenous (IV) administered from Day -6 to -3, Melphalan 140 mg/m^2 IV on Day -2 and Alemtuzumab 50 mg IV on Day -1. Day 0 Stem Cell infusion: Fresh or cryopreserved peripheral blood progenitor cells infused. Fludarabine 40 mg/m^2 intravenous (IV) administered from Day -6 to -3, Melphalan 140 mg/m^2 IV on Day -2 and Alemtuzumab 50 mg IV on Day -1. Day 0 Stem Cell infusion: Fresh or cryopreserved peripheral blood progenitor cells infused. Planned Donor Lymphocyte Infusion CD3+ cells: 1*10^6 CD3+ cells/kg between Day +56 & +64. Tacrolimus 0.015 mg/kg IV as continuous infusion daily to achieve therapeutic level of 5-15 ng/ml (target 10 ng/ml). Tacrolimus changed to oral dosing, tapering approximately Day +35 to off by Day +42. Methotrexate 5 mg/m^2 administered IV days +1, +3, +6. G-CSF 5 mcg/kg/day subcutaneously beginning Day +7, continuing until absolute neutrophil count (ANC)> 500*10/L for 3 consecutive days. Fludarabine 40 mg/m^2 intravenous (IV) administered from Day -6 to -3, Melphalan 140 mg/m^2 IV on Day -2 and Alemtuzumab 50 mg IV on Day -1. Day 0 Stem Cell infusion: Fresh or cryopreserved peripheral blood progenitor cells infused. Planned Donor Lymphocyte Infusion CD3+ cells: 3*10^6 CD3+ cells/kg between Day +56 & +64. Tacrolimus 0.015 mg/kg IV as continuous infusion daily to achieve therapeutic level of 5-15 ng/ml (target 10 ng/ml). Tacrolimus changed to oral dosing, tapering approximately Day +35 to off by Day +42. Methotrexate 5 mg/m^2 administered IV days +1, +3, +6. G-CSF 5 mcg/kg/day subcutaneously beginning Day +7, continuing until absolute neutrophil count (ANC)> 500*10/L for 3 consecutive days.
    Period Title: Stem Cell Transplant
    STARTED 16 0 0
    COMPLETED 7 0 0
    NOT COMPLETED 9 0 0
    Period Title: Stem Cell Transplant
    STARTED 0 3 4
    COMPLETED 0 1 3
    NOT COMPLETED 0 2 1

    Baseline Characteristics

    Arm/Group Title Stem Cell Transplant + Donor Lymphocyte Infusion
    Arm/Group Description Fludarabine 40 mg/m^2 intravenous (IV) administered from Day -6 to -3, Melphalan 140 mg/m^2 IV on Day -2 and Alemtuzumab 50 mg IV on Day -1. Day 0 Stem Cell infusion: Fresh or cryopreserved peripheral blood progenitor cells infused. Planned Donor Lymphocyte Infusion CD3+ cells: 1 x 10^6 CD3+ cells/kg or 3 x 10^6 CD3+ cells/kg between Day +56 & +64. Tacrolimus 0.015 mg/kg IV as continuous infusion daily to achieve therapeutic level of 5-15 ng/ml (target 10 ng/ml). Tacrolimus changed to oral dosing, tapering approximately Day +35 to off by Day +42. Methotrexate 5 mg/m^2 administered IV days +1, +3, +6. G-CSF 5 mcg/kg/day subcutaneously beginning Day +7, continuing until absolute neutrophil count (ANC)> 500*10/L for 3 consecutive days.
    Overall Participants 16
    Age (years) [Median (Full Range) ]
    Median (Full Range) [years]
    58
    Sex: Female, Male (Count of Participants)
    Female
    5
    31.3%
    Male
    11
    68.8%
    Region of Enrollment (participants) [Number]
    United States
    16
    100%

    Outcome Measures

    1. Primary Outcome
    Title Success Rate
    Description Success rate defined as alive, engrafted without grade 3 or 4 GvHD or relapse at day 100 post allogeneic stem cell transplantation followed by donor lymphocyte infusion (DLI).
    Time Frame 100 days

    Outcome Measure Data

    Analysis Population Description
    Sixteen participants have been treated on study and were evaluable for treatment response. Out of 16, 7 participants met the criteria to receive planned DLI. 9 participants did not meet the criteria to receive randomized planned DLI.
    Arm/Group Title Low Dose Donor T-Cells High Dose Donor T-Cells
    Arm/Group Description Fludarabine 40 mg/m^2 intravenous (IV) administered from Day -6 to -3, Melphalan 140 mg/m^2 IV on Day -2 and Alemtuzumab 50 mg IV on Day -1. Day 0 Stem Cell infusion: Fresh or cryopreserved peripheral blood progenitor cells infused. Planned Donor Lymphocyte Infusion CD3+ cells: 1*10^6 CD3+ cells/kg between Day +56 & +64. Tacrolimus 0.015 mg/kg IV as continuous infusion daily to achieve therapeutic level of 5-15 ng/ml (target 10 ng/ml). Tacrolimus changed to oral dosing, tapering approximately Day +35 to off by Day +42. Methotrexate 5 mg/m^2 administered IV days +1, +3, +6. G-CSF 5 mcg/kg/day subcutaneously beginning Day +7, continuing until absolute neutrophil count (ANC)> 500*10/L for 3 consecutive days. Fludarabine 40 mg/m^2 intravenous (IV) administered from Day -6 to -3, Melphalan 140 mg/m^2 IV on Day -2 and Alemtuzumab 50 mg IV on Day -1. Day 0 Stem Cell infusion: Fresh or cryopreserved peripheral blood progenitor cells infused. Planned Donor Lymphocyte Infusion CD3+ cells: 3*10^6 CD3+ cells/kg between Day +56 & +64. Tacrolimus 0.015 mg/kg IV as continuous infusion daily to achieve therapeutic level of 5-15 ng/ml (target 10 ng/ml). Tacrolimus changed to oral dosing, tapering approximately Day +35 to off by Day +42. Methotrexate 5 mg/m^2 administered IV days +1, +3, +6. G-CSF 5 mcg/kg/day subcutaneously beginning Day +7, continuing until absolute neutrophil count (ANC)> 500*10/L for 3 consecutive days.
    Measure Participants 3 4
    Number [participants]
    1
    6.3%
    3
    NaN
    2. Secondary Outcome
    Title Overall Survival (OS)
    Description Overall Survival is defined as the interval between day of transplant and day of death.
    Time Frame Every 3 months until day of death

    Outcome Measure Data

    Analysis Population Description
    Sixteen participants have been treated on study and were evaluable for treatment response. Out of 16, 7 participants met the criteria to receive planned DLI.
    Arm/Group Title Stem Cell Transplant + Donor Lymphocyte Infusion
    Arm/Group Description Fludarabine 40 mg/m^2 intravenous (IV) administered from Day -6 to -3, Melphalan 140 mg/m^2 IV on Day -2 and Alemtuzumab 50 mg IV on Day -1. Day 0 Stem Cell infusion: Fresh or cryopreserved peripheral blood progenitor cells infused. Planned Donor Lymphocyte Infusion CD3+ cells: 1 x 10^6 CD3+ cells/kg or 3 x 10^6 CD3+ cells/kg between Day +56 & +64. Tacrolimus 0.015 mg/kg IV as continuous infusion daily to achieve therapeutic level of 5-15 ng/ml (target 10 ng/ml). Tacrolimus changed to oral dosing, tapering approximately Day +35 to off by Day +42. Methotrexate 5 mg/m^2 administered IV days +1, +3, +6. G-CSF 5 mcg/kg/day subcutaneously beginning Day +7, continuing until absolute neutrophil count (ANC)> 500*10/L for 3 consecutive days.
    Measure Participants 16
    Median (Full Range) [days]
    246

    Adverse Events

    Time Frame Adverse events (AEs) were collected from the start of preparative regimen up to discontinuation of study treatment. Overall collection period: March 30, 2012 to April 15, 2014.
    Adverse Event Reporting Description
    Arm/Group Title Stem Cell Infusion Low Dose Donor T-Cells High Dose Donor T-Cells
    Arm/Group Description Fludarabine 40 mg/m^2 intravenous (IV) administered from Day -6 to -3, Melphalan 140 mg/m^2 IV on Day -2 and Alemtuzumab 50 mg IV on Day -1. Day 0 Stem Cell infusion: Fresh or cryopreserved peripheral blood progenitor cells infused. Fludarabine 40 mg/m^2 intravenous (IV) administered from Day -6 to -3, Melphalan 140 mg/m^2 IV on Day -2 and Alemtuzumab 50 mg IV on Day -1. Day 0 Stem Cell infusion: Fresh or cryopreserved peripheral blood progenitor cells infused. Planned Donor Lymphocyte Infusion CD3+ cells: 1*10^6 CD3+ cells/kg between Day +56 & +64. Tacrolimus 0.015 mg/kg IV as continuous infusion daily to achieve therapeutic level of 5-15 ng/ml (target 10 ng/ml). Tacrolimus changed to oral dosing, tapering approximately Day +35 to off by Day +42. Methotrexate 5 mg/m^2 administered IV days +1, +3, +6. G-CSF 5 mcg/kg/day subcutaneously beginning Day +7, continuing until absolute neutrophil count (ANC)> 500*10/L for 3 consecutive days. Fludarabine 40 mg/m^2 intravenous (IV) administered from Day -6 to -3, Melphalan 140 mg/m^2 IV on Day -2 and Alemtuzumab 50 mg IV on Day -1. Day 0 Stem Cell infusion: Fresh or cryopreserved peripheral blood progenitor cells infused. Planned Donor Lymphocyte Infusion CD3+ cells: 3*10^6 CD3+ cells/kg between Day +56 & +64. Tacrolimus 0.015 mg/kg IV as continuous infusion daily to achieve therapeutic level of 5-15 ng/ml (target 10 ng/ml). Tacrolimus changed to oral dosing, tapering approximately Day +35 to off by Day +42. Methotrexate 5 mg/m^2 administered IV days +1, +3, +6. G-CSF 5 mcg/kg/day subcutaneously beginning Day +7, continuing until absolute neutrophil count (ANC)> 500*10/L for 3 consecutive days.
    All Cause Mortality
    Stem Cell Infusion Low Dose Donor T-Cells High Dose Donor T-Cells
    Affected / at Risk (%) # Events Affected / at Risk (%) # Events Affected / at Risk (%) # Events
    Total / (NaN) / (NaN) / (NaN)
    Serious Adverse Events
    Stem Cell Infusion Low Dose Donor T-Cells High Dose Donor T-Cells
    Affected / at Risk (%) # Events Affected / at Risk (%) # Events Affected / at Risk (%) # Events
    Total 9/9 (100%) 2/3 (66.7%) 4/4 (100%)
    Blood and lymphatic system disorders
    Idiopathic Thrombocytopenic Purpura 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Deep Vein Thrombosis 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Anoxic Brain Injury 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Gastrointestinal disorders
    Enterococcus Faecium Stool Infection 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Gastrointestinal GvHD 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Diarrhea 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    General disorders
    Death 5/9 (55.6%) 5 2/3 (66.7%) 2 1/4 (25%) 1
    Neutropenic Fevers 1/9 (11.1%) 1 0/3 (0%) 0 1/4 (25%) 1
    Pansinusitis 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Hepatobiliary disorders
    Liver GvHD 0/9 (0%) 0 1/3 (33.3%) 1 3/4 (75%) 4
    Immune system disorders
    Secondary Graft Failure 1/9 (11.1%) 1 0/3 (0%) 0 1/4 (25%) 1
    Infections and infestations
    Parvovirus 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Disseminated Cytomegalovirus Infections 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Pseudomonas Bacteremia 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Viral Exanthem 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Staphylococcus Epidermidis Bacteremia 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Candida Albicans 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Pseudomonas Tracheitis 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    BK Virus Associated Hemorrhagic Cystitis 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Adenovirus Viremia 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    HSV Viremia 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Pseudomonas Aeruginosa Infection 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Varicella Zoster 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Clostridium Difficile 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Enterococcus/ASTR Sepsis 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Alpha Hemolytic Strep Bacteremia 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Epstein-Barr Virus Post-Transplant Lymphoproliferative Disease 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Renal and urinary disorders
    Escherichia Coli Urinary Tract Infection 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Staphylococcus Urinary Tract Infection 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Acute Tubular Necrosis 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Renal Insufficiency 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Respiratory, thoracic and mediastinal disorders
    Pneumonia 3/9 (33.3%) 3 0/3 (0%) 0 0/4 (0%) 0
    Pneumocystis Jiroveci (PCP) Pneumonia 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Fusarium Pneumonia 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Pulmonary Nocardiosis 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Pseudomonas Pneumonia 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Respiratory Syncytial Virus Upper Respiratory Illness 1/9 (11.1%) 1 1/3 (33.3%) 1 0/4 (0%) 0
    Aspergillus Terreus Pneumonia 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Vascular disorders
    Diffuse Alveolar Hemorrhage 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Other (Not Including Serious) Adverse Events
    Stem Cell Infusion Low Dose Donor T-Cells High Dose Donor T-Cells
    Affected / at Risk (%) # Events Affected / at Risk (%) # Events Affected / at Risk (%) # Events
    Total 9/9 (100%) 3/3 (100%) 4/4 (100%)
    Cardiac disorders
    Atrial Flutter 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Hypertension 0/9 (0%) 0 1/3 (33.3%) 1 0/4 (0%) 0
    Eye disorders
    Ocular GvHD 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Gastrointestinal disorders
    Diarrhea 4/9 (44.4%) 4 1/3 (33.3%) 1 2/4 (50%) 3
    Mucositis 4/9 (44.4%) 4 1/3 (33.3%) 1 1/4 (25%) 1
    Nausea 9/9 (100%) 9 3/3 (100%) 3 4/4 (100%) 4
    Gastrointestinal GvHD 2/9 (22.2%) 2 0/3 (0%) 0 2/4 (50%) 2
    Upper Gastrointestinal GvHD 1/9 (11.1%) 1 0/3 (0%) 0 3/4 (75%) 4
    Gastrointestinal Bleed 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    HSV Oral Lesions 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Neutropenic Colitis 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Clostridium Difficile Colitis 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    General disorders
    Tacrolimus Induced Headaches 2/9 (22.2%) 2 1/3 (33.3%) 1 0/4 (0%) 0
    Hepatobiliary disorders
    Liver GvHD 0/9 (0%) 0 0/3 (0%) 0 2/4 (50%) 3
    Immune system disorders
    Allergic Reaction due to Campath 0/9 (0%) 0 1/3 (33.3%) 1 1/4 (25%) 1
    Infections and infestations
    Cytomegalovirus Antigenemia 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Cytomegalovirus Reactivation 3/9 (33.3%) 3 3/3 (100%) 3 3/4 (75%) 3
    Enterococcus Faecalis Bacteremia 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Adenovirus Viremia 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Staphylococcus Epidermidis Bacteremia 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Epstein-Barr Viremia 0/9 (0%) 0 0/3 (0%) 0 1/4 (25%) 1
    Metabolism and nutrition disorders
    Fluid Overload 6/9 (66.7%) 6 0/3 (0%) 0 0/4 (0%) 0
    Elevated Alanine Aminotransferase 2/9 (22.2%) 2 2/3 (66.7%) 2 2/4 (50%) 2
    Elevated Bilirubin 4/9 (44.4%) 4 0/3 (0%) 0 1/4 (25%) 1
    Elevated Alkaline Phosphatase 1/9 (11.1%) 1 0/3 (0%) 0 1/4 (25%) 1
    Nervous system disorders
    Headaches 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Psychiatric disorders
    Altered Mental Status Change 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Renal and urinary disorders
    Tacrolimus Induced Renal Insufficiency 3/9 (33.3%) 3 0/3 (0%) 0 0/4 (0%) 0
    Renal Insufficiency 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Respiratory, thoracic and mediastinal disorders
    Pneumonia 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Fungal Pneumonia 1/9 (11.1%) 1 0/3 (0%) 0 1/4 (25%) 1
    Aspirated Pneumonia 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Multifocal Pneumonia 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Skin and subcutaneous tissue disorders
    Campath Induced Hives 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Skin GvHD 5/9 (55.6%) 6 2/3 (66.7%) 2 3/4 (75%) 4
    Campath Induced Rash 0/9 (0%) 0 1/3 (33.3%) 1 0/4 (0%) 0
    Fungal Dermatitis 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0
    Viral Lesion 1/9 (11.1%) 1 0/3 (0%) 0 0/4 (0%) 0

    Limitations/Caveats

    [Not Specified]

    More Information

    Certain Agreements

    All Principal Investigators ARE employed by the organization sponsoring the study.

    There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

    Results Point of Contact

    Name/Title Richard E. Champlin, MD/Chair, Stem Cell Transplantation
    Organization University of Texas (UT) MD Anderson Cancer Center
    Phone 713-792-8750
    Email CR_Study_Registration@mdanderson.org
    Responsible Party:
    M.D. Anderson Cancer Center
    ClinicalTrials.gov Identifier:
    NCT01518153
    Other Study ID Numbers:
    • 2011-1104
    • NCI-2012-00131
    First Posted:
    Jan 25, 2012
    Last Update Posted:
    Mar 17, 2016
    Last Verified:
    Feb 1, 2016