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Trial record 2 of 5 for:    multitaa

Administration of Donor Multi TAA-Specific T Cells for AML or MDS (ADSPAM)

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ClinicalTrials.gov Identifier: NCT02494167
Recruitment Status : Recruiting
First Posted : July 10, 2015
Last Update Posted : June 25, 2019
Sponsor:
Collaborators:
Texas Children's Hospital
The Methodist Hospital System
Center for Cell and Gene Therapy, Baylor College of Medicine
American Society for Blood and Marrow Transplantation (ASBMT)
Cancer Prevention Research Institute of Texas
Information provided by (Responsible Party):
Premal Lulla, Baylor College of Medicine

Tracking Information
First Submitted Date  ICMJE July 8, 2015
First Posted Date  ICMJE July 10, 2015
Last Update Posted Date June 25, 2019
Actual Study Start Date  ICMJE February 2016
Estimated Primary Completion Date April 2020   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: July 9, 2015)
Number of patients with dose-limiting toxicities (DLTs). [ Time Frame: 4 weeks ]
Maximum tolerated dose (MTD) of multiTAA-specific T cells among the three pre-specified dose levels.
Original Primary Outcome Measures  ICMJE Same as current
Change History Complete list of historical versions of study NCT02494167 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures  ICMJE
 (submitted: July 9, 2015)
  • Number of patients with a decrease in the marker of disease. [ Time Frame: 4 weeks ]
    To obtain information on the anti-tumor effects of adoptively transferred donor-derived multiTAA-specific T cells in patients with AML or MDS.
  • Median number of T cells post-infusion. [ Time Frame: 1 year ]
    To obtain information on the expansion and persistence of adoptively transferred donor-derived multiTAA-specific T cells in patients with AML or MDS.
Original Secondary Outcome Measures  ICMJE Same as current
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Administration of Donor Multi TAA-Specific T Cells for AML or MDS (ADSPAM)
Official Title  ICMJE Administration of Donor Derived Multi-Tumor-Associated Antigen (TAA)- Specific T Cells to Patients With AML or MDS (ADSPAM)
Brief Summary

This research study uses special blood cells called multiple tumor-associated antigen (TAA)-specific T cells (a new experimental therapy) to treat patients with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) which has come back, or may come back, or has not gone away after standard treatment, including an allogeneic hematopoietic stem cell transplant (HSCT).

The investigators have previously used this sort of therapy to treat Hodgkin or non-Hodgkin lymphomas that are infected with Epstein-Barr virus (EBV). EBV is found in cancer cells of up to half of all patients with Hodgkin and non-Hodgkin lymphoma. This suggests that it may play a role in causing lymphoma. The cancer cells infected by EBV are able to hide from the body's immune system and escape being killed. The investigators previously tested whether special white blood cells (called T cells) that were trained to kill EBV-infected cells could affect these tumors, and in many patients the investigators found that giving these trained T cells causes a complete or partial response.

Other cancers express specific proteins that can be targeted in the same way. The investigators have been able to infuse such tumor-targeted cells into up to 10 patients with lymphoma who do not have EBV, and seen some complete responses. Importantly, the treatment appears to be safe. Therefore, the investigators now want to test whether the investigators can direct these special T cells against other types of cancers that carry similar proteins called tumor-associated antigens (TAAs). These proteins are specific to the cancer cell, so they either do not show up, or show up in low quantities, or normal human cells.

The investigators will grow T cells from patients' stem cell donors in the laboratory in a way that will train them to recognize the tumor proteins WT1, NY-ESO-1, PRAME, and Survivin, which are expressed on most AML and MDS cancer cells. The cells will be infused at least 30 days post-allogeneic stem cell transplant. In this study, the investigators want see whether these cells will be able to recognize and kill cancer cells that express these proteins. These donor-derived multiTAA-specific T cells are an investigational product not yet approved by the U.S. Food and Drug Administration

The purpose of this study is to find the largest safe dose of donor-derived tumor protein multiTAA-specific T cells for patients with AML or MDS.

Detailed Description

To make donor derived multiTAA-specific T cells, the investigators will collect blood from the patient's stem cell donor, and mix the donor's T cells with small pieces of tumor proteins WT1, PRAME, NY-ESO-1, and Survivin. These protein fragments stimulate the donor T cells to grow and react against these proteins in such a way that they will recognize and kill cancer cells that express these proteins. Once sufficient numbers of multiTAA-specific T cells have been made, the investigators test them to make sure they target the patient's cancer cells, but not their normal healthy cells.

The multiTAA-specific T cells will be administered as a single intravenous (IV) infusion over 10 minutes. The patient's cancer will be assessed within 4 weeks prior to the T cell infusion, and then 4-6 weeks after the infusion. If at least 4 weeks after the infusion there is no change or a reduction in the number of cancer cells measured in the bone marrow, or a decline in cancer-specific markers in the blood, patients may receive up to six (6) additional doses of T cells at least 4 weeks apart. All of the treatments will be given by the Center for Cell and Gene Therapy at Houston Methodist Hospital or Texas Children's Hospital.

For at least 4 weeks after the infusion, patients may not receive any other anti-cancer treatments, such as radiation therapy, or chemotherapy. Patients who do receive any other therapies will be taken off treatment and will not be able to receive additional doses of T cells. However, drugs such as 5-azacytidine (Vidaza), decitabine (Dacogen), or lenalidomide (Revlimid) will be allowed during infusions.

This is a dose escalation study, which means that at the beginning, patients will be started on the lowest dose (1 of 5 different levels) of T cells. Once that dose level proves safe, the next group of patients will be started at the next highest dose. This process will continue until all 5 dose levels have been studied. If side-effects are too severe, the dose will be lowered or the T cells injections will be stopped.

MEDICAL TESTS BEFORE TREATMENT:

Before being treated, patients will undergo a series of standard medical tests:

  • Measurement of AML/MDS (done by bone marrow biopsy or tests on blood or other tissues)
  • Pregnancy test, if patient is a female who can have children.

MEDICAL TESTS DURING TREATMENT

Patients will undergo standard medical tests on the day of infusion:

  • Physical exam.
  • Blood test to measure blood cells, kidney and liver function.

MEDICAL TESTS AFTER TREATMENT:

  • Blood tests to measure blood cells, kidney and liver function on week 4.
  • Measurement of AML/MDS 4-6 weeks after the T cells infusion and 8-12 weeks after the infusion (done by bone marrow biopsy and tests done on your blood or other tissues).

To learn more about the way the T cells are working in the patient's body, an extra 20-40 mL (4-8 teaspoons) of blood will be taken before the infusion, and at weeks 1, 2, 4 and 8. Afterwards, blood will be collected at 3, 6, 9 and 12 months after the infusion. Blood should come from the central intravenous line, and should not require extra needle sticks. Investigators will use this blood to see how long the T cells last, and to look at the immune response to the patient's cancer. Investigators will also look at this in bone marrow and other tissue samples collected from the patient at the time points stated above (pre-infusion, 4 - 6 weeks and 8 - 12 weeks post infusion).

Patients will be followed for up to one year from the date of the last T cell infusion, so that the investigators can learn more about the way the T cells are working, how long the T cells last in the body, and to assess the immune response to the cancer. Patients who receive additional doses of T cells will undergo the same tests and evaluations performed for each dose as described above.

Patients will then be contacted once a year for up to 4 additional years (total of 5 years follow-up) to evaluate their disease response long-term.

Study Type  ICMJE Interventional
Study Phase  ICMJE Phase 1
Study Design  ICMJE Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Condition  ICMJE
  • Acute Myeloid Leukemia
  • Myelodysplastic Syndrome
Intervention  ICMJE Biological: MultiTAA-specific T cells

The 3 dose levels are:

Dose Level 1: 5 x 10e6 cells/m2; Dose Level 2: 1 x 10e7 cells/m2; Dose Level 3: 2 x 10e7 cells/m2; Dose Level Four: 5 x 107 cells/m2; Dose Level Five: 1 x 108 cells/m2

The T cells are given from 30 days post-HSCT. They are administered by intravenous injection over 1-10 minutes through either a peripheral or central lie.

If patients with residual disease (Group B) have a partial response, complete response or stable disease, they will be eligible to receive up to 6 further doses of multiTAA-specific T cells at the same dose as the initial infusions (or below the patient's original dose can be administered) at least 4 weeks apart.

Other Name: Multiple tumor-associated antigen (TAA)-specific T cells
Study Arms  ICMJE
  • Experimental: Group A
    Treatment with donor-derived multiTAA-specific T cells as adjuvant therapy following HSCT for AML or MDS
    Intervention: Biological: MultiTAA-specific T cells
  • Experimental: Group B
    Treatment with donor-derived multiTAA-specific T cells for relapsed/residual disease following HSCT for AML or MDS
    Intervention: Biological: MultiTAA-specific T cells
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Recruiting
Estimated Enrollment  ICMJE
 (submitted: June 24, 2019)
44
Original Estimated Enrollment  ICMJE
 (submitted: July 9, 2015)
28
Estimated Study Completion Date  ICMJE February 2025
Estimated Primary Completion Date April 2020   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  1. Patients will be eligible to receive donor-derived multiTAA-specific T cells following any type of allogeneic HSCT as;

    (i) Adjuvant therapy for AML/MDS (Group A) or

    (ii) Treatment for refractory/relapsed or minimal residual AML/MDS disease (Group B)

    Residual disease at the time of transplant or post transplant relapse is defined as PCR positivity, specific cytogenetic abnormalities, an abnormal population on flow cytometry or increased blasts on bone marrow biopsy, in the peripheral blood or any other extramedullary sites.

    Minimal residual disease (MRD) will be defined as detection in blood, bone marrow, or other tissues of any of the following:

    (i) Any leukemia specific marker such as t(8;21); inv 16; t (15;17), t(9;22) or t(4;11) documented in the patient's leukemia cells pre-transplant on a post-transplant evaluation.

    (ii) Expression of a leukemia associated antigen known to be a marker for residual disease like WT1.

    (iii) A leukemia-specific phenotype (e.g. expression of markers including CD13 and/or CD33 and/or CD117 and/or HLA-DR+) post-transplant at a level of ≥ 0.01%.

    (ix) Mixed donor chimerism (> 20%).

  2. Life expectancy ≥ 6 weeks.
  3. Karnofsky/Lansky score of ≥ 50.
  4. Patient or parent/guardian capable of providing informed consent.
  5. Bilirubin ≤ 2X upper limit of normal.
  6. AST ≤ 3X upper limit of normal.
  7. Undergoing stem cell transplant at CAGT.
  8. Serum creatinine ≤ 2X upper limit of normal.
  9. Hgb ≥ 7.0 g/dL (can be transfused).
  10. Pulse oximetry of > 90% on room air.
  11. Sexually active patients must be willing to utilize one of the more effective birth control methods for 6 months after the T cell infusion. Male partner should use a condom.
  12. Available donor-derived multiTAA-specific T cell line.
  13. No other investigational anti-neoplastic therapy for one month prior to entry in this study.

Exclusion Criteria:

  1. Patients receiving ATG or Campath within 28 days of infusion.
  2. Patients receiving a Donor Lymphocyte Infusion within 4 weeks of planned T cell infusion.
  3. Less than 30 days post-allogeneic stem cell transplant.
  4. Severe intercurrent infection.
  5. Evidence of GVHD > Grade II.
  6. Pregnant or lactating.
  7. Currently taking corticosteroids (> 0.5 mg/kg/day prednisone or equivalent).
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE Child, Adult, Older Adult
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE
Contact: Premal Lulla, MD 832-824-4847 lulla@bcm.edu
Contact: Josalind Randall 832-824-6835 jxrandal@txch.org
Listed Location Countries  ICMJE United States
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT02494167
Other Study ID Numbers  ICMJE H-36346 ADSPAM
Has Data Monitoring Committee Yes
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement  ICMJE Not Provided
Responsible Party Premal Lulla, Baylor College of Medicine
Study Sponsor  ICMJE Baylor College of Medicine
Collaborators  ICMJE
  • Texas Children's Hospital
  • The Methodist Hospital System
  • Center for Cell and Gene Therapy, Baylor College of Medicine
  • American Society for Blood and Marrow Transplantation (ASBMT)
  • Cancer Prevention Research Institute of Texas
Investigators  ICMJE
Principal Investigator: Premal Lulla, MD Baylor College of Medicine
PRS Account Baylor College of Medicine
Verification Date June 2019

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP