T Cell Depleted Allogeneic Hematopoietic Stem Cell Transplantation Conditioned With a Reduced Intensity Regimen in Patients With Hematologic Malignancies and Aplastic Anemia

Allogeneic Hematopoietic Stem Cell Transplantation of α/β T-Lymphocyte Depleted Graft Conditioned With a Reduced Intensity Regimen in Patients With Hematologic Malignancies and Aplastic Anemia

The main purpose of this study is to learn if a new combination of chemotherapy, in combination with low-dose radiation, will be safe for the patient, and at the same time provide the best opportunity to cure the bone marrow cancer. The combination of chemotherapy and radiation described in the study is considered 'low intensity.' Although the chemotherapy agents used in this study and for transplant are FDA approved, the chemotherapy treatment and conditioning regimens or combinations listed in this consent are not yet FDA approved.

The CliniMACS device is FDA approved for one type of T cell depletion (positive selection of the stem cells) but not approved yet for other type of T cell depletion, which is being studied on this protocol. This pilot study, along with other studies will serve as the basis for FDA approval, if outcomes are favorable.

Study Overview

• Status: Active, not recruiting
• Conditions: Myeloid Diseases
• Intervention / Treatment: Drug: Antithymocyte globulin (Rabbit); Drug: fludarabine; Radiation: total body irradiation; Drug: cyclophosphamide; Drug: Rituxan; Procedure: Allogeneic Hematopoietic Stem Cell Transplantation

• Study Type: Interventional
• Enrollment (Actual): 17
• Phase: Phase 1

Contacts and Locations

• Study Contact: Name: Roni Tamari, MD; Phone Number: 212-639-5987; Email: ABMTTrials@mskcc.org
• Study Contact Backup: Name: Miguel-Angel Perales, MD; Phone Number: 212-639-8682; Email: ABMTTrials@mskcc.org

Study Locations

• United States
  • New Jersey
    • Middletown, New Jersey, United States, 07748
      • Memorial Sloan Kettering Monmouth (Limited Protocol Activities)
  • New York
    • New York, New York, United States, 10065
      • Memorial Sloan Kettering Cancer Center

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Patients with one of the high risk myeloid diseases as outlined below. Patients must have ≤ 5% blasts on the last BM evaluation prior to starting the conditioning regimen. Diseases included on this protocol include:

  1. Acute Myeloid Leukemia (AML) in CR1 with intermediate or high risk features as defined below:

     °Cytogenetic abnormalities which are not considered "good risk" cytogenetic features (i.e t(8:21), t(15:17), inv 16 without c-kit mutations.

     And/or

     • Therapy related AML with history of antineoplastic therapy (radiation and/or chemotherapy) And/or
     • Normal karyotype with mutations of FLT3, RUNX1, TP53 mutation, ASXL1 or any others that are considered to be high risk
  2. AML in ≥ 2nd remission

  3. Myelodysplastic syndrome, myeloproliferative neoplasms, or MDS/MPN overlap syndrome with:

     °International prognostic scoring system risk score INT-2 or high risk at the time of transplant evaluation.

     And/or

     • Any risk category if life-threatening cytopenia exists And/or
     • Karyotype or genomic changes that indicate high risk for progression to acute myelogenous leukemia, including abnormalities of chromosome 7 or 3, mutations of TP53, or complex or monosomal karyotype.
  4. Chronic myelomonocytic leukemia (CMML)

  5. Chronic myeloid leukemia (CML) with the following features:

     °Patients who have failed or are intolerant to BCR-ABL tyrosine kinase inhibitors.

     And/or

     °CML with BCR-ABL mutation consistent with poor response to tyrosine kinase inhibition (e.g T351l mutation)

  6. Patients with severe aplastic anemia
• Chronic lymphocytic leukemia (CLL) with high risk disease as defined by the EBMT consensus criteria.

• Non-Hodgkin lymphoma meeting both of the following criteria:

  • Responding to therapy prior to enrollment.
  • Relapse after prior autologous bone marrow transplant or are ineligible for autologous bone marrow transplant.

• Multiple Myeloma with disease in the following categories:

  • Patients with relapsed multiple myeloma following autologous stem cell transplantation who have achieved at least partial response following additional chemotherapy
  • Patients with high risk cytogenetics at diagnosis must have achieved at least a partial response following autologous stem cell transplantation. Patients must have complex karyotype, del17p, t4;14, and/or t14;16 by FISH and/or del13 by karyotyping.
• Each patient must be willing to participate as a research participant and must sign an informed consent form.

• Organ Function and Performance Status Criteria:

  1. Patients be ≥ 18 years old.
  2. Patients must have a Karnofsky (adult) or Performance Status ≥ 70%.

  3. Patients must have adequate organ function measured by:

     • Cardiac: asymptomatic or if symptomatic, then LVEF at rest must be ≥ 40% and must improve with exercise.
     • Hepatic: < 5x ULN ALT and < 2x ULN total serum bilirubin, unless there is congenital benign hyperbilirubinemia.
     • Renal: CrCl >30ml/min (measured or calculated/estimated).
     • Pulmonary: asymptomatic or if symptomatic, DLCO > 50% of predicted (corrected for hemoglobin)

Exclusion Criteria:

• Prior allogenic hematopoietic stem cell transplantation
• Prior radiation therapy with 400cGY or more of TBI
• BM with increased fibrosis (Reticulin stain > 1/3)
• Active and uncontrolled infection at time of transplantation
• HIV infection
• Seropositivity for HTLV-1
• Inadequate performance status/ organ function
• Pregnancy or breast feeding
• Patient or guardian unable to give informed consent or unable to comply with the treatment protocol including appropriate supportive care, follow-up, and research tests.

Donor Inclusion and Exclusion Criteria:

• Must be a 10/10 HLA genotypically match related or unrelated donor at all A, B, C, DRB1, and DQB1 loci, as tested by DNA analysis
• Able to provide informed consent for the donation process per institutional standards
• Meet standard criteria for donor collection as defined by the National Marrow Donor Program Guidelines

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm

Intervention / Treatment

Experimental: Patients with Myeloid Malignancies & Aplastic Anemia; Transplant conditioning will consist of: ATG (2 mg/kg/day IV on days-8 through-6), fludarabine (30 mg/m^2/d on days -5 through -2), TBI 400 cGy in 2 divided doses (days -2 and -1) and high dose cyclophosphamide given post stem cell infusion (50 mg/kg on days +3 and +4). One dose of Rituxan (200 mg/m^2) will be given to reduce the risk of EBV viremia. The donor stem cell product will be derived from the peripheral blood with a target cell infusion of ≥8X10^6 CD34 cells per recipient kg. Patients will receive post-transplant G-CSF starting on day +7. Patients will undergo donor/recipient bone marrow and peripheral chimerism studies at 30 and 100, and 6, 12, 18 and 24 months post allo HCT and thereafter, at the discretion of the treating clinician. Immune function and disease restaging will be performed at day 100 and 6, 12, 18, and 24 months and as otherwise clinically indicated by the treating physician.

Drug: Antithymocyte globulin (Rabbit); ATG (2 mg/kg/d IV on days-8 through -7); Other Names: ATG; Drug: fludarabine; fludarabine (30 mg/m2/d on days -5 through -2); Radiation: total body irradiation; TBI 200 cGy (days -2 and -1) given post stem cell infusion; Other Names: TBI; Drug: cyclophosphamide; cyclophosphamide given post stem cell infusion (50 mg/kg on days +3 and +4); Drug: Rituxan; Rituxan (200 mg/m2) will be given to reduce the risk of EBV viremia; Procedure: Allogeneic Hematopoietic Stem Cell Transplantation; Allogeneic Hematopoietic Stem Cell Transplantation

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Rate of donor Neutrophil Engraftment	Neutrophil engraftment (recovery of ANC) defined by an ANC ≥ 500/mm^3 for 3 consecutive days	30 days post-transplant

Collaborators and Investigators

• Sponsor: Memorial Sloan Kettering Cancer Center
• Investigators: Principal Investigator: Roni Tamari, MD, Memorial Sloan Kettering Cancer Center

Publications and helpful links

Helpful Links

• Memorial Sloan Kettering Cancer Center

Study record dates

Study Major Dates

• Study Start (Actual): May 9, 2018
• Primary Completion (Estimated): May 1, 2025
• Study Completion (Estimated): May 1, 2025

Study Registration Dates

• First Submitted: May 9, 2018
• First Submitted That Met QC Criteria: May 9, 2018
• First Posted (Actual): May 22, 2018

Study Record Updates

• Last Update Posted (Actual): November 30, 2023
• Last Update Submitted That Met QC Criteria: November 29, 2023
• Last Verified: November 1, 2023

More Information

Terms related to this study

• Keywords: Allogeneic Hematopoietic Stem Cell Transplantation; intensity conditioning regimen; 17-639
• Additional Relevant MeSH Terms: Neoplasms; Neoplasms by Site; Bone Marrow Diseases; Hematologic Diseases; Anemia; Bone Marrow Failure Disorders; Hematologic Neoplasms; Anemia, Aplastic; Physiological Effects of Drugs; Molecular Mechanisms of Pharmacological Action; Antirheumatic Agents; Antineoplastic Agents; Immunosuppressive Agents; Immunologic Factors; Antineoplastic Agents, Alkylating; Alkylating Agents; Myeloablative Agonists; Antineoplastic Agents, Immunological; Cyclophosphamide; Rituximab; Fludarabine; Thymoglobulin; Antilymphocyte Serum
• Other Study ID Numbers: 17-639

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: UNDECIDED

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No