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

Sponsor

Memorial Sloan Kettering Cancer Center (Other)

Overall Status

Recruiting

CT.gov ID

NCT03531736

Collaborator

(none)

Enrollment

Locations

Arm

59.7

Anticipated Duration (Months)

7.5

Patients Per Site

0.1

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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.

Condition or Disease	Intervention/Treatment	Phase
Myeloid Diseases	Drug: Antithymocyte globulin (Rabbit) Drug: fludarabine Radiation: total body irradiation Drug: cyclophosphamide Drug: Rituxan Procedure: Allogeneic Hematopoietic Stem Cell Transplantation	Phase 1

Study Design

Study Type:

Interventional

Anticipated Enrollment :

15 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Intervention Model Description:

This is a pilot study to assess engraftment of a T cell depleted (TCD) graft following a reduced intensity conditioning regimen (RIC). The conditioning regimen will include total body irradiation (TBI), Fludarabine, anti-thymocyte globulin (ATG) and post transplant cyclophosphamide (PT-Cy). The graft will be TCD and will be composed of a TCR-α/β+ lymphocyte depletion stem cells and CD34+ selected stem cells.This is a pilot study to assess engraftment of a T cell depleted (TCD) graft following a reduced intensity conditioning regimen (RIC). The conditioning regimen will include total body irradiation (TBI), Fludarabine, anti-thymocyte globulin (ATG) and post transplant cyclophosphamide (PT-Cy). The graft will be TCD and will be composed of a TCR-α/β+ lymphocyte depletion stem cells and CD34+ selected stem cells.

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

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

Actual Study Start Date :

May 9, 2018

Anticipated Primary Completion Date :

May 1, 2023

Anticipated Study Completion Date :

May 1, 2023

Arms and Interventions

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

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

Outcome Measures

Primary Outcome Measures

Rate of donor Neutrophil Engraftment [30 days post-transplant]
Neutrophil engraftment (recovery of ANC) defined by an ANC ≥ 500/mm^3 for 3 consecutive days

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

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:

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

AML in ≥ 2nd remission
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.

Chronic myelomonocytic leukemia (CMML)
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)

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:

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

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Memoral Sloan Kettering Monmouth (Limited Protocol Activities)	Middletown	New Jersey	United States	07748
2	Memorial Sloan Kettering Cancer Center	New York	New York	United States	10065