Haploidentical HCT for Severe Aplastic Anemia

St. Jude Children's Research Hospital

Status and phase

Enrolling

Phase 2

Conditions

Bone Marrow Failure Syndrome

Aplastic Anemia

Treatments

Drug: Fludarabine

Drug: Mesna

Drug: Anti-Thymocyte Globulin (Rabbit)

Biological: CD45RA-depleted DLI

Drug: Cyclophosphamide

Radiation: Total Lymphoid Irradiation (TLI)

Biological: HPC, A Infusion

Device: CliniMACS

Drug: G-CSF

Study type

Interventional

Funder types

Other

Identifiers

NCT04558736

HAPSAA

Details and patient eligibility

About

This study is a prospective, single center phase II clinical trial in which patients with Severe Aplastic Anemia (SAA) ) will receive a haploidentical transplantation. The purpose of this study is to learn more about newer methods of transplanting blood forming cells donated by a family member that is not fully matched to the patient. This includes studying the effects of the chemotherapy, radiation, the transplanted cell product and additional white blood cell (lymphocyte) infusions on the patient's body, disease and overall survival. The primary objective is to assess the rate of engraftment at 30 days and overall survival (OS) and event free survival (EFS) at 1 year post-hematopoietic cell transplantation (HCT).

Primary Objectives

To estimate the rate of engraftment at 30 days after TCR αβ+ T-cell-depleted graft infusion in patients receiving a single dose of post graft infusion cyclophosphamide.
To estimate the overall survival and event free survival at 1-year post transplantation.

Secondary Objectives

To calculate the incidence of acute and chronic GVHD after HCT.
To calculate the rate of secondary graft rejection at 1-year post transplantation
To calculate the cumulative incidence of viral reactivation (CMV, EBV and adenovirus).
To describe the immune reconstitution after TCR αβ+ T-cell-depleted graft infusion at 1 month, 3 months, 6 months, 9 months, and 1 year.

Exploratory Objectives

To longitudinally assess the phenotype and epigenetic profile of T-cells in SAA patients receiving HCT for SAA.
To assess the phenotype and epigenetic profile of T-cells in DLI administered to SAA patients post HCT.
To longitudinally assess CD8 T cell differentiation status in SAA patients using an epigenetic atlas of human CD8 T cell differentiation.
To examine the effector functions and proliferative capacity of CD8 T cells isolated from SAA patients before and after DLI.
Quantify donor derived Treg cells at different time points in patients received HCT.
Determine Treg activation status at different stages after HCT.
Are specific features of the DLI product associated with particular immune repertoire profiles post-transplant?
How does the diversity and functional profile of the DLI product alter the response to pathogens in the recipient?
Do baseline features of the recipient's innate and adaptive immune cells correlate with post-transplant immune repertoires and response profiles?

Full description

Immunosuppressant therapy (IST) is the main treatment for SAA for patients who do not have an HLA-matched sibling donor available for transplant. But some patients with SAA do not respond to IST and some others relapse after IST. HCT using an unrelated but HLA-matched donor is the only curative option for these patients but many patients lack a suitable HLA-matched donor. St Jude is trying to increase donor options for these patients by using novel therapeutic strategies by combining two widely used of GVHD prophylaxis methods: i) selective T cell depletion and ii) use of post-transplant cyclophosphamide. This will allow expansion of the donor pool to include haploidentical donors as well as reduce the risk of GVHD. The goal of this protocol is to test whether combining these GVHD prophylaxis approaches will allow use of haploidentical donors, reduce risk of GVHD, reduce transfusion dependence and improve immune reconstitution.

For this study chemotherapy, antibodies and radiation will be given to prepare the body to receive donor cells. Participants will then be given the donor cell infusion.

Patients will receive two types of donor blood cell products - a progenitor blood cell infusion and then a donor lymphocyte infusion. Both the progenitor blood cell and the donor lymphocyte infusion will be processed in a laboratory at St. Jude using a machine called the CliniMACS™.

In this clinical trial, participants will receive a special type of progenitor blood cells (called TCRαβ- depleted blood cells) from the donor.

After the donor progenitor cells have started to grow within the body (engraftment), participants will receive a second product that contains mature immune cells. These immune cells called CD45RA-depleted lymphocytes or donor lymphocyte infusion (DLI) will help fight infections in the body after the transplant and strengthen the developing immune system.

Enrollment

21 estimated patients

Sex

All

Ages

Under 21 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for Transplant Recipient

Age less than or equal to 21 years at time of enrollment.
Confirmed diagnosis of SAA or a single lineage cytopenia

(a) SAA or single lineage cytopenia will be defined as follows:
- i. Bone marrow cellularity < 25% or hypocellular marrow for age, AND
- ii. One or more of the following (in peripheral blood): (i) Neutrophils < 0.5 x10^9/L (ii) Platelets < 20 x10^9/L, or platelet transfusion dependence (iii) Hemoglobin <8g/dL, or red blood cell transfusion dependence
Does not have a suitable HLA-matched sibling donor (MSD) or volunteer 10/10 HLA-matched unrelated donor (MUD) available in the necessary time for progenitor cell donation.
Failed at least one trial of immunosuppressive therapy (IST) by being refractory (persistence of severe cytopenias and fulfillment of SAA disease criteria at least 3 months after initial IST) or having relapsed (initial improvement of cytopenias after first-line IST but then a later return to fulfillment of SAA disease criteria when IST is decreased or ceased). IST could have included ATG based regimens, calcineurin inhibitors and/or other higher dose therapy directed at the treatment of primary SAA. Patients with very severe aplastic anemia who are likely not to benefit from IST do not need to have failed a trial of IST and can proceed directly to HCT if they meet the rest of the criteria.
Has a suitable single haplotype matched (≥ 3 of 6) family member donor.
Patient and/or legal guardian must sign informed consent for HCT.
Adequate organ function defined as:
1. Left ventricular ejection fraction > 40% or shortening fraction ≥ 25%.
2. Creatinine clearance (CrCl) or glomerular filtration rate (GFR) ≥ 50 ml/ min/1.73m2.
3. Forced vital capacity (FVC) ≥ 50% of predicted value; or pulse oximetry
4. ≥ 92% on room air if patient is unable to perform pulmonary function testing.
5. Karnofsky or Lansky (age-dependent) performance score ≥ 50.
6. Bilirubin ≤ 3 times the upper limit of normal for age.
7. Alanine aminotransferase (ALT) or Aspartate aminotransferase (AST) ≤ 5 times the upper limit of normal for age.
Females and males of childbearing potential must agree to practice 2 effective methods of contraception at the same time or agree to abstinence until after the last dose of chemotherapy has been administered

Exclusion Criteria for Transplant Recipient:

Diagnosis of Fanconi anemia. Fanconi anemia must be excluded by diepoxybutane (DEB) or equivalent testing.
Known clinical or genetic diagnosis of dyskeratosis congenita
Clonal cytogenetic abnormalities consistent with pre-myelodysplastic syndrome (pre- MDS) or MDS on marrow examination (e.g. Monosomy 7).
Diagnosis of myelodysplastic syndrome (MDS).
Presence of anti-donor HLA antibodies (positive anti-donor HLA antibody is defined as a positive cross-match test of any titer by complement- dependent cytotoxicity or flow cytometric testing or the presence of anti- donor HLA antibody to the high expression loci HLA-A, B, C, DRB1, or DPB1 with mean fluorescence intensity (MFI) > 1000 by solid phase immunoassay).
Prior allogeneic hematopoietic cell transplant.
Prior solid organ transplant.
Known life-threatening reaction (i.e., anaphylaxis) to ATG that would prohibit use for the patient.
Uncontrolled bacterial, viral, or fungal infection at the time of enrollment. Uncontrolled is defined as progression or no clinical improvement on appropriate medical treatment.
Female patients who are pregnant (per institutional practice) or breast- feeding.
Prior malignancies except resected basal cell carcinoma or treated cervical carcinoma in situ. Cancer treated with curative intent > 5 years previously will be allowed. Cancer treated with curative intent ≤ 5 years previously will not be allowed unless approved by the PI.
Alemtuzumab or ATG within 2 weeks of enrollment.

Inclusion Criteria for Haploidentical Donor

At least single haplotype matched (≥ 3 of 6) family member.
At least 18 years of age.
HIV negative.
Not pregnant as confirmed by negative serum or urine pregnancy test within 14 days prior to enrollment (if female).
Not breast feeding.
Related donors must be ruled out for telomere disease by appropriate clinical and diagnostic measures (for example, clinical evaluation, telomere length testing, genetic testing, and/or bone marrow examination).
The HAPLO donor and/or legal guardian must be able to sign informed consent documents.
The potential HAPLO donor must be willing and able to donate PBSCs.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

21 participants in 1 patient group

Haploidentical HCT

Experimental group

Description:

To assess the safety and efficacy of haploidentical donor transplantation for patients with severe aplastic anemia who lack an available HLA-matched donor. The goal of this study is to develop a novel, reduced-toxicity, post-transplant pharmacologic immunosuppression (GVHD prophylaxis)- free, highly tolerogenic haploidentical transplant regimen that is associated with few post- transplant complications or late toxicities and is available promptly to all patients, irrespective of matched donor availability. Cells for infusion are prepared using the CliniMACS System.

Treatment: