NCT04776850

Pre-transplant Immunosuppression and Donor Stem Cell Transplant for the Treatment of Severe Hemoglobinopathies

Pre-Transplant Immunosuppression and Related Haploidentical Hematopoietic Cell Transplantation for Patients With Severe Hemoglobinopathies

• Status: Withdrawn
• Phase: EARLY_Phase 1
• Study type: Interventional
• Enrollment: 0 (actual)
• Sponsor: M.D. Anderson Cancer Center · Academic / Other
• Sex: All
• Age: 2 Years – 30 Years
• Healthy volunteers: Not accepted

Summary

This clinical trial studies the effect of pre-transplant immunosuppression (PTIS) and donor stem cell transplant in treating patients with severe blood diseases (hemoglobinopathies). PTIS helps prepare the body for the transplant and lowers the risk of developing graft versus host disease (GVHD). Hematopoietic cells are found in the bone marrow and produce blood cells. Hematopoietic cell transplantation (HCT) injects healthy hematopoietic cells into the body to support blood cell production. PTIS and HCT may help to control severe hemoglobinopathies.

Detailed description

PRIMARY OBJECTIVE: I. To estimate event-free survival (EFS) at 2-years post HCT. SECONDARY OBJECTIVES: I. Assess event-free survival (EFS) at 100 days and 1 year post HCT. II. Assess overall survival (OS) at 100 days and 1 year post HCT. III. 30-day transplant-related mortality (TRM). IV. Time to platelet and neutrophil engraftment. V. Rate of graft failure (primary and secondary) through day 100. VI. Incidence of acute graft-versus-host disease (aGVHD) by day 100. VII. Incidence of chronic graft-versus-host disease (cGVHD) by 1 year and 2 years. VIII. Rate of grade II or greater organ toxicity through day 100. IX. Incidence of hepatic sinusoidal obstruction syndrome (SOS) by day 100. X. Incidence of central nervous system (CNS) toxicities including posterior reversible encephalopathy syndrome (PRES) by day 100. XI. Incidence of infectious complications through day 100. EXPLORATORY OBJECTIVES: I. Effect of HCT on clinical and laboratory manifestations of hemoglobinopathies by 1 and 2 years after HCT. II. Assess the pharmacokinetic profile of busulfan and thymoglobulin to better understand post-transplant outcomes. III. Assess immune reconstitution kinetics post HCT. OUTLINE: DONOR-SPECIFIC ANTI-HLA DESENSITIZATION: Patients with donor-specific anti-HLA antibody titers \>= 1:3,000 at the start of PTIS receive rituximab intravenously (IV) on days -69, -41, -28, and -13 and bortezomib IV over less than 1 minute on days -68, -65, -40, and -37 in the absence of unacceptable toxicity. Patients with donor-specific anti-HLA antibody titers \> 1:15,000 at the start of PTIS receive receive rituximab IV on days -69, -41, -28, and -13 and bortezomib IV over less than 1 minute on days -68, -65, -62, -58, -40, -37, -34, and -31 in the absence of unacceptable toxicity. Patients with donor-specific anti-HLA antibody titers \> 1:5,000 at the start of conditioning may also undergo plasmapheresis on day -12. PTIS: Patients receive fludarabine phosphate (fludarabine) IV over 1 hour and dexamethasone IV over less than 1 minute on days -68 to -64 and days -40 to -36 in the absence of disease progression or unacceptable toxicity. CONDITIONING: Patients receive lapine T-lymphocyte immune globulin (rATG) IV over 4-6 hours on days -12 to -10, fludarabine phosphate IV over 1 hour on days -8 to -4, and busulfan IV over 2 hours on days -7 to -4 in the absence of disease progression or unacceptable toxicity. TRANSPLANT: Patients undergo HCT on day 0. GVHD PROPHYLAXIS: Patients receive cyclophosphamide IV over 2-3 hours on days 3 and 4 in the absence of unacceptable toxicity. Beginning on day 5, patients also receive tacrolimus IV continuously daily and then orally (PO) twice daily (BID) at the discretion of the treating physician for up to 12 months, and mycophenolate mofetil IV or PO BID up to day 60 in the absence of unacceptable toxicity. After completion of HCT, patients are followed up periodically for up to 2 years.

Conditions

• Beta Thalassemia Major
• Sickle Beta 0 Thalassemia
• Sickle Beta Plus Thalassemia
• Sickle Beta Thalassemia
• Sickle Cell Disease
• Sickle Cell-SS Disease

Interventions

Type	Name	Description
DRUG	Bortezomib	Given IV
DRUG	Busulfan	Given IV
DRUG	Cyclophosphamide	Given IV
DRUG	Dexamethasone	Given IV
DRUG	Fludarabine Phosphate	Given IV
PROCEDURE	Hematopoietic Cell Transplantation	Undergo HCT
BIOLOGICAL	Lapine T-Lymphocyte Immune Globulin	Given IV
DRUG	Mycophenolate Mofetil	Given IV or PO
PROCEDURE	Plasmapheresis	Undergo plasmapheresis
BIOLOGICAL	Rituximab	Given IV
DRUG	Tacrolimus	Given IV or PO

Timeline

• Start date: 2020-12-29
• Primary completion: 2022-12-05
• Completion: 2022-12-05
• First posted: 2021-03-02
• Last updated: 2024-10-24

Regulatory

• FDA-regulated drug study