Randomized study of low versus moderate dose busulfan in transplant for severe combined immunodeficiency

低剂量与中剂量白消安治疗严重联合免疫缺陷移植的随机研究

• 批准号: 10474994
• 负责人: Leslie S Kean
• 金额: $ 99.52万
• 依托单位: CHILDREN'S HOSPITAL OF LOS ANGELES
• 依托单位国家: 美国
• 财政年份: 2017
• 资助国家: 美国
• 起止时间: 2017-08-24 至 2024-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10474994
• 关键词: 2 year old; Abnormal Cell; Acute; Adoptive Transfer; Affect; Age; Allogenic; American; Antibody Formation; Antibody Response; Antithymoglobulin; Area Under Curve; B cell reconstitution; B-Cell Antigen Receptor; B-Cell Development; B-Lymphocytes; Biological Markers; Biology; Birth; Blood; Bone Marrow Transplantation; Busulfan; CD19 gene; Cell Compartmentation; Cell Count; Cell physiology; Cells; Cellular Immunity; Chemotherapy-Oncologic Procedure; Child; Childhood; Chimerism; Data; Disease; Dose; Drug Kinetics; Engraftment; Enrollment; Funding; Future; Generations; Genetic; Genetic Diseases; Genotype; Goals; Gold; Graft Rejection; Growth; Hematopoietic stem cells; Hepatotoxicity; Host vs Graft Reaction; Hour; Humoral Immunities; IL2RG gene; Immune; Immune Tolerance; Immune system; Immunity; Immunoglobulin-Secreting Cells; Immunoglobulins; Immunologics; Immunosuppression; Incidence; Infant; Infection; Infertility; JAK3 gene; Kinetics; Life; Long-Term Effects; Lung; Mature T-Lymphocyte; Measures; Memory B-Lymphocyte; Molecular Abnormality; Monitor; Myelogenous; Myeloid Cells; National Institute of Allergy and Infectious Disease; Nature; Neonatal Screening; Non-Malignant; Opportunistic Infections; Oryctolagus cuniculus; Outcome; Output; Participant; Patients; Peripheral; Phase; Phenotype; Progenitor Cell Engraftment; Prophylactic treatment; Prospective Studies; Randomized; Recovery; Regimen; Regulation; Replacement Therapy; Retrospective Studies; Risk; Role; Safety; Second Primary Cancers; Severe Combined Immunodeficiency; Siblings; Source; Specialist; Subgroup; T cell reconstitution; T-Cell Development; T-Lymphocyte; Testing; Tetanus; Tetanus Vaccine; Thiotepa; Thymus Gland; Toxic effect; Transplantation; Transplantation Conditioning; United States; Vaccination; Viral Vaccines; base; cell type; cohort; conditioning; congenital immunodeficiency; cost; dose individualization; efficacy testing; exhaustion; fludarabine; hematopoietic cell transplantation; high risk; immune function; immune reconstitution; improved; insight; patient tolerability; phase II trial; primary endpoint; prospective; recruit; response; restoration; safety outcomes; secondary endpoint; standard care; stem cell engraftment; stem cells; virtual

Project Summary Severe combined immunodeficiency (SCID) is a group of genetic disorders that abrogate T cell development and function. Allogeneic hematopoietic cell transplantation (HCT) is the standard treatment, for the disease, which is typically fatal by age 2 years if not treated. HCT can be performed successfully in SCID patients without the high dose pre-HCT busulfan conditioning typically used, due to the lack of functional T cells. Despite restoration of T cell function, humoral immunity remains poor in many patients post-HCT. This project seeks to test the efficacy and safety of a regimen of low dose, individualized targeted busulfan compared to moderate dose in SCID patients at risk of poor humoral outcome undergoing non-matched sibling donor HCT. We will target patients without active infection, leveraging the widespread implementation of universal newborn screening in the United States. We hypothesize that in our proposed multi-institutional randomized phase II trial patients receiving low dose busulfan will achieve similar outcomes compared to those receiving moderate dose (myeloablative) busulfan, achieving both T and B cell immune reconstitution. In Aim 1, we will examine immunological and safety outcomes in trial participants. Patients who lack matched sibling donors, confirmed to have the appropriate genotype, and who do not have active infection will be recruited over 4 1/2 years. Within each of 2 genotype cohorts (IL2RG/JAK3, RAG1/RAG2), 32 patients will be randomized to cumulative area-under-the-curve exposure of busulfan of 30 mg*h/L versus 60 mg*h/L (32 patients per cohort, 64 patients total). IL2RG/JAK3 patients will also receive rATG and RAG1/RAG2 patients will receive rATG, fludarabine, and thiotepa. Stem cell sources include unrelated and haploidentical related donor products that will be TCRαβ+/CD19+ depleted with no post-HCT GVHD prophylaxis. The primary endpoint is protective antibody response to tetanus, a gold standard of normal humoral immune function in children, by 2 years post-HCT. Secondary endpoints include reconstitution of T cell number, thymic output, cell type specific chimerism, response to live viral vaccines at 3 years, survival, and incidence of HCT related complications. In Aim 2, we will examine the correction of T and B cell abnormalities in depth. The central question is whether mixed/split chimerism (donor-derived T cells with mixed chimerism in the B and myeloid compartments) will nevertheless be associated with normal immune phenotype, function, repertoire and tolerance in one or more genotypic cohorts. We hypothesize that generation of memory B cells, antibody- secreting cells and correction of pre-existing abnormalities of the B cell receptor repertoire post-HCT will be evident in all genotype cohorts and that the degree and quality of correction in the setting of mixed chimerism will vary according to the biology of each genetic abnormality. We hypothesize that T cell exhaustion seen in patients undergoing HCT in the absence of conditioning will be diminished or absent in trial participants due to improvements in thymic output associated with engraftment of donor-derived HSC. We hypothesize that T cell tolerance will occur by different mechanisms (central deletion versus peripheral regulation) according to donor type (haploidentical versus well matched unrelated donor) yet will be induced successfully in patients with mixed chimerism.

项目总结