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The objective of this study is to evaluate the efficacy of using a reduced-intensity condition (RIC) regimen with umbilical cord blood transplant (UCBT), double cord UCBT, matched unrelated donor (MUD) bone marrow transplant (BMT) or peripheral blood stem cell transplant (PBSCT) in patients with non-malignant disorders that are amenable to treatment with hematopoietic stem cell transplant (HSCT). After transplant, subjects will be followed for late effects and for ongoing graft success.
For some non-malignant diseases (NMD; i.e., thalassemia, sickle cell disease, most immune deficiencies) a hematopoietic stem cell transplant may be curative by healthy donor stem cell engraftment alone. HSCT in patients with NMD differs from that in malignant disorders for two important reasons: 1) these patients are typically naïve to chemotherapy and immunosuppression. This may potentially lead to difficulties with engraftment. And 2) RIC with subsequent bone marrow chimerism may be beneficial even in mixed chimerism and result in decreased transplant-related mortality (TRM). Nevertheless, any previous organ damage, as a result of the underlying disease, may remain present after the HSCT.
For other diseases (metabolic disorders, some immunodeficiencies, etc.), a transplant is not curative. For these diseases, the main intent of the transplant is to slow down, or stop, the progress of the disease. In select few cases/diseases, the presence of healthy bone marrow derived cells may even prevent progression and prevent neurological decline.
Research funds are not available to assist with enrollment on this trial.
In this research study, instead of using the standard myeloablative conditioning, the study doctor is using RIC, in which significantly lower doses of chemotherapy will be used. The lower doses may not eradicate every stem cell in the patient's bone marrow, however, in the presented combination, the intention is to eliminate already formed immune cells and provide maximum growth advantage to healthy donor stem cells. This paves the way to successful engraftment of donor stem cells. Engrafting donor stem cells can outcompete, and donor lymphocytes could suppress, the patients' surviving stem cells. With RIC, the side effects on the brain, heart, lung, liver, and other organ functions are less severe and late toxic effects should also be reduced.
The purpose of this study is to collect data from the patients undergoing reduced-intensity conditioning before HSCT, and compare it to the standard myeloablative conditioning. It is expected there will be therapeutic benefits, paired with better survival rate, less organ toxicity and improved quality of life, following the RIC compared to the myeloablative regimen.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| UCBT:transfusion dependent anemias or increased rejection risk | Experimental | Alemtuzumab, Hydroxyurea, Fludarabine, Melphalan, and Thiotepa conditioning regimen prior to allogenic HSCT. |
|
| BMT, PBSCT and not transfusion dependent UCBT | Experimental | Alemtuzumab, Hydroxyurea, Fludarabine, Melphalan, and Thiotepa conditioning regimen prior to allogenic HSCT. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Hydroxyurea | Drug | Oral administration |
|
| Measure | Description | Time Frame |
|---|---|---|
| Post-transplant treatment-related mortality (TRM) | The number of deaths related to the research intervention at day 100, 6 months, and 1 year post-transplant. | 1 year post-transplant |
| Neurodevelopmental milestones | Evaluation of the pace of attaining neurodevelopmental milestones after reduced-intensity conditioning as compared to myeloablative conditioning historical controls from the target population(s). | 1 year post-transplant |
| Immune Reconstitution | Evaluation of the pace of immune reconstitution. | 1 year post-transplant |
| Severe opportunistic infections | Evaluation of the incidence of severe opportunistic infections. | 1 year post-transplant |
| GVHD occurrence | Description of the incidence of acute graft versus host disease (GVHD) (II-IV) and chronic extensive GVHD. | 1 year post-transplant |
| Measure | Description | Time Frame |
|---|---|---|
| Donor cell engraftment | Determination of the feasibility of attaining robust donor cell engraftment (>50% donor chimerism at 6 months) following reduced-intensity conditioning (RIC) regimens prior to HSCT in the target population(s). | 6 months post-transplant |
| Normal enzyme level |
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Inclusion:
A 4/6, 5/6 or 6/6 HLA matched related or unrelated UCB unit available that will deliver a pre-cryopreservation total nucleated cell dose of ≥ 3 x 10e7 cells/kg, or double unit grafts, each cord blood unit delivering at least 2 x 10e7 cells/kg OR an 8 of 8 or 7 of 8 HLA allele level matched unrelated donor bone marrow or peripheral blood progenitor graft.
Adequate organ function as measured by:
Written informed consent and/or assent according to FDA guidelines.
Negative pregnancy test if pubertal and/or menstruating.
HIV negative.
A non-malignant disorder amenable to treatment by stem cell transplantation, including but not limited to:
Primary Immunodeficiency syndromes including but not limited to:
Congenital bone marrow failure syndromes including but not limited to:
Inherited Metabolic Disorders (IMD) including but not limited to:
Mucopolysaccharidoses
Leukodystrophies
Other inherited metabolic disorders
Other inheritable metabolic diseases where hematopoietic stem cell transplantation may be beneficial.
Hereditary anemias
Thalassemia major
Sickle cell disease (SCD) - patients with sickle disease must have one or more of the following:
Diamond Blackfan Anemia (DBA)
Other congenital transfusion dependent anemias
Inflammatory Conditions
Exclusion:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Paul Szabolcs, MD | Contact | 412-692-5427 | paul.szabolcs@chp.edu | |
| Shawna McIntyre, RN | Contact | 412-692-5552 | mcintyresm@upmc.edu |
| Name | Affiliation | Role |
|---|---|---|
| Paul Szabolcs, MD | University of Pittsburgh | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| UPMC Children's Hospital of Pittsburgh | Recruiting | Pittsburgh | Pennsylvania | 15224 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 32750127 | Result | Vander Lugt MT, Chen X, Escolar ML, et al. Reduced-intensity single-unit unrelated cord blood transplant with optional immune boost for nonmalignant disorders. Blood Adv. 2020;4(13):3041-3052. Blood Adv. 2020 Aug 11;4(15):3508. doi: 10.1182/bloodadvances.2020002967. No abstract available. | |
| 32634238 | Derived | Vander Lugt MT, Chen X, Escolar ML, Carella BA, Barnum JL, Windreich RM, Hill MJ, Poe M, Marsh RA, Stanczak H, Stenger EO, Szabolcs P. Reduced-intensity single-unit unrelated cord blood transplant with optional immune boost for nonmalignant disorders. Blood Adv. 2020 Jul 14;4(13):3041-3052. doi: 10.1182/bloodadvances.2020001940. |
| Label | URL |
|---|---|
| Reduced-intensity single-unit unrelated cord blood transplant with optional immune boost for nonmalignant disorders | View source |
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| Alemtuzumab | Drug | Intravenous (IV) administration. |
|
|
| Fludarabine | Drug | IV administration |
|
|
| Melphalan | Drug | IV administration |
|
|
| Thiotepa | Drug | IV administration |
|
Determination of the feasibility of attaining and sustaining normal enzyme levels in the target population(s). |
| 1 year post-transplant |
| Neutrophil recovery | Determination of the pace of neutrophil recovery. | 1 year post-transplant |
| Platelet recovery | Determination of the pace of platelet recovery. | 1 year post-transplant |
| Grade 3-4 organ toxicity | The number of grade 3-4 organ adverse events. | 1 year post-transplant |
| Late graft failure | Evaluation of the incidence of late graft failure. | 1 year post-transplant |
| ID | Term |
|---|---|
| D000081207 | Primary Immunodeficiency Diseases |
| D000080984 | Congenital Bone Marrow Failure Syndromes |
| D001171 | Arthritis, Juvenile |
| D016511 | Severe Combined Immunodeficiency |
| D013577 | Syndrome |
| D014923 | Wiskott-Aldrich Syndrome |
| C535887 | Leukocyte adhesion deficiency type 1 |
| D006105 | Granulomatous Disease, Chronic |
| C580192 | Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome |
| D002609 | Chediak-Higashi Syndrome |
| D056735 | Autoimmune Lymphoproliferative Syndrome |
| D051359 | Lymphohistiocytosis, Hemophagocytic |
| D019871 | Dyskeratosis Congenita |
| C535982 | Congenital amegakaryocytic thrombocytopenia |
| D010022 | Osteopetrosis |
| D009083 | Mucopolysaccharidoses |
| D008059 | Mucopolysaccharidosis I |
| D016532 | Mucopolysaccharidosis II |
| D013398 | Sudden Infant Death |
| D007965 | Leukodystrophy, Globoid Cell |
| D007966 | Leukodystrophy, Metachromatic |
| D000326 | Adrenoleukodystrophy |
| D008363 | alpha-Mannosidosis |
| D005776 | Gaucher Disease |
| D017086 | beta-Thalassemia |
| D000755 | Anemia, Sickle Cell |
| D029503 | Anemia, Diamond-Blackfan |
| D003424 | Crohn Disease |
| D015212 | Inflammatory Bowel Diseases |
| C580150 | Hereditary Diffuse Leukoencephalopathy with Spheroids |
| ID | Term |
|---|---|
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D007153 | Immunologic Deficiency Syndromes |
| D007154 | Immune System Diseases |
| D000080983 | Bone Marrow Failure Disorders |
| D001855 | Bone Marrow Diseases |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D007232 | Infant, Newborn, Diseases |
| D001168 | Arthritis |
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
| D012216 | Rheumatic Diseases |
| D003240 | Connective Tissue Diseases |
| D017437 | Skin and Connective Tissue Diseases |
| D001327 | Autoimmune Diseases |
| D049914 | DNA Repair-Deficiency Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D004194 | Disease |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D025861 | Blood Coagulation Disorders, Inherited |
| D001778 | Blood Coagulation Disorders |
| D008231 | Lymphopenia |
| D007970 | Leukopenia |
| D000095542 | Cytopenia |
| D006474 | Hemorrhagic Disorders |
| D007960 | Leukocyte Disorders |
| D040181 | Genetic Diseases, X-Linked |
| D010585 | Phagocyte Bactericidal Dysfunction |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D000417 | Albinism |
| D015785 | Eye Diseases, Hereditary |
| D005128 | Eye Diseases |
| D008232 | Lymphoproliferative Disorders |
| D008206 | Lymphatic Diseases |
| D007160 | Immunoproliferative Disorders |
| D015616 | Histiocytosis, Non-Langerhans-Cell |
| D015614 | Histiocytosis |
| D012868 | Skin Abnormalities |
| D000013 | Congenital Abnormalities |
| D012873 | Skin Diseases, Genetic |
| D012871 | Skin Diseases |
| D010026 | Osteosclerosis |
| D010009 | Osteochondrodysplasias |
| D001848 | Bone Diseases, Developmental |
| D001847 | Bone Diseases |
| D002239 | Carbohydrate Metabolism, Inborn Errors |
| D008661 | Metabolism, Inborn Errors |
| D016464 | Lysosomal Storage Diseases |
| D017520 | Mucinoses |
| D038901 | X-Linked Intellectual Disability |
| D008607 | Intellectual Disability |
| D019954 | Neurobehavioral Manifestations |
| D009461 | Neurologic Manifestations |
| D009422 | Nervous System Diseases |
| D020271 | Heredodegenerative Disorders, Nervous System |
| D003645 | Death, Sudden |
| D003643 | Death |
| D066088 | Infant Death |
| D020279 | Hereditary Central Nervous System Demyelinating Diseases |
| D020739 | Brain Diseases, Metabolic, Inborn |
| D001928 | Brain Diseases, Metabolic |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D013106 | Sphingolipidoses |
| D020140 | Lysosomal Storage Diseases, Nervous System |
| D056784 | Leukoencephalopathies |
| D003711 | Demyelinating Diseases |
| D008064 | Lipidoses |
| D008052 | Lipid Metabolism, Inborn Errors |
| D052439 | Lipid Metabolism Disorders |
| D052516 | Sulfatidosis |
| D018901 | Peroxisomal Disorders |
| D000309 | Adrenal Insufficiency |
| D000307 | Adrenal Gland Diseases |
| D004700 | Endocrine System Diseases |
| D044904 | Mannosidase Deficiency Diseases |
| D013789 | Thalassemia |
| D000745 | Anemia, Hemolytic, Congenital |
| D000743 | Anemia, Hemolytic |
| D000740 | Anemia |
| D006453 | Hemoglobinopathies |
| D029502 | Anemia, Hypoplastic, Congenital |
| D000741 | Anemia, Aplastic |
| D012010 | Red-Cell Aplasia, Pure |
| D005759 | Gastroenteritis |
| D005767 | Gastrointestinal Diseases |
| D004066 | Digestive System Diseases |
| D007410 | Intestinal Diseases |
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| ID | Term |
|---|---|
| D006918 | Hydroxyurea |
| D000074323 | Alemtuzumab |
| C024352 | fludarabine |
| C042382 | fludarabine phosphate |
| D008558 | Melphalan |
| D013852 | Thiotepa |
| ID | Term |
|---|---|
| D014508 | Urea |
| D000577 | Amides |
| D009930 | Organic Chemicals |
| D061067 | Antibodies, Monoclonal, Humanized |
| D000911 | Antibodies, Monoclonal |
| D000906 | Antibodies |
| D007136 | Immunoglobulins |
| D007162 | Immunoproteins |
| D001798 | Blood Proteins |
| D011506 | Proteins |
| D000602 | Amino Acids, Peptides, and Proteins |
| D012712 | Serum Globulins |
| D005916 | Globulins |
| D009588 | Nitrogen Mustard Compounds |
| D009150 | Mustard Compounds |
| D006846 | Hydrocarbons, Halogenated |
| D006838 | Hydrocarbons |
| D010649 | Phenylalanine |
| D024322 | Amino Acids, Aromatic |
| D000598 | Amino Acids, Cyclic |
| D000596 | Amino Acids |
| D063088 | Phosphoramides |
| D009943 | Organophosphorus Compounds |
| D013721 | Triethylenephosphoramide |
| D001388 | Aziridines |
| D001389 | Azirines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
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