Discarded Bone Marrow for Hematology Research

NCT ID: NCT04671212

Last Updated: 2025-11-10

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 50 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2022-07-26
• Study Completion Date: 2035-01-31

Brief Summary

The primary objective of this study is to establish a mechanism to obtain discarded bone marrow-containing bone samples from hemoglobinopathy, as well as non-hemoglobinopathy individuals. The processing of samples will help to understand how best to manipulate HSPC's from hemoglobinopathy patients with gene therapy and gene technologies in the laboratory environment. It will also allow us to establish a reservoir of samples that can be studied in the future to assess cellular function and fitness for transplant.

Secondary objectives

• To develop gene transfer and gene editing strategies as potentially curative therapy for hemoglobinopathies (e.g. sickle cell disease (SCD) and β-thalassemia).
• To develop a drug treatment strategy which elevates the expression of fetal hemoglobin to a potentially curative level for hemoglobinopathies.
• To examine the biology of bone marrow cells isolated from patients with hemoglobinopathies.

Detailed Description

The hemoglobinopathies (e.g. sickle cell disease (SCD) and thalassemia) are devastating inherited anemias that shorten and reduce quality of life. The only current curative therapy for SCD is bone marrow transplantation. However, many patients lack access to suitable donors for transplant. Alternative treatments based on gene therapy, gene editing and novel drugs are currently being developed and show great promise for hemoglobinopathies. Gene therapy and gene editing are especially appealing because they eliminate both the need for donors and the potentially devastating side effects of Graft-versus-Host Disease because they take advantage of the patients own cells. In gene therapy approaches, hematopoietic stem and progenitor cells (HSPCs) are collected from a patient and then treated to 'correct' or 'replace' the disease-causing mutation. However, much work remains to develop optimal gene therapy and gene editing protocols, as well as better understand the inherent biology of HSPCs in patients with hemoglobinopathies.

Researchers at St. Jude want to learn how to best manipulate HSPCs from hemoglobinopathy patients with gene therapy and gene editing technologies to achieve optimal gene correction and/or replacement, as well as optimal engraftment of 'corrected' HSPCs after transplantation. St. Jude researchers also seek to test candidate drugs on SCD HSPCs that might ameliorate the symptoms of SCD. Finally, St. Jude researchers seek to thoroughly characterize the basic biology and function of HSPCs isolated from hemoglobinopathy patients.

Bone marrow-containing bone samples that are typically discarded during orthopedic surgery will be saved from hemoglobinopathy patients, as well as non- hemoglobinopathy patients, undergoing these surgeries. These samples will be shipped to the St. Jude Hematology Department for experimental research aimed at addressing the primary and secondary objectives of this protocol.

Conditions

Hemoglobinopathies

Keywords

Bone samples; Bone marrow; Discarded; Hemoglobinopathies; Non-hemoglobinopathies

Study Design

• Observational Model Type: OTHER
• Study Time Perspective: PROSPECTIVE

Study Groups

Orthopedic Surgery Patients

Participants receiving orthopedic surgery for clinical management that involve bone marrow containing bone discard.

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Patients of any age receiving orthopedic surgery for clinical management that involve bone marrow containing bone discard.
• Patients receiving orthopedic surgery for clinical management will be considered for this study if they have the following diagnosis and criteria:

• Homozygous S/S disease or doubly heterozygous for S and β thalassemia who are two years or older are eligible.
• HbE-β- thalassemia or homozygous (severe) β-thalassemia. including those who are transfusion dependent (major) or severely anemic but relatively transfusion independent (intermedia). Diagnostic criteria include standard hematological parameters, red cell indices, hemoglobin electrophoresis and quantitative determination of HbF and HbA2.

Exclusion Criteria

• Active, acute manifestations of sickle cell disease including painful crisis, acute chest syndrome, cerebrovascular events or active infection.
• Pregnant women will not be eligible for study enrollment
• Inability or unwillingness of the research participant or legal guardian/representative to give written informed consent will preclude enrollment on this research protocol.
• Platelet count < 150,000/mm^3
• Neutrophil count < 2000/mm^3
• Neutrophil count < 1000/mm^3 for patients on hydroxyurea therapy
• Prothrombin Time > 17 seconds
• Partial thromboplastin Time > 43 seconds
• History of excessive bleeding in the context of previous procedures including surgery and dental extractions

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

St. Jude Children's Research Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Shannon McKinney-Freeman, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

St. Jude Children's Research Hospital

Locations

St. Jude Children's Research Hospital

Memphis, Tennessee, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Shannon McKinney-Freeman, Ph.D.

Role: CONTACT

Phone: 866-278-5833

Email: referralinfo@stjude.org

Facility Contacts

Shannon McKinney-Freeman, Ph.D.

Role: primary

Related Links

https://www.stjude.org

St. Jude Children's Research Hospital

https://www.stjude.org/protocols

Clinical Trials Open at St. Jude

Other Identifiers

BMHR

Identifier Type: -

Identifier Source: org_study_id