RUNX1 Familial Platelet Disorder
Conditions
Brief summary
To evaluate the safety and feasibility of collecting hematopoietic stem cells (HSC) in participants with RUNX1-FPD.
Detailed description
Primary Objective: \- To evaluate the safety of harvesting HSCs in participants with RUNX1 FPD Secondary Objective \- To evaluate the feasibility and other relevant information of collecting HSCs from participants with RUNX1 FPD
Interventions
DRUGG-CSF (filgrastim or biosimilar)
Given by IV or SC
PROCEDUREApheresis
Given by procedure
DRUGPlerixafor
Given by IV
Sponsors
M.D. Anderson Cancer Center
RUNX1 Foundation
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes
Inclusion criteria
Participants who meet all of the following criteria are eligible to be included in the study: 1. Are aged ≥ 18 to 75 years a. Once a favorable review of safety has been completed by the SMC in 3 participants aged ≥ 18 years, the study will be opened to participants aged ≥ 12 years. 2. Are willing and able to provide informed consent, as appropriate (either directly or through a legally authorized representative \[LAR\]), as described in Appendix 1, Section 13.1 3. Have a confirmed diagnosis of RUNX1 FPD, verified by a Clinical Laboratory Improvement Amendments (CLIA)-certified genetic sequencing report. 4. Clearance by apheresis team to proceed 5. Have systolic blood pressure ≤ 170 mm Hg and diastolic blood pressure ≤ 95 mmHg 6. Are eligible for HSCT per institution requirements 7. Have a Lansky (age \< 16 years)/Karnofsky performance status of ≥ 70 (see Appendix 2, Section 13.2). 8. Are willing and able to comply with protocol-defined contraceptive requirements (see Appendix 3 Section 13.3) 9. Have a platelet count ≥ 50,000/μL for initiation of apheresis, assessed within 24 hours prior to the procedure, or, if \< 50,000/μL are administered platelets on the day of the collection a. If the apheresis team decides that a central venous catheter (CVC) is to be placed, platelet count should be ≥ 50,000 prior to catheter placement. 10. Have hemoglobin ≥ 7.5 g/dL as assessed within 24 hours prior to the procedure
Exclusion criteria
Participants who meet any of the following criteria are excluded from the study: 1. Participants with cognitive impairments and/or any serious unstable pre-existing medical condition or psychiatric disorder that can interfere with safety or with obtaining informed consent or compliance with study procedures. 2. Have uncontrolled bleeding 3. Are using supplemental oxygen 4. Have known severe splenomegaly (≥ 20 cm) 5. Have a diagnosis of MDS or hematologic malignancies, as defined by WHO hematolymphoid tumor classification fifth edition (Khourey et al 2022) hematolymphoid tumor classification fifth edition (Khourey et al 2022) 6. Have recent prior malignancies except resected basal cell carcinoma or treated cervical carcinoma in situ Note: Cancer treated with curative intent \< 5 years previously may be allowed following approval from the study investigator. Cancer treated with curative intent \> 5 years previously is allowed. 7. Have any prior or current myeloproliferative or a significant coagulation or immunodeficiency disorder 8. Have advanced liver disease, defined as any of the following: 1. Persistent aspartate transaminase, alanine transaminase, or direct bilirubin value \> 5× the upper limit of normal (ULN) at screening 2. Screening prothrombin time (PT) or partial thromboplastin time (PTT) \> 1.5× ULN 9. Have had prior HSCT or gene therapy 10. Have history of concomitant sickle cell disease 11. Have been treated with an investigational drug within 30 days of screening or 5 half-lives (whichever is longer) 12. Have a positive test result for HIV, hepatitis B virus (HBV), or hepatitis C virus (HCV) at screening 1. Participants with positive hepatitis B core antibody (HbcAb) and/or hepatitis B-e antibody (HbeAb) are eligible provided viral load is negative by quantitative polymerase chain reaction (qPCR). 2. Participants who are positive for anti-hepatitis C antibody are eligible as long as they have a negative HCV viral load by qPCR. 13. Have a positive infectious disease panel at screening for human T-lymphotropic virus 1 or 2 (HTLV-1 and HTLV-2), or syphilis (rapid plasma 24 reagin \[RPR\]) 14. Have clinically significant and active bacterial, viral, fungal, or parasitic infection at screening 15. Have a white blood cell (WBC) count \< 2 × 109/L 16. Have a left ventricular ejection fraction \< 45% 17. Have a screening estimated glomerular filtration rate \< 60 mL/min/1.73 m2 18. Have a diagnosis of a significant psychiatric disorder that could seriously impede the ability to participate in the study 19. For women of childbearing potential: are pregnant or breastfeeding or lack adequate contraception 20. Are unable to comply with the study procedures, as assessed by the investigator
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Safety and adverse events (AEs) | Through study completion; an average of 1 year. | Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0 |
Countries
United States
Contacts
CONTACTChitra Hosing, MD
PRINCIPAL_INVESTIGATORChitra Hosing
M.D. Anderson Cancer Center
Outcome results
None listed