Backtracking Leukemia-Typical Somatic Mutations in Cord Blood
NCT05014165 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 300
Last updated 2026-04-08
Summary
A comprehensive mechanistic and epidemiological study to obtain banked cord blood samples from consecutive childhood leukemia patients enrolled in the COG Project:EveryChild (APEC14B1) study. Will attempt to backtrack the initiating genomic alteration identified in the matched diagnostic leukemia sample and molecularly characterize pre-leukemic cells. The ultimate goal of this research is to pinpoint the cell of origin of leukemogenic alterations formed in utero, elucidating the etiology of these initiating mutations (as opposed to frank leukemia), and devising a test for circulating pre-leukemia that can be applied on a population-wide basis.
Conditions
Interventions
- OTHER
-
Cord blood Sample Collection
Obtain banked cord blood samples from consecutive childhood leukemia patients
- OTHER
-
Case identification and recruitment
Cases meeting eligibility and who have given consent through APEC14B1 for future contact for non-therapeutic studies
- OTHER
-
Questionnaire Administration
The family will be given an option to complete questionnaire on paper, online, or over the telephone.
Sponsors & Collaborators
-
National Cancer Institute (NCI)
collaborator NIH -
Children's Oncology Group
lead NETWORK
Principal Investigators
-
Adam de Smith, PhD · Beckman Research Institute of the City of Hope
-
Logan Spector, PhD · University of Minnesota Masonic Cancer Center
Eligibility
- Max Age
- 25 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-08-25
- Primary Completion
- 2026-09-30
- Completion
- 2026-09-30
Countries
- United States
Study Locations
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