Prediction of risk for myeloid malignancy in clonal hematopoiesis.
Lachelle D Weeks, Abhishek Niroula, Donna Neuberg...
https://pubmed.ncbi.nlm.nih.gov/37483562/Actively Recruiting
Led by Dana-Farber Cancer Institute · Updated on 2026-06-30
5000
Participants Needed
1
Research Sites
352 weeks
Total Duration
Researchers are studying how clonal hematopoiesis CH affects people receiving chemotherapy and radiation for solid cancers. The goal is to understand clinical and molecular factors that predict high-risk CH in patients treated with cancer therapies. This research aims to identify cancer patients and survivors at increased risk for therapy-related myeloid neoplasms t-MNs, potentially leading to new ways to intercept progression to these serious conditions. Participants will provide tissue samples such as blood, buccal swabs, urine, stool, biopsy or surgical tissue, and other bodily fluids during routine visits or through remote collection at home. They will also complete intake surveys covering demographics, medical history, and family history. This observational study involves up to about 5,000 people diagnosed with solid malignancies who are planning to receive chemotherapy or radiation. During the study, participants samples and clinical data will be collected to analyze changes in CH and related outcomes over time, up to 5 to 10 years. Researchers will assess CH prevalence, gene distribution, variant changes, cancer progression, survival, hematologic toxicity, and development of therapy-related myeloid neoplasms. The study also aims to develop a predictive algorithm for adverse outcomes in patients with CH, with ongoing monitoring and data collection throughout the follow-up period.
CONDITIONS
Clonal Hematopoiesis Chemotherapy and Radiation Effects Study
C
Cindy Amaya Lopez, BA
J
Jenna Beckwith, MPH
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Dana-Farber Cancer Institute
Lead Sponsor
You may qualify if you...
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote)
Duration - Up to 10 years
Participants provide tissue samples such as blood, saliva, urine, stool, or other bodily fluids during routine visits or via remote collection at home. They also complete surveys about demographics, medical history, and family history.
Periodic sample collections and surveys over time
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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Lead Sponsor