Risk Assessment With Ultra-Low-Pass Whole-Genome Sequencing of Cell-Free DNA for Large B-Cell Lymphoma.
Davidson Zhao, Noémie Lang, Ting Liu...
https://pubmed.ncbi.nlm.nih.gov/40632977/Actively Recruiting
Led by University Health Network, Toronto · Updated on 2025-11-26
2500
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are developing a liquid biopsy protocol at the University Health Networks Princess Margaret Cancer Centre. This observational study focuses on collecting blood samples and archived tumor specimens from patients with confirmed solid tumors, hematological cancers, or those at high risk for cancer due to genetic predisposition or family history. The goal is to enable non-invasive monitoring of tumor progression and treatment response using circulating cell-free nucleic acids such as DNA and RNA. Participants will provide peripheral blood samples, called liquid biopsies, at multiple points during their disease course. These samples will be used for future research to better understand cancer behavior and treatment effects. The study includes patients with various cancers including breast, lung, colon, ovarian, melanoma, lymphoma, leukemia, and others. There is a single observational arm named LIBERATE. During the study, researchers will collect and annotate biospecimens over a period of up to five years. Participants will also complete electronic consent and correlative studies questionnaires throughout this time. No interventions or treatments are administered as part of the study. The data collected aims to provide diagnostic and prognostic information, helping inform future cancer research and care.
CONDITIONS
Liquid Biopsy Evaluation and Repository Development at Princess Margaret
C
Celeste Yu, MSc
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University Health Network, Toronto
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 5 years
Participants provide biospecimens and complete questionnaires for research purposes over the course of the study.
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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https://pubmed.ncbi.nlm.nih.gov/35705312/University Health Network, Toronto
Lead Sponsor