Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID03702309

Liquid Biopsy Evaluation and Repository Development at Princess Margaret Cancer Centre

Led by University Health Network, Toronto · Updated on 2025-11-26

2500

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are developing a liquid biopsy protocol at the University Health Network's 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

Brief Title

Liquid Biopsy Evaluation and Repository Development at Princess Margaret

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with histological confirmation of a solid tumor or blood cancer, OR identified as high-risk for cancer due to gene mutation or family/hormonal history
  • Age 18 years or older
  • Signed and dated informed consent for this LIBERATE study
  • If co-consented for another primary research study, must meet that study's eligibility criteria
Not Eligible

You will not qualify if you...

  • None

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Long-term Monitoring

Duration - Up to 5 years

Participants provide biospecimens and complete questionnaires for research purposes over the course of the study.

Trial Site Locations

Total: 1 location

1

Princess Margaret Cancer Centre

Toronto, Ontario, Canada, M5G2M9

Actively Recruiting

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Research Team

C

Celeste Yu, MSc

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

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https://pubmed.ncbi.nlm.nih.gov/37972346

Tumor-Naïve Circulating Tumor DNA as an Early Response Biomarker for Patients Treated With Immunotherapy in Early Phase Clinical Trials.

Enrique Sanz-Garcia, Sofia Genta, Xiaoxi Chen...

https://pubmed.ncbi.nlm.nih.gov/37027812

Longitudinal efficacy and toxicity of SARS-CoV-2 vaccination in cancer patients treated with immunotherapy.

Pavlina Spiliopoulou, Helena J Janse van Rensburg, Lisa Avery...

https://pubmed.ncbi.nlm.nih.gov/36670100

Increase in serum choline levels predicts for improved progression-free survival (PFS) in patients with advanced cancers receiving pembrolizumab.

Geoffrey Alan Watson, Enrique Sanz-Garcia, Wen-Jiang Zhang...

https://pubmed.ncbi.nlm.nih.gov/35705312