Actively Recruiting

Age: 18Years +
All Genders
ID02906943

Ontario-wide Cancer Targeted Nucleic Acid Evaluation to Study Advanced Solid Tumors Using Next Generation Sequencing

Led by University Health Network, Toronto · Updated on 2026-06-05

10000

Participants Needed

7

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University Health Network, Toronto

Lead Sponsor

P

Princess Margaret Hospital, Canada

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating the use of targeted gene sequencing to better understand advanced, incurable solid tumors in patients receiving standard palliative treatments. The study aims to collect biomarker data from previously collected tumor samples to help guide future treatment decisions and identify suitable clinical trials. This research also seeks to develop a province-wide registry of gene sequencing results and a biobank of tumor and blood samples to support cancer research in Ontario. Participants will provide archival formalin-fixed paraffin embedded (FFPE) tumor tissue for targeted next generation sequencing (NGS) panel testing. Additional tumor tissue and blood samples will be collected for future research and stored in a centralized biorepository. The results of selected gene tests will be shared securely with the treating oncologist through a web portal. Remaining tumor DNA and blood samples may undergo further analysis to support test development and research. During the study, participants' health records will be reviewed and linked to health databases to gather information about their medical treatments and outcomes. Researchers will monitor how gene sequencing data is used in clinical care and research, including the number of patients included in the registry and biobank. The study will last for several years, with ongoing collection and analysis of data to improve understanding of cancer and its treatment.

CONDITIONS

Brief Title

Ontario-wide Cancer TArgeted Nucleic Acid Evaluation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with histological confirmation of advanced solid tumor malignancies who are candidates for systemic therapy.
  • Patients must have sufficient archived formalin-fixed paraffin embedded (FFPE) tumor tissue for molecular profiling.
  • Patients must be 18 years old or older.
  • Patients must have an ECOG performance status of 0 or 1.
  • Patients must have a life expectancy of more than 6 months.
  • Patients must have adequate organ functions.
  • Patients must have signed and dated an informed consent form.
Not Eligible

You will not qualify if you...

  • Patients who have received more than 2 lines of prior cytotoxic therapy for their recurrent or metastatic disease, except Phase I trial candidates who may have had more than 2 prior treatments.

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.

1 visit (in-person)

Surveillance

Duration - Up to 5 years

Participants with advanced solid tumors who are receiving standard palliative treatments are observed while archival tumor tissue and blood samples are collected for targeted next generation sequencing and future research.

Single visit for sample collection; follow-up assessments occur through medical record review and data collection

Trial Site Locations

Total: 7 locations

1

Juravinski Cancer Centre

Hamilton, Ontario, Canada

Active, Not Recruiting

2

Kingston General Hospital

Kingston, Ontario, Canada

Active, Not Recruiting

3

London Health Sciences Centre

London, Ontario, Canada

Active, Not Recruiting

4

The Ottawa Hospital Cancer Centre

Ottawa, Ontario, Canada

Actively Recruiting

5

Princess Margaret Hospital

Toronto, Ontario, Canada, M5G 2M9

Actively Recruiting

6

Mount Sinai Hospital

Toronto, Ontario, Canada

Active, Not Recruiting

7

Sunnybrook Health Sciences Centre

Toronto, Ontario, Canada

Active, Not Recruiting

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Research Team

S

Samanta Del Rossi

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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Frequently Asked Questions

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Published Research Related To This Trial

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https://pubmed.ncbi.nlm.nih.gov/35337750