Actively Recruiting

Age: 18Years +
All Genders
NCT04665388

LANDscape MApping of Epitopes and T Cell Receptors for Selected Cancers

Led by University Health Network, Toronto · Updated on 2025-07-02

105

Participants Needed

1

Research Sites

273 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a correlative research project aimed at characterizing the T cell mediated immune responses to hepatocellular carcinoma (HCC), as well as Epstein-Barr virus (EBV)- and human papillomavirus (HPV)-related cancers. This study will enroll approximately 105 patients over 48 months. Of these 105 patients, 30 are EBV-related cancer, 45 are HPV-related cancer, and 30 are HCC. Patients will have blood samples collected one time to identify cancer specific T cells and T cell receptors in their blood. They will also have tissue samples collected one time to study the different types of immune cells, especially the T cells and their receptors. The 105 patients enrolled in this study will be compared to retrospective samples (N=210; 30 from EBV-related cancer cohort, 180 from HPV-related cancer cohort).

CONDITIONS

Official Title

LANDscape MApping of Epitopes and T Cell Receptors for Selected Cancers

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with a confirmed diagnosis of EBV-related cancers such as nasopharyngeal cancer
  • Patients with HPV-related cancers including squamous cell carcinoma of the head and neck, cervix, vulva, or anal canal; HPV positivity required for head and neck cancers, p16 positivity acceptable; not required for other sites
  • For anal canal cancers, late-stage metastatic tissue preferred; early-stage primary tissue acceptable if uncontaminated
  • Patients with hepatocellular carcinoma (HCC) having alpha-fetoprotein levels above the upper normal limit
  • Patients aged 18 years or older
  • Patients who have provided voluntary written informed consent
Not Eligible

You will not qualify if you...

  • Any condition that may interfere with patient safety, specimen evaluation, or study result interpretation as determined by the investigator

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Trial Site Locations

Total: 1 location

1

Princess Margaret Cancer Centre

Toronto, Ontario, Canada, M5G 2M9

Actively Recruiting

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Research Team

K

Kathy Han, MD

CONTACT

K

Kendra Ross

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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