Tumor-Informed ctDNA Testing for MRD Following Treatment of Squamous Cell Carcinoma

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of California, San Francisco

About this trial

This is a single-center, non-interventional, observational study that evaluates the correlation of circulating tumor DNA (ctDNA) testing to cancer relapse for participants with squamous cell carcinomas (HNC) of the head and neck mucosa and skin after curative-intent primary radiation or surgery.

Eligibility criteria

Qualifiers

Participants must have histologically or cytologically confirmed squamous cell carcinoma of the head and neck mucosa and skin.

Participants must be age >=18 years.

Participants must be planning to receive curative-intent surgery or radiation-based treatment as part of standard of care treatment.

Participants must have the ability to understand and the willingness to sign a written informed consent document.

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Blood Specimen Collection
  • Tumor Tissue Collection
  • Medical Record Review

Treatment groups

250 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University of California, San Francisco

Lead sponsor

Haystack Oncology, Inc.

Collaborator