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NCT06744296Recruiting

Measurable Residual Disease Detection Using Tumor-Informed ctDNA Surveillance After Curative-Intent Treatment in HPV-Independent Squamous Cell Carcinoma of the Head and Neck

Source: ClinicalTrials.gov · Last updated 18 May 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This study will test the ability of a personalized blood test to determine which head and neck cancer patients will have a recurrence after treatment.

Status (registry)
Recruiting
Study type
Observational
Enrollment
75 (estimated)
First submitted
9 Dec 2024
Start date
Feb 2025
Primary completion date
Jan 2027
Lead sponsor
Massachusetts Eye and Ear Infirmary
NCT number
NCT06744296

What you commit to

  • Study type: Observational
  • Planned participants: 75
  • From Feb 2025 to the primary completion date, Jan 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients receiving non-standard of care therapy as determined by the clinical investigator
  • Participants who have undergone prior surgical resection, excisional biopsy, radiation, and/or chemotherapy for the treatment of HNSCC. Prior incisional biopsies are permitted. Discrepant cases will be reviewed by study PI.
  • Participants who are receiving any investigational agents at the time of enrollment.

Other illness

  • Active non-HNSCC malignancy.

Age

  • Patients \<18 years of age

Other

  • Participants with AJCC Stage IVC HNSCC, which includes patients with biopsy-confirmed distant metastatic HNSCC, including but not limited to metastatic spread to the lungs, bones, or liver.
  • Active pregnancy during treatment.

Who the study is looking for

  • Newly diagnosed AJCC 8th edition Stage III-IVB mucosal SCC of the head and neck, which includes tumors arising from the oral cavity, nasal cavity, paranasal sinuses, nasopharynx, oropharynx, hypopharynx, and larynx.
  • Available tissue for tumor-informed ctDNA panel creation.
  • Definitive treatment with standard of care surgery or chemoradiotherapy is planned to be administered at Massachusetts Eye and Ear Institute (MEEI) or within the Massachusetts General Hospital (MGH) Cancer Center (including but not limited to the Boston, Danvers, and Newton-Wellesley locations).

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Massachusetts Eye and Ear
Coordinator of this site? Confirm its status
BostonUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.