RecruitingPhase 1NCT06997094

Decitabine in Combination With Standard of Care Therapy for the Treatment of Surgically Resectable HPV-Negative Head and Neck Cancer

Phase I Decitabine Dose-Tolerance in Surgically Resectable HPV-Negative Head and Neck Cancer


Sponsor

Mayo Clinic

Enrollment

24 participants

Start Date

Jan 23, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This phase I trial tests the safety, side effects, and best dose of decitabine in combination with standard of care surgery, radiation, and/or chemotherapy and the effectiveness of the combination in treating patients with head and neck squamous cell cancers that are not caused by human papilloma virus (HPV-negative) and that can be removed by surgery (resectable). Decitabine, an antimetabolite, stops cells from making deoxyribonucleic acid (DNA) and may kill tumor cells. Studies have shown that medications like decitabine can make some types of solid tumors more sensitive to chemotherapy. This allows the chemotherapy to be more effective, with slower progression and longer survival. Decitabine is also a clinically active demethylating agent, and may help make tumor cells more sensitive to radiation therapy. Radiation therapy uses high energy x-rays, particles, or radioactive seeds to kill tumor cells and shrink tumors. External beam radiation therapy (EBRT) is a type of radiation that uses a machine to aim high-energy rays at the tumor from outside the body. Chemotherapy drugs work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving decitabine in combination with standard of care surgery, radiation and/or chemotherapy may be safe, tolerable, and/or effective in treating patients with surgically resectable HPV-negative head and neck squamous cell cancers.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether adding decitabine (a drug that affects how genes are turned on or off) before and after surgery can improve outcomes for patients with HPV-negative head and neck squamous cell carcinoma — a type of head and neck cancer not caused by the HPV virus — that is eligible for surgical removal. **You may be eligible if...** - You are 18 or older with a confirmed HPV-negative squamous cell carcinoma of the head and neck that can be surgically removed - You have measurable disease before surgery - Your blood counts, liver, and kidney function are adequate - Your cancer has not spread to distant organs **You may NOT be eligible if...** - You are pregnant or breastfeeding, or not willing to use contraception - You have had prior radiation to the same area of the head and neck - You have had systemic chemotherapy in the past 5 years for another cancer - You have serious uncontrolled illnesses (heart failure, active infection, psychiatric conditions) - You have HIV with immune suppression Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREBiospecimen Collection

Undergo blood sample collection

DRUGChemotherapy

Given concurrent chemotherapy

DRUGDecitabine

Given IV

RADIATIONExternal Beam Radiation Therapy

Undergo EBRT

OTHERQuestionnaire Administration

Ancillary studies

PROCEDURESurgical Procedure

Undergo standard of care surgery


Locations(1)

Mayo Clinic in Florida

Jacksonville, Florida, United States

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NCT06997094


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