RecruitingPhase 2NCT07058805

Compartmentalized Postoperative Radiotherapy in Head and Neck Cancer

COMPORT: Compartmentalization in Postoperative Radiotherapy for Head and Neck Squamous Cell Carcinoma - A Phase II Clinical Trial


Sponsor

Olgun Elicin

Enrollment

50 participants

Start Date

Jan 15, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

COMPORT is a multicenter phase II clinical trial evaluating a personalized approach to postoperative radiotherapy in patients with head and neck squamous cell carcinoma (HNSCC). The study investigates whether a risk-adapted, compartmentalized radiotherapy strategy can safely reduce the treatment volume, and thus the side effects, without increasing the risk of tumor recurrence. Eligible patients are those with surgically treated cancers of the oral cavity, oropharynx, larynx, or hypopharynx who have a standard indication for postoperative radiotherapy. The primary outcome is the rate of recurrence in anatomical compartments that would normally be irradiated but are intentionally omitted in this study. COMPORT aims to generate high-level evidence to support a more personalized and less toxic standard of care in postoperative head and neck cancer management.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Compartmentalized Postoperative Radiotherapy for people with head and neck cancer, head and neck squamous cell carcinoma, and other related conditions. The study is currently recruiting participants at 3 locations. People eligible for this study include aged 18 Years and older.

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

RADIATIONCompartmentalized Postoperative Radiotherapy

Pathology- and imaging-guided compartmentalized postoperative radiotherapy (PORT), with or without concurrent systemic treatment. Based on a predefined algorithm, PORT or specific anatomical volumes may be omitted. Dose prescription and volumes are risk-adapted.


Locations(3)

University Hospital of Basel

Basel, Switzerland

Inselspital, Bern University Hospital

Bern, Switzerland

University Hospital of Zurich

Zurich, Switzerland

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NCT07058805


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