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Clinical Trial RTOG 0920

A Phase III Study of Postoperative Radiation Therapy (IMRT) +/- Cetuximab for Locally-Advanced Resected Head and Neck Cancer
Principal Investigator
Eric Donnelly
  • Status: Accepting New Patients
  • Study Type: Therapeutic, Treatment
  • Protocol No:.RTOG 0920
The purpose of this study is to compare the effects, good and/or bad, of radiation therapy alone versus radiation therapy and cetuximab on head and neck cancer after surgery.
It is standard treatment to remove head and/or neck tumors surgically when able to do so. After surgery it is common to have radiation therapy to help stop tumors from growing back or spreading to other parts of the body. Cetuximab is a drug that may slow down or prevent tumor growth. It works by blocking certain pathways that lead to tumor growth. This study will see if the addition of this drug with radiation therapy can improve overall outcomes over radiation alone.
Some of the eligibility criteria include:
  • Participants must be 18 years of age or older.
  • Participants must have had surgery for a head and/or neck tumor.
  • Participants with primary hypopharynx tumors are not eligible.
Note: This is only a partial list of eligibility criteria. Please contact the Lurie Cancer Center for complete screening information if you are interested in this clinical trial.
Description of Treatment
There are two groups in this study, Group 1 and Group 2. Participants will be randomized like flipping a coin)into one or the other group. Both groups will receive radiation therapy for about 6 weeks. Group 2 will be given cetuximab intravenously (through a vein) once a week and may receive up to 11 doses.
Sara Duffey
Clinical Research and Education Specialist
Robert H. Lurie Comprehensive Cancer Center

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last updated: 05-Oct-15 04:33 PM


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