A Study Comparing Personalized Radiation Therapy With Standard Radiation Therapy in People With HPV-Positive Throat Cancer (NCT06563479)
Phase III Randomized and Double-blinded Trial of De-escalated Radiation in FMISO PET-selected Good Risk Versus Standard of Care Radiation in Unselected HPV Positive Oropharyngeal Cancer
๐ฉบ Plain-English Summary (8th-Grade Level)
The researchers are doing this study to find out if a personalized approach to chemoradiation therapy (which may include a lower dose of radiation) is as effective as the standard chemoradiation therapy in people with HPV-positive throat cancer. Other purposes of this study include looking at the following: * Whether a lower dose of radiation in combination with standard chemotherapy causes fewer side effects than the standard dose of radiation therapy in combination with standard chemotherapy * How the study approaches (lower dose of radiation therapy + standard chemotherapy and standard dose of radiation therapy + standard chemotherapy) affect participants' quality of life. The researchers will measure quality of life by having participants fill out questionnaires.
Who can join: Review the eligibility criteria below.
Location: Hartford Healthcare (Data Collection Only) โ Hartford, Connecticut
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (9 Sites)
- Hartford Healthcare (Data Collection Only) โ Hartford, Connecticut
- Baptist Alliance MCI (Data Collection Only) โ Miami, Florida
- Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities) โ Basking Ridge, New Jersey
- Memorial Sloan Kettering Monmouth (Limited Protocol Activities) โ Middletown, New Jersey
- Memorial Sloan Kettering Bergen (Limited Protocol Activities) โ Montvale, New Jersey
- Memorial Sloan Kettering Suffolk- Commack (Limited Protocol Activities) โ Commack, New York
- Memorial Sloan Kettering Westchester (Limited Protocol Activities) โ Harrison, New York
- Memorial Sloan Kettering Cancer Center (All Protocol Activities) โ New York, New York
- Memorial Sloan Kettering Nassau (Limited Protocol Activities) โ Uniondale, New York
๐ Contact the Study Coordinator
Phone: (212) 639-3341
Email: leen2@mskcc.org
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in HPV-Related Squamous Cell Carcinoma
- Trial of Cemiplimab, or Cemip-Chemo Followed by Biomarker-guided Treatment for Pts w/HPV H&N Ca โ Baltimore, Maryland
Explore by condition: All HPV-Related Squamous Cell Carcinoma clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.