De-escalated Radiation for Human Papillomavirus-Positive Squamous Cell Carcinoma of the Oropharynx
Part of paid clinical trials in Orange, California.
- Sponsor
- University of California, Irvine
- Study ID
- NCT05600842
- Status
- Recruiting
Conditions
- HPV Positive Oropharyngeal Squamous Cell Carcinoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Intensity-Modulated Radiation Therapy (IMRT) — RADIATIONIMRT will be given in 30 daily fractions at 2 Gy per fraction (60 Gy total) beginning Day 1; Six fractions will be delivered per week. High risk patients will receive induction chemotherapy with 2 cycles of carboplatin and paclitaxel.
Study Details
This is a single-arm, observational registry study determining the effects of reduced radiation dose in select patients with human papillomavirus (HPV) positive oropharyngeal cancer.
Key Dates
- Start date
- Nov 3, 2022
- Status verified
- Mar 2026
- Primary completion
- Nov 30, 2026
- Completion
- Nov 30, 2026
Study Design
- Enrollment
- 111 participants (estimated)
Arms
- Arm: De-escalated radiotherapy
Primary Outcome Measure
2-Year Progression-Free Survival [ Time Frame: Given the natural history of this disease, PFS will be monitored up to 2 years from registration ]
Central Contacts
- Chao Family Comprehensive Cancer Center University of California, Irvine877-827-8839
- University of California Irvine Medical
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Chao Family Comprehensive Cancer Center, University of California, Irvine | Orange | California | 92868 |
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