Trial of Individualized Adaptive RT in HPV-related High Risk Oropharynx Cancer

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

19

Participants

Timeline

Start Date

December 20, 2023

Primary Completion Date

July 31, 2026

Study Completion Date

July 31, 2026

Conditions
Oropharynx CancerHPV-Related Carcinoma
Interventions
RADIATION

Radiation

"Patients will undergo 2 phases of RT replanning:~1. Based on 2-week DCE-MRI low BV tumor subvolume, patients will have a PTVboost1 that will start to receive 2.5Gy/day with fraction 16. PTVboost1=(persistent lowBVsubvolume\_2 wks+ MTV3\_2 weeks)+ 3mm margin.~2. Based on 4-week FDG-PET MTV3, patients with have a PTVboost2 cone down that will receive 2.5Gy/day starting with fraction 23. PTVboost2=(LBV\_2 wks + MTV3\_4wks)+ 3mm margin~3. Thus, the tumor subvolumes that are included in the boost from fx16-35 will receive 86 Gy EQD2 (80Gy physical dose) and the FDG-avid subvolumes which start boost at 2 weeks but are not persistently avid at 4 wks will receive 76Gy EQD2 (74Gy physical dose)."

DRUG

Platinum based chemotherapy

Standard of care therapy, weekly, with either Cisplatin or Carboplatin

Trial Locations (1)

48109

University of Michigan Rogel Cancer Center, Ann Arbor

All Listed Sponsors
lead

University of Michigan Rogel Cancer Center

OTHER

NCT06234748 - Trial of Individualized Adaptive RT in HPV-related High Risk Oropharynx Cancer | Biotech Hunter | Biotech Hunter