Pilot Study of Chemotherapy for HPV-Associated Oropharyngeal Cancer

PHASE1CompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

October 1, 2020

Primary Completion Date

January 9, 2023

Study Completion Date

January 9, 2023

Conditions
Oropharyngeal Squamous Cell Carcinoma
Interventions
OTHER

Transoral Robotic Surgery (TORS) or Radiotherapy

Participants assigned to this group will receive transoral robotic surgery (TORs) or radiotherapy. Radiotherapy is given once a day for 5 weeks. A percentage of subjects who undergo surgery may need further radiotherapy with or without chemotherapy based on the results of the surgery. TORs is surgery in which a robot with arms is used to remove cancer from hard-to-reach areas of the mouth and throat.

OTHER

Chemotherapy and Low-Dose Radiotherapy

Participants assigned to this group will receive 5 weeks of chemotherapy combined with low- dose radiotherapy.

OTHER

Chemotherapy and High-Dose Radiotherapy

Participants assigned to this group will receive 7 weeks of chemotherapy combined with high- dose radiotherapy.

DRUG

Paclitaxel

This drug will be combined with carboplatin during induction therapy for 9 weeks.

DRUG

Carboplatin

This drug will be combined with paclitaxel during induction therapy for 9 weeks.

Trial Locations (1)

60637

University of Chicago Medical Center, Chicago

All Listed Sponsors
lead

University of Chicago

OTHER

NCT04572100 - Pilot Study of Chemotherapy for HPV-Associated Oropharyngeal Cancer | Biotech Hunter | Biotech Hunter