CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 74 target
Drug / intervention
Chemoradiation +2 morecombination
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06984861
NCT06984861Phase 2RecruitingHigh Momentum

Major Radiation Dose De-Escalation Concurrent With Chemotherapy for Advanced Stage Human Papilloma Virus Associated Oropharyngeal Carcinoma

Memorial Sloan Kettering Cancer Center·interventional·Posted May 22, 2025·Updated May 11, 2026

In Brief

A Phase 2 clinical trial evaluating 18F-FMISO PET/CT Scan, Chemoradiation, and 1 other intervention for Oropharyngeal Carcinoma. Currently recruiting, targeting 74 participants across 7 sites.

Signals

Enrolling ahead of pace

Detailed Summary

The researchers are doing this study is to find out if lower doses (given in fewer treatments over a shorter period of time) of radiation therapy in combination with standard-of-care chemotherapy is an effective treatment for people with Human Papilloma Virus (HPV)-positive throat cancer and works as well as the standard doses of radiation therapy in combination with standard-of-care chemotherapy. The chemotherapy drugs used in combination with radiation therapy in this study include cisplatin, carboplatin, and 5-fluorouracil (5-FU).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2Recruiting
202620272028
First PostedMay 22, 2025
Enrollment StartMay 13, 2025
Primary CompletionMay 1, 2028
TodayJul 1, 2026
Enrollment to primary: 3.0 yearsPosted 1.1 years agoPrimary completion in 1.8 years

Interventions

18F-FMISO PET/CT Scanother

The 18F-FMISO PET/CT Scan Protocol consists first of an IV bolus injection of approximately 5-10 mCi of the radiotracer. Subjects will undergo 18F-FMISO scan (only 1 injection) occurs at 8-10 treatment days\* into chemoradiation. Each patient will have a baseline staging FDG PET scan which is used to localize the tumor at the primary site and all suspicious cervical neck nodes (\> 1 cm in short axis diameter with focal abnormal increased FDG avidity). These lesions are then assessed on the respective 18F-FMISO PET/CT.

Chemoradiationcombination

Patients will start with induction chemotherapy of carboplatin, paclitaxel and cetuximab for 6 weeks and when downstaged to T1-2 and \< N3, the patient is eligible to receive concurrent chemoradiation per protocol. All subjects will undergo radiation treatments (IMRT and/or proton therapy). A total radiation therapy of 30Gy will be delivered to the oropharynx and neck at 2Gy per fraction per day over 15 days for patients who exhibited no evidence of hypoxia on the intra-treatment 18F-FMISO PET/CT. Concurrent chemotherapy (2 cycles) will be given. After completion of chemotherapy and radiation therapy, a 4 month (+/-4 weeks)

Questionnairesother

EQ-5D-5L, MDADI-HN, COST-FACIT