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Clinical trialNCT06088381RecruitingPhase 2Interventional

Selective Adjuvant Therapy for HPV-mediated Oropharynx SCCs Based on Residual Circulating Tumor DNA Levels (SAVAL)

SponsorUniversity of Maryland, BaltimoreEnrollment61HPV Positive Oropharyngeal Squamous Cell CarcinomaHead and Neck CancerHead and Neck Squamous Cell CarcinomaOropharynx CancerOropharynx Squamous Cell Carcinoma
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

Patients with human papillomavirus (HPV)-related oropharyngeal cancer generally have favorable outcomes and how well they do depends on the specific details about the patient and their cancer. How well they do isn't as related to the kinds of treatment they get. However, there are significant side effects for the various types of treatments they may get. Because these patients generally have favorable outcomes no matter the kind of treatment, reducing side effects should be a priority when choosing their treatment. The goal of this clinical research study is to evaluate whether a new blood test called a Circulating Tumor DNA test (ctDNA test) can decrease the number of people that require radiation after surgery. This blood test is often elevated in people when they are diagnosed with head and neck cancer. There are studies that show that cancer most often returns when this blood test is positive after treatment. This study will test patients' blood before and after surgery. In cases where the test is negative after surgery, people on the study will not receive radiation unless they are considered high risk based on surgery findings. The hope is that radiation and its potential side effects can be limited to only people that need the treatment.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

  • Jason K Molitoris, MD, PhD

    University of Maryland/Maryland Proton Treatment Center

    Principal Investigator

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

5 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Maryland Proton Treatment Center

    Baltimore, Maryland, United States

    Recruiting
  • University of Maryland Greenebaum Cancer Center

    Baltimore, Maryland, United States

    Recruiting
  • Upper Chesapeake Health

    Bel Air, Maryland, United States

    Not, yet, recruiting
  • Central Maryland Radiation Oncology

    Columbia, Maryland, United States

    Not, yet, recruiting
  • Baltimore Washington Medical Center

    Glen Burnie, Maryland, United States

    Not, yet, recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
7 Mar 2024
Primary completion
18 Dec 2028
Completion
18 Dec 2030
Last update posted
10 Nov 2025
Registered enrollment
61
Registry id
NCT06088381

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.