SAVAL Study: HPV-related Oropharynx Cancer and ctDNA Testing
This study, called SAVAL, is looking at a new way to decide who needs radiation after surgery for HPV-related oropharyngeal (throat) cancer. People with this type of cancer often do well, but treatments can have significant side effects. The study wants to see if a blood test called a Circulating Tumor DNA test (ctDNA test) can help reduce the number of people who need radiation. You might be able to join if you are 18 or older and have a confirmed diagnosis of p16+ squamous cell carcinoma of the oropharynx. The main goal is to see how long people live without their cancer progressing (Progression-free Survival) after two years. The current status of the study is unclear, and it plans to enroll 61 people.
- Study design
- This is an interventional study planning to enroll 61 participants. It involves different groups: some will be observed, and others will receive standard radiation treatment.
- What's involved
- You will undergo a ctDNA blood test before and after surgery, and then every three months for two years after treatment.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your progression-free survival will be measured for two years after your last treatment.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Selective Adjuvant Therapy for HPV-mediated Oropharynx SCCs Based on Residual Circulating Tumor DNA Levels (SAVAL)
At a glance
Conditions
Where it's being run
5 sites across 1 statesStudy leadership
- Jason K Molitoris, MD, PhD · PRINCIPAL_INVESTIGATOR · University of Maryland/Maryland Proton Treatment Center
Who to contact
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What this trial measures
- Progression-free Survival (PFS)2 year post last treatment
Percent PFS at 2 year post last treatment inclusive of patients undergoing salvage treatment for LRR.