Plain-English translation of NCT04900623 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Phase 2 — Testing in a bigger group (up to a few hundred people) to see if the treatment actually works and is still safe.
The ReACT Study is testing whether a blood test called NavDx® HPV ctDNA can help personalize treatment for people with HPV-positive throat cancer. Instead of giving everyone the same radiation and chemotherapy doses, this study uses the blood test results to identify patients who might do well with lower doses. The goal is to reduce side effects while keeping the cancer treatment effective.
Currently, all patients with HPV-positive throat cancer receive standard-dose radiation and chemotherapy, even though some patients may not need full doses. This research wants to see if the blood test can safely identify which patients can tolerate lower treatment doses, which could mean fewer long-term side effects like difficulty swallowing, dry mouth, and other complications.
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You will have blood tests before, during, and after your radiation therapy to measure HPV DNA levels. Based on your blood test results and other factors, your doctor will assign you to either low-dose or standard-dose radiation therapy, sometimes combined with chemotherapy. Treatment lasts 5–7 weeks, and you'll have regular follow-up visits and additional blood tests for the next 5 years to monitor how well the treatment worked and watch for any cancer recurrence.
AI-generated summary from trial data · Aug 10, 2026 · Not medical advice
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