Precision proton beams and chemo aim to beat childhood muscle cancer
NCT ID NCT01871766
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a personalized treatment plan for children with a rare muscle cancer called rhabdomyosarcoma. Depending on their risk level, patients receive standard or stronger chemotherapy, plus focused proton beam radiation and/or surgery to remove the tumor. The goal is to improve survival while limiting damage to healthy tissue.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- Vincristine, dactinomycin, cyclophosphamide, and anti-angiogenic maintenance therapy
- What this could lead to
- If successful, this approach could improve event-free survival for children with intermediate- and high-risk rhabdomyosarcoma while reducing side effects from radiation.
- What could go wrong
- This is a Phase 2 trial with a relatively small number of participants (115). The results may not generalize to all patients, and intensified chemotherapy carries risks of serious side effects.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Cook Children's Medical Center
Fort Worth, Texas, 76104, United States
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Nemours Children's Clinic
Jacksonville, Florida, 32207, United States
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St. Jude Children's Research Hospital
Memphis, Tennessee, 38105, United States
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University of Florida Proton Therapy Institute
Jacksonville, Florida, 32206, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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