RecruitingPhase 2NCT05357794
Effectiveness of Concurrent Ultra-Low-Dose Total-Skin Electron Beam Therapy and Brentuximab Vedotin Given Quarterly Over 12 Months for Patients With Mycosis Fungoides
Sponsor
M.D. Anderson Cancer Center
Enrollment
30 participants
Start Date
Oct 13, 2022
Study Type
INTERVENTIONAL
Conditions
Summary
To learn if a form of radiation therapy (called ultra-low-dose - total skin electron beam therapy \[ULD-TSEBT\]) in combination with brentuximab vedotin can help to control mycosis fungoides
Eligibility
Min Age: 18 Years
Plain Language Summary
Simplified for easier understanding
This study is testing a combined treatment approach for mycosis fungoides — a type of skin lymphoma — using low-dose full-body radiation (electron beam therapy) given alongside a targeted drug called brentuximab vedotin, delivered quarterly over 12 months.
**You may be eligible if...**
- You have biopsy-confirmed mycosis fungoides at any stage (I–IV)
- Your cancer has returned or stopped responding to previous treatments
- Your tumor cells express at least 1% of a protein called CD30
- You have received prior treatments for this cancer
**You may NOT be eligible if...**
- Your Sezary cell count in the blood is 1,000 or more per microliter at the time of enrollment
- You have had prior brentuximab vedotin treatment with unacceptable toxicity
- You have significant nerve damage (peripheral neuropathy) of grade 2 or higher
- You have active serious infections or other major health conditions
- You are pregnant or breastfeeding
Talk to your doctor to see if this trial is right for you.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
DRUGBrentuximab vedotin
Given by Vein (IV)
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT05357794
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