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)

MD Anderson Cancer Center

Houston, Texas, United States

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NCT05357794


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