Exploratory Pilot Study of Brentuximab Vedotin (SGN-35) in Patients With Mycosis Fungoides and SÚzary Syndrome With Variable CD30 Expression Level

The purpose of this study is to learn the effects of an investigational medication, SGN 35, on patients with mycosis fungoides. Despite a wide range of therapeutic options, the treatments are associated with short response duration, thus this condition is largely incurable. This investigational drug may offer less toxicity than standard treatments and have better tumor specific targeting.

Stanford is not currently accepting new patients for this trial. You may want to check clinicaltrials.gov to see if other locations are recruiting.



  • drug : Brentuximab vedotin

Phase: N/A


Ages Eligible For Study:

18 Years - N/A

Inclusion Criteria

1. Patient has biopsy-proven MF/SS, stage IB-IVB, and failed one standard systemic therapy. - Skin biopsy will be obtained within 3 months of beginning study medication, for assessment of CD30 expression by immunohistochemistry (IHC). This data will be used to ensure equal enrollment of patients in the 3 groups of varying CD30 expression (low, intermediate, high). If patient has different lesion morphology (patch, plaque, tumor), a biopsy will be obtained from each morphologic lesion. If the patient has one type of lesion morphology, a biopsy from 2 separate anatomic sites will be obtained. - The highest CD30 expression value among biopsies will be used to determine which of the 3 groups the subject will be assigned to. 2. Patients must have the following minimum wash-out from previous treatments: - >= 3 weeks for local radiation therapy, systemic cytotoxic anticancer therapy, treatment with other anti-cancer investigational agents (including monoclonal antibody). - > 3 weeks for retinoids, interferons, vorinostat, romidepsin, denileukin diftitox. - > 3 wks for phototherapy. - > 2 wks for topical therapy (including topical steroid, retinoid, nitrogen mustard, or imiquimod). 3. At least 18 years of age. 4. ECOG performance status of <= 2. 5. Patients must be available for study treatment, blood sampling, study assessments, and management of toxicity at the treating institution. 6. Adequate baseline laboratory data: absolute neutrophil count (ANC) >= 1000/uL, platelets >= 50,000/uL, bilirubin <= 2X upper limit of normal (ULN) or <= 3X ULN for patients with Gilbert's disease, serum creatinine <= 2X ULN, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) <= 3X ULN. 7. Women of childbearing potential (WOCBP) must have a negative serum beta-HCG pregnancy test result within seven days of treatment. 8. Ability to understand and the willingness to sign a written informed consent document.

External Links

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Contact information

Primary Contact:

Kokil Bakshi 650-421-6370

Stanford University School of Medicine 300 Pasteur Drive Stanford, CA 94305

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