Optimizing Dosing of Brentuximab Vedotin for Mycosis Fungoides, Sezary Syndrome, and Lymphomatoid Papulosis

Who is this study for? Patients with Mycosis Fungoides, Lymphomatoid Papulosis, Sezary Syndrome
What treatments are being studied? Brentuximab Vedotin
Status: Recruiting
Location: See all (8) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The purpose of this study is to test any good and bad effects of the study drug called brentuximab vedotin at a lower dose than is FDA-approved.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ Mycosis fungoides (MF) and Sezary Syndrome (SS)

• Pathologically confirmed mycosis fungoides/sezary syndrome at the enrolling institution, disease stage IB (defined as patches, plaque, or papules that involve 10% of the skin surface viscera) or higher

• ° CD30 negative mycosis fungoides patients are eligible.

• Age ≥ 18 years

• ECOG Performance Score ≤ 2

• For Cohort 1, patients who have not received brentuximab vedotin are eligible.

• For Cohort 2, patients who have previously had brentuximab vedotin for MF/SS are eligible. Patients previously treated on Cohort 1 who were discontinued due to toxicity are not eligible for Cohort 2.

• Previous systemic anti-cancer therapy must have been discontinued at least 2 weeks prior to treatment.

• ° See section 6.2 Subject Exclusion Criteria for guidelines regarding adjuvant and maintenance therapy for prior malignancy.

• Topical or systemic steroids (equivalent to ≤ 10 mg/day of prednisone) may be considered if dose has been constant and discontinuation may lead to rebound flare in disease, adrenal insufficiency, and/or unnecessary suffering, after discussion with PI.

• If HIV+, patient must be on stable anti-retroviral treatment for 12 weeks prior to C1D1, with CD4 count \>200 within 7 days prior to C1D1.

• Females of childbearing potential must be on acceptable form of birth control per instutional standard.

⁃ Lymphomatoid papulosis (LyP)

• Pathologically confirmed lymphomatoid papulosis at the enrolling institution

• Requiring systemic treatment per investigator's discretion

• Age ≥ 18 years

• ECOG Performance Score ≤ 2

• Previous systemic anti-cancer therapy must have been discontinued at least 2 weeks prior to treatment.

• Topical or systemic steroids (equivalent to ≤ 10 mg/day of prednisone) may be considered if dose has been constant and discontinuation may lead to rebound flare in disease, adrenal insufficiency, and/or unnecessary suffering.

• If HIV+, patient must be on stable anti-retroviral treatment for 12 weeks prior to C1D1, with CD4 count \>200 within 7 days prior to C1D1.

• Females of childbearing potential must be on acceptable form of birth control per institutional standard

Locations
United States
California
Stanford University Medical Center
RECRUITING
Stanford
New Jersey
Memorial Sloan Kettering Basking Ridge
RECRUITING
Basking Ridge
Memorial Sloan Kettering Monmouth
RECRUITING
Middletown
Memorial Sloan Kettering Bergen
RECRUITING
Montvale
New York
Memorial Sloan Kettering Commack
RECRUITING
Commack
Memorial Sloan Kettering Westchester
RECRUITING
Harrison
Memorial Sloan Kettering Cancer Center
RECRUITING
New York
Memorial Sloan Kettering Nassau
RECRUITING
Uniondale
Contact Information
Primary
Alison Moskowitz, MD
moskowia@mskcc.org
646-608-3726
Backup
Patricia Myskowski, MD
646-608-2351
Time Frame
Start Date: 2018-07-03
Estimated Completion Date: 2026-07
Participants
Target number of participants: 58
Treatments
Experimental: not been previously treated with brentuximab vedotin.
Patients with MF/SS who have not been previously treated with brentuximab vedotin. For MF patients: Treatment delays lasting longer than 8 weeks for toxicity will result in removal from study. As of October 2020, the Simon two stage design for Cohort 1 has restarted at the 1.2 mg/kg dose.
Experimental: treated with reduced dose brentuximab vedotin
Patients with MF/SS who were previously treated with brentuximab vedotin. Up to 10 patients will be enrolled onto this cohort. Following identification of a promising dose after the completion of the full Cohort 1 Simon two stage design, enrollment will initiate onto cohort 2 at the dose found to be promising in cohort 1. For MF patients: Treatment delays lasting longer than 8 weeks for toxicity will result in removal from study. The 0.9mg/kg dose did not meet the primary endpoint for response, therefore 1.2 mg/kg has been chosen as the dose for Cohort 2. As of October 2020, enrollment on our exploratory Cohort 2 has opened at the 1.2 mg/kg dose.
Experimental: Patients with LyP
Patients with LyP patients with lymphomatoid papulosis will receive brentuximab vedotin 0.9 mg/kg as an intravenous infusion over 30 minutes every three weeks. Cohort 3 will enroll patients concurrently with Cohort 1. Treatment may be held if felt to be in patient's best interest (for example: for toxicity or no active disease). Treatment can be reinitiated after discussion with MSK PI as long as the study is still open and patient has not received alternate systemic therapy.
Sponsors
Leads: Memorial Sloan Kettering Cancer Center
Collaborators: Seagen Inc.

This content was sourced from clinicaltrials.gov