Expired Study
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Los Angeles, California 90095


RATIONALE: Bortezomib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. PURPOSE: This phase II trial is studying how well bortezomib works in treating patients with relapsed or refractory cutaneous T-cell lymphoma.

Study summary:

OBJECTIVES: - Determine the response rates (complete response and partial response) and duration of response in patients with relapsed or refractory cutaneous T-cell lymphoma treated with bortezomib. - Determine the safety and tolerability of this drug in these patients. OUTLINE: This is an open-label study. Patients receive bortezomib IV over 3-5 seconds on days 1, 4, 8, and 11. Treatment repeats every 21 days for up to 8 courses in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed at 1 month and then at least every 3 months for 2 years or until disease progression. PROJECTED ACCRUAL: A total of 15-25 patients will be accrued for this study.


Inclusion Criteria: - Histologically confirmed cutaneous T-cell lymphoma, including mycosis fungoides/Sézary syndrome - Stage IB-IV disease - Relapsed or refractory disease OR intolerant to ≥ 1 prior systemic therapy - Measurable disease by radiological imaging or clinical finding - Age Over 18 - Performance status Karnofsky 70-100% - Hematopoietic - WBC > 2,000/mm^3 - Absolute neutrophil count > 1,500/mm^3 - Platelet count > 75,000/mm^3 - Hemoglobin > 8.0 g/dL - Hepatic - Bilirubin < 2 times upper limit of normal (ULN) - AST and ALT < 3 times ULN - Renal - Creatinine < 1.5 times ULN - Creatinine clearance ≥ 30 mL/min - Negative pregnancy test - Fertile patients must use effective contraception - More than 3 months since prior high-dose chemotherapy - More than 30 days since prior and no other concurrent investigational drugs Exclusion Criteria: - history of myelodysplastic syndromes - evidence of CNS disease - pregnant or nursing - peripheral neuropathy ≥ grade 2 - hypersensitivity to bortezomib, boron, or mannitol - serious medical condition or psychiatric illness that would preclude study participation - concurrent immunotherapy - concurrent chemotherapy - concurrent steroid dose > 10 mg/day of prednisone or its equivalent - concurrent radiotherapy - concurrent surgery for the malignancy



Primary Contact:

Principal Investigator
Lauren C. Pinter-Brown, MD
Jonsson Comprehensive Cancer Center

Backup Contact:


Location Contact:

Los Angeles, California 90095
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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