Lymphoma Clinical Trial
Official title:
Phase II Trial of Doxorubicin HCl Liposome Injection (Doxil®) in Advanced Stage Cutaneous T-Cell Lymphoma Followed by Bexarotene (Targretin®)
RATIONALE: Drugs used in chemotherapy, such as liposomal doxorubicin and bexarotene, work in
different ways to stop the growth of cancer cells, either by killing the cells or by stopping
them from dividing. Bexarotene may also cause cutaneous T-cell lymphoma cells to look more
like normal cells, and to grow and spread more slowly. Giving liposomal doxorubicin followed
by bexarotene may be an effective treatment for cutaneous T-cell lymphoma.
PURPOSE: This phase II trial is studying how well giving liposomal doxorubicin followed by
bexarotene works in treating patients with cutaneous T-cell lymphoma.
OBJECTIVES:
Primary
- Determine the progression-free survival of patients with stage IB-IV cutaneous T-cell
lymphoma treated with doxorubicin HCl liposome followed by bexarotene.
Secondary
- Determine the complete and partial response rate in patients treated with this regimen.
OUTLINE: This is an open-label, multicenter study.
Patients receive doxorubicin HCl liposome IV over 30-90 minutes once on day 1. Treatment
repeats every 2 weeks for 8 courses. Beginning within 4 weeks after the last dose of
doxorubicin HCl liposome, patients receive oral bexarotene once daily for at least 16 weeks.
Patients who achieve a complete or partial response may continue to receive bexarotene in the
absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed periodically for 5 years.
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