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A phase II trial of miltefosine in patients with cutaneous T-cell lymphoma


Bulletin du Cancer. Volume 93, Number 11, 10115-8, Novembre 2006, Electronic Journal of Oncology

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Author(s) : Charles Dumontet, Luc Thomas, Frédéric Bérard, Jean François Gimonet, Bertrand Coiffier

Summary : A phase II trial evaluating 6% topical miltefosine solution was performed in 12 pretreated patients with cutaneous T-cell lymphoma. Miltefosine (Miltex ®) was administered for 8 weeks, once per day during the first week then twice every day for seven weeks. Main side effects consisted in moderate to mild pruritus or desquamation in 57 % and 50 % of patients, respectively. No systemic nor biological toxicity was observed. This treatment was administered on an outpatient basis exclusively. The overall response rate was 58 % with a median duration of response of 12 months. Miltefosine is a safe, simple and effective treatment in certain patients with cutaneous T-cell lymphoma.

Keywords : miltefosine, cutaneous T-cell lymphoma

 

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