Abstract
Introduction: Cutaneous T cell lymphomas are a heterogeneous group of malignancies characterized by the accumulation of malignantly transformed skin homing T cells. Mycosis fungoides, a typically indolent form of cutaneous T cell lymphoma characterized by patches, plaques, and tumors, and Sézary syndrome, a leukemic variant, make up the majority of cutaneous T cell lymphomas, and prognosis in advanced-stage disease remains poor. The defucosylated monoclonal antibody, mogamulizumab, targets the CC chemokine receptor 4 on malignant cells of cutaneous T cell lymphoma and offers a novel approach to treating advanced-stage disease. Areas covered: Mogamulizumab has shown efficacy in phase I/II clinical trials in patients with cutaneous T cell lymphoma, with overall response rates between 35–36.8%. Currently, a phase III trial is underway comparing mogamulizumab to vorinostat in the treatment of cutaneous T cell lymphoma. Expert opinion: Mogamulizumab has already been approved in Japan for the treatment of relapsed/refractory adult T cell leukemia/lymphoma. Clinical trials, currently in progress, are investigating the efficacy of mogamulizumab for advanced and metastatic solid tumors. Depletion of regulatory T cells, and the resulting boost in anti-tumor immunity caused by mogamulizumab, have great potential in the treatment of a wide range of malignancies, including cutaneous T cell lymphomas.
Original language | English (US) |
---|---|
Pages (from-to) | 1277-1280 |
Number of pages | 4 |
Journal | Expert Opinion on Orphan Drugs |
Volume | 4 |
Issue number | 12 |
DOIs | |
State | Published - Dec 1 2016 |
Externally published | Yes |
Keywords
- CC Chemokine receptor 4 (CCR4)
- Sézary Syndrome (SS)
- cutaneous T cell lymphoma (CTCL)
- mycosis fungoides (MF)
- regulator T cells (Tregs)
ASJC Scopus subject areas
- Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
- Health Policy
- Pharmacology (medical)