Seminars in Oncology
Volume 34, Supplement 5 , Pages S21-S28, December 2007

Mycosis Fungoides: Pathophysiology and Emerging Therapies

  • Madeleine Duvic

      Affiliations

    • Department of Dermatology, University of Texas M.D. Anderson Cancer Center, Houston, TX.
    • Corresponding Author InformationAddress reprint requests to Madeleine Duvic, MD, Professor of Internal Medicine and Dermatology, University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Blvd. #434, Houston, TX 77030
    • Dr Duvic has received research grant support from Merck, Ligand, Gloucester, Curagen, Biogen, BioCryst, Yaupon, Cyclacel, Celgene, Novartis, and Allos. She has received honoraria from Merck, Ligand, and Novartis.
  • ,
  • Francine M. Foss

      Affiliations

    • Yale Cancer Center, New Haven, CT.

Primary cutaneous T-cell lymphomas (CTCLs) are a heterogeneous group of non-Hodgkin’s lymphomas characterized by skin infiltration of neoplastic T lymphocytes. Mycosis fungoides and its leukemic variant Sézary syndrome represent the most common CTCL subtypes. Current treatment for patients with mycosis fungoides involves topical and systemic therapies for the cutaneous manifestations. However, no therapy is curative and patients often progress to advanced extracutaneous CTCL with visceral organ complications or relapsed disease that is frequently refractory to most topical and aggressive systemic regimens. The emergence of novel targeted therapies such as biologic agents, histone deacetylase inhibitors, and purine nucleoside phosphorylase inhibitors offers promise for more effective and safer treatment strategies for refractory CTCLs.

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PII: S0093-7754(07)00225-4

doi:10.1053/j.seminoncol.2007.11.006

Seminars in Oncology
Volume 34, Supplement 5 , Pages S21-S28, December 2007