Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Jul-Aug;96(4):458-471.
doi: 10.1016/j.abd.2020.12.007. Epub 2021 May 28.

Mycosis fungoides and Sézary syndrome: focus on the current treatment scenario

Affiliations
Review

Mycosis fungoides and Sézary syndrome: focus on the current treatment scenario

José Antonio Sanches et al. An Bras Dermatol. 2021 Jul-Aug.

Abstract

Cutaneous T-cell lymphomas are a heterogeneous group of lymphoproliferative disorders, characterized by infiltration of the skin by mature malignant T cells. Mycosis fungoides is the most common form of cutaneous T-cell lymphoma, accounting for more than 60% of cases. Mycosis fungoides in the early-stage is generally an indolent disease, progressing slowly from some patches or plaques to more widespread skin involvement. However, 20% to 25% of patients progress to advanced stages, with the development of skin tumors, extracutaneous spread and poor prognosis. Treatment modalities can be divided into two groups: skin-directed therapies and systemic therapies. Therapies targeting the skin include topical agents, phototherapy and radiotherapy. Systemic therapies include biological response modifiers, immunotherapies and chemotherapeutic agents. For early-stage mycosis fungoides, skin-directed therapies are preferred, to control the disease, improve symptoms and quality of life. When refractory or in advanced-stage disease, systemic treatment is necessary. In this article, the authors present a compilation of current treatment options for mycosis fungoides and Sézary syndrome.

Keywords: Lymphoma, T-cell, cutaneous; Mycosis fungoides; Sezary syndrome; Therapeutics.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Willemze R., Cerroni L., Kempf W., Berti E., Facchetti F., Swerdlow S.H. The 2018 update of the WHO-EORTC classification for primary cutaneous lymphomas. Blood. 2019;133:1703–1714. - PMC - PubMed
    1. Olsen E.A. Evaluation, Diagnosis, and Staging of Cutaneous Lymphoma. Dermatol Clin. 2015;33:643–644. - PubMed
    1. Kadin M.E., Hughey L.C., Wood G.S. Large-cell transformation of mycosis fungoides-differential diagnosis with implications for clinical management: a consensus statement of the US Cutaneous Lymphoma Consortium. J Am Acad Dermatol. 2014;70:374–376. - PubMed
    1. Miyashiro D., Sanches J.A. Cutaneous manifestations of adult T-cell leukemia/lymphoma. Semin Diagn Pathol. 2020;37:81–91. - PubMed
    1. Olsen E.A., Whittaker S., Kim Y.H., Duvic M., Prince H.M., Lessin S.R. Clinical end points and response criteria in mycosis fungoides and Sezary syndrome: a consensus statement of the International Society for Cutaneous Lymphomas, the United States Cutaneous Lymphoma Consortium, and the Cutaneous Lymphoma Task Force of the European Organisation for Research and Treatment of Cancer. J Clin Oncol. 2011;29:2598–2607. - PMC - PubMed