Multidisciplinary Management of Mycosis Fungoides/Sézary Syndrome

Curr Hematol Malig Rep. 2017 Jun;12(3):234-243. doi: 10.1007/s11899-017-0387-9.

Abstract

Purpose of review: Diagnosis and management of mycosis fungoides and Sézary syndrome (MF/SS) require accurate clinicopathological correlation and a multidisciplinary approach. We reviewed major advances in the field regarding diagnostic and prognostic tools as well as skin-directed therapies (SDTs) and systemic agents for MF/SS published in the past 2 years.

Recent findings: Improved technology (T-cell receptor high-throughput sequencing) and increased multicenter collaboration (Cutaneous Lymphoma International Consortium) have led to diagnostic/prognostic advances. Concurrently, numerous genomic studies have enhanced understanding of disease pathogenesis. Advances in SDTs include topical resiquimod, a novel potent Toll-like receptor (TLR) agonist; consensus CTCL phototherapy guidelines; and use of low-dose radiation therapy. Novel systemic therapies for advanced disease of note include targeted antibody drug conjugates (brentuximab vedotin), immune checkpoint inhibitors, and allogeneic hematopoietic stem cell transplantation (HSCT). Our "toolbox" to diagnose and treat the spectrum of MF/SS continues to expand. Further characterization of genomic data going forward will enable a rational approach to selecting and combining therapies to improve patient care.

Keywords: Consensus CTCL phototherapy; Cutaneous Lymphoma International Consortium; MF/SS; Mycosis fungoides and Sézary syndrome; Toll-like receptor agonist.

Publication types

  • Review

MeSH terms

  • Biomarkers, Tumor
  • Combined Modality Therapy
  • Disease Management
  • Genomics / methods
  • Humans
  • Mycosis Fungoides / diagnosis*
  • Mycosis Fungoides / etiology
  • Mycosis Fungoides / therapy*
  • Prognosis
  • Sezary Syndrome / diagnosis*
  • Sezary Syndrome / etiology
  • Sezary Syndrome / therapy*
  • Skin Neoplasms / diagnosis*
  • Skin Neoplasms / etiology
  • Skin Neoplasms / therapy*
  • Treatment Outcome

Substances

  • Biomarkers, Tumor