TY - JOUR
T1 - EORTC consensus recommendations for the treatment of mycosis fungoides/Sézary syndrome - Update 2023
AU - Latzka, Johanna
AU - Assaf, Chalid
AU - Bagot, Martine
AU - Cozzio, Antonio
AU - Dummer, Reinhard
AU - Guenova, Emmanuella
AU - Gniadecki, Robert
AU - Hodak, Emmilia
AU - Jonak, Constanze
AU - Klemke, Claus-Detlev
AU - Knobler, Robert
AU - Morrris, Stephen
AU - Nicolay, Jan P
AU - Ortiz-Romero, Pablo L
AU - Papadavid, Evangelia
AU - Pimpinelli, Nicola
AU - Quaglino, Pietro
AU - Ranki, Annamari
AU - Scarisbrick, Julia
AU - Stadler, Rudolf
AU - Väkevä, Liisa
AU - Vermeer, Maarten H
AU - Wehkamp, Ulrike
AU - Whittaker, Sean
AU - Willemze, Rein
AU - Trautinger, Franz
N1 - Publisher Copyright:
© 2023 The Authors
PY - 2023/12
Y1 - 2023/12
N2 - On behalf of the EORTC Cutaneous Lymphoma Tumours Group (EORTC-CLTG) and following up on earlier versions published in 2006 and 2017 this document provides an updated standard for the treatment of mycosis fungoides and Sézary syndrome (MF/SS). It considers recent relevant publications and treatment options introduced into clinical practice after 2017. Consensus was established among the authors through a series of consecutive consultations in writing and a round of discussion. Treatment options are assigned to each disease stage and, whenever possible and clinically useful, separated into first- and second line options annotated with levels of evidence. Major changes to the previous version include the incorporation of chlormethine, brentuximab vedotin, and mogamulizumab, recommendations on the use of pegylated interferon α (after withdrawal of recombinant unpegylated interferons), and the addition of paragraphs on supportive therapy and on the care of older patients. Still, skin-directed therapies are the most appropriate option for early-stage MF and most patients have a normal life expectancy but may suffer morbidity and impaired quality of life. In advanced disease treatment options have expanded recently. Most patients receive multiple consecutive therapies with treatments often having a relatively short duration of response. For those patients prognosis is still poor and only for a highly selected subset long term remission can be achieved with allogeneic stem cell transplantation. Understanding of the disease, its epidemiology and clinical course, and its most appropriate management are gradually advancing, and there is well-founded hope that this will lead to further improvements in the care of patients with MF/SS.
AB - On behalf of the EORTC Cutaneous Lymphoma Tumours Group (EORTC-CLTG) and following up on earlier versions published in 2006 and 2017 this document provides an updated standard for the treatment of mycosis fungoides and Sézary syndrome (MF/SS). It considers recent relevant publications and treatment options introduced into clinical practice after 2017. Consensus was established among the authors through a series of consecutive consultations in writing and a round of discussion. Treatment options are assigned to each disease stage and, whenever possible and clinically useful, separated into first- and second line options annotated with levels of evidence. Major changes to the previous version include the incorporation of chlormethine, brentuximab vedotin, and mogamulizumab, recommendations on the use of pegylated interferon α (after withdrawal of recombinant unpegylated interferons), and the addition of paragraphs on supportive therapy and on the care of older patients. Still, skin-directed therapies are the most appropriate option for early-stage MF and most patients have a normal life expectancy but may suffer morbidity and impaired quality of life. In advanced disease treatment options have expanded recently. Most patients receive multiple consecutive therapies with treatments often having a relatively short duration of response. For those patients prognosis is still poor and only for a highly selected subset long term remission can be achieved with allogeneic stem cell transplantation. Understanding of the disease, its epidemiology and clinical course, and its most appropriate management are gradually advancing, and there is well-founded hope that this will lead to further improvements in the care of patients with MF/SS.
KW - Consensus
KW - Humans
KW - Immunologic Factors/therapeutic use
KW - Lymphoma, T-Cell, Cutaneous/drug therapy
KW - Mycosis Fungoides/pathology
KW - Quality of Life
KW - Sezary Syndrome/therapy
KW - Skin Neoplasms/drug therapy
UR - http://www.scopus.com/inward/record.url?scp=85174679979&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2023.113343
DO - 10.1016/j.ejca.2023.113343
M3 - Review article
C2 - 37890355
SN - 0959-8049
VL - 195
SP - 113343
JO - European Journal of Cancer
JF - European Journal of Cancer
M1 - 113343
ER -