TY - JOUR
T1 - Novel therapies for cutaneous T-cell lymphoma
T2 - What does the future hold?
AU - Guenova, Emmanuella
AU - Hoetzenecker, Wolfram
AU - Rozati, Sima
AU - Levesque, Mitchell P.
AU - Dummer, Reinhard
AU - Cozzio, Antonio
N1 - Funding Information:
This work was supported in part by the ‘Krebsforschung-Schweiz’ (Cancer Research in Switzerland) and by the German Research Foundation (GU1271/2-1 to E Guenova). R Dummer receives research funding from AstraZeneca, Novartis, Cephalon, Merck Sharp and Dohme, Transgene, Bristol-Myers Squibb, Roche, GlaxoSmithKline and Bayer, and has a consultant or advisory board relationship with AstraZeneca, Novartis, Cephalon, Merck Sharp & Dohme, Transgene, Genta, Bayer, Roche, Bristol-Myers Squibb, GlaxoSmithKline and Spirig.
PY - 2014/4
Y1 - 2014/4
N2 - Introduction: Cutaneous T-cell lymphomas (CTCLs) represent a group of extranodal non-Hodgkin lymphomas, of which mycosis fungoides (MF) is the most frequent. Standard therapeutic approaches are well established and often achieve stable disease. However, cure for MF is rare and thus novel therapies are needed. Areas covered: This review provides a discussion of the most promising new therapeutic approaches in the management of MF and other rare CTCLs. It includes targeted therapies with antibodies against surface molecules on malignant T cells (e.g., brentuximab), novel chemotherapeutic agents (e.g., pralatrexate), small-molecule compounds (e.g., panobinostat) and evidence of emerging targets in CTCLs (e.g., anti-IL-31). It also provides discussion of immune checkpoint inhibitors such as anti-PD1 that are worth considering in the treatment of leukaemic CTCL variants. Finally, it gives a brief overview of the possible use of stem-cell transplantation. Expert opinion: There is no doubt that progress has been made in the treatment of CTCLs with new, innovative and promising therapies approaching. However, there is still an urgent need to identify and test additional targets in well-designed clinical trials.
AB - Introduction: Cutaneous T-cell lymphomas (CTCLs) represent a group of extranodal non-Hodgkin lymphomas, of which mycosis fungoides (MF) is the most frequent. Standard therapeutic approaches are well established and often achieve stable disease. However, cure for MF is rare and thus novel therapies are needed. Areas covered: This review provides a discussion of the most promising new therapeutic approaches in the management of MF and other rare CTCLs. It includes targeted therapies with antibodies against surface molecules on malignant T cells (e.g., brentuximab), novel chemotherapeutic agents (e.g., pralatrexate), small-molecule compounds (e.g., panobinostat) and evidence of emerging targets in CTCLs (e.g., anti-IL-31). It also provides discussion of immune checkpoint inhibitors such as anti-PD1 that are worth considering in the treatment of leukaemic CTCL variants. Finally, it gives a brief overview of the possible use of stem-cell transplantation. Expert opinion: There is no doubt that progress has been made in the treatment of CTCLs with new, innovative and promising therapies approaching. However, there is still an urgent need to identify and test additional targets in well-designed clinical trials.
KW - Alemtuzumab
KW - Brentuximab
KW - Cutaneous lymphoma
KW - Mycosis fungoides
KW - Panobinostat
KW - Pralatrexate
KW - Sezary syndrome
KW - Th1
KW - Th2
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U2 - 10.1517/13543784.2014.876407
DO - 10.1517/13543784.2014.876407
M3 - Review article
C2 - 24397291
AN - SCOPUS:84896128144
SN - 1354-3784
VL - 23
SP - 457
EP - 467
JO - Expert Opinion on Investigational Drugs
JF - Expert Opinion on Investigational Drugs
IS - 4
ER -