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
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 - Animals
KW - Antineoplastic Agents/therapeutic use
KW - Humans
KW - Lymphoma, T-Cell, Cutaneous/drug therapy
KW - Skin Neoplasms/drug therapy
UR - https://www.scopus.com/pages/publications/84896128144
U2 - 10.1517/13543784.2014.876407
DO - 10.1517/13543784.2014.876407
M3 - Review article
C2 - 24397291
SN - 1354-3784
VL - 23
SP - 457
EP - 467
JO - Expert opinion on investigational drugs
JF - Expert opinion on investigational drugs
IS - 4
ER -