TY - JOUR
T1 - Emerging therapies for the treatment of essential thrombocythemia
AU - Diaz, Adolfo Enrique
AU - Scherber, Robin M.
AU - Mesa, Ruben A.
N1 - Publisher Copyright:
© 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2018/10/3
Y1 - 2018/10/3
N2 - Introduction: Historically the treatment of essential thrombocythemia (ET) has focused on decreasing the risk of thrombotic and hemorrhagic complications. Despite numerous available therapies with a long history of clinical use, there remains only one Federal Drug Administration approved therapy for high-risk ET patient populations. Areas covered: In recent years, the treatment landscape for ET has been evolving at a fast pace. Therapies such as JAK1/JAK2 inhibitors have demonstrated promising safety, tolerability, and efficacy. Alternative targeted agents are also in development, including Histone Deacetylase Inhibitors, Telomerase Inhibitors, and Human Double Minute 2 Inhibitors. Herein, authors provide an overview of emerging therapies for the treatment of ET. Expert opinion: Patients with ET often have a near-normal life expectancy. Treatments are targeted to primary and secondary prevention of complications such as thrombosis and hemorrhagic events. To date, no therapies have demonstrated a definitive alteration of the natural history of ET. Since several exciting agents are in development, well designed prospective trials would offer more facts regarding choice of therapy, sequence of use and/or association with established therapies.
AB - Introduction: Historically the treatment of essential thrombocythemia (ET) has focused on decreasing the risk of thrombotic and hemorrhagic complications. Despite numerous available therapies with a long history of clinical use, there remains only one Federal Drug Administration approved therapy for high-risk ET patient populations. Areas covered: In recent years, the treatment landscape for ET has been evolving at a fast pace. Therapies such as JAK1/JAK2 inhibitors have demonstrated promising safety, tolerability, and efficacy. Alternative targeted agents are also in development, including Histone Deacetylase Inhibitors, Telomerase Inhibitors, and Human Double Minute 2 Inhibitors. Herein, authors provide an overview of emerging therapies for the treatment of ET. Expert opinion: Patients with ET often have a near-normal life expectancy. Treatments are targeted to primary and secondary prevention of complications such as thrombosis and hemorrhagic events. To date, no therapies have demonstrated a definitive alteration of the natural history of ET. Since several exciting agents are in development, well designed prospective trials would offer more facts regarding choice of therapy, sequence of use and/or association with established therapies.
KW - JAK2 inhibitors
KW - Myeloproliferative neoplasms
KW - essential thrombocythemia
KW - interferon
KW - newer therapies
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U2 - 10.1080/21678707.2018.1520091
DO - 10.1080/21678707.2018.1520091
M3 - Review article
AN - SCOPUS:85055175072
SN - 2167-8707
VL - 6
SP - 567
EP - 575
JO - Expert Opinion on Orphan Drugs
JF - Expert Opinion on Orphan Drugs
IS - 10
ER -