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Glasdegib: A Novel Hedgehog Pathway Inhibitor for Acute Myeloid Leukemia

Acute myeloid leukemia (AML) is an aggressive myeloid disorder that is associated with a generally poor prognosis. Effective treatment options have been limited for older patients with AML who are not able to undergo intensive remission induction chemotherapy due to advanced age or comorbidities. Ne...

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Detalles Bibliográficos
Autores principales: Thompson, Daniel L., Moore, Donald C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Harborside Press LLC 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848813/
https://www.ncbi.nlm.nih.gov/pubmed/33532119
http://dx.doi.org/10.6004/jadpro.2020.11.2.8
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author Thompson, Daniel L.
Moore, Donald C.
author_facet Thompson, Daniel L.
Moore, Donald C.
author_sort Thompson, Daniel L.
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description Acute myeloid leukemia (AML) is an aggressive myeloid disorder that is associated with a generally poor prognosis. Effective treatment options have been limited for older patients with AML who are not able to undergo intensive remission induction chemotherapy due to advanced age or comorbidities. New and novel agents are needed to improve treatment outcomes for this patient population. Glasdegib is a novel Hedgehog signaling pathway inhibitor approved by the U.S. Food & Drug Administration for the treatment of patients with newly diagnosed AML who are 75 years of age or older or who have comorbidities that preclude intensive induction chemotherapy. Glasdegib is approved in combination with low-dose cytarabine (LDAC). This approval is based on the results of a multicenter, open-label, randomized trial of glasdegib plus LDAC vs. LDAC monotherapy in which the addition of glasdegib resulted in an improvement in median overall survival.
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spelling pubmed-78488132021-02-01 Glasdegib: A Novel Hedgehog Pathway Inhibitor for Acute Myeloid Leukemia Thompson, Daniel L. Moore, Donald C. J Adv Pract Oncol Prescriber's Corner Acute myeloid leukemia (AML) is an aggressive myeloid disorder that is associated with a generally poor prognosis. Effective treatment options have been limited for older patients with AML who are not able to undergo intensive remission induction chemotherapy due to advanced age or comorbidities. New and novel agents are needed to improve treatment outcomes for this patient population. Glasdegib is a novel Hedgehog signaling pathway inhibitor approved by the U.S. Food & Drug Administration for the treatment of patients with newly diagnosed AML who are 75 years of age or older or who have comorbidities that preclude intensive induction chemotherapy. Glasdegib is approved in combination with low-dose cytarabine (LDAC). This approval is based on the results of a multicenter, open-label, randomized trial of glasdegib plus LDAC vs. LDAC monotherapy in which the addition of glasdegib resulted in an improvement in median overall survival. Harborside Press LLC 2020-03 2020-03-01 /pmc/articles/PMC7848813/ /pubmed/33532119 http://dx.doi.org/10.6004/jadpro.2020.11.2.8 Text en © 2020 Harborside™ http://creativecommons.org/licenses/by-nc-nd/3.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial Non-Derivative License, which permits unrestricted non-commercial and non-derivative use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Prescriber's Corner
Thompson, Daniel L.
Moore, Donald C.
Glasdegib: A Novel Hedgehog Pathway Inhibitor for Acute Myeloid Leukemia
title Glasdegib: A Novel Hedgehog Pathway Inhibitor for Acute Myeloid Leukemia
title_full Glasdegib: A Novel Hedgehog Pathway Inhibitor for Acute Myeloid Leukemia
title_fullStr Glasdegib: A Novel Hedgehog Pathway Inhibitor for Acute Myeloid Leukemia
title_full_unstemmed Glasdegib: A Novel Hedgehog Pathway Inhibitor for Acute Myeloid Leukemia
title_short Glasdegib: A Novel Hedgehog Pathway Inhibitor for Acute Myeloid Leukemia
title_sort glasdegib: a novel hedgehog pathway inhibitor for acute myeloid leukemia
topic Prescriber's Corner
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848813/
https://www.ncbi.nlm.nih.gov/pubmed/33532119
http://dx.doi.org/10.6004/jadpro.2020.11.2.8
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