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Future Oncol ; 17(20): 2563-2571, 2021 Jul.
Article in English | MEDLINE | ID: mdl-33769069

ABSTRACT

Two oral hypomethylating agents, oral azacitidine (CC-486) and decitabine/cedazuridine (ASTX727), have recently entered the clinical domain. CC-486 has been shown to improve overall survival as maintenance therapy for older patients with acute myeloid leukemia in complete remission, whereas the combination of decitabine with cedazuridine, a cytidine deaminase inhibitor, is indicated for the treatment of adult patients with myelodysplastic syndromes and chronic myelomonocytic leukemia with intermediate-1, or higher, International Prognostic Scoring System risk. This article briefly summarizes the clinical development of both drugs, the pivotal studies that led to their approval and some of the issues faced in extending the use of these drugs to other indications.


Lay abstract One of the key challenges in treating acute myeloid leukemia is to prevent relapse after remission has been achieved. This means that developing an effective maintenance treatment is very important. Maintenance treatment is given for a prolonged period and so it needs to be easy to give and well tolerated. Oral azacitidine is an example of this type of treatment and is the first drug that has been shown to improve survival as maintenance therapy for acute myeloid leukemia patients. This article describes the key studies that led to the approval of this important therapy.


Subject(s)
Antimetabolites, Antineoplastic/administration & dosage , Decitabine/administration & dosage , Drug Approval , Leukemia, Myeloid, Acute/drug therapy , Myelodysplastic Syndromes/drug therapy , Uridine/analogs & derivatives , Antimetabolites, Antineoplastic/adverse effects , Antimetabolites, Antineoplastic/pharmacokinetics , Azacitidine/administration & dosage , Azacitidine/adverse effects , Azacitidine/pharmacokinetics , Biological Availability , Clinical Trials, Phase III as Topic , DNA Methylation/drug effects , Decitabine/adverse effects , Decitabine/pharmacokinetics , Drug Combinations , Humans , Randomized Controlled Trials as Topic , Remission Induction/methods , Uridine/administration & dosage , Uridine/adverse effects , Uridine/pharmacokinetics
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