Ontology highlight
ABSTRACT: Purpose
Patients with acute myeloid leukemia (AML) unfit for, or resistant to, intensive chemotherapy are often treated with DNA methyltransferase inhibitors (DNMTi). Novel combinations may increase efficacy. In addition to demethylating CpG island gene promoter regions, DNMTis enhance PARP1 recruitment and tight binding to chromatin, preventing PARP-mediated DNA repair, downregulating homologous recombination (HR) DNA repair, and sensitizing cells to PARP inhibitor (PARPi). We previously demonstrated DNMTi and PARPi combination efficacy in AML in vitro and in vivo. Here, we report a phase I clinical trial combining the DNMTi decitabine and the PARPi talazoparib in relapsed/refractory AML.Patients and methods
Decitabine and talazoparib doses were escalated using a 3 + 3 des
SUBMITTER: Baer MR
PROVIDER: S-EPMC8976746 | biostudies-literature | 2022 Apr
REPOSITORIES: biostudies-literature