| Literature DB >> 29616864 |
Robert L Redner1,2, Jan H Beumer1,2,3, Patricia Kropf2, Mounzer Agha1,2, Michael Boyiadzis1,2, Kathleen Dorritie1,2, Rafic Farah1,2, Jing-Zhao Hou1,2, Annie Im1,2, Seah H Lim2, Anastasios Raptis1,2, Alison Sehgal1,2, Susan M Christner1, Daniel Normolle4, Daniel E Johnson2.
Abstract
Src family kinases (SFKs) are hyperactivated in acute myeloid leukemia (AML). SFKs impede the retinoic acid receptor, and SFK inhibitors enhance all-trans retinoic acid (ATRA)-mediated cellular differentiation in AML cell lines and primary blasts. To translate these findings into the clinic, we undertook a phase-I dose-escalation study of the combination of the SFK inhibitor dasatinib and ATRA in patients with high-risk myeloid neoplasms. Nine subjects were enrolled: six received 70 mg dasatinib plus 45 mg/m2 ATRA daily, and three received 100 mg dasatinib plus 45 mg/m2 ATRA daily for 28 days. Headache and QTc prolongations were the only two grade 3 adverse events observed. No significant clinical responses were observed. We conclude that the combination of 70 mg dasatinib and 45 mg/m2 ATRA daily is safe with acceptable toxicity. Our results provide the safety profile for further investigations into the clinical efficacy of this combination therapy in myeloid malignancies.Entities:
Keywords: AML; ATRA; dasatinib; pharmacodynamics; pharmacokinetics; phase I
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Year: 2018 PMID: 29616864 PMCID: PMC6201295 DOI: 10.1080/10428194.2018.1443330
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022