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A phase-1 study of dasatinib plus all-trans retinoic acid in acute myeloid leukemia.

Robert L RednerJan H BeumerPatricia KropfMounzer AghaMichael BoyiadzisKathleen DorritieRafic FarahJing-Zhao HouAnnie ImSeah H LimAnastasios RaptisAlison SehgalSusan M ChristnerDaniel P NormolleDaniel E Johnson
Published in: Leukemia & lymphoma (2018)
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.
Keyphrases
  • acute myeloid leukemia
  • combination therapy
  • chronic myeloid leukemia
  • physical activity
  • bone marrow
  • open label
  • clinical trial
  • allogeneic hematopoietic stem cell transplantation
  • immune response
  • tyrosine kinase