Literature DB >> 29616864

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

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

Mesh:

Substances:

Year:  2018        PMID: 29616864      PMCID: PMC6201295          DOI: 10.1080/10428194.2018.1443330

Source DB:  PubMed          Journal:  Leuk Lymphoma        ISSN: 1026-8022


  31 in total

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Journal:  Leukemia       Date:  2007-04-19       Impact factor: 11.528

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Journal:  Blood       Date:  2006-06-13       Impact factor: 22.113

7.  Phase I dose-escalation and pharmacokinetic study of dasatinib in patients with advanced solid tumors.

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Review 8.  The role of retinoids and retinoic acid receptors in normal hematopoiesis.

Authors:  S J Collins
Journal:  Leukemia       Date:  2002-10       Impact factor: 11.528

9.  Isocitrate dehydrogenase 1 mutations prime the all-trans retinoic acid myeloid differentiation pathway in acute myeloid leukemia.

Authors:  Héléna Boutzen; Estelle Saland; Clément Larrue; Fabienne de Toni; Lara Gales; Florence A Castelli; Mathilde Cathebas; Sonia Zaghdoudi; Lucille Stuani; Tony Kaoma; Romain Riscal; Guangli Yang; Pierre Hirsch; Marion David; Véronique De Mas-Mansat; Eric Delabesse; Laurent Vallar; François Delhommeau; Isabelle Jouanin; Ouathek Ouerfelli; Laurent Le Cam; Laetitia K Linares; Christophe Junot; Jean-Charles Portais; François Vergez; Christian Récher; Jean-Emmanuel Sarry
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10.  All-trans retinoic acid as adjunct to intensive treatment in younger adult patients with acute myeloid leukemia: results of the randomized AMLSG 07-04 study.

Authors:  Richard F Schlenk; Michael Lübbert; Axel Benner; Alexander Lamparter; Jürgen Krauter; Wolfgang Herr; Hans Martin; Helmut R Salih; Andrea Kündgen; Heinz-A Horst; Peter Brossart; Katharina Götze; David Nachbaur; Mohammed Wattad; Claus-Henning Köhne; Walter Fiedler; Martin Bentz; Gerald Wulf; Gerhard Held; Bernd Hertenstein; Hans Salwender; Verena I Gaidzik; Brigitte Schlegelberger; Daniela Weber; Konstanze Döhner; Arnold Ganser; Hartmut Döhner
Journal:  Ann Hematol       Date:  2016-10-03       Impact factor: 3.673

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Review 2.  Src-family Protein Tyrosine Kinases: A promising target for treating Cardiovascular Diseases.

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