Literature DB >> 20072833

Dasatinib.

Markus Lindauer1, Andreas Hochhaus.   

Abstract

Dasatinib, (former BMS 354825), is an orally available small-molecule multikinase inhibitor. It potently inhibits BCR-ABL and SRC-family kinases (SRC, LCK, YES, FYN), but also c-KIT, PDGFR-alpha and beta, and ephrin receptor kinase.Dasatinib is about 300 times more potent than imatinib in cells expressing unmutated BCR-ABL in vitro. The drug has demonstrated activity against clinically relevant mutations, including those associated with poor prognosis during ongoing imatinib therapy.Dasatinib is approved for the treatment of patients with BCR-ABL-positive chronic myeloid leukemia (CML), resistant or intolerant to imatinib in chronic, accelerated, and blast phase. It also is approved for the treatment of Philadelphia Chromosome positive (Ph+) acute lymphoblastic leukemia (ALL) resistant or intolerant to imatinib.A single daily dose of 100 mg in chronic phase CML results in high hematologic and molecular remission rates and prolongation of survival. In accelerated and blastic phase as well as in ALL, 70 mg twice daily is recommended. Complete hematologic and cytogenetic remissions (CR) frequently occur even in this patient group with poor prognosis. Remissions however are very short.Side effects of dasatinib are frequent but mostly moderate and manageable and include cytopenias and pleural effusions. The role of dasatinib in other diseases, including solid tumors, has to be identified.

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Year:  2010        PMID: 20072833     DOI: 10.1007/978-3-642-01222-8_7

Source DB:  PubMed          Journal:  Recent Results Cancer Res        ISSN: 0080-0015


  19 in total

Review 1.  Role of chemokines and their receptors in chronic lymphocytic leukemia: function in microenvironment and targeted therapy.

Authors:  Ting-Ting Han; Lei Fan; Jian-Yong Li; Wei Xu
Journal:  Cancer Biol Ther       Date:  2013-10-22       Impact factor: 4.742

2.  Dasatinib therapy results in decreased B cell proliferation, splenomegaly, and tumor growth in a murine model of lymphoma expressing Myc and Epstein-Barr virus LMP2A.

Authors:  Jamie L Dargart; Kamonwan Fish; Leo I Gordon; Richard Longnecker; Osman Cen
Journal:  Antiviral Res       Date:  2012-05-16       Impact factor: 5.970

Review 3.  Development of an effective therapy for chronic myelogenous leukemia.

Authors:  David W Woessner; Carol S Lim; Michael W Deininger
Journal:  Cancer J       Date:  2011 Nov-Dec       Impact factor: 3.360

Review 4.  Changing paradigm of the treatment of Philadelphia chromosome-positive acute lymphoblastic leukemia.

Authors:  Ryuzo Ohno
Journal:  Curr Hematol Malig Rep       Date:  2010-10       Impact factor: 3.952

5.  Single-cell mass cytometry of differential immune and drug responses across a human hematopoietic continuum.

Authors:  Sean C Bendall; Erin F Simonds; Peng Qiu; El-ad D Amir; Peter O Krutzik; Rachel Finck; Robert V Bruggner; Rachel Melamed; Angelica Trejo; Olga I Ornatsky; Robert S Balderas; Sylvia K Plevritis; Karen Sachs; Dana Pe'er; Scott D Tanner; Garry P Nolan
Journal:  Science       Date:  2011-05-06       Impact factor: 47.728

Review 6.  Targeting cytoskeleton reorganisation as antimetastatic treatment.

Authors:  Miguel Quintela-Fandino; Antonio González-Martín; Ramon Colomer
Journal:  Clin Transl Oncol       Date:  2010-10       Impact factor: 3.405

Review 7.  Co-operating STAT5 and AKT signaling pathways in chronic myeloid leukemia and mastocytosis: possible new targets of therapy.

Authors:  Siham Bibi; Melis Dilara Arslanhan; Florent Langenfeld; Sylvie Jeanningros; Sabine Cerny-Reiterer; Emir Hadzijusufovic; Luba Tchertanov; Richard Moriggl; Peter Valent; Michel Arock
Journal:  Haematologica       Date:  2014-03       Impact factor: 9.941

8.  Dasatinib inhibits proinflammatory functions of mature human neutrophils.

Authors:  Krisztina Futosi; Tamás Németh; Robert Pick; Tibor Vántus; Barbara Walzog; Attila Mócsai
Journal:  Blood       Date:  2012-03-12       Impact factor: 22.113

9.  The FGFR4-G388R polymorphism promotes mitochondrial STAT3 serine phosphorylation to facilitate pituitary growth hormone cell tumorigenesis.

Authors:  Toru Tateno; Sylvia L Asa; Lei Zheng; Thomas Mayr; Axel Ullrich; Shereen Ezzat
Journal:  PLoS Genet       Date:  2011-12-08       Impact factor: 5.917

Review 10.  Emerging Agents for the Treatment of Advanced, Imatinib-Resistant Gastrointestinal Stromal Tumors: Current Status and Future Directions.

Authors:  Sebastian Bauer; Heikki Joensuu
Journal:  Drugs       Date:  2015-08       Impact factor: 9.546

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