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Leukemia Research
Volume 33, Issue 11
, Pages 1481-1484
, November 2009
Phase II study of imatinib mesylate as therapy for patients with systemic mastocytosis
References
- . Mastocytosis: state of the art. Pathobiology. 2007;74:121–132
- . Kit: molecule of interest for the diagnosis and treatment of mastocytosis and other neoplastic disorders. Curr Cancer Drug Target. 2007;7:492–503
- Identifications of mutations in the coding sequence of the proto-oncogen c-kit in a human mast cell leukemia cell line causing ligand-independent activation of c-kit product. J Clin Invest. 1993;92:1736–1744
- Novel approaches in the treatment of systemic mastocytosis. Cancer. 2006;107:1429–1439
- The c-KIT mutation causing human mastocytosis is resistant to STI571 and other KIT kinase inhibitors; kinases with enzymatic site mutations show different inhibitor sensitivity profiles than wild-type kinases and those with regulatory-type mutations. Blood. 2002;99:1741–1744
- Imatinib mesylate in the treatment of systemic mastocytosis: a phase II trial. Cancer. 2006;107:345–351
- Diagnostic criteria and classification of mastocytosis: a consensus proposal. Leuk Res. 2001;25(7):603–625
- Imatinib mesylate in the treatment of hematologic malignancies. Expert Opin Biol Ther. 2007;7:1597–1611
- Imatinib for systemic mast cell disease. Lancet. 2003;362:535–537
- A novel form of mastocytosis associated with a transmembrane c-kit mutation and response to imatinib. Blood. 2004;103:3222–3225
- Juxtamembrane mutant V560Gkit is more sensitive to imatinib (STI571) compared with wild-type c-kit whereas the kinase mutant D816Vkit is resistant. Mol Cancer Ther. 2002;1:1115–1124
PII: S0145-2126(08)00567-5
doi: 10.1016/j.leukres.2008.12.020
© 2008 Elsevier Ltd. All rights reserved.
« Previous
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Leukemia Research
Volume 33, Issue 11
, Pages 1481-1484
, November 2009
