3.8 Article Proceedings Paper

Second-line Therapy and Beyond Resistance for the Treatment of Patients With Chronic Myeloid Leukemia Post Imatinib Failure

期刊

CLINICAL LYMPHOMA & MYELOMA
卷 9, 期 -, 页码 S272-S279

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CIG MEDIA GROUP, LP
DOI: 10.3816/CLM.2009.s.023

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Farnesyltransferase inhibitors; Histone deacetylases; Kinase inhibitors; Omacetaxine; T3151 mutations

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Chronic myeloid leukemia (CML) is characterized at the molecular level by the presence of the Philadelphia chromosome (Ph) and the resultant oncogenic signaling by the BCR-ABL fusion protein. The treatment and outlook for CML were revolutionized by the introduction of imatinib, but resistance is a substantial barrier to successful treatment in many patients. Introduction of the second-generation tyrosine kinase inhibitors (TKI) dasatinib and nilotinib has provided effective therapeutic options for many patients with resistance to front-line imatinib. However, the T3151 mutation remains a significant clinical issue because it is insensitive to all currently available agents. A number of new agents are in development and many hold the promise of activity in T3151-mutated disease. Successful treatment of patients with disease harboring T3151 might lie in the effective combination or sequencing of these new agents with existing TKI therapies.

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