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New Drugs for Chronic Myelogenous Leukemia

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Abstract

The introduction of tyrosine kinase inhibitors (TKIs) has changed the landscape of therapy for chronic myelogenous leukemia (CML). Once considered an incurable malignancy, CML now has become a manageable chronic condition. Despite the great advances that imatinib has brought to the treatment of CML, some patients still develop resistance to imatinib and other TKIs, such as dasatinib and nilotinib. Furthermore, none of the clinically available TKIs is capable of eradicating leukemia stem cells and therefore curing CML. Several new compounds have been developed in recent years in an attempt to manage TKI-resistant CML. These include third-generation TKIs (ponatinib, danusertib) and even old compounds such as omacetaxine, which were developed before imatinib and now find a possible niche in the treatment of imatinib-resistant CML. We review the current preclinical and clinical data on the most promising new compounds for the treatment of CML.

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Authors and Affiliations

  1. Department of Leukemia, Unit 428, M. D. Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA

    Alfonso Quintás-Cardama

  2. Hematology Department, Hospital Israelita Albert Einstein, São Paulo, Brazil

    Fabio P. S. Santos

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  1. Fabio P. S. Santos
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  2. Alfonso Quintás-Cardama
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Correspondence to Alfonso Quintás-Cardama.

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Santos, F.P.S., Quintás-Cardama, A. New Drugs for Chronic Myelogenous Leukemia. Curr Hematol Malig Rep 6, 96–103 (2011). https://doi.org/10.1007/s11899-011-0079-9

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