Literature DB >> 31739705

Complexity of chronic-phase CML management after failing a second-generation TKI.

Riad El Fakih1, Naeem Chaudhri1, Feras Alfraih1, Caitlin R Rausch2, Kiran Naqvi2, Elias Jabbour2.   

Abstract

The treatment landscape of chronic myeloid leukemia (CML) was radically changed with the introduction of imatinib in 2001. With the emergence of treatment failure with imatinib, more specific and potent second- and third-generation tyrosine kinase inhibitors (TKIs) were developed. Currently, 6 TKIs and one protein synthesis inhibitor are available on the market for CML treatment. Despite the availability of these agents, it is not uncommon for some patients to experience treatment failure across several lines of therapy. Sequencing the available treatment options is a challenging task that becomes more complex after patients fail the more potent second- and third-generation TKIs. The ability to successfully salvage such patients is limited. In this paper, we will briefly review the mechanisms of treatment failure in chronic-phase CML (CP-CML) and focus on the complexity of managing patients who fail a second-generation TKI.

Entities:  

Keywords:  CML; Failure of second-generation TKI; Resistance to TKI

Mesh:

Substances:

Year:  2019        PMID: 31739705     DOI: 10.1080/10428194.2019.1691196

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


  3 in total

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Journal:  Int J Hematol Oncol       Date:  2022-06-30

3.  Cryptotanshinone enhances the efficacy of Bcr-Abl tyrosine kinase inhibitors via inhibiting STAT3 and eIF4E signalling pathways in chronic myeloid leukaemia.

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  3 in total

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