Abstract |
Current treatment recommendations for chronic myeloid leukemia (CML) are guided by results from multiple clinical trials involving tyrosine kinase inhibitors that target BCR-ABL1. Consideration of the unique clinical benefits and potential risks associated with each tyrosine kinase inhibitor approved for the treatment of CML is crucial for physicians when recommending the most appropriate therapy for each patient. Monitoring for and prompt management of adverse events may increase adherence to therapy and optimize patient outcomes. Here we provide an overview of the efficacy and safety of tyrosine kinase inhibitors approved for the treatment of CML, as well as recommendations for the management of key adverse events reported with these agents in clinical trials involving patients with CML.
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Authors | Benedito A Carneiro, Jason B Kaplan, Francis J Giles |
Journal | Expert review of hematology
(Expert Rev Hematol)
Vol. 8
Issue 4
Pg. 457-79
(Aug 2015)
ISSN: 1747-4094 [Electronic] England |
PMID | 25938861
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
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Chemical References |
- Antineoplastic Agents
- Protein Kinase Inhibitors
- Fusion Proteins, bcr-abl
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Topics |
- Antineoplastic Agents
(adverse effects, therapeutic use)
- Clinical Trials as Topic
- Disease Management
- Drug-Related Side Effects and Adverse Reactions
(diagnosis, therapy)
- Fusion Proteins, bcr-abl
(antagonists & inhibitors)
- Humans
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive
(complications, drug therapy, metabolism)
- Protein Kinase Inhibitors
(adverse effects, therapeutic use)
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