Abstract |
Lymphoplasmacytic lymphoma is an indolent B-cell, non-Hodgkin lymphoma (NHL), the majority of which are characterized by production of a monoclonal immunoglobulin M ( IgM) protein and are known as Waldenström macroglobulinemia. Identification of highly recurrent activating somatic mutation in MYD88 has improved our understanding of the pathogenesis of Waldenström macroglobulinemia and has therapeutic implications. Here, we review novel therapeutic agents in Waldenström macroglobulinemia/lymphoplasmacytic lymphoma, which have emerged in the past decade and discuss their comparative efficacy and safety, with emphasis on a Bruton's tyrosine kinase (BTK) inhibitor, which has been recently approved by the US FDA, specifically for Waldenström macroglobulinemia/lymphoplasmacytic lymphoma. Future research should focus on identifying targeted agents against activating mutations and long-term data for currently available novel agents should be critically evaluated, both in treatment-naïve and in relapsed/refractory settings.
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Authors | Rajshekhar Chakraborty, Prashant Kapoor, Stephen M Ansell, Morie A Gertz |
Journal | Expert review of anticancer therapy
(Expert Rev Anticancer Ther)
Vol. 15
Issue 10
Pg. 1143-56
( 2015)
ISSN: 1744-8328 [Electronic] England |
PMID | 26196236
(Publication Type: Journal Article, Review)
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Chemical References |
- Antineoplastic Agents
- Myeloid Differentiation Factor 88
- Protein Kinase Inhibitors
- Protein-Tyrosine Kinases
- Agammaglobulinaemia Tyrosine Kinase
- BTK protein, human
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Topics |
- Agammaglobulinaemia Tyrosine Kinase
- Antineoplastic Agents
(adverse effects, pharmacology, therapeutic use)
- Drug Design
- Humans
- Molecular Targeted Therapy
- Mutation
- Myeloid Differentiation Factor 88
(genetics)
- Protein Kinase Inhibitors
(adverse effects, pharmacology, therapeutic use)
- Protein-Tyrosine Kinases
(antagonists & inhibitors)
- Waldenstrom Macroglobulinemia
(drug therapy, genetics, pathology)
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