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• W2130853856 abstract "Abstract It is well known that signals emanating from the B-cell receptor (BCR) activate downstream pathways to regulate the development and survival of normal B cells. In B-cell malignancies, it is increasingly understood that similar pathways are activated through both tonic and chronic active BCR signaling to promote tumor viability and resistance to therapy. Recently, several active and oral agents have emerged that target key proximal kinases in the BCR pathway, including Bruton tyrosine kinase, PI3K, and spleen tyrosine kinase. In early clinical studies, these agents have shown significant activity across a broad range of B-cell lymphomas and chronic lymphocytic leukemia. Especially impressive responses have been reported in mantle cell lymphoma and chronic lymphocytic leukemia, and many patients remain on treatment with continued disease control. Toxicity profiles have been mild in the majority of early studies, without significant myelosuppression over prolonged dosing. Due to these attractive attributes, several agents targeting the BCR pathway are now entering early combination studies with traditional chemotherapeutics and/or other novel agents. It is clear that agents targeting the BCR pathway will significantly affect the design of future therapeutic regimens for B-cell malignancies. Future research will focus on understanding potential mechanisms of resistance, identifying biomarkers of response, and defining optimal combination regimens." @default.
• W2130853856 created "2016-06-24" @default.
• W2130853856 creator A5017385023 @default.
• W2130853856 creator A5044284041 @default.
• W2130853856 date "2013-12-06" @default.
• W2130853856 modified "2023-10-03" @default.
• W2130853856 title "Targeting B-cell receptor signaling: changing the paradigm" @default.
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• W2130853856 doi "https://doi.org/10.1182/asheducation-2013.1.553" @default.
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