| Literature DB >> 30069634 |
Katja Zirlik1,2, Hendrik Veelken3.
Abstract
Idelalisib (GS-1101, CAL-101, Zydelig®) is an orally bioavailable, small-molecule inhibitor of the delta isoform (p110δ) of the enzyme phosphoinositide 3-kinase (PI3K). In contrast to the other PI3K isoforms, PI3Kδ is expressed selectively in hematopoietic cells. PI3Kδ signaling is active in many B-cell leukemias and lymphomas. By inhibiting the PI3Kδ protein, idelalisib blocks several cellular signaling pathways that maintain B-cell viability. Idelalisib is the first PI3K inhibitor approved by the US Food and Drug Administration (FDA). Treatment with idelalisib is indicated in relapsed/refractory chronic lymphocytic leukemia (CLL), follicular lymphoma (FL), and small lymphocytic lymphoma (SLL). This review presents the preclinical and clinical activity of idelalisib with a focus on clinical studies in CLL.Entities:
Keywords: Chronic lymphocytic leukemia (CLL); Idelalisib; Kinase inhibitor; PI 3 Kinase
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Year: 2018 PMID: 30069634 DOI: 10.1007/978-3-319-91439-8_12
Source DB: PubMed Journal: Recent Results Cancer Res ISSN: 0080-0015