PI3Kδ Inhibition by Idelalisib in Patients with Relapsed Indolent Lymphoma
Author(s) -
Ajay K. Gopal,
Brad S. Kahl,
Sven de Vos,
Nina D. WagnerJohnston,
Stephen J. Schuster,
Wojciech Jurczak,
Ian W. Flinn,
Christopher R. Flowers,
Peter Martin,
Andreas Viardot,
Kristie A. Blum,
André Goy,
Andrew Davies,
Pier Luigi Zinzani,
Martin Dreyling,
Dave Johnson,
Langdon L. Miller,
Leanne Holes,
Daniel Li,
Roger Dansey,
Wayne R. Godfrey,
Gilles Salles
Publication year - 2014
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa1314583
Subject(s) - idelalisib , pi3k/akt/mtor pathway , lymphoma , phosphatidylinositol , cancer research , kinase , medicine , chemistry , signal transduction , chronic lymphocytic leukemia , leukemia , ibrutinib , biochemistry
Phosphatidylinositol-3-kinase delta (PI3Kδ) mediates B-cell receptor signaling and microenvironmental support signals that promote the growth and survival of malignant B lymphocytes. In a phase 1 study, idelalisib, an orally active selective PI3Kδ inhibitor, showed antitumor activity in patients with previously treated indolent non-Hodgkin's lymphomas.
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