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PI3K signaling pathway in normal B cells and indolent B-cell malignancies
被引:31
作者:
Pongas, Georgios
[1
,2
]
Cheson, Bruce D.
[3
]
机构:
[1] NCI, Med Oncol Serv, NIH, Bethesda, MD 20892 USA
[2] NCI, Womens Malignancies Branch, NIH, Bethesda, MD 20892 USA
[3] Georgetown Univ Hosp, Lombardi Comprehens Canc Ctr, Washington, DC 20007 USA
关键词:
Chronic lymphocytic leukemia;
Indolent non-Hodgkin lymphoma;
PI3K;
Lymphoma;
Leukemia;
Idelalisib;
CHRONIC LYMPHOCYTIC-LEUKEMIA;
PHOSPHOINOSITIDE;
3-KINASE;
TYROSINE PHOSPHORYLATION;
EMBRYONIC LETHALITY;
IDELALISIB;
RECEPTOR;
INHIBITOR;
CD19;
P110-DELTA;
ACTIVATION;
D O I:
10.1053/j.seminoncol.2016.11.011
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
In chronic lymphocytic leukemia (CLL) and non-Hodgkin lymphomas (NHLs), B-cell receptor signaling leads to activation of the phosphatidylinositol 3-kinase (PI3K) pathway. Idelalisib, a PI3K delta inhibitor was approved in 2014 by the US Food and Drug Administration (FDA) in combination with rituximab for the treatment of patients with CLL for whom single-agent rituximab would be considered appropriate and as a single agent for patients with relapsed small lymphocytic lymphoma (SLL) and relapsed follicular lymphoma (FL). Following its approval, several trials investigating various PI3K delta inhibitors as single agents or in combination with chemoimmunotherapy or other molecular targeted agents in CLL and indolent NHL (iNHL) have uncovered some severe autoimmune related toxicities. This review discusses and summarizes the biologic basis and the clinical experience of the PI3K delta inhibitors in indolent B-cell malignancies. Published by Elsevier Inc.
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页码:647 / 654
页数:8
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