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Targeting BTK with Ibrutinib in Relapsed or Refractory Mantle-Cell Lymphoma
Author(s) -
Michael Wang,
Simon Rule,
Peter Martin,
André Goy,
Rebecca Auer,
Brad S. Kahl,
Wojciech Jurczak,
Ranjana H. Advani,
Jorge Romaguera,
Michael E. Williams,
Jacqueline C. Barrientos,
Ewa Chmielowska,
John Radford,
Stephan Stilgenbauer,
Martin Dreyling,
W Wiktor-Jędrzejczak,
Peter Johnson,
Stephen E. Spurgeon,
Lei Li,
Liang Zhang,
Kate J. Newberry,
Zhishuo Ou,
Nancy Cheng,
Bingliang Fang,
Jesse McGreivy,
Fong Clow,
Joseph J. Buggy,
Betty Chang,
Darrin M. Beaupre,
Lori Kunkel,
Kristie A. Blum
Publication year - 2013
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/nejmoa1306220
Subject(s) - ibrutinib , bruton's tyrosine kinase , mantle cell lymphoma , cancer research , lymphoma , tyrosine kinase , medicine , pathogenesis , immunology , leukemia , receptor , chronic lymphocytic leukemia
Bruton's tyrosine kinase (BTK) is a mediator of the B-cell-receptor signaling pathway implicated in the pathogenesis of B-cell cancers. In a phase 1 study, ibrutinib, a BTK inhibitor, showed antitumor activity in several types of non-Hodgkin's lymphoma, including mantle-cell lymphoma.

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