Results 1 to 10 of about 30,894 (205)

Ibrutinib inhibits SDF1/CXCR4 mediated migration in AML [PDF]

open access: gold, 2014
Pharmacological targeting of BTK using ibrutinib has recently shown encouraging clinical activity in a range of lymphoid malignancies. Recently we reported that ibrutinib inhibits human acute myeloid leukemia (AML) blast proliferation and leukemic cell ...
Lyubov Zaitseva   +6 more
core   +7 more sources

Ibrutinib Unmasks Critical Role of Bruton Tyrosine Kinase in Primary CNS Lymphoma [PDF]

open access: yesCancer Discovery, 2017
Bruton tyrosine kinase (BTK) links the B-cell antigen receptor (BCR) and Toll-like receptors with NF-κB. The role of BTK in primary central nervous system (CNS) lymphoma (PCNSL) is unknown.
Christian Grommes   +2 more
exaly   +3 more sources

Long-term efficacy and safety of first-line ibrutinib treatment for patients with CLL/SLL: 5 years of follow-up from the phase 3 RESONATE-2 study [PDF]

open access: yesLeukemia, 2019
RESONATE-2 is a phase 3 study of first-line ibrutinib versus chlorambucil in chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL). Patients aged ≥65 years (n = 269) were randomized 1:1 to once-daily ibrutinib 420 mg continuously or ...
Jan A Burger, Paul M Barr, Tadeusz Robak
exaly   +5 more sources

Efficacy in the margins of NHL with ibrutinib [PDF]

open access: bronzeBlood, 2017
In this issue of Blood, Noy et al report on the efficacy of single-agent ibrutinib in patients with relapsed or refractory marginal zone lymphoma (MZL). They demonstrate an overall response rate of 48% and a median progression-free survival of 14 months, establishing the Bruton tyrosine kinase (BTK) inhibitor ibrutinib as a therapeutic option for this ...
Paul M. Barr
openalex   +4 more sources

Targeting BTK with Ibrutinib in Relapsed Chronic Lymphocytic Leukemia [PDF]

open access: bronzeNew England Journal of Medicine, 2013
John C Byrd, Ian W Flinn, Jan A Burger
exaly   +2 more sources

Therapeutic antitumor immunity by checkpoint blockade is enhanced by ibrutinib, an inhibitor of both BTK and ITK [PDF]

open access: bronzeProceedings of the National Academy of Sciences of the United States of America, 2015
Idit Sagiv-Barfi, Ronald Levy
exaly   +2 more sources

High-throughput combinatorial screening identifies drugs that cooperate with ibrutinib to kill activated B-cell–like diffuse large B-cell lymphoma cells

open access: bronzeProceedings of the National Academy of Sciences of the United States of America, 2014
Rajarshi Guha, Ryan M Young, Adam Yasgar
exaly   +2 more sources

Extrahepatic metabolism of ibrutinib [PDF]

open access: yesInvestigational New Drugs, 2020
SummaryIbrutinib is a first-in-class Bruton’s kinase inhibitor used in the treatment of multiple lymphomas. In addition to CYP3A4-mediated metabolism, glutathione conjugation can be observed. Subsequently, metabolism of the conjugates and finally their excretion in feces and urine occurs. These metabolites, however, can reach substantial concentrations
Rosalinde Masereeuw   +13 more
openaire   +5 more sources

Arrhythmia Patterns in Patients on Ibrutinib [PDF]

open access: yesFrontiers in Cardiovascular Medicine, 2022
Introduction: Ibrutinib, a Bruton's tyrosine kinase inhibitor (TKI) used primarily in the treatment of hematologic malignancies, has been associated with increased incidence of atrial fibrillation (AF), with limited data on its association with other tachyarrhythmias.
Muhammad Fazal   +9 more
openaire   +3 more sources

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