Results 41 to 50 of about 29,210 (297)
PURPOSE To present primary and final analyses from the randomized, double-blind, placebo-controlled, phase III iNTEGRATE study, which evaluated the safety and efficacy of ibrutinib with prednisone in previously untreated patients with chronic graft ...
D. Miklos +20 more
semanticscholar +1 more source
Ibrutinib-based therapies are costly and require continuous administration. We hypothesized combining BTK inhibition with anti-CD20 monoclonal antibodies would yield deep remissions allowing discontinuation.
Januario E. Castro +11 more
doaj +1 more source
Ibrutinib Inhibits Angiogenesis and Tumorigenesis in a BTK-Independent Manner
BTK inhibitor (BTKi) Ibrutinib carries an increased bleeding risk compared to more selective BTKis Acalabrutinib and Zanubrutinib, however, its impact on vascular endothelium remains unknown.
Jia Liu +6 more
doaj +1 more source
Ibrutinib plus Bendamustine and Rituximab in Untreated Mantle-Cell Lymphoma.
BACKGROUND Ibrutinib, a Bruton's tyrosine kinase inhibitor, may have clinical benefit when administered in combination with bendamustine and rituximab and followed by rituximab maintenance therapy in older patients with untreated mantle-cell lymphoma ...
Michael L. Wang +30 more
semanticscholar +1 more source
Choosing ibrutinib wisely [PDF]
In this issue of Blood , Bartlett et al share their experience with the use of ibrutinib in patients with relapsed or refractory follicular lymphoma (FL ...
openaire +3 more sources
Background In preclinical studies of pancreatic ductal adenocarcinoma (PDAC), ibrutinib improved the antitumor efficacy of the standard of care chemotherapy.
Li Zhang +28 more
doaj +1 more source
Purpose: The CAPTIVATE study investigated first-line ibrutinib plus venetoclax for chronic lymphocytic leukemia in 2 cohorts: minimal residual disease (MRD)-guided randomized discontinuation (MRD cohort) and Fixed Duration (FD cohort). We report outcomes
J. Allan +16 more
semanticscholar +1 more source
Ibrutinib (IBR) is an oral anticancer medication that inhibits Bruton tyrosine kinase irreversibly. Due to the high risk of adverse effects and its pharmacokinetic variability, the safe and effective use of IBR is expected to be facilitated by precision dosing. Delivering suitable clinical laboratory information on IBR is a prerequisite of constructing
Gellért Balázs Karvaly +5 more
openaire +3 more sources
ROR1 – a receptor tyrosine kinase – is overexpressed in CLL. Ibrutinib, a Bruton's tyrosine kinase inhibitor, is clinically effective in CLL but patients may develop resistance. We evaluated the effect of an ROR1 inhibitor, KAN0441571C, in CLL cells from
Amineh Ghaderi +9 more
doaj +1 more source
Key Points • The combination of ibrutinib and venetoclax induced deep and durable responses in treatment-naïve patients with Waldenström macroglobulinemia.• Planned study therapy was stopped early due to a higher-than-expected occurrence of ventricular ...
J. J. Castillo +18 more
semanticscholar +1 more source

