Results 141 to 150 of about 29,210 (297)
ABSTRACT Background Hairy cell leukemia (HCL) is a rare disorder characterized by splenomegaly, pancytopenia, and proliferation with “hairy” lymphocytes. Treatment is based on purine analogs and anti‐CD20 antibodies, often resulting in significant adverse effects.
M. Garcia Fasanella +4 more
wiley +1 more source
Yang Cao +9 more
openalex +1 more source
Abstract Waldenström's macroglobulinemia (WM) is a rare, indolent lymphoproliferative disorder, genetically characterized by the presence of the L265P mutation in the MYD88 gene in almost all cases, resulting in constitutive activation of NF‐kappa B (NF‐κB). Despite its slow progression, WM remains incurable due to the lack of specific treatments.
Quentin Lemasson +7 more
wiley +1 more source
Ibrutinib inhibits SDF1/CXCR4 mediated migration in AML [PDF]
Lyubov Zaitseva +6 more
openalex +1 more source
Ibrutinib Resistance in Chronic Lymphocytic Leukemia [PDF]
Gustaaf Reurink +7 more
openalex +1 more source
Ibrutinib is an effective treatment of autoimmune haemolytic anaemia in chronic lymphocytic leukaemia [PDF]
Sudhir Manda +3 more
openalex +1 more source
Ibrutinib and Rituximab in Waldenström’s Macroglobulinemia [PDF]
Gian Matteo Rigolin +2 more
openaire +4 more sources
Background: Ibrutinib, a potent Bruton’s tyrosine kinase inhibitor with marked efficacy against hematological malignancies, is associated with the heightened risk of atrial fibrillation (AF).
Yukun Li +16 more
doaj +1 more source
ABSTRACT Background Chronic lymphocytic leukemia (CLL) treatment choice remains a challenge in the era of molecular biology and targeted therapy. Methods We conducted a bicentric retrospective analysis of the impact of NOTCH1 mutation according to the treatment of CLL patients in real life.
Clémence Haméon +9 more
wiley +1 more source
Life after ibrutinib? A new unmet need in CLL [PDF]
Javier Pinilla‐Ibarz, Julio C. Chávez
openalex +1 more source

