Study Provides Support for TKI Discontinuation in Some Patients With CML
This population-based study of patients with chronic phase CML evaluated the BCR/ABL1 TKI discontinuation rates for patients treated on and off a clinical trial.
This population-based study of patients with chronic phase CML evaluated the BCR/ABL1 TKI discontinuation rates for patients treated on and off a clinical trial.
In this study, obinutuzumab, ibrutinib, and venoclax were administered as first-line therapy in patients with CLL characterized by del(17p) and/or TP53 mutation.
The addition of venetoclax to azacitidine was associated with a 34% reduction in risk of death.
Genetic mutations associated with the heterogeneity of hemophilia B Leyden may also be linked to mechanisms that increase factor IX levels with age.
Due to phenotypic overlap between bone marrow failure and primary immunodeficiency, researchers recommend accurate immunologic work-up.
Modifications of ABVD or CHOP were common among elderly patients with cHL and may contribute to their disproportionate excess mortality, signaling a need for less toxic regimens.
Few population-based studies have compared treatment approaches in the setting of mantle cell lymphoma.
Ixazomib maintenance therapy prolonged PFS compared with placebo among patients with newly diagnosed MM who were not eligible for transplant.
Ixazomib, lenalidomide, and dexamethasone are all oral agents and each one has been approved by the FDA in the setting of multiple myeloma.
VTE-BLEED prognostic scores did not accurately identify patients with VTE who were at high risk of bleeding events.