Addressing Barriers to the Use of Gene Therapies and CAR-T Therapies
Researchers sought to determine factors limiting access to gene and CAR-T therapies for patients with hematologic disorders.
Researchers sought to determine factors limiting access to gene and CAR-T therapies for patients with hematologic disorders.
Patients were randomly assigned (1:1) to receive either 6 cycles of FCR every 28 days or IR for up to 6 years.
Researchers sought to create a prediction model to identify patients with unprovoked venous thromboembolism who are at low risk of recurrence.
Researchers sought to determine whether the COVID-19 mRNA vaccines were safe and effective in patients with transfusion-dependent beta-thalassemia.
Researchers sought to determine the educational burdens of children with SCD in the US compared with other nations.
Researchers sought to determine whether luspatercept would improve outcomes in patients with nontransfusion-dependent β-thalassemia.
Researchers sought to determine whether pegcetacoplan would be better than standard of care for treating patients with PNH.
Predictors of worse progression-free survival included ISS stage II, ISS stage III, and adverse cytogenetics.
Researchers sought to determine whether fitusiran prophylaxis would reduce the rate of bleeding events among patients with hemophilia A or B with inhibitors.
Researchers sought to determine whether there was an association between the presence of clonal hematopoiesis of indeterminate potential and protection from Alzheimer’s disease.