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The US Food and Drug Administration (FDA) has approved isatuximab-irfc (Sarclisa), in combination with pomalidomide and dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least 2 prior therapies including lenalidomide and a proteasome inhibitor....
Treatment with cord blood-derived chimeric antigen receptor (CAR) natural killer (NK)-cell therapy targeting CD19 resulted in clinical responses in a majority of patients with relapsed or refractory non-Hodgkin’s lymphoma (NHL) and chronic lymphocytic leukemia (CLL), with no major toxicities...
A pooled analysis of 9 prospective studies involving more than 750,000 adults finds that recommended amounts of leisure-time physical activity were linked to a lower risk for 7 cancers, with several cancer types having a dose/response relationship. Updated guidelines for activity now state that...
Single-agent belantamab mafodotin shows anti-myeloma activity with a manageable safety profile in patients with relapsed or refractory multiple myeloma, according to a study published in The Lancet Oncology. Belantamab mafodotin, an immunoconjugate targeting B-cell maturation antigen, showed...
The US Food and Drug Administration (FDA) has granted supplemental approval to acalabrutinib (Calquence) for the treatment of adults with chronic lymphocytic leukaemia (CLL) or small lymphocytic lymphoma (SLL). This new approved indication for acalabrutinib provides a new treatment option for...

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