The survey of oncologists outside the US examined global access to 14 myeloma chemoimmunotherapy options and autologous stem cell transplant (ASCT), and included questions on demographics and perceived barriers.
Targeted next-generation sequencing of the full UBA1 locus was used to profile diagnostic and treatment-naïve samples.
Patients in the COMMANDS study were randomly assigned to luspatercept or epoetin alfa.
Of the patients included in the study, 67.6% were not transfusion dependent before initiating luspatercept.
Adults older than 65 and newly diagnosed with DLBCL or DLBCL/high-grade BCL with MYC and BCL2 rearrangements were surveyed.
There was previously a gap in evidence when it came to how the drug works after treatment with covalent BTK inhibitors.
The retrospective study evaluated if pacritinib increased PLT counts in the phase III PERSIST-2 and phase II PAC203 studies.
The results suggest a possible treatment strategy of selinexor followed by immunotherapy.
Tasquinimod inhibited interaction of A9, a protein associated with poor prognosis.
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