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Minimal residual disease (MRD) negativity and its duration led to significantly better progression-free survival (PFS) in patients with relapsed/refractory multiple myeloma, new analyses of two randomized trials showed.
MRD-negative rates increased significantly with the addition of daratumumab (Darzalex) to standard therapy, from 6.7% with lenalidomide (Revlimid) and dexamethasone (Rd) to 32.5% with the addition of the anti-CD38 antibody (DRd) and from 1.6% with bortezomib (Velcade)-dexamethasone (Vd) to 15.1% with daratumumab-VD (DVd). The proportion of patients who had MRD-negative status for 6 months or longer increased about 10-fold when daratumumab was added to Rd or Vd.
Progression-free survival (PFS) increased with MRD-negativity and its duration, Hervé Avet-Loiseau, MD, of University Cancer Institute-Oncopole in Toulouse, France, and co-authors reported in the
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