The MagnetisMM-6 study investigated the combination of the BCMA-CD3 bispecific antibody elranatamab added to lenalidomide and daratumumab in patients with transplant-ineligible, previously untreated MM. Part 1 of the study evaluated the optimal dose of the experimental treatment regimen. Dr Meletios Dimopoulos (University of Athens, Greece) presented findings of cohort G, which included 37 patients who were exposed to 76 mg elranatamab, subcutaneously administered every 4 weeks, plus lenalidomide and daratumumab [1].
The most common grade 3 or 4 treatment-emergent adverse events were haematologic toxicity (78.4%) and infections (18.9%). Cytokine release syndrome was observed in 62.2% of the patients, but these were all grade 1 or 2 events. “One patient died from a Candida pneumonia infection,” mentioned Dr Dimopoulos. “Other grade 3 or 4 infections were urinary tract infections, cytomegalovirus reactivation, and pneumonia.”
Except for the patient who had deceased early, all patients responded to therapy (97.3%) after a median follow-up of 7.9 months. In addition, 27.0% of the patients reached at least a complete response. “The follow-up time was short and we expect that the responses will deepen over time,” commented Dr Dimopoulos.
The initial results from the MagnetisMM-6 part-1 dose level G indicated that the combination of elranatamab (every 4 weeks), daratumumab and lenalidomide is effective and manageable in transplant-ineligible, untreated MM. “MagnetisMM-6 part 2, which is a randomised phase 3 study, will evaluate dose level G from part 1,” Dr Dimopoulos concluded his talk.
- Dimopoulos M-A, et al. Elranatamab in combination with daratumumab and lenalidomide in patients with newly diagnosed multiple myeloma not eligible for transplant: initial results from MagnetisMM-6 Part 1. S206, EHA2025 Congress, 12–15 June, Milan, Italy.
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Table of Contents: EHA 2025
Featured articles
Letter from the Editor
Multiple Myeloma/Plasma Cell Disorders
Large pooled analysis reveals prognostic utility of circulating tumour cells in MM
RedirecTT-1: Dual antigen-targeting treatment associated with promising efficacy in EMD myeloma
Prognostic impact of circulating tumour cells in AL amyloidosis
IRAKLIA: Novel isatuximab delivery system improves patient satisfaction in MM
MagnetisMM-6: Excellent early results of elranatamab in MM
MIDAS: Is ASCT needed in MM after reaching MRD-negativity with IsaKRD?
Novel trispecific antibody may be a game-changer for relapsed/refractory MMF
Lymphoma
GAIA/CLL13: Positive 5-year efficacy outcomes for GIV in CLL
ELM-2: Survival benefit for patients with FL on odronextamab
inMIND: Positive phase 3 results for tafasitamab combination in FL
Unravelling real-world safety and effectiveness of axi-cel in LBCL
STARGLO: Long-term clinical benefits of Glofit-GemOx over R-GemOx in DLBCL
ECHO: Older patients with high-risk MCL benefit from acalabrutinib added to BR
POLARGO: Pola-R-GemOx delivers overall survival benefit in second-line DLBCL
Acute Leukaemia (AML and ALL)
Refined AML risk prediction by improved understanding of genetics
TUSCANY: Promising data for the addition of tuspetinib in untreated chemo-ineligible AML
Chemogenomic profiling appears reliable strategy to improve outcomes in T-ALL/ETP-ALL
Dasatinib does not cross the finish line in the phase 3 AML study
Myeloid Neoplasms
ASC4START: asciminib showed superior tolerability to nilotinib in CML
Encouraging results for new mutation-specific targeted therapy in CALR-mutated ET
Improving diagnosis, classification, and prognosis of MDN with an AI-based model
SURPASS-ET: Ropeg meets primary endpoint in essential thrombocythemia
MANIFEST-2: Sustained benefits of pelabresib plus ruxolitinib in myelofibrosis
Stem Cell Transplantation
Targeted anti-thymocyte globulin dosing improves transplantation outcomes
HCT Frailty Scale may refine the allo-HCT selection process
Ravulizumab shows tolerability and efficacy in HSCT-thrombotic microangiopathy
ALLG BM12 CAST: improved GRFS through novel GVHD prophylaxis
Non-Malignant Haematology
Promising safety and efficacy data for novel anti-CD38 treatment in ITP
Novel investigational gene-editing therapy for TDT and SCD
HSCT may reduce risk of ocular complications in SCD
Are PBSCs a viable source for haplo-HSCT in SCD?
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