Teclistamab significantly improves progression-free and overall survival in relapsed or refractory multiple myeloma patients with 1-3 prior therapies, achieving 69.8% 18-month progression-free survival.
- 19 cites
Moving in Blood, New England Journal of Medicine.
Rebuilt
Teclistamab significantly improves progression-free and overall survival in relapsed or refractory multiple myeloma patients with 1-3 prior therapies, achieving 69.8% 18-month progression-free survival.
Newest first · last 60 days
Menin-MLL inhibitors increase JUND activity in MLL-rearranged leukemic cells, contributing to tumor growth and therapy resistance.
Degrading NSD2 with a targeted ligand degrader reverses oncogenic chromatin changes and improves survival in t(4;14) multiple myeloma models.
Fibrocytes are the main collagen-producing cells in JAK2V617F-mutated myelofibrosis, accounting for nearly two-thirds of collagen production in the bone marrow.
PKMYT1 inhibition induces DNA damage and cell death specifically in del(17p) multiple myeloma cells, offering a targeted therapeutic approach.
Epigenetic plasticity driven by genomic and cytogenetic changes enables therapy resistance and disease progression in multiple myeloma, with nearly 900 patient samples revealing key transitions.
Tambotatug pelitecan significantly improves survival and response rates in relapsed small-cell lung cancer compared to topotecan, with fewer severe adverse events.
Elevated NF-κB activity in CD4 CAR-T cells predicts durable responses and improved survival in multiple myeloma patients treated with ide-cel.
Arlocabtagene autoleucel achieves an 87% overall response rate with durable responses in heavily pretreated relapsed/refractory multiple myeloma patients.
Loss of DNA methylation in multiple myeloma leads to variable LINE-1 activation, with high L1 activity linked to increased proliferation and altered gene expression.
Mezigdomide reverses T-cell exhaustion by degrading IKZF1/IKZF3, restoring cytokine production and enhancing target cell killing in multiple myeloma.
Anti-BCMA/GPRC5D bispecific CAR T cells achieved a 97% overall response rate in patients with relapsed or refractory multiple myeloma with extraosseous extramedullary disease.
Talquetamab combined with daratumumab and pomalidomide significantly prolongs progression-free survival in relapsed or refractory multiple myeloma, with 24-month estimates over 81%.
Journals this month
Moving areas, week to 3 Oct 2026