Blinatumomab consolidation reduces relapse and improves survival in high-risk Ph- B-ALL patients, with 5-year relapse at 23% versus 49% in controls.
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Blinatumomab consolidation reduces relapse and improves survival in high-risk Ph- B-ALL patients, with 5-year relapse at 23% versus 49% in controls.
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Venetoclax combined with pediatric-inspired chemotherapy achieves a 91% remission rate and improves survival in adolescents and adults with newly diagnosed Ph-negative ALL.
Ablating endothelial PERK enhances DLL4-NOTCH3 signaling, boosting lymphoid regeneration by 50% after irradiation in hematopoietic recovery.
Inhibiting WNK1, an atypical kinase overexpressed in T-ALL, induces cell cycle arrest and disrupts mitosis, offering a promising therapeutic target with significant effects.
Genomic and epigenomic profiling reveal over 40 molecular subtypes of acute lymphoblastic leukemia, enhancing classification and informing treatment strategies.
Combining genetics and MRD assessment identifies adult Ph- ALL patients who benefit from allo-HSCT, with a 3-year OS of up to 81% in low-risk groups.
IGH::FENDRR and KRAS mutations define a novel B-ALL subtype with 85% poor chemotherapy response.
IDH2 mutations and IKAROS loss define a distinct subtype of lenalidomide-associated B-ALL, with IDH2 R140Q mutations enriched 23% in this condition.
The gut microbiota directs a three-day pathway of vitamin A derivatives from epithelial cells to T cells, shaping intestinal adaptive immunity.
Consensus guidelines for administering CAR T-cell therapy in adult B-ALL reached agreement on 33 key recommendations, guiding clinical practice amid limited randomized trials.
The miR-15b/16-2 cluster acts as a tumor suppressor in T-cell acute lymphoblastic leukemia, impairing leukemic growth and progression by downregulating key oncogenes.
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