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The phase III ECOG-ACRIN E1910 trial (NCT02003222) demonstrated that adding blinatumomab to consolidation chemotherapy significantly improved 3-year overall survival (85% vs 68%) and improved relapse-free survival (80% vs 64%) compared with chemotherapy alone in patients aged 30–70 years with newly diagnosed BCR::ABL1-negative B-cell precursor acute lymphoblastic leukemia (B-ALL) in MRD-negative remission. With a median follow-up of 43 months, the combination therapy showed a higher incidence of Grade 3 non-hematologic adverse events and treatment-related psychiatric or neurological events (43% vs 36% and 23% vs 5%, respectively).
These results led to FDA (2024) and EC (2025) approvals of blinatumomab as consolidation therapy for CD19+ Ph- B-ALL, regardless of MRD status. The findings support the inclusion of immunotherapy in initial treatment for B-ALL, changing the frontline standard of care for patients with ALL.
Blinatumomab. Prescribing Information. Amgen Inc; 2014. Revised Jul 2018.
Litzow M, et al. N Engl J Med. 2024;391:320–333.
PR Newswire. https://www.prnewswire.co.uk/news-releases/european-commission-approves-blincyto-in-philadelphia-chromosome-negative-cd19-positive-b-cell-precursor-acute-lymphoblastic-leukemia-in-the-consolidation-phase-302363668.html. Published Jan 29, 2025. Accessed Jun 3, 2025.
Dinner S. Abstract #S110. Presented at: European Hematology Association 2025 Congress; Jun 12–15, 2025; Milan, IT.
This educational resource is independently supported by Amgen. All content was developed by SES in collaboration with an expert steering committee; funders were allowed no influence on the content of this resource.
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