THE HAGUE, Netherlands, June 11, 2021 /PRNewswire/ -- The non-transfusion-dependent (NTD) form of β-thalassemia, an inherited blood disorder with impaired production of hemoglobin, is characterized by chronic anemia of mild-moderate severity and iron overload. Despite their transfusion-independence, patients with NTD β-thalassemia can
Treatment with luspatercept significantly improved anemia compared with placebo. Patients showed increased hemoglobin and almost 90% of luspatercept-treated patients remained transfusion-free through Week 24. Consequently, patients in the intervention arm reported a higher quality of life score, indicating a reduction in clinical symptoms such as tiredness and weakness. The improvement in quality of life significantly correlated with hemoglobin increase. Importantly, the incidence of treatment-emergent adverse events was comparable between the luspatercept and placebo groups and no thromboembolic or thrombophlebitis events occurred in the trial. In conclusion, luspatercept is efficacious and safe for treating patients with NTD β-thalassemia.
The results of this study will be presented by Professor Ali Taher in the Presidential Symposium.
Presenter: Professor Ali T. Taher
Affiliation: American University of Beirut Medical Center, Beirut, Lebanon
Abstract: #S101 THE BEYOND STUDY: RESULTS OF A PHASE 2, DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED MULTICENTER STUDY OF LUSPATERCEPT IN ADULT PATIENTS WITH NON-TRANSFUSION DEPENDENT BETA-THALASSEMIA
About the EHA Annual Congress: Every June, EHA organizes its Annual Congress in a major European city. This year, due to the persisting COVID19 pandemic, EHA organizes a virtual Congress for the second time. The Congress is aimed at health professionals working in or interested in the field of hematology.
Website: www.ehaweb.org
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