Profile of Luspatercept in the Treatment of Anemia in Adults with Non-Transfusion-Dependent β-Thalassemia (NTDT): Design, Development and Potential Place in Therapy

Abstract

Over the past decade, evidence has been mounting on the detrimental clinical sequelae of untreated anemia in patients with non-transfusion-dependent β-thalassemia (NTDT). There are no pharmacologic agents that are specifically approved for the management of anemia in NTDT, and available options such as splenectomy, transfusion therapy, and hydroxyurea each come with their own shortcomings, especially for long-term use. Luspatercept is an erythroid maturation agent that has been evaluated in a Phase 2, randomized trial and showed a significant benefit in raising hemoglobin level by at least 1 g/dL in adults with NTDT and a baseline hemoglobin level ≤10 g/dL. These data led to luspatercept’s approval by the European Commission for the treatment of anemia in adults with NTDT and presents the first evidence-based approach for a novel agent that is able to ameliorate anemia in this patient population. © 2023 Musallam et al.

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Keywords

Anemia, Ineffective erythropoiesis, Iron, Management, Thalassemia, Transfusion, Activin receptors, type ii, Adult, Beta-thalassemia, Hemoglobins, Humans, Immunoglobulin fc fragments, Hemoglobin, Hydroxyurea, Iron chelating agent, Luspatercept, Activin receptor 2, Immunoglobulin fc fragment, Arthralgia, Article, Beta thalassemia, Blood transfusion, Bone pain, Drug approval, Drug design, Drug efficacy, Drug mechanism, Drug research, Drug safety, Drug tolerability, Dyserythropoiesis, Evidence based practice, Headache, Hemoglobin blood level, Human, Iron chelation, Iron overload, Myalgia, Non transfusion dependent beta thalassemia, Nonhuman, Pathophysiology, Patient care, Population research, Randomized controlled trial (topic), Risk benefit analysis, Splenectomy, Treatment duration, Treatment response, Unmet medical need, Complication

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