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

dc.contributor.authorMusallam, Khaled M.
dc.contributor.authorTaher, Ali T.
dc.contributor.authorKattamis, Antonis C.
dc.contributor.authorKuo, Kevin H.M.
dc.contributor.authorSheth, Sujit S.
dc.contributor.authorCappellini, Maria Teresa
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:45:55Z
dc.date.available2025-01-24T11:45:55Z
dc.date.issued2023
dc.description.abstractOver 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.
dc.identifier.doihttps://doi.org/10.2147/DDDT.S368584
dc.identifier.eid2-s2.0-85160602581
dc.identifier.pmid37255740
dc.identifier.urihttp://hdl.handle.net/10938/30613
dc.language.isoen
dc.publisherDove Medical Press Ltd
dc.relation.ispartofDrug Design, Development and Therapy
dc.sourceScopus
dc.subjectAnemia
dc.subjectIneffective erythropoiesis
dc.subjectIron
dc.subjectManagement
dc.subjectThalassemia
dc.subjectTransfusion
dc.subjectActivin receptors, type ii
dc.subjectAdult
dc.subjectBeta-thalassemia
dc.subjectHemoglobins
dc.subjectHumans
dc.subjectImmunoglobulin fc fragments
dc.subjectHemoglobin
dc.subjectHydroxyurea
dc.subjectIron chelating agent
dc.subjectLuspatercept
dc.subjectActivin receptor 2
dc.subjectImmunoglobulin fc fragment
dc.subjectArthralgia
dc.subjectArticle
dc.subjectBeta thalassemia
dc.subjectBlood transfusion
dc.subjectBone pain
dc.subjectDrug approval
dc.subjectDrug design
dc.subjectDrug efficacy
dc.subjectDrug mechanism
dc.subjectDrug research
dc.subjectDrug safety
dc.subjectDrug tolerability
dc.subjectDyserythropoiesis
dc.subjectEvidence based practice
dc.subjectHeadache
dc.subjectHemoglobin blood level
dc.subjectHuman
dc.subjectIron chelation
dc.subjectIron overload
dc.subjectMyalgia
dc.subjectNon transfusion dependent beta thalassemia
dc.subjectNonhuman
dc.subjectPathophysiology
dc.subjectPatient care
dc.subjectPopulation research
dc.subjectRandomized controlled trial (topic)
dc.subjectRisk benefit analysis
dc.subjectSplenectomy
dc.subjectTreatment duration
dc.subjectTreatment response
dc.subjectUnmet medical need
dc.subjectComplication
dc.titleProfile of Luspatercept in the Treatment of Anemia in Adults with Non-Transfusion-Dependent β-Thalassemia (NTDT): Design, Development and Potential Place in Therapy
dc.typeArticle

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