2021
DOI: 10.1136/bmjopen-2020-044885
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Phase 3 randomised trial of eltrombopag versus standard first-line pharmacological management for newly diagnosed immune thrombocytopaenia (ITP) in children: study protocol

Abstract: IntroductionImmune thrombocytopaenia (ITP) is an acquired disorder of low platelets and risk of bleeding. Although many children can be observed until spontaneous remission, others require treatment due to bleeding or impact on health-related quality of life. Standard first-line therapies for those who need intervention include corticosteroids, intravenous immunoglobulin and anti-D globulin, though response to these agents may be only transient. Eltrombopag is an oral thrombopoietin receptor agonist approved f… Show more

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Cited by 6 publications
(7 citation statements)
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References 49 publications
(55 reference statements)
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“…Indeed, the results of a multicenter, open-label, phase 3 RCT (NCT03939637) that compares eltrombopag to standard first-line management (steroids vs. immunoglobulins vs. Rho(D) immunoglobulin) in children (n ¼ 162) with newly diagnosed ITP ( 3 months from diagnosis) are expected in 2024. 54 The fact that eltrombopag binds to the transmembrane and juxtamembrane but not to the classical extracellular binding domains of the TPO-R makes this substance appealing for use in rare inherited thrombocytopenia, especially in CAMT. This group of congenital thrombocytopenias is characterized by ineffective megakaryopoiesis without typical features of syndromic conditions.…”
Section: Schlüsselwörtermentioning
confidence: 99%
“…Indeed, the results of a multicenter, open-label, phase 3 RCT (NCT03939637) that compares eltrombopag to standard first-line management (steroids vs. immunoglobulins vs. Rho(D) immunoglobulin) in children (n ¼ 162) with newly diagnosed ITP ( 3 months from diagnosis) are expected in 2024. 54 The fact that eltrombopag binds to the transmembrane and juxtamembrane but not to the classical extracellular binding domains of the TPO-R makes this substance appealing for use in rare inherited thrombocytopenia, especially in CAMT. This group of congenital thrombocytopenias is characterized by ineffective megakaryopoiesis without typical features of syndromic conditions.…”
Section: Schlüsselwörtermentioning
confidence: 99%
“…The sample size for the study was determined based on the results from previous studies [38,[57][58][59], which have a power of 80-90%. In addition, the highest number of patients in previous randomized studies was 55 and 62 [60][61][62].…”
Section: Sample Sizementioning
confidence: 99%
“…ITP is usually a self-limiting and mild disease, without life-threatening bleeding episodes or the need for hospitalization or treatment intervention [1,2]. Although most children with ndITP achieve remission spontaneously, others require therapy for minor or moderate bleedings and improvements in their health related quality of life [3,4]. The first-line treatment for ndITP includes corticosteroids, intravenous immunoglobulin, and anti-D globulin [1,3,5].…”
Section: Introductionmentioning
confidence: 99%
“…However, 10-20% of children with ITP do not respond to the recommended first-line therapies, going on to develop pITP or cITP. In addition, some patients become steroid--dependent or refractory, and this leads to adverse events and challenges in logistical and economic terms [4].…”
Section: Introductionmentioning
confidence: 99%
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