A single-arm, long-term efficacy and safety study of subcutaneous romiplostim in children with immune thrombocytopenia.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
14 02 2023
Historique:
accepted: 27 03 2022
received: 25 08 2021
pubmed: 13 4 2022
medline: 2 2 2023
entrez: 12 4 2022
Statut: ppublish

Résumé

Romiplostim is a thrombopoietin (TPO) receptor agonist approved for children and adults with immune thrombocytopenia (ITP) for ≥6 months, recommended as second-line treatment. This phase 3b, single-arm, multicenter study investigated long-term efficacy and safety of romiplostim in children ≥1 to <18 years old with ≥6 months' ITP duration and platelet counts ≤30 × 109/L. Children received weekly subcutaneous romiplostim (1 μg/kg titrated to 10 μg/kg) to maintain platelets within 50 to 200 × 109/L. A subset underwent bone marrow examinations. The primary end point was percentage of time with platelet response during the first 6 months' treatment (counts ≥50 × 109/L without rescue medication within the preceding 4 weeks). Overall, 203 patients (median age, 10.0 years) received ≥1 dose of romiplostim, median treatment duration was ∼3 years, and median average weekly dose was 6.9 μg/kg. Ninety-five (46.8%) discontinued (lack of efficacy, n = 43 [21.2%]). Platelet responses were achieved a median (interquartile range) of 50.0% (16.7%-83.3%) of the time during the first 6 months, increasing to 78.2% (26.7%-90.4%) during the overall 36-month treatment period. Eleven patients (5.4%) achieved sustained responses (consecutive counts ≥50 × 109/L without ITP medications for ≥24 weeks). Treatment-related adverse events (AEs) occurred in 56 patients (27.6%), with 8 (3.9%) experiencing serious treatment-related AEs; all of these led to discontinuation, including 4 cases of neutralizing antibodies (romiplostim, n = 3; TPO, n = 1). Bleeding occurred in 141 patients (69.5%), decreasing over time; grade ≥3 bleeding events occurred in 20 (9.9%). At year 2, eight of 63 evaluable patients (12.7%) had grade 2 reticulin. Long-term romiplostim resulted in sustained on-treatment platelet responses with an overall safety profile consistent with previous studies. This trial was registered at www.clinicaltrials.gov as #NCT02279173.

Identifiants

pubmed: 35413092
pii: 484880
doi: 10.1182/bloodadvances.2021006014
pmc: PMC9979726
doi:

Substances chimiques

romiplostim GN5XU2DXKV
Thrombopoietin 9014-42-0
Receptors, Fc 0
Recombinant Fusion Proteins 0

Banques de données

ClinicalTrials.gov
['NCT02279173']

Types de publication

Multicenter Study Clinical Trial, Phase III Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

396-405

Informations de copyright

© 2023 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.

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Auteurs

John Grainger (J)

Department of Haematology, Royal Manchester Children's Hospital, Faculty of Medical & Human Sciences, University of Manchester, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.

James Bussel (J)

Department of Pediatrics, Division of Hematology, Weill Cornell Medicine, New York, NY.

Michael Tarantino (M)

The Bleeding and Clotting Disorders Institute, University of Illinois College of Medicine-Peoria, Peoria, IL.

Nichola Cooper (N)

Department of Haematology, Hammersmith Hospital, Imperial College, London, UK.

Donald Beam (D)

Cook Children's Medical Center, Fort Worth, TX.

Jenny Despotovic (J)

Texas Children's Hematology Center, Houston, TX.

Alexey Maschan (A)

Dmitry Rogachev National Research Center for Pediatric Hematology, Oncology and Immunology, Moscow, Russian Federation.

Kejia Wang (K)

Amgen Inc., Thousand Oaks, CA.

Melissa Eisen (M)

Amgen Inc., Thousand Oaks, CA.

Charles Bowers (C)

Amgen Inc., Thousand Oaks, CA.

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Classifications MeSH