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

Author:

Grainger John1ORCID,Bussel James2,Tarantino Michael3,Cooper Nichola4,Beam Donald5,Despotovic Jenny6,Maschan Alexey7ORCID,Wang Kejia8,Eisen Melissa8,Bowers Charles8

Affiliation:

1. 1Department 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

2. 2Department of Pediatrics, Division of Hematology, Weill Cornell Medicine, New York, NY

3. 3The Bleeding and Clotting Disorders Institute, University of Illinois College of Medicine–Peoria, Peoria, IL

4. 4Department of Haematology, Hammersmith Hospital, Imperial College, London, UK

5. 5Cook Children’s Medical Center, Fort Worth, TX

6. 6Texas Children’s Hematology Center, Houston, TX

7. 7Dmitry Rogachev National Research Center for Pediatric Hematology, Oncology and Immunology, Moscow, Russian Federation

8. 8Amgen Inc., Thousand Oaks, CA

Abstract

Abstract 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.

Publisher

American Society of Hematology

Subject

Hematology

Reference27 articles.

1. Romiplostim as a treatment for immune thrombocytopenia: a review;Chalmers;J Blood Med,2015

2. American Society of Hematology 2019 guidelines for immune thrombocytopenia;Neunert;Blood Adv,2019

3. The incidence of immune thrombocytopenic purpura in children and adults: a critical review of published reports;Terrell;Am J Hematol,2010

4. Updated international consensus report on the investigation and management of primary immune thrombocytopenia;Provan;Blood Adv,2019

5. International consensus report on the investigation and management of primary immune thrombocytopenia;Provan;Blood,2010

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