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      Long-Term Use of the Thrombopoietin-Mimetic Romiplostim in Children With Severe Chronic Immune Thrombocytopenia (ITP)

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          Abstract

          Background

          Treatment of chronic severe pediatric ITP is not well studied. In a phase 1/2 12–16-week study, 15/17 romiplostim-treated patients achieved platelet counts ≥50 × 10 9/L, and romiplostim treatment was well tolerated. In a subsequent open-label extension (≤109 weeks), 20/22 patients received romiplostim; all achieved platelet counts >50 × 10 9/L. Twelve patients continued in a second extension (≤127 weeks). Longitudinal data from start of romiplostim treatment through the two extensions were evaluated to investigate the safety and efficacy of long-term romiplostim treatment in chronic severe pediatric ITP.

          Procedure

          Patients received weekly subcutaneous romiplostim, adjusted by 1 µg/kg/week to maintain platelet counts (50–200 × 10 9/L, maximum dose 10 µg/kg). Bone marrow examinations were not required.

          Results

          At baseline, patients were median age 10.0 years; median ITP duration 2.4 years; median platelet count 13 × 10 9/L; 73% were male; and 36% had prior splenectomy. Median romiplostim treatment duration was 167 weeks (Q1, Q3: 78,227 weeks), and median average weekly dose was 5.4 µg/kg (Q1, Q3: 4.3, 8.0 µg/kg). Seven patients discontinued treatment: four withdrew consent, two were noncompliant, and one received alternative therapy. None withdrew because of adverse events (AEs). After the first 12 weeks, median platelet counts remained >50 × 10 9/L. Eight (36.4%) patients received rescue medication, and 14 (63.6%) used concurrent ITP therapy. Seven patients (31.8%) reported serious AEs, and two (9.1%) reported life-threatening AEs (both thrombocytopenia); there were no serious AEs attributed to treatment and no fatalities.

          Conclusions

          Long-term romiplostim treatment in this small cohort increased and maintained platelet counts for over 4 years in children with ITP with good tolerability and without significant toxicity. Pediatr Blood Cancer 2015;62:208–213. © 2014. The Authors. Pediatr Blood & Cancer published by Wiley Periodicals, Inc.

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          Most cited references24

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          International consensus report on the investigation and management of primary immune thrombocytopenia.

          Previously published guidelines for the diagnosis and management of primary immune thrombocytopenia (ITP) require updating largely due to the introduction of new classes of therapeutic agents, and a greater understanding of the disease pathophysiology. However, treatment-related decisions still remain principally dependent on clinical expertise or patient preference rather than high-quality clinical trial evidence. This consensus document aims to report on new data and provide consensus-based recommendations relating to diagnosis and treatment of ITP in adults, in children, and during pregnancy. The inclusion of summary tables within this document, supported by information tables in the online appendices, is intended to aid in clinical decision making.
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            Efficacy of romiplostim in patients with chronic immune thrombocytopenic purpura: a double-blind randomised controlled trial.

            Chronic immune thrombocytopenic purpura (ITP) is characterised by accelerated platelet destruction and decreased platelet production. Short-term administration of the thrombopoiesis-stimulating protein, romiplostim, has been shown to increase platelet counts in most patients with chronic ITP. We assessed the long-term administration of romiplostim in splenectomised and non-splenectomised patients with ITP. In two parallel trials, 63 splenectomised and 62 non-splenectomised patients with ITP and a mean of three platelet counts 30x10(9)/L or less were randomly assigned 2:1 to subcutaneous injections of romiplostim (n=42 in splenectomised study and n=41 in non-splenectomised study) or placebo (n=21 in both studies) every week for 24 weeks. Doses of study drug were adjusted to maintain platelet counts of 50x10(9)/L to 200x10(9)/L. The primary objectives were to assess the efficacy of romiplostim as measured by a durable platelet response (platelet count > or =50x10(9)/L during 6 or more of the last 8 weeks of treatment) and treatment safety. Analysis was per protocol. These studies are registered with ClinicalTrials.gov, numbers NCT00102323 and NCT00102336. A durable platelet response was achieved by 16 of 42 splenectomised patients given romplostim versus none of 21 given placebo (difference in proportion of patients responding 38% [95% CI 23.4-52.8], p=0.0013), and by 25 of 41 non-splenectomised patients given romplostim versus one of 21 given placebo (56% [38.7-73.7], p<0.0001). The overall platelet response rate (either durable or transient platelet response) was noted in 88% (36/41) of non-splenectomised and 79% (33/42) of splenectomised patients given romiplostim compared with 14% (three of 21) of non-splenectomised and no splenectomised patients given placebo (p<0.0001). Patients given romiplostim achieved platelet counts of 50x10(9)/L or more on a mean of 13.8 (SE 0.9) weeks (mean 12.3 [1.2] weeks in splenectomised group vs 15.2 [1.2] weeks in non-splenectomised group) compared with 0.8 (0.4) weeks for those given placebo (0.2 [0.1] weeks vs 1.3 [0.8] weeks). 87% (20/23) of patients given romiplostim (12/12 splenectomised and eight of 11 non-splenectomised patients) reduced or discontinued concurrent therapy compared with 38% (six of 16) of those given placebo (one of six splenectomised and five of ten non-splenectomised patients). Adverse events were much the same in patients given romiplostim and placebo. No antibodies against romiplostim or thrombopoietin were detected. Romiplostim was well tolerated, and increased and maintained platelet counts in splenectomised and non-splenectomised patients with ITP. Many patients were able to reduce or discontinue other ITP medications. Stimulation of platelet production by romiplostim may provide a new therapeutic option for patients with ITP.
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              Idiopathic thrombocytopenic purpura: a practice guideline developed by explicit methods for the American Society of Hematology.

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                Author and article information

                Journal
                Pediatr Blood Cancer
                Pediatr Blood Cancer
                pbc
                Pediatric Blood & Cancer
                Blackwell Publishing Ltd (Oxford, UK )
                1545-5009
                1545-5017
                February 2015
                24 October 2014
                : 62
                : 2
                : 208-213
                Affiliations
                [1 ]Department of Pediatrics, Division of Hematology, Weill Medical College of Cornell University New York, New York
                [2 ]Children's Hospital of Orange County/University of California Irvine, California
                [3 ]Department of Pediatrics, University of Texas Southwestern Medical Center Dallas, Texas
                [4 ]Arkansas Children's Hospital Little Rock, Arkansas
                [5 ]Children's Mercy Hospital Kansas City, Missouri
                [6 ]Children's Hospital and Medical Center, University of Nebraska Medical Center Omaha, Nebraska
                [7 ]Department of Pediatrics, Monroe Carell Jr. Children's Hospital at Vanderbilt Nashville, Tennessee
                [8 ]Amgen Inc. Thousand Oaks, California
                Author notes
                *Correspondence to: James B. Bussel, Weill Medical College of Cornell University, 525 East 68th Street, Payson Pavilion–695, New York, NY 10065., E-mail: jbussel@ 123456med.cornell.edu

                Conflicts of interest: Dr. Bussel has received research funding from Amgen, Cangene, GlaxoSmithKline (GSK), Genzyme, IgG of America, Immunomedics, Ligand, Eisai, Shionogi and Sysmex; his family owns stock in Amgen and GSK; he has served on advisory boards for Amgen, GSK, Ligand, Shionogi, and Eisai; and he has consulted for Portola. Dr. Stine has served on advisory boards for Kedrion, Octapharma, and Biogen Idec. Dr. Nie and Dr. Eisen are employees and stockholders of Amgen. The other authors do not have any disclosures.

                Article
                10.1002/pbc.25136
                4309514
                25345874
                0219ad40-ef5f-4e32-ad41-65084d037b05
                © 2014 The Authors. Pediatric Blood & Cancer published by Wiley Periodicals, Inc.

                This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

                History
                : 29 October 2013
                : 14 May 2014
                Categories
                Research Articles

                Pediatrics
                autoimmunity,bleeding,platelets,thrombopoietin
                Pediatrics
                autoimmunity, bleeding, platelets, thrombopoietin

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