Turkish Journal of Hematology (Aug 2020)

Outcomes of Eltrombopag Treatment and Development of Iron Deficiency in Children with Immune Thrombocytopenia in Turkey

  • Ayça Koca Yozgat,
  • Göksel Leblebisatan,
  • Sinan Akbayram,
  • Simge Çınar Özel,
  • Zeynep Karakaş,
  • Erol Erduran,
  • Şebnem Yılmaz,
  • Ülker Koçak,
  • Şule Ünal,
  • Gül Nihal Özdemir,
  • Meryem Albayrak,
  • Emine Zengin,
  • Yeşim Oymak,
  • Özcan Bör,
  • Hasan Fatih Çakmaklı,
  • Murat Söker,
  • Dilek Gürlek Gökçebay,
  • Hüseyin Tokgöz,
  • Barış Malbora,
  • Serap Karaman,
  • Tiraje Celkan,
  • İlgen Şaşmaz,
  • Neşe Yaralı,
  • Hale Ören,
  • Ayşegül Ünüvar

DOI
https://doi.org/10.4274/tjh.galenos.2020.2019.0380
Journal volume & issue
Vol. 37, no. 3
pp. 139 – 144

Abstract

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Objective: Immune thrombocytopenia (ITP) is a rare autoimmune disease and hematologic disorder characterized by reduced platelet counts that can result in significant symptoms, such as bleeding, bruising, epistaxis, or petechiae. The thrombopoietin receptor agonist eltrombopag (EPAG) is a second-line agent used to treat chronic ITP purpura in adults and children. Materials and Methods: The present retrospective study evaluated the efficacy, safety, and side effects of EPAG treatment in pediatric patients with acute refractory and chronic immune thrombocytopenia, particularly focusing on iron-deficiency anemia. Results: The diagnosis was chronic ITP in 89 patients and acute refractory ITP in 16 patients. The mean age of patients was 9.5+-4.5 years (minimum-maximum: 1.2-18 years) at the beginning of EPAG treatment. The overall response rate was 74.3% (n=78). The mean time for platelet count of ≥50x109/L was 11.6+-8 weeks (range: 1-34 weeks). The treatment was stopped for 27 patients (25.7%) at an average of 6.8+-9 months (range: 1-38 months). The reason for discontinuation was lack of response in 18 patients, nonadherence in 4 patients, and hepatotoxicity in 2 patients. Response to treatment continued for an average of 4 months after cessation of EPAG in 3 patients. Conclusion: Results of the current study imply that EPAG is an effective therapeutic option in pediatric patients with acute refractory and chronic ITP. However, patients must be closely monitored for response and side effects during treatment, and especially for iron deficiency.

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