Experience of 2<sup>nd</sup> line therapy with eltrombopag in patients with immune thrombocytopenia

Q4 Medicine
S. G. Zakharov, T. A. Mitina, R. V. Vardanyan, Z. R. Tekeeva, I. N. Kontievskiy, Yu. Yu. Chuksina, A. V. Zakharova
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引用次数: 0

Abstract

Background. Immune thrombocytopenia (ITP), or idiopathic thrombocytopenic purpura, is a hematological autoimmune disease characterized by bleeding and an isolated decrease in platelet count <100 × 10 9 / l. The decision to start treatment for ITP depends on several factors. The ITP treatment strategy is based on the clinical symptoms, with a focus on reducing the risk of severe bleeding and increasing platelet counts. Aim. To evaluate the efficacy of 2 nd line therapy with the thrombopoietin receptor agonist eltrombopag in patients with ITP. Materials and methods. 490 patients with ITP are under observation at the center for orphan diseases of M. F. Vladimirskiy Moscow Regional Research Clinical Institute. The present study included 186 patients with primary ITP after 1 st line glucocorticosteroid therapy. eltrombopag, a thrombopoietin receptor agonist, was prescribed as the 2 nd line of therapy. Results. The median platelet count prior to eltrombopag therapy in all patients was 27.5 × 10 9 / l. after eltrombopag therapy, a significant (by 490 %) increase in platelet levels (median 135 × 10 9 / l) and a complete response according to clinical recommendations were noted. Conclusion. Glucocorticosteroids (prednisolone, dexamethasone) remain the drugs of choice for the 1 st line of therapy. Treatment with drugs of this group in most cases allows achieving an optimal platelet level and preventing bleeding. In case of inefficiency, intolerance, occurrence of side effects, the appointment of thrombopoietin receptor agonists eltrombopag or romiplostim is recommended. therapy with eltrombopag at a dose of 50 mg daily for several weeks has been able to achieve an increase in platelet levels, correct hemorrhagic syndrome, reduce the number of side effects during first-line glucocorticosteroid therapy, and improve the patient’s quality of life.
2< supit>和</ supit>在免疫性血小板减少症患者中使用埃曲波帕进行一线治疗
背景。免疫性血小板减少症(ITP),或特发性血小板减少性紫癜,是一种血液学自身免疫性疾病,其特征是出血和孤立性血小板计数减少(100 × 10 / l)。ITP治疗策略以临床症状为基础,重点是减少严重出血的风险和增加血小板计数。的目标。评价血小板生成素受体激动剂埃曲巴格二线治疗ITP患者的疗效。材料和方法。莫斯科地区临床研究所的孤儿病中心正在观察490名ITP患者。本研究纳入186例经一线糖皮质激素治疗的原发性ITP患者。血栓生成素受体激动剂埃曲巴格被列为第二线治疗药物。结果。所有患者在接受依曲波包治疗前的中位血小板计数为27.5 × 109 / l,接受依曲波包治疗后,血小板水平显著(490%)增加(中位135 × 109 / l),并根据临床推荐达到完全缓解。结论。糖皮质激素(强的松龙、地塞米松)仍然是一线治疗的首选药物。在大多数情况下,使用该组药物治疗可以达到最佳血小板水平并防止出血。在无效、不耐受、出现副作用的情况下,推荐使用血小板生成素受体激动剂埃曲巴格或罗米普罗stim。使用每日50mg的伊曲波巴治疗数周,可以提高血小板水平,纠正出血性综合征,减少一线糖皮质激素治疗期间的副作用,并改善患者的生活质量。
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来源期刊
Oncogematologiya
Oncogematologiya Medicine-Hematology
CiteScore
0.50
自引率
0.00%
发文量
67
审稿时长
10 weeks
期刊介绍: The main purpose of the Oncohematology journal is to publish up-to-date information on clinical, experimental and fundamental scientific research, diagnostics and treatment options, as well as other materials on all relevant issues in oncohematology. The journal’s objectives are to inform various specialists who provide advisory and therapeutic assistance to patients with oncohematological diseases about current advances, including the latest methods for the diagnosis and treatment of malignant blood diseases. The journal is an interdisciplinary scientific publication uniting doctors of various specialties ‒ hematologists, oncologists, surgeons, radiation therapists, intensive care specialist, pathologists, etc. ‒ to form an interdisciplinary therapy approach in order to improve the treatment efficacy of patients with hematological malignancies.
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