Alternatives for managing patients with newly diagnosed immune thrombocytopenia: a narrative review

医学 美罗华 免疫性血小板减少症 重症监护医学 耐受性 叙述性评论 心理干预 一线治疗 不利影响 外科 内科学 血小板 淋巴瘤 精神科
作者
David Gómez‐Almaguer,Edgar A. Rojas-Guerrero,Andrés Gómez‐De León,Perla R. Colunga‐Pedraza,José Carlos Jaime‐Pérez
出处
期刊:Expert Review of Hematology [Informa]
卷期号:15 (6): 493-501 被引量:1
标识
DOI:10.1080/17474086.2022.2082936
摘要

Introduction Primary immune thrombocytopenia (ITP) is an acquired bleeding disorder. Conventionally, first-line ITP therapy aims to obtain a rapid response and stop or decrease the risk of bleeding by increasing the platelet count. At this point, the duration of the response, the tolerability, and the long-term safety of pharmacologic interventions are considered less of a priority. Combination treatments that simultaneously address multiple disease mechanisms are an attractive strategy to increase efficacy in acute ITP therapy. In this review, we discuss the treatment of newly diagnosed ITP patients, emphasizing the use of new combinations to benefit from their synergy.Areas covered This article summarizes conventional treatment, recent and novel combinations, and COVID-19 management recommendations of newly diagnosed ITP patients.Expert opinion The key areas for improvement consider the long-term effects of conventional first-line therapy, reducing relapse rates, and extending responses to achieve long-term remission. Although corticosteroids remain a first-line therapy, restricting their use to avoid toxicity and the increasing use of rituximab and TPO-RAs in the first three months after diagnosis open the landscape for future interventions in frontline therapy for ITP. First-line therapy intensification or synergistic drug combination offers a potential and realistic shift in future treatment guidelines.
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