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难治性原发性免疫性血小板减少症的标志物。

Markers of refractory primary immune thrombocytopenia.

机构信息

Department of Internal Medicine, Referral Center for Autoimmune Cytopenia, Toulouse University Hospital, Toulouse, France.

Clinical Investigation Center 1436, Team PEPSS, Toulouse University Hospital, Toulouse, France.

出版信息

Br J Haematol. 2023 Oct;203(1):112-118. doi: 10.1111/bjh.19076. Epub 2023 Aug 30.

Abstract

Refractory immune thrombocytopenia (ITP) is a challenging disease that can be defined by refractoriness to second-line treatments. In this review, we list and comment available evidence about clinical and biological factors associated with refractoriness to splenectomy, thrombopoietin receptor agonists (TPO-RAs), rituximab and fostamatinib, as well as those associated with multirefractory ITP (active disease with failure of rituximab, TPO-RAs and splenectomy).

摘要

难治性免疫性血小板减少症(ITP)是一种具有挑战性的疾病,其可以通过对二线治疗的抵抗来定义。在这篇综述中,我们列出并评论了与脾切除术、血小板生成素受体激动剂(TPO-RAs)、利妥昔单抗和 fostamatinib 抵抗以及与多难治性 ITP(利妥昔单抗、TPO-RAs 和脾切除术失败的活动性疾病)相关的临床和生物学因素的现有证据。

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