Management of immune thrombotic thrombocytopenic purpura without therapeutic plasma exchange.

IF 21 1区 医学 Q1 HEMATOLOGY
Blood Pub Date : 2024-10-03 DOI:10.1182/blood.2023023780
Lucas Kühne, Paul Knöbl, Kathrin Eller, Johannes Thaler, Wolfgang R Sperr, Karoline Gleixner, Thomas Osterholt, Jessica Kaufeld, Jan Menne, Veronika Buxhofer-Ausch, Anja Mühlfeld, Evelyn Seelow, Adrian Schreiber, Polina Todorova, Sadrija Cukoski, Wolfram J Jabs, Fedai Özcan, Anja Gäckler, Kristina Schönfelder, Felix S Seibert, Timm Westhoff, Vedat Schwenger, Dennis A Eichenauer, Linus A Völker, Paul T Brinkkoetter
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引用次数: 0

Abstract

Abstract: Immune thrombotic thrombocytopenic purpura (iTTP) is a rare, life-threatening autoimmune disorder caused by a disintegrin and metalloproteinase with thrombospondin type 1 motif, member 13 (ADAMTS13) deficiency. Caplacizumab, an anti-von Willebrand factor nanobody, is approved for iTTP treatment, reducing the need for therapeutic plasma exchange (TPE) and improving platelet count recovery and survival. We conducted a retrospective study on 42 acute iTTP cases in Austria and Germany, treated with a modified regimen aimed at avoiding TPE if platelet count increased after the first caplacizumab dose. Baseline characteristics and patient outcomes were compared with a control group of 59 patients with iTTP receiving frontline treatment with TPE, caplacizumab, and immunosuppression. The main outcome was the time to platelet count normalization. Secondary outcomes included clinical response, exacerbation, refractory iTTP, iTTP-related deaths, and the time to platelet count doubling. The median time to platelet count normalization was similar between the 2 cohorts (3 and 4 days; P = .31). There were no significant differences in clinical response, exacerbations, refractoriness, iTTP-related deaths, or time to platelet count doubling, reflecting the short-term treatment response. Four patients did not respond to the first caplacizumab dose, and TPE was subsequently initiated. Cytomegalovirus infection, HIV/hepatitis B virus coinfection, an ovarian teratoma with associated antiplatelet antibodies, and multiple platelet transfusions before the correct diagnosis may have impeded the immediate treatment response in these patients. In conclusion, caplacizumab and immunosuppression alone, without TPE, rapidly controlled thrombotic microangiopathy and achieved a sustained clinical response in iTTP. Our study provides a basis for TPE-free iTTP management in experienced centers via shared decision-making between patients and treating physicians.

不进行治疗性血浆置换的免疫性血栓性血小板减少性紫癜治疗方法
免疫性血栓性血小板减少性紫癜(iTTP)是一种罕见的、危及生命的自身免疫性疾病,由 ADAMTS13 缺乏症引起。卡普拉珠单抗是一种抗 VWF 纳米抗体,已被批准用于 iTTP 治疗,可减少治疗性血浆置换(TPE)的需要,改善血小板计数恢复和存活率。我们对奥地利和德国的 42 例急性 iTTP 病例进行了一项回顾性研究,这些病例在首次服用卡普单抗后,如果血小板计数增加,则采用旨在避免 TPE 的改良方案进行治疗。该研究将基线特征和患者预后与接受 TPE、卡普珠单抗和免疫抑制一线治疗的 59 例 iTTP 患者组成的对照组进行了比较。主要结果是血小板计数恢复正常的时间。次要结果包括临床反应、病情加重、难治性 iTTP、iTTP 相关死亡以及血小板计数翻倍的时间。两组患者血小板计数恢复正常的中位时间相似(3 天和 4 天;P = 0.31)。在反映短期治疗反应的临床反应、病情加重、难治性、iTTP 相关死亡或血小板计数翻倍时间方面没有明显差异。四名患者对第一剂卡普珠单抗没有反应,随后开始使用 TPE。巨细胞病毒感染、HIV/乙型肝炎合并感染、卵巢畸胎瘤伴有抗血小板抗体,以及在正确诊断前多次输注血小板可能阻碍了这些患者的即时治疗反应。总之,单用卡普拉珠单抗和免疫抑制,而不使用 TPE,可迅速控制血栓性微血管病变,并在 iTTP 中获得持续的临床反应。我们的研究为有经验的中心通过患者和主治医生共同决策来管理无 TPE 的 iTTP 提供了依据。
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来源期刊
Blood
Blood 医学-血液学
CiteScore
23.60
自引率
3.90%
发文量
955
审稿时长
1 months
期刊介绍: Blood, the official journal of the American Society of Hematology, published online and in print, provides an international forum for the publication of original articles describing basic laboratory, translational, and clinical investigations in hematology. Primary research articles will be published under the following scientific categories: Clinical Trials and Observations; Gene Therapy; Hematopoiesis and Stem Cells; Immunobiology and Immunotherapy scope; Myeloid Neoplasia; Lymphoid Neoplasia; Phagocytes, Granulocytes and Myelopoiesis; Platelets and Thrombopoiesis; Red Cells, Iron and Erythropoiesis; Thrombosis and Hemostasis; Transfusion Medicine; Transplantation; and Vascular Biology. Papers can be listed under more than one category as appropriate.
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