Zheng X Long, Vesely Sara K, Cataland Spero R, Coppo Paul, Geldziler Brian, Iorio Alfonso, Matsumoto Masanori, Mustafa Reem A, Pai Menaka, Rock Gail, Russell Lene, Tarawneh Rawan, Valdes Julie, Peyvandi Flora
Department of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS, USA.
Hudson College of Public Health, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
J Thromb Haemost. 2020 Oct;18(10):2496-2502. doi: 10.1111/jth.15010. Epub 2020 Sep 11.
Despite advances in treatment options for thrombotic thrombocytopenic purpura (TTP), there are still limited high quality data to inform clinicians regarding its appropriate treatment.
In June 2018, the ISTH formed a multidisciplinary guideline panel to issue recommendations about treatment of TTP. The panel discussed 12 treatment questions related to immune-mediated TTP (iTTP) and hereditary or congenital TTP (cTTP). The panel used the Grading of Recommendations Assessment, Development, and Evaluation approach, including evidence-to-decision frameworks, to appraise evidence and formulate recommendations.
The panel agreed on 11 recommendations based on evidence ranging from very low to moderate certainty. For first acute episode and relapses of iTTP, the panel made a strong recommendation for adding corticosteroids to therapeutic plasma exchange (TPE) and a conditional recommendation for adding rituximab and caplacizumab. For asymptomatic iTTP with low plasma ADAMTS13 activity, the panel made a conditional recommendation for the use of rituximab outside of pregnancy, but prophylactic TPE during pregnancy. For asymptomatic cTTP, the panel made a strong recommendation for prophylactic plasma infusion during pregnancy, and a conditional recommendation for plasma infusion or a wait and watch approach outside of pregnancy.
The panel's recommendations are based on all the available evidence for the effects of an individual component of various treatment approaches, including suppressing inflammation, blocking platelet clumping, replacing the missing and/or inhibited ADAMTS13, and suppressing the formation of ADAMTS13 autoantibody. There was insufficient evidence for further comparing different treatment approaches (eg, TPE, corticosteroids, rituximab, and caplacizumab, etc.), for which high quality studies are needed.
尽管血栓性血小板减少性紫癜(TTP)的治疗选择有所进展,但仍缺乏高质量数据为临床医生提供关于其恰当治疗的信息。
2018年6月,国际血栓与止血学会(ISTH)成立了一个多学科指南小组,以发布关于TTP治疗的建议。该小组讨论了12个与免疫介导的TTP(iTTP)和遗传性或先天性TTP(cTTP)相关的治疗问题。该小组采用推荐分级评估、制定和评价方法,包括证据到决策框架,来评估证据并制定建议。
该小组基于从极低到中等确定性的证据达成了11项建议。对于iTTP的首次急性发作和复发,该小组强烈建议在治疗性血浆置换(TPE)中添加皮质类固醇,并有条件地建议添加利妥昔单抗和卡泊单抗。对于血浆ADAMTS13活性低的无症状iTTP,该小组有条件地建议在非孕期使用利妥昔单抗,但在孕期进行预防性TPE。对于无症状cTTP,该小组强烈建议在孕期进行预防性血浆输注,并有条件地建议在非孕期进行血浆输注或采取观察等待的方法。
该小组的建议基于各种治疗方法中各个组成部分作用的所有现有证据,包括抑制炎症、阻止血小板聚集、替代缺失和/或受抑制的ADAMTS13以及抑制ADAMTS13自身抗体的形成。没有足够的证据进一步比较不同的治疗方法(如TPE、皮质类固醇、利妥昔单抗和卡泊单抗等),为此需要高质量的研究。