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血小板生成素受体激动剂和利妥昔单抗治疗儿童免疫性血小板减少症:前瞻性临床试验的系统评价和荟萃分析

Thrombopoietin receptor agonists and rituximab for treatment of pediatric immune thrombocytopenia: A systematic review and meta-analysis of prospective clinical trials.

作者信息

Ayad Nardeen, Grace Rachael F, Al-Samkari Hanny

机构信息

Harvard Medical School, Boston, Massachusetts, USA.

Dana-Farber/Boston Children's Cancer and Blood Disorder Center, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Pediatr Blood Cancer. 2022 Mar;69(3):e29447. doi: 10.1002/pbc.29447. Epub 2021 Dec 28.

Abstract

BACKGROUND

Children with immune thrombocytopenia (ITP) may require second-line ITP therapies. The high remission rate in pediatric patients, need for extended-duration use of thrombopoietin receptor agonists (TPO-RAs), drug adherence, potential side effects, monitoring, and cost effectiveness are factors that should be considered in decision-making about second-line therapies. Rituximab (RTX) has been used off-label for years to treat ITP but there are limited studies about its efficacy and safety in children. To date, no studies have directly compared TPO-RAs with RTX for the treatment of childhood ITP.

METHODS

This systematic review analyzed the overall platelet response, durability of treatment effect, and safety for RTX use in comparison to TPO-RAs in pediatric ITP. MEDLINE/PubMed, EMBASE, Cochrane Library, and Web of Science databases were searched through December 2020 and meta-analysis was conducted using proportions of success/failure for each intervention in the selected studies.

RESULTS

The proportion of participants achieving the primary endpoint of a platelet response above 50,000 was similar for TPO-RAs (proportion = 0.71, 95% CI: 0.63-0.78) and RTX (proportion = 0.68, 95% CI: 0.53-0.82). However, considerable variation was found between the two groups with regards to the sustainability of the response and other secondary outcomes such as need for rescue and adverse events. RTX was associated with higher rates of rescue therapy.

CONCLUSIONS

In this analysis of prospective pediatric ITP studies, RTX and TPO-RAs had similar rates of overall platelet response but differed in other important measures. Prospective comparative studies are needed to better characterize second-line treatments for pediatric ITP.

摘要

背景

免疫性血小板减少症(ITP)患儿可能需要二线ITP治疗。小儿患者的高缓解率、血小板生成素受体激动剂(TPO-RAs)的长期使用需求、药物依从性、潜在副作用、监测以及成本效益是二线治疗决策中应考虑的因素。利妥昔单抗(RTX)多年来一直被用于ITP的非标签治疗,但关于其在儿童中的疗效和安全性的研究有限。迄今为止,尚无研究直接比较TPO-RAs与RTX治疗儿童ITP的效果。

方法

本系统评价分析了RTX与TPO-RAs相比,在儿童ITP中使用时的总体血小板反应、治疗效果的持久性和安全性。检索了截至2020年12月的MEDLINE/PubMed、EMBASE、Cochrane图书馆和Web of Science数据库,并使用所选研究中每种干预措施的成功/失败比例进行荟萃分析。

结果

TPO-RAs组(比例 = 0.71,95%CI:0.63 - 0.78)和RTX组(比例 = 0.68,95%CI:0.53 - 0.82)达到血小板反应高于50,000的主要终点的参与者比例相似。然而,两组在反应的可持续性以及其他次要结局(如抢救需求和不良事件)方面存在相当大的差异。RTX与更高的抢救治疗率相关。

结论

在这项对前瞻性儿童ITP研究的分析中,RTX和TPO-RAs的总体血小板反应率相似,但在其他重要指标上有所不同。需要进行前瞻性比较研究,以更好地描述儿童ITP的二线治疗。

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