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促血小板生成素受体激动剂治疗造血干细胞移植后血小板减少症的疗效和安全性:Meta 分析和系统评价。

Efficacy and safety of thrombopoietin receptor agonists in the treatment of thrombocytopenia after hematopoietic stem cell transplantation: a meta-analysis and systematic review.

机构信息

National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, the First Affiliated Hospital of Soochow University, Suzhou, China.

Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, China.

出版信息

Expert Rev Hematol. 2021 Nov;14(11):1041-1048. doi: 10.1080/17474086.2021.2009337. Epub 2021 Dec 1.

Abstract

Thrombocytopenia is a tough complication after hematopoietic stem cell transplantation (HSCT) with elusive pathogenesis and lack of well-established therapies. Thrombopoietin receptor agonists (TPO-RAs) have been used for thrombocytopenia post HSCT in recent years, but the outcomes remain debatable. We conducted this meta-analysis and systematic-review to evaluate the efficacy and safety of TPO-RAs for platelet recovery after HSCT. We searched PubMed, EMBASE, and Cochrane databases for studies on the application of TPO-RAs (eltrombopag and romiplostim) in the settings of primary or secondary thrombocytopenia after HSCT by 17 March 2021. Efficacy outcomes included response rate and survival rate, and adverse events were also evaluated. A total of 19 studies involving 378 patients were included. The pooled response rate was 73% (95%CI: 68-78%), which was significantly higher than recombinant human thrombopoietin (rhTPO) (27.8%). The pooled survival rate was 66% (95%CI: 54-77%), and infection was found to be the main cause of death. In addition, the pooled rate of adverse events was 3% (95%CI: 1-7%), with no severe adverse events reported. TPO-RAs could effectively and safely promote the recovery of platelets in patients after HSCT.

摘要

血小板减少症是造血干细胞移植(HSCT)后的一种严重并发症,发病机制尚不清楚,且缺乏成熟的治疗方法。近年来,血小板生成素受体激动剂(TPO-RAs)已被用于 HSCT 后血小板减少症的治疗,但疗效仍存在争议。我们进行了这项荟萃分析和系统评价,以评估 TPO-RAs 在 HSCT 后血小板恢复中的疗效和安全性。我们检索了 PubMed、EMBASE 和 Cochrane 数据库,以获取 2021 年 3 月 17 日前关于 TPO-RAs(艾曲泊帕和罗米司亭)在 HSCT 后原发性或继发性血小板减少症治疗中应用的研究。疗效结局包括反应率和生存率,同时还评估了不良反应事件。共纳入 19 项研究,涉及 378 例患者。汇总的反应率为 73%(95%CI:68-78%),明显高于重组人血小板生成素(rhTPO)(27.8%)。汇总的生存率为 66%(95%CI:54-77%),感染是导致死亡的主要原因。此外,汇总的不良反应发生率为 3%(95%CI:1-7%),无严重不良反应报告。TPO-RAs 可有效且安全地促进 HSCT 后患者血小板的恢复。

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