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艾曲泊帕治疗结缔组织病合并难治性免疫性血小板减少症的有效性和安全性:一项回顾性研究

Effectiveness and safety of eltrombopag in connective tissue disease patients with refractory immune thrombocytopenia: a retrospective study.

作者信息

Jiang Xiangpin, Shu Xiaoming, Ge Yongpeng

机构信息

Department of Rheumatology, Jining No. 1 People's Hospital, Jining, China.

Department of Rheumatology, Key Laboratory of Myositis, China-Japan Friendship Hospital, Beijing, China.

出版信息

Rheumatol Adv Pract. 2024 Mar 4;8(2):rkae029. doi: 10.1093/rap/rkae029. eCollection 2024.

Abstract

OBJECTIVES

We aimed to investigate the safety and effectiveness of eltrombopag for adult patients with refractory immune thrombocytopenia (ITP) secondary to connective tissue disease (CTD).

METHODS

This is a single-centre, retrospective cohort and propensity score-matched study. Data from CTD-ITP patients treated with eltrombopag between January 2019 and January 2023 were retrospectively analysed. Baseline characteristics and follow-up information were recorded. CTD patients without ITP were matched to identify the risk factors associated with CTD-ITP performed by Logistic regression analysis.

RESULTS

Twenty patients were enrolled, including 5 systemic lupus erythematosus (SLE), 9 Sjögren's syndrome (SS) and 6 undifferentiated connective tissue disease (UCTD). Nineteen (95%) patients were female, and the median age was 59 years. Logistic regression analysis showed that anaemia (OR = 8.832, =0.007) was associated with increased risk of ITP, while non-erosive arthritis (OR = 0.045, =0.001) and interstitial lung disease (OR = 0.075, =0.031) were associated with reduced risk. Fourteen patients (70%) achieved a complete response (CR) and one (5%) achieved a partial response (PR). The median response time was 14 days. The median platelet count was 8.5 × 10/l at baseline of eltrombopag and increased to 122 × 10/l after 4 weeks. No adverse events were observed.

CONCLUSIONS

Eltrombopag appears to be effective, safe and well-tolerated in refractory ITP patients with CTD; larger studies are needed to confirm the generalizability of these findings.

摘要

目的

我们旨在研究艾曲泊帕对结缔组织病(CTD)继发的难治性免疫性血小板减少症(ITP)成年患者的安全性和有效性。

方法

这是一项单中心、回顾性队列和倾向评分匹配研究。对2019年1月至2023年1月期间接受艾曲泊帕治疗的CTD-ITP患者的数据进行回顾性分析。记录基线特征和随访信息。将无ITP的CTD患者进行匹配,通过逻辑回归分析确定与CTD-ITP相关的危险因素。

结果

共纳入20例患者,其中5例为系统性红斑狼疮(SLE),9例为干燥综合征(SS),6例为未分化结缔组织病(UCTD)。19例(95%)患者为女性,中位年龄为59岁。逻辑回归分析显示,贫血(OR = 8.832,P = 0.007)与ITP风险增加相关,而非侵蚀性关节炎(OR = 0.045,P = 0.001)和间质性肺病(OR = 0.075,P = 0.031)与风险降低相关。14例(70%)患者达到完全缓解(CR),1例(5%)达到部分缓解(PR)。中位缓解时间为14天。艾曲泊帕基线时中位血小板计数为8.5×10⁹/L,4周后升至122×10⁹/L。未观察到不良事件。

结论

艾曲泊帕在CTD难治性ITP患者中似乎有效、安全且耐受性良好;需要更大规模的研究来证实这些发现的普遍性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b86/10942842/1c66a59d4b4d/rkae029f2.jpg

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本文引用的文献

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