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艾曲泊帕治疗结缔组织病继发的严重免疫性血小板减少症:17例病例报告及文献综述

Eltrombopag in severe immune thrombocytopenia secondary to connective tissue disease: a report of 17 patients and literature review.

作者信息

Li Wenjing, Wang Dandan, Ma Ling, Zhu Yun, Wang Fan, Hua Bingzhu, Wang Hong, Feng Xuebing

机构信息

Department of Rheumatology and Immunology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, 321 Zhongshan Road, Nanjing, 210008, China.

出版信息

Clin Rheumatol. 2023 May;42(5):1451-1457. doi: 10.1007/s10067-022-06464-w. Epub 2023 Jan 3.

Abstract

To assess the remission rate of eltrombopag in the treatment of severe immune thrombocytopenia (ITP) secondary to connective tissue disease (CTD) and to explore factors related to drug efficacy in the context of literature reports, seventeen CTD patients accompanied with severe ITP treated with eltrombopag between June 2019 and February 2021 were included, with their follow-up information recorded. Combined with literature review, patients were divided into two groups depending on whether the treatment was effective or not to determine efficacy-related factors. Totally, 7 patients with systemic lupus erythematosus, 6 with Sjögren's syndrome, and 4 with undifferentiated connective tissue disease were enrolled. The median duration of eltrombopag treatment was 8 weeks, and the median time to response was 4 weeks. Twelve (70.6%) patients responded to eltrombopag. Patients with higher serum white blood cell counts, lower serum triglyceride levels, or previously received multiple immunosuppressants achieved a better efficacy (p < 0.05), while those with megakaryocytopenia in bone marrow tended to have lower remission rate (p = 0.08). By using pooled data including literature reported cases, we demonstrated that evidence of leukopenia, megakaryocytopenia, and being treated with fewer prior immunosuppressants were still associated with poor remission (p < 0.05). Meanwhile, there was a trend indicating the primary disease might affect the treatment efficacy (p = 0.06). Eltrombopag is a viable option for treating severe ITP secondary to CTDs, yet it may be less effective for patients with leukopenia, megakaryocytopenia, and being treated with fewer prior immunosuppressants. Key Points • Eltrombopag provides an alternative to the current treatment of CTD-ITP. • White blood cell levels, bone marrow megakaryocyte counts, and prior use of immunosuppressants may affect the efficacy of eltrombopag.

摘要

为评估艾曲泊帕治疗结缔组织病(CTD)继发的重度免疫性血小板减少症(ITP)的缓解率,并结合文献报道探讨与药物疗效相关的因素,纳入了2019年6月至2021年2月期间接受艾曲泊帕治疗的17例伴有重度ITP的CTD患者,并记录其随访信息。结合文献复习,根据治疗是否有效将患者分为两组以确定疗效相关因素。共纳入7例系统性红斑狼疮患者、6例干燥综合征患者和4例未分化结缔组织病患者。艾曲泊帕治疗的中位持续时间为8周,中位起效时间为4周。12例(70.6%)患者对艾曲泊帕有反应。血清白细胞计数较高、血清甘油三酯水平较低或既往接受过多种免疫抑制剂治疗的患者疗效较好(p<0.05),而骨髓中巨核细胞减少的患者缓解率往往较低(p = 0.08)。通过使用包括文献报道病例的汇总数据,我们证明白细胞减少、巨核细胞减少以及既往接受免疫抑制剂治疗较少的证据仍与缓解不佳相关(p<0.05)。同时,有趋势表明原发性疾病可能影响治疗效果(p = 0.06)。艾曲泊帕是治疗CTD继发重度ITP的可行选择,但对于白细胞减少、巨核细胞减少以及既往接受免疫抑制剂治疗较少的患者可能效果较差。要点 • 艾曲泊帕为目前CTD-ITP的治疗提供了一种替代方案。 • 白细胞水平、骨髓巨核细胞计数和既往免疫抑制剂的使用可能影响艾曲泊帕的疗效。

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