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Progressive multifocal leukoencephalopathy in rituximab-treated rheumatic diseases: a rare event.利妥昔单抗治疗风湿性疾病后进展性多灶性白质脑病:罕见事件。
J Neurovirol. 2018 Jun;24(3):323-331. doi: 10.1007/s13365-018-0615-7. Epub 2018 Mar 5.
2
Diminished expression of β2-GPI is associated with a reduced ability to mitigate complement activation in anti-GPIIb/IIIa-mediated immune thrombocytopenia.β2-糖蛋白表达降低与抗糖蛋白IIb/IIIa介导的免疫性血小板减少症中减轻补体激活的能力降低有关。
Ann Hematol. 2018 Apr;97(4):641-654. doi: 10.1007/s00277-017-3215-3. Epub 2017 Dec 29.
3
Eltrombopag, low-dose rituximab, and dexamethasone combination as frontline treatment of newly diagnosed immune thrombocytopaenia.艾曲泊帕、低剂量利妥昔单抗和地塞米松联合用药作为新诊断免疫性血小板减少症的一线治疗方案
Br J Haematol. 2019 Jan;184(2):288-290. doi: 10.1111/bjh.15070. Epub 2017 Dec 21.
4
Treatment of Children with Persistent and Chronic Idiopathic Thrombocytopenic Purpura: 4 Infusions of Rituximab and Three 4-Day Cycles of Dexamethasone.持续性和慢性特发性血小板减少性紫癜患儿的治疗:4次利妥昔单抗输注及三个4天疗程的地塞米松治疗
J Pediatr. 2017 Dec;191:225-231. doi: 10.1016/j.jpeds.2017.08.036.
5
Progressive Multifocal Leukoencephalopathy and Monoclonal Antibodies: A Review.进行性多灶性白质脑病与单克隆抗体:综述
Cancer Control. 2017 Oct-Dec;24(4):1073274817729901. doi: 10.1177/1073274817729901.
6
Effects of rituximab and dexamethasone on regulatory and proinflammatory B-cell subsets in patients with primary immune thrombocytopenia.利妥昔单抗和地塞米松对原发性免疫性血小板减少症患者调节性和促炎性 B 细胞亚群的影响。
Eur J Haematol. 2018 Jan;100(1):45-52. doi: 10.1111/ejh.12978. Epub 2017 Oct 18.
7
GPIIb/IIIa autoantibody predicts better rituximab response in ITP.糖蛋白IIb/IIIa自身抗体可预测免疫性血小板减少症患者对利妥昔单抗的反应更佳。
Br J Haematol. 2018 Jul;182(2):305-307. doi: 10.1111/bjh.14782. Epub 2017 May 23.
8
Lack of detectable platelet autoantibodies is correlated with nonresponsiveness to rituximab treatment in ITP patients.血小板自身抗体检测不到与免疫性血小板减少症(ITP)患者对利妥昔单抗治疗无反应相关。
Blood. 2017 Jun 22;129(25):3389-3391. doi: 10.1182/blood-2016-11-751719. Epub 2017 May 3.
9
The effect of rituximab on anti-platelet autoantibody levels in patients with immune thrombocytopenia.利妥昔单抗对免疫性血小板减少症患者抗血小板自身抗体水平的影响。
Br J Haematol. 2017 Jul;178(2):302-307. doi: 10.1111/bjh.14664. Epub 2017 Apr 25.
10
Pathogenesis of immune thrombocytopenia.免疫性血小板减少症的发病机制。
Autoimmun Rev. 2017 Jun;16(6):620-632. doi: 10.1016/j.autrev.2017.04.012. Epub 2017 Apr 17.

利妥昔单抗治疗免疫性血小板减少症:2019 年该药的作用是什么?

Rituximab in the treatment of immune thrombocytopenia: what is the role of this agent in 2019?

机构信息

SC Ematologia, Azienda Sanitaria Universitaria Integrata Trieste, Italy.

SC Ematologia, Azienda Sanitaria Universitaria Integrata Trieste, Italy

出版信息

Haematologica. 2019 Jun;104(6):1124-1135. doi: 10.3324/haematol.2019.218883. Epub 2019 May 24.

DOI:10.3324/haematol.2019.218883
PMID:31126963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6545833/
Abstract

The use of rituximab for the treatment of immune thrombocytopenia was greeted enthusiastically: it led to up to 60% response rates, making it, nearly 20 years ago, the main alternative to splenectomy, with far fewer side effects. However, long-term follow-up data showed that only 20-30% of patients maintained the remission. No significant changes have been registered using different dose schedules and timing of administration, while the combination with other drugs seemed promising. Higher response rates have been observed in young women before the chronic phase, but apart from that, other clinical factors or biomarkers predictive of response are still lacking. In this review we examine the historical and current role of rituximab in the management of immune thrombocytopenia, 20 years after its first use for the treatment of autoimmune diseases.

摘要

利妥昔单抗治疗免疫性血小板减少症的应用受到了热烈欢迎

它使反应率高达 60%,使其在近 20 年前成为脾切除术的主要替代疗法,且副作用要少得多。然而,长期随访数据显示,只有 20-30%的患者能维持缓解。不同的剂量方案和给药时间并没有显著改变,而与其他药物联合使用似乎很有前景。在慢性期之前,年轻女性的反应率较高,但除此之外,其他预测反应的临床因素或生物标志物仍然缺乏。在这篇综述中,我们探讨了利妥昔单抗在免疫性血小板减少症治疗中的历史和当前作用,这是它首次用于治疗自身免疫性疾病后的 20 年。