首页|程序性死亡受体1单抗诱发重度免疫性血小板减少(附3例报告)

程序性死亡受体1单抗诱发重度免疫性血小板减少(附3例报告)

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目的 分析程序性死亡受体1(PD-1)单抗诱发重度免疫性血小板减少(SIT)的诊断与治疗。方法 选取浙江省舟山市普陀区人民医院2020年3月至2022年10月因PD-1单抗治疗导致SIT患者3例,分析其诊疗过程和病情转归。结果 3例患者术后病理均确诊恶性肿瘤给予PD-1单抗后诱发SIT,其中1例患者死亡,2例患者经治疗后好转。结论 PD-1诱发SIT多发生于12周以后,可结合患者用药史、血小板抗体、骨髓检查明确临床诊断。在治疗上,激素有序减量,血小板生成素、血小板受体激动剂等联合治疗可促进患者恢复。此外,必要时可使用CD20单抗治疗以拮抗血小板抗体。
Severe Immune thrombocytopenia induced by programmed death-1 monoclonal antibody:report of 3 cases
Objective To retrospectively explore the diagnosis and treatment of severe immune thrombocytopenia(SIT)induced by programmed death-1(PD-1)monoclonal antibody.Methods Three patients with SIT caused by PD-1 monoclonal antibody treatment at Putuo District People's Hospital,Zhoushan City,Zhejiang Province from March 2020 to October 2022 were selected,and the diagnosis and treatment process and disease outcome were analyzed.Results All three patients were diagnosed with malignant tumors after postoperative pathological examination,and SIT was induced after PD-1 monoclonal antibody treatment,of which one patient died,and two patients improved after the treatment.Conclusion PD-1 induced SIT often occurs after 12 weeks,and clinical diagnosis can be confirmed by combining patients'medication history,platelet antibodies,and bone marrow examination.In terms of treatment,combination therapy such as ordered reduction of hormones,thrombopoietin,and platelet receptor agonists can promote the recovery of the patient.In addition,if necessary,CD20 monoclonal antibody therapy can be applied to antagonize platelet antibodies.

Programmed death-1Severe thrombocytopeniaDiagnosisTreatment

王振华、虞飞燕、楼芳、陈舒、徐志

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浙江省舟山市普陀区人民医院血液科(浙江舟山 316000)

浙江大学医学院附属邵逸夫医院肿瘤科(杭州 310020)

浙江省血液中心血液科(杭州 310052)

程序性死亡受体1 重度血小板减少 诊断 治疗

浙江省医药卫生科技计划

2018RC029

2024

中国药师
国家药品监督管理局高级研修学院,武汉医药(集团)股份有限公司

中国药师

CSTPCD
影响因子:0.944
ISSN:1008-049X
年,卷(期):2024.27(8)