艾曲波帕成功治疗atezolizumab诱导的严重免疫相关血小板减少症一例:病例报告。

IF 0.7 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Saki Harada, Takeshi Imakura, Seidai Sato, Hiroshi Nokihara, Yasuhiko Nishioka
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引用次数: 1

摘要

免疫检查点抑制剂(ICIs)对多种恶性肿瘤显示出令人印象深刻的抗肿瘤作用。在各种各样的免疫相关不良事件(irAE)中,免疫相关血小板减少症(ITP)相对罕见,但通常具有临床意义并危及生命。然而,严重ITP的适当治疗方法尚未确定。我们在此报告一名82岁的男性非小细胞肺癌癌症患者,他在开始第三个疗程的atezolizumab后三周出现严重的ITP。大剂量泼尼松、静脉注射免疫球蛋白和血小板输注的初始联合治疗无效。然而,使用血小板生成素受体激动剂eltrombopag进行额外治疗,可显著改善血小板减少症。J.Med.Invest。70:516-5202023年8月。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of successful treatment with eltrombopag for severe immune-related thrombocytopenia induced by atezolizumab:Case report.

Immune checkpoint inhibitors (ICIs) have shown impressive anti-tumor effects against multiple types of malignancies. Among the wide variety of immune-related adverse events (irAEs), immune-related thrombocytopenia (ITP) is relatively rare but often clinically significant and life-threatening. However, the appropriate treatment for severe ITP has not been determined. We herein report an 82-year-old male patient with non-small-cell lung cancer who developed severe ITP three weeks after starting the third course of atezolizumab. The initial combination therapy with high-dose prednisolone, intravenous immunoglobulin and platelet transfusion was ineffective. However, additional treatment with eltrombopag, a thrombopoietin receptor agonist, resulted in remarkable improvement in the thrombocytopenia. J. Med. Invest. 70 : 516-520, August, 2023.

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来源期刊
JOURNAL OF MEDICAL INVESTIGATION
JOURNAL OF MEDICAL INVESTIGATION MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
1.20
自引率
0.00%
发文量
55
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