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低丙种球蛋白血症与抗 CD20 治疗诱导的急性血小板减少症:或许并非巧合?

Hypogammaglobulinemia and Anti-CD20 Therapy-Induced Acute Thrombocytopenia: Perhaps More than a Coincidence?

机构信息

Department of Hematology, Oncology and Cell Therapy, Medical Center, Otto-von-Guericke University, Magdeburg, Germany.

出版信息

Oncol Res Treat. 2024;47(9):434-438. doi: 10.1159/000539919. Epub 2024 Jun 21.

DOI:10.1159/000539919
PMID:38901415
Abstract

INTRODUCTION

The development of secondary hypogammaglobulinemia (sHGG) because of tumor treatment and/or the primary underlying hematologic disorder holds substantial clinical significance. B-cell-derived malignancies and anti-CD20 monoclonal antibodies (mAbs) represent important risk factors for the development of sHGG. In addition, the occurrence of acute thrombocytopenia (AT) induced by anti-CD20 therapy is a known, albeit rare, phenomenon.

CASE PRESENTATION

A 54-year-old patient experiencing the first relapse of classical follicular lymphoma has commenced salvage therapy following the R-DHAP protocol. After rituximab infusion, platelet count dropped from 116 × 109/L to 13 × 109/L within 24 h. Reduced immunoglobulin G levels indicated moderate HGG; thus, we immediately administered intravenous immunoglobulins (IVIg). Within 5 days after initiation of IVIg, platelet count increased and stabilized at >50 × 109/L.

CONCLUSIONS

It seems possible that anti-CD20 mAbs act like or activate similar mechanisms as autoantibodies in immune thrombocytopenia (ITP). Assuming that anti-CD20 therapy-induced AT is an ITP-like condition, HGG could be considered a potential risk factor. Thus, appropriate treatment of HGG with IVIg prior to anti-CD20 mAb therapy could potentially alleviate anti-CD20 therapy-induced AT.

摘要

简介

由于肿瘤治疗和/或潜在的血液系统疾病,继发性低丙种球蛋白血症(sHGG)的发展具有重要的临床意义。B 细胞来源的恶性肿瘤和抗 CD20 单克隆抗体(mAbs)是 sHGG 发展的重要危险因素。此外,抗 CD20 治疗引起的急性血小板减少症(AT)是一种已知的、尽管罕见的现象。

病例介绍

一名 54 岁的患者在经历了经典滤泡淋巴瘤的首次复发后,开始接受 R-DHAP 方案的挽救治疗。利妥昔单抗输注后,血小板计数在 24 小时内从 116×109/L 降至 13×109/L。免疫球蛋白 G 水平降低表明存在中度 HGG,因此我们立即给予静脉注射免疫球蛋白(IVIg)。在开始 IVIg 治疗后的 5 天内,血小板计数增加并稳定在>50×109/L。

结论

抗 CD20 mAbs 似乎可以像免疫性血小板减少症(ITP)中的自身抗体一样或通过类似的机制发挥作用。假设抗 CD20 治疗引起的 AT 是一种 ITP 样情况,则 HGG 可被视为潜在的危险因素。因此,在接受抗 CD20 mAb 治疗之前,用 IVIg 适当治疗 HGG 可能有助于缓解抗 CD20 治疗引起的 AT。

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