Sudden unexpected death after initial infusion of rituximab for Waldenström macroglobulinemia/lymphoplasmacytic lymphoma: an autopsy case.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-06-28 DOI:10.1186/s13000-024-01519-9
Shojiro Ichimata, Yukiko Hata, Kazuhiro Nomoto, Tsutomu Sato, Naoki Nishida
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Abstract

Background: Waldenström's macroglobulinemia (WM) is defined as a lymphoplasmacytic lymphoma (LPL) involving the bone marrow (BM) with presence of IgM monoclonal protein, and comprises > 95% of all LPL cases. Rituximab-based regimens have been predominant in the management of WM. Infusion-related reactions (IRRs) are a primary concern with rituximab, although it is generally better tolerated with less toxicity than conventional anticancer agents. Here, we present an autopsy case of an elderly man who died suddenly after receiving the initial infusion of rituximab for WM/LPL.

Case presentation: An 84-year-old man was found dead in his bedroom. He had undergone the initial intravenous rituximab infusion for progressive anemia related to Waldenström's macroglobulinemia/lymphoplasmacytic lymphoma (WM/LPL) approximately 15 h before death. Although the protocol for rituximab administration and additional medication was considered appropriate, he exhibited several symptoms consistent with infusion-related reactions (IRRs) during the infusion. Autopsy revealed monotonous proliferation of small-to-medium-sized lymphocytic cells in the bone marrow, consistent with the premortem diagnosis of WM/LPL. Additionally, immunoglobulin λ-light chain-derived amyloid (ALλ) deposition was identified in all organs other than the brain. Although ALλ deposition and LPL infiltration were found in the heart, they were not severe enough to cause severe functional impairment. Severe congestion and/or edema were observed in the lungs, liver, and brain. Although significant inflammatory cell infiltration was not found in any organs, laboratory tests revealed elevated serum levels of inflammatory cytokines, including interleukin-1β, interleukin-6, tumor necrosis factor-α and the presence of IgM-λ monoclonal protein.

Conclusion: Acute IRRs associated with the initial rituximab infusion were the major contributing factor to his sudden unexpected death. The autopsy findings of present case suggest the necessity for thorough monitoring of older patients with WM/LPL undergoing rituximab treatment, particularly when pronounced IRRs occur during the first administration, in addition to investigating complications of WM/LPL before infusion.

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瓦尔登斯特伦巨球蛋白血症/淋巴细胞性淋巴瘤首次输注利妥昔单抗后意外猝死:一例尸检病例。
背景:瓦尔登斯特伦巨球蛋白血症(WM)被定义为累及骨髓(BM)并存在IgM单克隆蛋白的淋巴浆细胞性淋巴瘤(LPL),占所有LPL病例的95%以上。利妥昔单抗是治疗 WM 的主要方案。输注相关反应(IRRs)是利妥昔单抗的主要问题,尽管与传统抗癌药物相比,利妥昔单抗的耐受性更好,毒性更小。在此,我们介绍了一例尸检病例,该病例是一名老人在接受了治疗 WM/LPL 的首次利妥昔单抗输注后突然死亡:一名 84 岁的老人被发现死于自己的卧室。死亡前约15小时,他因患与瓦登斯特伦巨球蛋白血症/淋巴细胞性淋巴瘤(WM/LPL)相关的进行性贫血而接受了首次静脉注射利妥昔单抗治疗。虽然利妥昔单抗给药和额外用药的方案被认为是适当的,但他在输液过程中出现了一些与输液相关反应(IRR)一致的症状。尸检显示,骨髓中单个的中小型淋巴细胞增生,与尸检前诊断的WM/LPL一致。此外,免疫球蛋白λ轻链衍生的淀粉样蛋白(ALλ)沉积在除大脑以外的所有器官中。虽然在心脏中发现了 ALλ 沉积和 LPL 浸润,但其严重程度不足以导致严重的功能损害。肺部、肝脏和大脑出现严重充血和/或水肿。虽然没有在任何器官中发现明显的炎症细胞浸润,但实验室检查发现血清中炎症细胞因子水平升高,包括白细胞介素-1β、白细胞介素-6、肿瘤坏死因子-α,以及 IgM-λ 单克隆蛋白:结论:与首次利妥昔单抗输注相关的急性IRR是导致患者意外猝死的主要原因。本病例的尸检结果表明,有必要对接受利妥昔单抗治疗的老年 WM/LPL 患者进行全面监测,尤其是在首次给药时出现明显的 IRR 时,此外还需在输注前对 WM/LPL 的并发症进行调查。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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