Pein Romy, Steinberg Amir
Hematology and Oncology, New York Medical College, Valhalla, USA.
Hematology and Oncology, Westchester Medical Center, Valhalla, USA.
Cureus. 2025 Apr 9;17(4):e81946. doi: 10.7759/cureus.81946. eCollection 2025 Apr.
The objective of this paper is to report a case of anti-myelin-associated glycoprotein (anti-MAG) antibody neuropathy treated with zanubrutinib, offering insight into a potential therapeutic avenue for this challenging neurological disorder. A 65-year-old male initially presented with peripheral neuropathy in the lower distal extremities. Hematologic evaluation revealed an elevated M-spike of IgM and a high MAG antibody titer. His initial titer was measured at 1:102400 on February 28, 2023. These findings were consistent with the diagnosis of Waldenström macroglobulinemia (WM) with associated anti-MAG antibody neuropathy. The patient was started on rituximab and reported a slight improvement in symptoms. However, the patient felt the efficacy of rituximab diminished with each subsequent dose. Due to this, the patient was initiated on zanubrutinib. Close monitoring of clinical symptoms and laboratory parameters was conducted to assess treatment response and potential side effects. Following zanubrutinib therapy, the patient exhibited mild improvement in neuropathic symptoms, which have stabilized, although still present. Serologic examination demonstrated a decrease in anti-MAG-antibody titer at 1:25600 in the spring of 2023 and 1:51200 in November of 2023. Patient reports increased fatigue and musculoskeletal pain. This clinical vignette highlights the outcomes of zanubrutinib in the management of anti-MAG antibody neuropathy in a patient with WM. Further research and larger clinical trials are warranted to validate these findings and establish zanubrutinib as a viable therapeutic option for this rare and often challenging neurological disorder.
本文的目的是报告1例接受泽布替尼治疗的抗髓鞘相关糖蛋白(anti-MAG)抗体神经病病例,为这种具有挑战性的神经系统疾病提供一种潜在的治疗途径。一名65岁男性最初表现为下肢远端周围神经病变。血液学评估显示IgM的M峰升高和MAG抗体滴度高。其初始滴度于2023年2月28日测得为1:102400。这些发现与伴有抗MAG抗体神经病的华氏巨球蛋白血症(WM)诊断一致。患者开始使用利妥昔单抗治疗,症状略有改善。然而,患者感觉利妥昔单抗的疗效在后续每次给药时都会降低。因此,患者开始使用泽布替尼。密切监测临床症状和实验室参数以评估治疗反应和潜在副作用。接受泽布替尼治疗后,患者的神经病变症状有轻度改善,症状已稳定,尽管仍然存在。血清学检查显示抗MAG抗体滴度在2023年春季降至1:25600,在2023年11月降至1:51200。患者报告疲劳和肌肉骨骼疼痛加重。这个临床病例突出了泽布替尼在治疗WM患者抗MAG抗体神经病方面的疗效。需要进一步的研究和更大规模的临床试验来验证这些发现,并确立泽布替尼作为这种罕见且通常具有挑战性的神经系统疾病的一种可行治疗选择。