Division of Hematology and Oncology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Division of Infectious Diseases, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Oncology. 2018;95(5):319-322. doi: 10.1159/000490617. Epub 2018 Jul 25.
Progressive multifocal leukoencephalopathy (PML) is a fatal demyelinating disease associated with immunocompromised states. We describe a case of PML, which developed after prolonged ibrutinib use and a low burden of chronic lymphocytic leukemia disease. The delay in diagnosis of the patient despite multiple presentations to medical providers across different facilities suggests that there is a lack of awareness of PML as a potential complication of ibrutinib. Treatments with postulated anti-John Cunningham polyomavirus agents and IL-2 were ineffective, likely due to the advanced state of the patient's disease. Although recent evidence indicates that ibrutinib may enhance cell-mediated immunity, consistent with elevated CD4+ and CD8+ T cells and appropriate T-cell response to mitogens in the patient, ibrutinib-mediated inhibition of the humoral function may contribute to PML pathogenesis. As the duration of ibrutinib use is often indefinite, and the number of indications for ibrutinib continues to grow, recognition and further evaluation of the link between PML and ibrutinib is warranted.
进行性多灶性白质脑病(PML)是一种与免疫功能低下状态相关的致命脱髓鞘疾病。我们描述了一例 PML 病例,该病例发生在长期使用伊布替尼和慢性淋巴细胞白血病疾病负担较低之后。尽管该患者在不同医疗机构多次就诊,但仍未能及时诊断,这表明人们对 PML 作为伊布替尼潜在并发症的认识不足。针对 JC 多瘤病毒的假定治疗药物和白细胞介素 2 的治疗均无效,可能是由于患者疾病已处于晚期。尽管最近的证据表明伊布替尼可能增强细胞介导的免疫,与患者 CD4+和 CD8+T 细胞升高以及对有丝分裂原的适当 T 细胞反应一致,但伊布替尼介导的体液功能抑制可能有助于 PML 的发病机制。由于伊布替尼的使用时间通常不确定,而且伊布替尼的适应证数量不断增加,因此有必要进一步认识和评估 PML 与伊布替尼之间的联系。