Progressive multifocal leukoencephalitis (PML) in three patients treated with standard-dose fludarabine (FAMP).

H Gonzalez, F Bolgert, P Camporo, V Leblond
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引用次数: 58

Abstract

Since 1990 we have treated 60 patients with standard-dose fludarabine for chronic lymphocytic leukemia (B-CLL), on a compassionate basis. Three patients developed grade IV neurologic complications after treatment, with demyelination of white matter on magnetic resonance imaging (MRI) in patient # 1, diffuse demyelination, abnormal oligodendroglia and enlarged astrocytes at brain biopsy in patient no 2, and progressive multifocal leukoencephalitis (PML) with JC virus on brain biopsy in patient # 3. The neurotoxicity of fludarabine was often observed after administration of high doses (90-120 mg/m2). At standard doses (18-25 mg/m2) neurologic complications were observed in very few cases (0.2%). PML was observed in only 0.52% of patients with chronic lymphocytic leukemia (CLL), particularly those with advanced CLL. Our findings are consistent with the results of published studies and show an increase in neurologic complications in patients with advanced CLL treated with fludarabine. This increased vulnerability is probably multifactorial, but may be secondary to the immunodeficiency.

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标准剂量氟达拉滨(FAMP)治疗3例进行性多灶性脑白质炎(PML)
自1990年以来,我们在同情的基础上用标准剂量氟达拉滨治疗了60名慢性淋巴细胞白血病(B-CLL)患者。3例患者治疗后出现IV级神经系统并发症,患者1号磁共振成像(MRI)显示白质脱髓鞘,患者2号脑活检显示弥漫性脱髓鞘、少突胶质细胞异常和星形胶质细胞增大,患者3号脑活检显示进展性多灶性脑白质炎(PML)伴JC病毒。高剂量(90 ~ 120mg /m2)给药后常观察到氟达拉滨的神经毒性。在标准剂量(18- 25mg /m2)下,很少有病例(0.2%)出现神经系统并发症。慢性淋巴细胞白血病(CLL)患者中PML的发生率仅为0.52%,尤其是晚期CLL患者。我们的发现与已发表的研究结果一致,表明氟达拉滨治疗晚期CLL患者的神经系统并发症增加。这种增加的脆弱性可能是多因素的,但可能是继发于免疫缺陷。
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