Department of Neurology, St. Josef-Hospital, Ruhr University Bochum, Bochum, Germany.
J Neurol Neurosurg Psychiatry. 2013 Oct;84(10):1068-74. doi: 10.1136/jnnp-2013-304897. Epub 2013 Apr 19.
Although the prognosis of natalizumab-associated progressive multifocal leukoencephalopathy (PML) seems to be better than HIV-associated PML, little is known about the long-term functional outcome in multiple sclerosis (MS) patients and the subsequent return of MS disease activity. We evaluated retrospectively 15 patients with natalizumab-associated PML treated at our centre.
Fifteen MS-PML patients (nine women, six men) were referred to us from adjacent local centres. The patients had a median natalizumab exposure of 34 months at PML diagnosis. They received standardised treatment as described in previous work. Expanded Disability Status Scale (EDSS) and Karnofsky score in the year pre-PML, at PML-diagnosis (pre-immune reconstitution inflammatory syndrome (IRIS)) and post-PML were determined in 3-6 monthly intervals.
The median follow-up of these 15 patients was 21.5 months. None of the 15 patients died. Three patients had a Karnofsky score of 80 or higher, nine patients between 50-70 and three patients of 40 or lower at latest examination. Eight of the 15 patients developed seizures during acute PML phase. Fifty percent of those patients were not seizure-free one year post PML, despite continuation of antiepileptic treatment. The median EDSS in the year pre-PML was 2.5, 4.5 at PML diagnosis, 6.5 post-IRIS and 5.5 at latest examination. CSF became virus-free in eight of the 15 patients after a median time of 4.5 months. In nine patients, disease reappeared after a median time of seven months from PML diagnosis.
Although the clinical outcome of natalizumab-treated PML patients is much better than in patients with HIV-associated PML, this may be further improved by treatment at reference centres using standardised therapy regimens and transient intensive care if needed. Systematic studies of appropriate MS immunotherapies after PML are critically needed.
尽管纳武单抗相关性进行性多灶性白质脑病(PML)的预后似乎优于 HIV 相关性 PML,但我们对多发性硬化症(MS)患者的长期功能结局以及随后 MS 疾病活动的恢复知之甚少。我们回顾性评估了在我们中心治疗的 15 例纳武单抗相关性 PML 患者。
15 例 MS-PML 患者(9 名女性,6 名男性)从邻近的当地中心转诊至我们中心。这些患者在 PML 诊断时的中位纳武单抗暴露时间为 34 个月。他们接受了之前研究中描述的标准化治疗。在 PML 诊断前(免疫重建炎症综合征 [IRIS] 前)、PML 诊断时以及 PML 后,使用扩展残疾状态量表(EDSS)和卡诺夫斯基评分评估 15 例患者。
这些 15 例患者的中位随访时间为 21.5 个月。这 15 例患者中均无死亡病例。在最新的检查中,3 例患者的卡诺夫斯基评分≥80 分,9 例患者的评分在 50-70 分之间,3 例患者的评分在 40 分或以下。在急性 PML 期间,有 8 例患者发生癫痫发作。尽管继续抗癫痫治疗,但 PML 后一年仍有 50%的患者癫痫发作未得到控制。在 PML 诊断前的一年,EDSS 的中位数为 2.5,在 PML 诊断时为 4.5,在 IRIS 后为 6.5,在最新的检查时为 5.5。在 15 例患者中,8 例患者在中位时间为 4.5 个月后 CSF 病毒载量转为阴性。在 PML 诊断后,有 9 例患者的疾病在中位时间为 7 个月后再次出现。
尽管纳武单抗治疗的 PML 患者的临床结局明显优于 HIV 相关性 PML 患者,但在参考中心使用标准化治疗方案并在需要时进行短暂强化治疗可能会进一步改善这一结果。迫切需要进行 PML 后适当的 MS 免疫治疗的系统研究。