Obradović Dragana, Tukić Ljiljana, Radovinović-Tasić Sanja, Petrović Boris, Elez Marija, Ostojić Gordana, Balint Bela
Vojnosanit Pregl. 2016 May;73(5):504-8. doi: 10.2298/vsp150304045o.
Multiple sclerosis (MS) is an immune-mediated disease of the central nervous system that affects young individuals and leads to severe disability. High dose immunoablation followed by autologous hemopoietic stem cell transplantation (AHSCT) has been considered in the last 15 years as potentialy effective therapeutic approach for aggressive MS. The most recent long-time follow-up results suggest that AHSCT is not only effective for highly-aggressive MS, but for relapsing-remitting MS as well, providing long-term remission, or maybe even cure. We presented a 10-year follow-up of the first MS patient being treated by immunoablation therapy and AHSCT.
A 27-year-old male experienced the first symptoms--intermitent numbness and paresthesia of arms and legs of what was treated for two years by psychiatrist as anxiety disorder. After he developed severe paraparesis he was admitted to the Neurology Clinic and diagnosed with MS. Our patient developed aggressive MS with frequent relapses, rapid disability progression and transition to secondary progressive form 6 years after MS onset[the Expanded Disability Status Scale (EDSS) 7.0 Ambulation Index (AI) 7]. AHSCT was performed, cyclophosphamide was used for hemopoietic stem cell mobilization and the BEAM protocol was used as conditionig regimen. No major adverse events followed the AHSCT. Neurological impairment improved, EDSS 6.5, AI 6 and during a 10-year follow-up remained unchanged. Brain MRI follow-up showed the absence of gadolinium enhancing lesions and a mild progression of brain atrophy.
The patient with rapidly evolving, aggressive, noninflammatory MS initialy improved and remained stable, without disability progression for 10 years, after AHSCT. This kind of treatment should be considered in aggressive MS, or in disease modifying treatment nonresponsive MS patients, since appropriately timed AHSCT treatment may not only prevent disability progression but reduce the achieved level of disability, as well.
多发性硬化症(MS)是一种中枢神经系统的免疫介导疾病,影响年轻人并导致严重残疾。在过去15年中,高剂量免疫消融后进行自体造血干细胞移植(AHSCT)被认为是治疗侵袭性MS的一种潜在有效治疗方法。最新的长期随访结果表明,AHSCT不仅对高度侵袭性MS有效,对复发缓解型MS也有效,可实现长期缓解,甚至可能治愈。我们报告了首例接受免疫消融治疗和AHSCT的MS患者的10年随访情况。
一名27岁男性出现了最初症状——手臂和腿部间歇性麻木和感觉异常,精神科医生将其作为焦虑症治疗了两年。在他出现严重截瘫后,被收治入神经科诊所并被诊断为MS。我们的患者在MS发病6年后发展为侵袭性MS,频繁复发,残疾进展迅速并转变为继发进展型[扩展残疾状态量表(EDSS)7.0,步行指数(AI)7]。进行了AHSCT,使用环磷酰胺进行造血干细胞动员,并采用BEAM方案作为预处理方案。AHSCT后未出现重大不良事件。神经功能障碍有所改善,EDSS为6.5,AI为6,在10年随访期间保持不变。脑部MRI随访显示无钆增强病灶,脑萎缩有轻度进展。
该快速进展、侵袭性、非炎性MS患者在AHSCT后最初有所改善并保持稳定,10年无残疾进展。对于侵袭性MS或对疾病修饰治疗无反应的MS患者,应考虑这种治疗方法,因为适时的AHSCT治疗不仅可以防止残疾进展,还可以降低已达到的残疾水平。