Can autologous stem cell transplantation be a treatment option in a patient diagnosed with secondary progressive multiple sclerosis?:Case report

Kemal Fıdan, Gülşah Akyol, Ali Ünal
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Abstract

Case report: İntroduction

Multiple sclerosis (MS) manifests itself with plaque formation as a result of defensive T and B cells in the immune system perceiving the myelin sheath around nerve cells as a foreign substance to the body and trying to destroy it, for an unknown reason.In short, it is an autoimmune inflammatory demyelinating disease of the central nervous system.

In multiple sclerosis, various interventions such as medication, physical therapy, and stem cell therapy are used to improve patients' quality of life. The goal of autologous hematopoietic stem cell transplantation (AHSCT) is to eliminate and replace the patient's pathogenic immune system to achieve long-term remission of MS.

Here, we will present our experience with autologous stem cell transplantation performed in our center for an MS case that had previously received both medical and physical therapy and failed to respond.

Key words: multiple sclerosis, autologous stem cell transplantation

Case report

The 41-year-old male patient was diagnosed with MS in 2012 and has been wheelchair-bound for about 3 years. Glatiramer acetate was started at the time of diagnosis. As the patient's complaints increased, fampridine and ocrelizumab treatments were given, respectively. The patient, who did not respond to treatment, was evaluated as having secondary progressive MS and an autologous stem cell transplant was planned. Mobilization was performed with cyclophosphamide + G-CSF in July 2023. In September 2023, AHSCT was performed with cyclophosphamide (40 mg/kg, 2400 mg in total, 5 days), Mesna (40 mg/kg/day, 2400 mg in total, 5 days) and ATG (360 mg in total) protocol. The patient, who had platelet engraftment on day +9 and neutrophil engraftment on day +11 after AHSCT, was discharged with outpatient clinic control.

Discussion and conclusion

Despite many advances in MS treatment, there is still no definitive treatment answer. Autologous hematopoietic stem cell transplantation may be promising, as observed in several studies. The aim of AHSCT is to eliminate and replace the patient's pathogenic immune system to ensure long-term remission of MS (1).

In the MIST study; One group of patients with relapse-refractory MS (RRMS) underwent myeloablative AHSCT with cyclophosphamide (200 mg/kg) and antithymocyte globulin (ATG), and the other group was given disease-modifying therapy. During an average follow-up of 2 years, disease progression was 5% in the AHSCT group and 62% in the other group. In addition, those who underwent AHSCT had fewer relapses, and the rate of lesion healing on MRI was observed to be higher in the AHSCT group (2). In the HALT-MS study, event-free survival and improvement in neurological functions were observed at higher rates in patients who underwent AHSCT after high-dose immunotherapy (3-4). In a study conducted in Sweden, no recurrence or progression was observed in the first 3 years of treatment after AHSCT, and it was also stated that no new lesions developed on MRI (5).

Although studies show the potential benefits of AHSCT, more long-term data from randomized controlled trials are needed to evaluate the effectiveness and safety of this intervention in the treatment of RRMS.

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自体干细胞移植能否成为继发性进展型多发性硬化症患者的治疗选择?
病例报告:多发性硬化症(MS)表现为斑块形成,这是由于免疫系统中的防御性T细胞和B细胞将神经细胞周围的髓鞘视为人体的异物,并试图破坏它,原因不明。简而言之,这是一种中枢神经系统自身免疫性炎症性脱髓鞘疾病。自体造血干细胞移植(AHSCT)的目标是消除和替代患者的致病免疫系统,以实现多发性硬化症的长期缓解。在此,我们将介绍本中心为一名既往接受过药物和物理治疗但无效的多发性硬化症病例实施自体干细胞移植的经验。确诊时开始使用醋酸格拉替雷。随着患者主诉的增加,患者分别接受了芬必得和奥克立珠单抗治疗。患者对治疗无反应,被评估为继发性进展型多发性硬化症,并计划进行自体干细胞移植。2023年7月,患者接受了环磷酰胺+G-CSF治疗。2023年9月,采用环磷酰胺(40毫克/公斤,共2400毫克,5天)、Mesna(40毫克/公斤/天,共2400毫克,5天)和ATG(共360毫克)方案进行了自体干细胞移植。该患者在 AHSCT 后第 +9 天出现血小板移植,第 +11 天出现中性粒细胞移植,经门诊控制后出院。自体造血干细胞移植可能很有希望,这一点已在多项研究中观察到。在MIST研究中,一组复发难治多发性硬化症(RRMS)患者接受了环磷酰胺(200毫克/千克)和抗胸腺细胞球蛋白(ATG)的髓鞘脱落AHSCT,另一组接受了疾病修饰治疗。在平均 2 年的随访期间,AHSCT 组的疾病进展率为 5%,另一组为 62%。此外,接受 AHSCT 治疗的患者复发率较低,而且据观察,AHSCT 组的磁共振成像病灶愈合率较高(2)。在 HALT-MS 研究中,高剂量免疫疗法后接受 AHSCT 治疗的患者的无事件生存率和神经功能改善率更高(3-4)。在瑞典进行的一项研究中,AHSCT 治疗后的前 3 年未发现复发或进展,MRI 上也未发现新的病灶(5)。尽管研究显示了 AHSCT 的潜在益处,但仍需要更多来自随机对照试验的长期数据来评估这种干预措施在 RRMS 治疗中的有效性和安全性。
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来源期刊
CiteScore
2.40
自引率
4.80%
发文量
1419
审稿时长
30 weeks
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