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自体造血干细胞移植与阿仑单抗治疗复发缓解型多发性硬化症的比较:一项观察性研究。

Autologous haematopoietic stem cell transplantation compared with alemtuzumab for relapsing-remitting multiple sclerosis: an observational study.

机构信息

Department of Neuroscience, Uppsala University, Uppsala, Sweden.

Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, Gothenburg, Sweden.

出版信息

J Neurol Neurosurg Psychiatry. 2021 Feb;92(2):189-194. doi: 10.1136/jnnp-2020-323992. Epub 2020 Oct 26.

Abstract

OBJECTIVE

To compare outcomes after treatment with autologous haematopoietic stem cell transplantation (AHSCT) and alemtuzumab (ALZ) in patients with relapsing-remitting multiple sclerosis.

METHODS

Patients treated with AHSCT (n=69) received a conditioning regimen of cyclophosphamide (200 mg/kg) and rabbit anti-thymocyte globulinerG (6.0 mg/kg). Patients treated with ALZ (n=75) received a dose of 60 mg over 5 days, a repeated dose of 36 mg over 3 days after 1 year and then as needed. Follow-up visits with assessment of the expanded disability status scale score, adverse events and MR investigations were made at least yearly.

RESULTS

The Kaplan-Meier estimates of the primary outcome measure 'no evidence of disease activity' was 88% for AHSCT and 37% for ALZ at 3 years, p<0.0001. The secondary endpoint of annualised relapse rate was 0.04 for AHSCT and 0.1 for ALZ, p=0.03. At last follow-up, the proportions of patients who improved, were stable or worsened were 57%/41%/1% (AHSCT) and 45%/43%/12% (ALZ), p=0.06 Adverse events grade three or higher were present in 48/69 patients treated with AHSCT and 0/75 treated with ALZ in the first 100 days after treatment initiation. The most common long-term adverse event was thyroid disease with Kaplan-Meier estimates at 3 years of 21% for AHSCT and 46% for ALZ, p=0.005.

CONCLUSIONS

In this observational cohort study, treatment with AHSCT was associated with a higher likelihood of maintaining 'no evidence of disease activity'. Adverse events were more frequent with AHSCT in the first 100 days, but thereafter more common in patients treated with ALZ.

摘要

目的

比较自体造血干细胞移植(AHSCT)和阿仑单抗(ALZ)治疗复发性多发性硬化症患者的疗效。

方法

接受 AHSCT 治疗的患者(n=69)接受环磷酰胺(200mg/kg)和兔抗胸腺细胞球蛋白 G(6.0mg/kg)的预处理方案。接受 ALZ 治疗的患者(n=75)接受 60mg 剂量 5 天,1 年后 3 天重复 36mg 剂量,然后按需使用。至少每年进行一次随访,评估扩展残疾状况量表评分、不良事件和磁共振成像检查结果。

结果

Kaplan-Meier 估计 AHSCT 组的主要疗效终点“无疾病活动证据”为 88%,ALZ 组为 37%,3 年时差异有统计学意义(p<0.0001)。AHSCT 组的年复发率为 0.04,ALZ 组为 0.1,差异有统计学意义(p=0.03)。末次随访时,改善、稳定和恶化的患者比例分别为 57%/41%/1%(AHSCT)和 45%/43%/12%(ALZ),差异无统计学意义(p=0.06)。在治疗开始后的 100 天内,AHSCT 组有 48/69 例患者出现 3 级或以上不良事件,ALZ 组为 0/75 例。最常见的长期不良事件是甲状腺疾病,3 年时 AHSCT 组和 ALZ 组的 Kaplan-Meier 估计值分别为 21%和 46%,差异有统计学意义(p=0.005)。

结论

在这项观察性队列研究中,AHSCT 治疗与维持“无疾病活动证据”的可能性更高相关。在治疗开始后的 100 天内,AHSCT 组的不良事件更为常见,但此后,ALZ 组更为常见。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b34/7841472/206b34b72e46/jnnp-2020-323992f01.jpg

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