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自体造血干细胞移植治疗多发性硬化症的疗效和安全性:系统评价和荟萃分析。

Efficacy and safety of autologous hematopoietic stem-cell transplantation in multiple sclerosis: a systematic review and meta-analysis.

机构信息

Department of Neurology, Tangdu Hospital, the Fourth Military Medical University, Xi'an, Shaanxi Province, People's Republic of China.

出版信息

Neurol Sci. 2019 Mar;40(3):479-487. doi: 10.1007/s10072-018-3670-1. Epub 2018 Dec 10.

Abstract

BACKGROUND

Autologous hematopoietic stem-cell transplantation (AHSCT) has been utilized as a treatment option for multiple sclerosis (MS) since 1995. However, this procedure has not been widely implemented in clinical practice owing to its mortality risk. Here, we conduct a meta-analysis to evaluate the long-term efficacy and safety of AHSCT in MS treatment, aiming to optimize the benefit/risk ratio of this therapeutic strategy.

METHODS

We searched the PubMed Web site and clinicaltrials.gov databases. The efficacy endpoints were progression-free survival (PFS) and disease activity-free survival. The safety outcomes were transplant-related mortality (TRM) and overall deaths.

RESULTS

Eighteen eligible studies with a total of 732 participants were enrolled. The PFS was 75% (95% CI, 0.69-0.81), and the estimate of disease activity-free survival was 61% with 48-month follow-up. Subgroups analysis showed that low- and intermediate-intensity regimens were associated with higher PFS 80%. Relapsing remitting MS (RRMS) benefited more from AHSCT than other MS subtypes with PFS 85%. Patients with Gd+ lesions at baseline MRI responded better to AHSCT with PFS 77%. The estimate of TRM was 1.34% (95% CI, 0.39-2.30), and the overall mortality was 3.58%. TRM was significantly higher in high-intensity regimen studies (3.13%) and in older studies (1.93%) performed before 2006.

CONCLUSIONS

This meta-analysis provides evidences that AHSCT can induce long-term remissions for MS patients with a high degree of safety. We indicate low- and intermediate-intensity regimens and RRMS patients with the presence of Gd+ lesions at baseline MRI can obtain the optimal benefit/risk ratio from AHSCT.

摘要

背景

自 1995 年以来,自体造血干细胞移植(AHSCT)已被用作治疗多发性硬化症(MS)的一种选择。然而,由于其死亡率,该方法并未在临床实践中广泛实施。在这里,我们进行了一项荟萃分析,以评估 AHSCT 在 MS 治疗中的长期疗效和安全性,旨在优化该治疗策略的获益/风险比。

方法

我们搜索了 PubMed 网站和 clinicaltrials.gov 数据库。疗效终点是无进展生存期(PFS)和疾病活动无进展生存期。安全性结果是与移植相关的死亡率(TRM)和总死亡率。

结果

纳入了 18 项符合条件的研究,共 732 名参与者。PFS 为 75%(95%CI,0.69-0.81),在 48 个月的随访中,疾病活动无进展生存率的估计值为 61%。亚组分析表明,低强度和中强度方案与较高的 PFS(80%)相关。与其他 MS 亚型相比,缓解复发型 MS(RRMS)从 AHSCT 中获益更多,PFS 为 85%。基线 MRI 上有 Gd+病变的患者对 AHSCT 的反应更好,PFS 为 77%。TRM 的估计值为 1.34%(95%CI,0.39-2.30),总死亡率为 3.58%。高强度方案研究(3.13%)和 2006 年之前进行的较老研究(1.93%)中的 TRM 明显更高。

结论

这项荟萃分析提供了证据,表明 AHSCT 可以诱导 MS 患者长期缓解,且具有高度安全性。我们表明,低强度和中强度方案以及基线 MRI 上有 Gd+病变的 RRMS 患者可以从 AHSCT 中获得最佳的获益/风险比。

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