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关节内注射自体脂肪来源间充质干细胞治疗膝骨关节炎的临床疗效和安全性:一项 III 期、随机、双盲、安慰剂对照试验。

Clinical Efficacy and Safety of the Intra-articular Injection of Autologous Adipose-Derived Mesenchymal Stem Cells for Knee Osteoarthritis: A Phase III, Randomized, Double-Blind, Placebo-Controlled Trial.

机构信息

Department of Orthopaedic Surgery, Center for Joint Diseases, Kyung Hee University Hospital at Gangdong, Seoul, Korea; Department of Orthopaedic Surgery, School of Medicine, Kyung Hee University, Seoul, Korea.

Investigation performed at Kyung Hee University Hospital at Gangdong, Seoul, Korea.

出版信息

Am J Sports Med. 2023 Jul;51(9):2243-2253. doi: 10.1177/03635465231179223. Epub 2023 Jun 21.

Abstract

BACKGROUND

Intra-articular injection of autologous culture-expanded adipose-derived mesenchymal stem cells (ADMSCs) has introduced a promising treatment option for knee osteoarthritis. Although the clinical efficacy and safety of ADMSCs have been reported, the treatment remains controversial owing to the small sample sizes and heterogeneous osteoarthritis grades in previous studies.

PURPOSE

To assess the efficacy and safety of intra-articular injection of ADMSCs as compared with placebo in alleviating pain and improving functional capacity in a large sample of patients with knee osteoarthritis of Kellgren-Lawrence (K-L) grade 3.

STUDY DESIGN

Randomized controlled trial; Level of evidence, 1.

METHODS

This phase III multicenter clinical trial was a double-blind randomized controlled study that included 261 patients with K-L grade 3 symptomatic knee osteoarthritis who were administered a single injection of autologous culture-expanded ADMSCs or placebo. Clinical data were assessed at baseline and at 3 and 6 months after the injection. The primary endpoints were improvements in 100-mm visual analog scale (VAS) for pain and Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) for function at 6 months after the injection. The secondary endpoints included clinical and radiologic examinations and safety after injection. The changes in cartilage defects after injection were assessed by magnetic resonance imaging at 6 months.

RESULTS

The ADMSC and control groups included 125 and 127 patients available for follow-up, respectively. At 6 months, the ADMSC group showed significantly better improvements in 100-mm VAS (ADMSC vs control, 25.2 vs 15.5; = .004) and total WOMAC score (21.7 vs 14.3; = .002) as compared with the control group. The linear mixed model analysis indicated significantly better improvements in all clinical outcomes in the ADMSC group after 6 months. At 6 months, the ADMSC group achieved significantly higher proportions of patients above the minimal clinically important difference in 100-mm VAS and WOMAC score. Radiologic outcomes and adverse events did not demonstrate significant differences between the groups. No serious treatment-related adverse events were observed. Magnetic resonance imaging revealed no significant difference in change of cartilage defects between the groups at 6 months.

CONCLUSION

Intra-articular injection of autologous culture-expanded ADMSCs provided significant pain relief and functional improvements in patients with K-L grade 3 osteoarthritis. Long-term results are needed to determine the disease-modifying effects of ADMSCs, such as structural changes, and the duration of effect of intra-articular injection of ADMSCs in knee osteoarthritis.

REGISTRATION

NCT03990805 (ClinicalTrials.gov identifier).

摘要

背景

关节内注射自体培养扩增的脂肪间充质干细胞(ADMSCs)为膝骨关节炎提供了一种有前景的治疗选择。尽管 ADMSCs 的临床疗效和安全性已被报道,但由于先前研究的样本量小和骨关节炎分级不均,该治疗仍存在争议。

目的

在大样本膝骨关节炎 K-L 分级 3 级患者中,评估关节内注射 ADMSCs 与安慰剂相比在缓解疼痛和改善功能能力方面的疗效和安全性。

研究设计

随机对照试验;证据水平,1 级。

方法

这是一项 III 期多中心临床试验,是一项双盲随机对照研究,纳入 261 例 K-L 分级 3 级有症状的膝骨关节炎患者,给予单次关节内注射自体培养扩增的 ADMSCs 或安慰剂。在注射后 3 个月和 6 个月评估临床数据。主要终点是注射后 6 个月时 100-mm 视觉模拟量表(VAS)疼痛评分和西部安大略省和麦克马斯特大学骨关节炎指数(WOMAC)功能评分的改善。次要终点包括注射后的临床和放射学检查以及安全性。注射后 6 个月时通过磁共振成像评估软骨缺损的变化。

结果

ADMSC 组和对照组分别有 125 例和 127 例患者可进行随访。6 个月时,ADMSC 组在 100-mm VAS(ADMSC 组 vs 对照组,25.2 vs 15.5; =.004)和总 WOMAC 评分(21.7 vs 14.3; =.002)方面的改善明显优于对照组。线性混合模型分析表明,6 个月后 ADMSC 组的所有临床结局均有明显改善。6 个月时,ADMSC 组在 100-mm VAS 和 WOMAC 评分方面达到最小临床重要差异以上的患者比例明显更高。两组的放射学结果和不良事件无显著差异。未观察到与治疗相关的严重不良事件。磁共振成像显示,6 个月时两组之间的软骨缺损变化无显著差异。

结论

关节内注射自体培养扩增的 ADMSCs 可显著缓解 K-L 分级 3 级骨关节炎患者的疼痛并改善其功能。需要长期结果来确定 ADMSCs 的疾病修饰作用,例如结构变化,以及 ADMSCs 关节内注射对膝骨关节炎的疗效持续时间。

登记

NCT03990805(ClinicalTrials.gov 标识符)。

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