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Stempeucel 治疗膝关节骨关节炎的疗效和安全性:一项 3 期随机、双盲、多中心、安慰剂对照研究。

Efficacy and Safety of Stempeucel in Osteoarthritis of the Knee: A Phase 3 Randomized, Double-Blind, Multicenter, Placebo-Controlled Study.

机构信息

Stempeutics Research, Bangalore, India.

Investigation performed at Post Graduate Institute of Medical Education & Research, Chandigarh and St. John's Medical College Hospital, Bengaluru, India.

出版信息

Am J Sports Med. 2023 Jul;51(9):2254-2266. doi: 10.1177/03635465231180323. Epub 2023 Jun 27.

Abstract

BACKGROUND

Osteoarthritis is a chronic, progressive, and degenerative condition with limited therapy options. Recently, biologic therapies have been an evolving option for the management of osteoarthritis.

PURPOSE

To assess whether allogenic mesenchymal stromal cells (MSCs) have the potential to improve functional parameters and induce cartilage regeneration in patients with osteoarthritis.

STUDY DESIGN

Randomized controlled trial; Level of evidence, 1.

METHODS

A total of 146 patients with grade 2 and 3 osteoarthritis were randomized to either an MSC group or placebo group with a ratio of 1:1. There were 73 patients per group who received either a single intra-articular injection of bone marrow-derived MSCs (BMMSCs; 25 million cells) or placebo, followed by 20 mg per 2 mL of hyaluronic acid under ultrasound guidance. The primary endpoint was the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) total score. The secondary endpoints were WOMAC subscores for pain, stiffness, and physical function; the visual analog scale score for pain; and magnetic resonance imaging findings using T2 mapping and cartilage volume.

RESULTS

Overall, 65 patients from the BMMSC group and 68 patients from the placebo group completed 12-month follow-up. The BMMSC group showed significant improvements in the WOMAC total score compared with the placebo group at 6 and 12 months (percentage change: -23.64% [95% CI, -32.88 to -14.40] at 6 months and -45.60% [95% CI, -55.97 to -35.23] at 12 months < .001; percentage change, -44.3%). BMMSCs significantly improved WOMAC pain, stiffness, and physical function subscores as well as visual analog scale scores at 6 and 12 months ( < .001). T2 mapping showed that there was no worsening of deep cartilage in the medial femorotibial compartment of the knee in the BMMSC group at 12-month follow-up, whereas in the placebo group, there was significant and gradual worsening of cartilage ( < .001). Cartilage volume did not change significantly in the BMMSC group. There were 5 adverse events that were possibly/probably related to the study drug and consisted of injection-site swelling and pain, which improved within a few days.

CONCLUSION

In this small randomized trial, BMMSCs proved to be safe and effective for the treatment of grade 2 and 3 osteoarthritis. The intervention was simple and easy to administer, provided sustained relief of pain and stiffness, improved physical function, and prevented worsening of cartilage quality for ≥12 months.

REGISTRATION

CTRI/2018/09/015785 (National Institutes of Health and Clinical Trials Registry-India).

摘要

背景

骨关节炎是一种慢性、进行性和退行性疾病,治疗选择有限。最近,生物疗法已成为骨关节炎治疗的一种新兴选择。

目的

评估同种异体间充质基质细胞(MSCs)是否有潜力改善功能参数并诱导骨关节炎患者的软骨再生。

研究设计

随机对照试验;证据水平,1 级。

方法

146 例 2 级和 3 级骨关节炎患者随机分为 MSC 组或安慰剂组,比例为 1:1。每组各有 73 例患者,接受单次关节内注射骨髓来源的 MSCs(BMMSCs;2500 万个细胞)或安慰剂,随后在超声引导下每 2 毫升 20 毫克透明质酸。主要终点是西安大略和麦克马斯特大学骨关节炎指数(WOMAC)总分。次要终点是 WOMAC 疼痛、僵硬和身体功能子评分;疼痛的视觉模拟评分;以及使用 T2 映射和软骨体积的磁共振成像发现。

结果

总体而言,BMMSC 组有 65 例患者和安慰剂组有 68 例患者完成了 12 个月的随访。与安慰剂组相比,BMMSC 组在 6 个月和 12 个月时 WOMAC 总分均有显著改善(6 个月时百分比变化:-23.64%[95%CI,-32.88 至-14.40];12 个月时百分比变化:-45.60%[95%CI,-55.97 至-35.23] <.001;百分比变化,-44.3%)。BMMSCs 还显著改善了 WOMAC 疼痛、僵硬和身体功能子评分以及视觉模拟评分(均 <.001)。T2 映射显示,在 12 个月的随访中,BMMSC 组膝关节内侧股胫关节的深层软骨没有恶化,而安慰剂组的软骨则逐渐恶化( <.001)。BMMSC 组的软骨体积没有明显变化。有 5 起不良事件可能/可能与研究药物有关,包括注射部位肿胀和疼痛,这些不良事件在几天内得到改善。

结论

在这项小型随机试验中,BMMSCs 被证明对 2 级和 3 级骨关节炎的治疗是安全有效的。该干预措施简单易用,可持续缓解疼痛和僵硬,改善身体功能,并在至少 12 个月内防止软骨质量恶化。

注册

CTRI/2018/09/015785(美国国立卫生研究院和印度临床试验注册中心)。

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