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采用培养扩增的自体间充质干细胞治疗与腰椎退行性椎间盘疾病相关的根性疼痛:安全性和疗效的初步研究。

Treatment of lumbar degenerative disc disease-associated radicular pain with culture-expanded autologous mesenchymal stem cells: a pilot study on safety and efficacy.

机构信息

Centeno-Schultz Clinic, Broomfield, CO, 80021, USA.

Regenerative Sciences, LLC, 403 Summit Blvd Suite 201, Broomfield, CO, 80021, USA.

出版信息

J Transl Med. 2017 Sep 22;15(1):197. doi: 10.1186/s12967-017-1300-y.


DOI:10.1186/s12967-017-1300-y
PMID:28938891
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5610473/
Abstract

BACKGROUND: Degenerative disc disease (DDD) is a common cause of lower back pain with radicular symptoms and has a significant socioeconomic impact given the associated disability. Limited effective conservative therapeutic options result in many turning to surgical alternatives for management, which vary in the rate of success and also carry an increased risk of morbidity and mortality associated with the procedures. Several animal based studies and a few human pilot studies have demonstrated safety and suggest efficacy in the treatment of DDD with mesenchymal stem cells (MSCs). The use of bone marrow-derived MSCs for the treatment of DDD is promising and in the present study we report on the safety and efficacy findings from a registry based proof of concept study using a percutaneous intradiscal injection of cultured MSCs for the management of DDD with associated radicular symptoms. METHODS: Thirty-three patients with lower back pain and disc degeneration with a posterior disc bulge diagnosed on magnetic resonance imaging (MRI) met the inclusion criteria and were treated with culture-expanded, autologous, bone marrow-derived MSCs. Prospective registry data was obtained at multiple time intervals up to 6 years post-treatment. Collected outcomes included numeric pain score (NPS), a modified single assessment numeric evaluation (SANE) rating, functional rating index (FRI), measurement of the intervertebral disc posterior dimension, and adverse events. RESULTS: Three patients reported pain related to procedure that resolved. There were no serious adverse events (i.e. death, infection, or tumor) associated with the procedure. NPS change scores relative to baseline were significant at 3, 36, 48, 60, and 72 months post-treatment. The average modified SANE ratings showed a mean improvement of 60% at 3 years post-treatment. FRI post-treatment change score averages exceeded the minimal clinically important difference at all time points except 12 months. Twenty of the patients treated underwent post-treatment MRI and 85% had a reduction in disc bulge size, with an average reduction size of 23% post-treatment. CONCLUSIONS: Patients treated with autologous cultured MSCs for lower back pain with radicular symptoms in the setting of DDD reported minor adverse events and significant improvements in pain, function, and overall subjective improvement through 6 years of follow-up. NCT03011398. A Clinical Registry of Orthobiologics Procedures. https://clinicaltrials.gov/ct2/show/NCT03011398?term=orthobiologics&rank=1.

摘要

背景:退行性椎间盘疾病(DDD)是导致下腰痛和神经根症状的常见原因,由于相关残疾,对社会经济有重大影响。由于有效的保守治疗选择有限,许多人转向手术治疗,这些治疗方法的成功率不同,而且与手术相关的发病率和死亡率也更高。一些基于动物的研究和少数人类试点研究已经证明了间充质干细胞(MSCs)治疗 DDD 的安全性和有效性。骨髓来源的 MSCs 用于治疗 DDD 具有很大的潜力,在本研究中,我们报告了一项基于注册的概念验证研究的安全性和疗效发现,该研究使用经皮椎间盘内注射培养的 MSCs 治疗伴有神经根症状的 DDD。

方法:33 名患有下腰痛和椎间盘退变的患者,其磁共振成像(MRI)诊断为后椎间盘膨出,符合纳入标准,并接受了培养的、自体、骨髓来源的 MSCs 治疗。在治疗后 6 年的多个时间间隔内,前瞻性地获得了注册数据。收集的结果包括数字疼痛评分(NPS)、改良的单一评估数字评估(SANE)评分、功能评分指数(FRI)、椎间盘后径测量和不良事件。

结果:3 名患者报告与手术相关的疼痛,但已缓解。与手术相关的严重不良事件(即死亡、感染或肿瘤)无发生。与基线相比,治疗后 3、36、48、60 和 72 个月时 NPS 变化评分均有显著差异。治疗后 3 年平均改良 SANE 评分显示 60%的平均改善。除 12 个月外,FRI 治疗后变化评分平均值均超过最小临床重要差异。20 名接受治疗的患者接受了治疗后的 MRI,85%的患者椎间盘膨出尺寸减小,治疗后平均减小 23%。

结论:在 DDD 背景下,患有下腰痛伴神经根症状的患者接受自体培养的 MSCs 治疗后,报告有轻微的不良事件,并在 6 年的随访中显著改善了疼痛、功能和整体主观改善。NCT03011398. 骨科生物制剂程序临床注册。https://clinicaltrials.gov/ct2/show/NCT03011398?term=orthobiologics&rank=1.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d050/5610473/5b02134b6e71/12967_2017_1300_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d050/5610473/1497b4bcca8c/12967_2017_1300_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d050/5610473/c2014acfb478/12967_2017_1300_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d050/5610473/0005cbd703fa/12967_2017_1300_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d050/5610473/f4b2be0290b8/12967_2017_1300_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d050/5610473/5b02134b6e71/12967_2017_1300_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d050/5610473/1497b4bcca8c/12967_2017_1300_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d050/5610473/c2014acfb478/12967_2017_1300_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d050/5610473/0005cbd703fa/12967_2017_1300_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d050/5610473/f4b2be0290b8/12967_2017_1300_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d050/5610473/5b02134b6e71/12967_2017_1300_Fig5_HTML.jpg

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