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标签扩展、单臂、III 期研究显示 stempeucel®在因动脉粥样硬化性外周动脉疾病导致的临界肢体缺血患者中的疗效和安全性。

Label extension, single-arm, phase III study shows efficacy and safety of stempeucel® in patients with critical limb ischemia due to atherosclerotic peripheral arterial disease.

机构信息

Stempeutics Research Pvt. Ltd., 3rd Floor, Manipal Hospitals Whitefield #143, EPIP Industrial Area, ITPL Main Road, Bangalore, 560 048, India.

Vijaya Hospital, Chennai, India.

出版信息

Stem Cell Res Ther. 2023 Apr 1;14(1):60. doi: 10.1186/s13287-023-03292-w.

Abstract

BACKGROUND

Peripheral arterial disease (PAD) of lower extremities comprises a clinical spectrum that extends from asymptomatic patients to critical limb ischemia (CLI) patients. 10% to 40% of the patients are at the risk of primary amputation. This study was planned in "no-option" patients of CLI due to atherosclerotic PAD to assess the efficacy and safety of pooled, allogeneic, adult human bone marrow-derived mesenchymal stromal cells which is already approved for marketing in India for CLI due to Buerger's disease.

METHODS

This was a single-arm, multi-centric, phase III study where mesenchymal stromal cells was injected as 2 million cells/kg body weight in the calf muscle and around the ulcer. Twenty-four patients of lower extremity CLI due to PAD with Rutherford III-5 or III-6 and ankle-brachial pressure index ≤ 0.6 and having have at least one ulcer with area between 0.5 and 10 cm were included in the study. These patients were evaluated over 12 months from drug administration.

RESULTS

Over a period of 12 months, statistical significant reduction of rest pain and ulcer size along with improvement in ankle-brachial pressure index and ankle systolic was observed. The quality of life of patients improved together with increase in total walking distance and major amputation-free survival time.

CONCLUSION

Mesenchymal stromal cells may be a feasible option to treat "no-option" patients with atherosclerotic PAD. Trial registration This study is registered prospectively in National Institutes of Health and Clinical Trials Registry-India (CTRI) website: CTRI/2018/06/014436. Registered 6th June 2018. http://ctri.nic.in/Clinicaltrials/pmaindet2.php?trialid=24050&EncHid=&userName=stempeutics .

摘要

背景

下肢外周动脉疾病(PAD)包括从无症状患者到严重肢体缺血(CLI)患者的临床谱。10%至 40%的患者有截肢的风险。本研究计划纳入因动脉粥样硬化性 PAD 导致 CLI 的“别无选择”患者,评估已在印度获得 Buerger 病 CLI 营销批准的同种异体、成人骨髓来源间充质基质细胞的疗效和安全性。

方法

这是一项单臂、多中心、III 期研究,在小腿肌肉和溃疡周围注射 200 万细胞/公斤体重的间充质基质细胞。纳入 24 例因 PAD 导致的下肢 CLI 患者,Rutherford III-5 或 III-6,踝肱压指数≤0.6,至少有一处溃疡,面积在 0.5 至 10cm 之间。这些患者在给药后 12 个月内进行评估。

结果

在 12 个月的时间内,观察到静息痛和溃疡面积的统计学显著减少,同时踝肱压指数和踝部收缩压改善。患者的生活质量得到改善,总步行距离增加,主要免于截肢的生存时间延长。

结论

间充质基质细胞可能是治疗动脉粥样硬化性 PAD“别无选择”患者的可行选择。

试验注册

本研究在国立卫生研究院和印度临床试验注册处(CTRI)网站进行了前瞻性注册:CTRI/2018/06/014436。于 2018 年 6 月 6 日注册。http://ctri.nic.in/Clinicaltrials/pmaindet2.php?trialid=24050&EncHid=&userName=stempeutics。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7954/10068167/22d31ef15695/13287_2023_3292_Fig1_HTML.jpg

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