Stempeutics Research Pvt. Ltd., 3rd Floor, Manipal Hospitals Whitefield #143, EPIP Industrial Area, ITPL Main Road, Bangalore, 560 048, India.
Vijaya Hospital, Chennai, India.
Stem Cell Res Ther. 2023 Apr 1;14(1):60. doi: 10.1186/s13287-023-03292-w.
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.
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.
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.
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 .
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。
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。
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。
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。
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。