Matoba Satoaki, Tatsumi Tetsuya, Murohara Toyoaki, Imaizumi Tsutomu, Katsuda Yousuke, Ito Masaaki, Saito Yoshihiko, Uemura Shiro, Suzuki Hiroshi, Fukumoto Shinya, Yamamoto Yasutaka, Onodera Rie, Teramukai Satoshi, Fukushima Masanori, Matsubara Hiroaki
Department of Cardiovascular Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Am Heart J. 2008 Nov;156(5):1010-8. doi: 10.1016/j.ahj.2008.06.025. Epub 2008 Sep 19.
Angiogenic cell therapy by intramuscular injection of autologous bone marrow mononuclear cells was first attempted in patients with peripheral artery disease (PAD) with critical limb ischemia, and the feasibility was shown by a randomized controlled Therapeutic Angiogenesis by Cell Transplantation (TACT) study.
The present study was designed to assess the 3-year safety and clinical outcomes of this angiogenic cell therapy by investigating the mortality and leg amputation-free interval as primary end points. The median follow-up time for surviving patients was 25.3 months (range, 0.8-69.0 months), and 3-year overall survival rates were 80% (95% CI 68-91) in patients with atherosclerotic peripheral arterial disease (11 died in 74 patients) and 100% (no death) in 41 patients with thromboangiitis obliterans (TAO; Buerger's disease). Three-year amputation-free rate was 60% (95% CI 46-74) in PAD and 91% (95% CI 82-100) in patients with TAO. The multivariate analysis revealed that the severity of rest pain and repeated experience of bypass surgery were the prognostic factors negatively affecting amputation-free interval. The significant improvement in the leg pain scale, ulcer size, and pain-free walking distance was maintained during at least 2 years after the therapy, although the ankle brachial index and transcutaneous oxygen pressure value did not significantly change.
The angiogenic cell therapy using bone marrow mononuclear cells can induce a long-term improvement in limb ischemia, leading to extension of amputation-free interval. The safety and efficacy are not inferior to the conventional revascularization therapies.
首次尝试通过肌肉注射自体骨髓单个核细胞进行血管生成细胞治疗外周动脉疾病(PAD)合并严重肢体缺血的患者,一项随机对照的细胞移植治疗性血管生成(TACT)研究证明了其可行性。
本研究旨在通过调查死亡率和无腿截肢间隔作为主要终点,评估这种血管生成细胞治疗的3年安全性和临床结果。存活患者的中位随访时间为25.3个月(范围0.8 - 69.0个月),动脉粥样硬化性外周动脉疾病患者的3年总生存率为80%(95%CI 68 - 91)(74例患者中有11例死亡),41例血栓闭塞性脉管炎(TAO;伯格氏病)患者的3年总生存率为100%(无死亡)。PAD患者的3年无截肢率为60%(95%CI 46 - 74),TAO患者为91%(95%CI 82 - 100)。多变量分析显示,静息痛的严重程度和搭桥手术的反复经历是对无截肢间隔有负面影响的预后因素。尽管踝肱指数和经皮氧分压值没有显著变化,但在治疗后至少2年内,腿痛量表、溃疡大小和无痛步行距离有显著改善。
使用骨髓单个核细胞的血管生成细胞治疗可诱导肢体缺血的长期改善,从而延长无截肢间隔。其安全性和有效性不低于传统的血管重建治疗。