Sheppard Richard, Eisenberg Mark J, Donath David, Meerkin David
Division of Cardiology, Royal Victoria Hospital, Montreal, Quebec, Canada.
Am Heart J. 2003 Nov;146(5):775-86. doi: 10.1016/S0002-8703(03)00389-2.
The purpose of this article is to review the current literature pertaining to intracoronary brachytherapy for the prevention of restenosis after percutaneous coronary revascularization (PCR).
English-language articles were identified through a MEDLINE search (January 1984 to January 2003) using the keywords brachytherapy, radioactive stents, and coronary arteries. In addition, pertinent reference citations from relevant articles were reviewed.
Restenosis after PCR is a complex process, thought to be due to a combination of vessel wall remodeling and neointimal proliferation. To date, catheter-based delivery of intracoronary brachytherapy has been found to prevent vessel wall remodeling and causes a reduction in the proliferation of the neointima. Neointimal proliferation, as measured by mean neointimal area, was reduced in all animal studies (range 26%-91%). In contrast, animal studies examining radioactive stents demonstrated an increase in neointimal proliferation, suggesting that they may not be helpful at preventing post-PCR restenosis. All human studies using catheter-based intracoronary brachytherapy for in-stent restenosis have employed either beta (beta) or gamma (gamma) radiation sources with variable doses of radiation (range 7-56 Grays [Gy]). Restenosis occurred in 12% to 40% of patients in nonrandomized studies, and clinical events occurred in 13% to 50% of patients. To date, there have been 7 published randomized trials in humans comparing catheter-based intracoronary brachytherapy to placebo, with a total of 1047 patients. The dose of radiation in the trials ranged from 14 Gy to 30 Gy. During follow-up, 8% to 33% of patients who received brachytherapy had restenosis versus 39% to 64% of patients receiving placebo. Clinical events occurred in 19% to 50% among patients who received brachytherapy versus 29% to 79% among patients receiving placebo. The majority of human studies examining radioactive stents do not demonstrate a reduction in restenosis in patients post-PCR. There are no randomized trials examining radioactive stents in humans.
Nonrandomized studies of radioactive stents suggest they are not effective at preventing in-stent restenosis. In contrast, data from animal and human studies suggest that catheter-based intracoronary brachytherapy can prevent in-stent restenosis and reduce clinical events post-PCR.
本文旨在综述目前有关冠状动脉内近距离放射治疗预防经皮冠状动脉血运重建术(PCR)后再狭窄的文献。
通过MEDLINE检索(1984年1月至2003年1月),使用关键词近距离放射治疗、放射性支架和冠状动脉来识别英文文献。此外,还对相关文章的参考文献进行了审查。
PCR后再狭窄是一个复杂的过程,被认为是血管壁重塑和新生内膜增殖共同作用的结果。迄今为止,已发现基于导管的冠状动脉内近距离放射治疗可预防血管壁重塑并减少新生内膜的增殖。在所有动物研究中,以平均新生内膜面积衡量的新生内膜增殖均有所减少(范围为26% - 91%)。相比之下,对放射性支架的动物研究显示新生内膜增殖增加,这表明它们可能无助于预防PCR后再狭窄。所有使用基于导管的冠状动脉内近距离放射治疗治疗支架内再狭窄的人体研究均采用了β或γ放射源,放射剂量各不相同(范围为7 - 56格雷[Gy])。在非随机研究中,12%至40%的患者出现再狭窄,13%至50%的患者发生临床事件。迄今为止,已有7项关于人体的随机试验发表,比较了基于导管的冠状动脉内近距离放射治疗与安慰剂,共有1047例患者。试验中的放射剂量范围为14 Gy至30 Gy。在随访期间,接受近距离放射治疗的患者中有8%至33%发生再狭窄,而接受安慰剂的患者中这一比例为39%至64%。接受近距离放射治疗的患者中19%至