Cardiovascular Center, Seoul National University Hospital, Seoul, Korea.
Circ Cardiovasc Interv. 2010 Jun 1;3(3):243-8. doi: 10.1161/CIRCINTERVENTIONS.109.889881. Epub 2010 May 18.
In the COREA-TAXUS trial ("Effect of Celecoxib On REstenosis after coronary Angioplasty with a TAXUS stent"), celecoxib reduced late luminal loss and adverse cardiac events at follow-up around 6 months. The objective of this study was to assess the long-term outcome of short-term adjunctive celecoxib treatment after paclitaxel-eluting stent implantation.
This is a 2-year clinical follow-up of the COREA-TAXUS trial, an open-label randomized controlled study. A total 274 patients were randomized to receive or not receive celecoxib (400 mg before the intervention and 200 mg twice daily for 6 months after the procedure), and 271 underwent successful paclitaxel-eluting stent implantation. All patients were given aspirin (100 mg daily indefinitely) and clopidogrel (75 mg daily for at least 6 months). Among the 271 patients, 267 (98.5%) completed the 2-year clinical follow-up. From the previous follow-up to 2 years, there was no difference in the rate of adverse cardiac events between the celecoxib and control groups (1.6% versus 4.3%, P=0.27). Thus, at 2 years, the rate of adverse cardiac events was consistently lower in the celecoxib group (6.9% versus 19.7%, P=0.002). A significant reduction in need for target lesion revascularization was observed (6.2% versus 18.2%, P=0.003). The efficacy benefit in the celecoxib group was not undermined by an increased risk for cardiac death or myocardial infarction at 2 years (1.5% versus 1.4%).
Six-month adjunctive celecoxib treatment after paclitaxel-eluting stent implantation was associated with durable long-term efficacy up to 2 years. However, the inconclusive evidence for the long-term safety of this treatment warrants caution.
URL: http://www.clinicaltrials.gov. Unique identifier: NCT 00292721.
在 COREA-TAXUS 试验(“塞来昔布对紫杉醇支架置入后再狭窄的影响”)中,塞来昔布降低了 6 个月左右随访时的晚期管腔丢失和不良心脏事件。本研究的目的是评估紫杉醇洗脱支架置入后短期辅助塞来昔布治疗的长期结果。
这是 COREA-TAXUS 试验的 2 年临床随访,这是一项开放标签的随机对照研究。共 274 例患者随机分为接受或不接受塞来昔布治疗组(介入前 400mg,术后 6 个月每天 2 次 200mg),271 例患者成功接受紫杉醇洗脱支架置入。所有患者均给予阿司匹林(每日 100mg 无限期使用)和氯吡格雷(至少 6 个月每日 75mg)。在 271 例患者中,267 例(98.5%)完成了 2 年的临床随访。从上次随访到 2 年时,塞来昔布组和对照组不良心脏事件的发生率无差异(1.6%比 4.3%,P=0.27)。因此,2 年时,塞来昔布组不良心脏事件的发生率持续较低(6.9%比 19.7%,P=0.002)。需要靶病变血运重建的比例显著降低(6.2%比 18.2%,P=0.003)。在 2 年时,塞来昔布组的心脏死亡或心肌梗死风险增加并没有破坏这种治疗的疗效获益(1.5%比 1.4%)。
紫杉醇洗脱支架置入后 6 个月辅助塞来昔布治疗可带来长达 2 年的持久长期疗效。然而,这种治疗长期安全性的证据尚不明确,需要谨慎。
网址:http://www.clinicaltrials.gov。唯一标识符:NCT 00292721。