Should we rely on OCT to assess the improvements of new generation drug-eluting stents?

Abstract

Drug-eluting stents have changed the landscape of interventional cardiology. Since their introduction, over a decade ago, their primary and ultimate effect— the ability to decrease neointimal proliferation—still remains undisputable. The reduction of restenosis after drug-eluting stents pushed the borders of percutaneous coronary intervention towards the treatment of patients with complex anatomies, while improving the durability of the procedure. However, the intense modulation of vascular healing by drug-eluting stents may also have potential drawbacks, namely impaired re-endothelialization. Newer generation drug-eluting stents, therefore, face the challenge of maintaining the efficacy levels of early stent formulations, and, at the same time, improving the quality of tissue response to these devices. Several new drug-eluting stents have already been released for clinical use, providing theoretical improvements in the platform, coating, and the drug. In practice, however, proving the superiority of newer stents is not an easy task. First-generation drug-eluting stents are associated with a low frequency of clinical complications. Particularly, the odds of stent thrombosis, perhaps the most feared safety event commonly do not surpass 3% during an observation period of several years. Therefore, a conclusive clinical trial would need the inclusion of thousands of patients, followed-up for a long period of time, in order to be powered to confirm a decrease in thrombosis. Surrogate endpoints are important tools to overcome the difficulties in assessing low-frequency adverse events. Optical coherence tomography (OCT) imaging has been recently introduced in interventional cardiology as a candidate method to evaluate the subtleties of the stent-to-vessel wall interaction. Indeed, stent apposition, strut coverage, and abnormal intraluminal tissue all seem to be reliably assessed by OCT. In the present issue of the International Journal of Cardiovascular Imaging, Jung-Sun Kim et al. show that the newer zotarolimus-eluting Resolute stent was less prone to present uncovered or malapposed stent struts and intracoronary thrombus than the sirolimus-eluting Cypher stent at 9 months, by OCT imaging. Taken together, in theory, these results would imply in an improved vascular response for the zotarolimus stent. Previous studies have shown that new-generation biolimus-eluting stents had better strut coverage at 9 months by OCT than sirolimus-eluting stents [1], but were not associated with a clear improvement in stent thrombosis after 2 years [2]. Conversely, newgeneration zotarolimus-eluting stents had similar 13-month OCT findings compared to new-generation everolimus stents [3], but tended to have more definite thrombotic events at 12 months [4]. These somewhat P. A. Lemos (&) Heart Institute (InCor), University of Sao Paulo Medical School, & Hospital Sirio-Libanes, Av. Dr. Eneas de Carvalho Aguiar, 44, Bloco I, 38 andar, Hemodinâmica, Sao Paulo, SP 05403-000, Brazil e-mail: pedro.lemos@incor.usp.br