A pooled analysis involving 1,748 patients in 4 randomized trials contradicts the results of recent trials that have demonstrated that the risks for death and myocardial infarction (MI) are potentially higher in patients receiving drug-eluting stents (particularlysirolimus-eluting stents) compared with patients receiving bare-metal stents.
A pooled analysis published in the New England Journal of Medicine (NEJM) involving 1,748 patients in 4 randomized trials contradicts the results of recent trials that have demonstrated that the risks for death and myocardial infarction (MI) are potentially higher in patients receiving drug-eluting stents (particularly sirolimus-eluting stents) compared with patients receiving bare-metal stents.
The trials included in this study were the Sirolimus-Coated Bx Velocity Balloon-Expandable Stent in the Treatment of Patients with De Novo Native Coronary Artery Lesions (RAVEL) study, the Sirolimus-Eluting Balloon-Expandable Stent in the Treatment of Patients with De Novo Native Coronary-Artery Lesions (SIRIUS) trial, the European SIRIUS (ESIRIUS) trial, and the Canadian SIRIUS (C-SIRIUS) trial. Each of these double-blinded trials randomized patients (1:1) to receive either a sirolimus-eluting stent or a bare-metal stent implanted into previously untreated lesions in a single, native coronary artery.
The primary safety end point in this study was all-cause mortality. After 4 years of patient follow-up, there was no statistically significant difference in the risk of death between the sirolimus-coated stent group (57 of 878) and the bare-metal stent group (46 of 870) (HR=1.24; 95% CI, 0.84–1.83; P=.28). In addition, the risk of MI or stent thrombosis was demonstrated to be similar between groups (HR=1.03; 95% CI, 0.71–1.51; P=.86 and HR=1.07; 95% CI, 0.64–1.79; P=.80, respectively). Sirolimus-eluting stents were associated with a greater percentage of complex lesions compared with bare-metal stents (22.5% vs 18.5%; P=.04). A greater percentage of patients with bare-metal stents had diabetes than patients with sirolimus-eluting stents (26.8% vs 22.2%; P=.02).
An estimated 664,000 percutaneous coronary intervention (PCI) procedures were performed in 2003 in the United States; drug-eluting or bare-metal stents were used in 84% of the procedures.
With regard to the previous studies that have demonstrated increased risk with drug-eluting stents, the authors stated: "The divergence of the Kaplan–Meier survival curves over time could be interpreted as a growing trend toward a lower survival rate among patients treated with sirolimus-eluting stents as compared with those treated with bare-metal stents, although a larger number of patients, a longer follow-up period, or both would be necessary to confirm this interpretation."
SOURCES
Spaulding C, Daemen J, Boersma E, Cutlip DE, Serruys PW. A pooled analysis of data comparing sirolimus-eluting stents with bare-metal stents. New Engl J Med. 2007;356:989–997.
Heart disease and stroke statistics-2007 update. A report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. http:// http://www.americanheart.org/statistics/. Accessed July 10, 2007.
David Calabrese of OptumRx Talks Top Three Drugs in Pipeline, Industry Trends in Q2
July 1st 2020In this week's episode of Tuning Into The C-Suite podcast, MHE's Briana Contreras chatted with David Calabrese, R.Ph, MHP, who is senior vice president and chief pharmacy officer of pharmacy care services company, OptumRx. David is also a member of Managed Healthcare Executives’ Editorial Advisory Board. During the discussion, he shared the OptumRx Quarter 2 Drug Pipeline Insights Report of 2020. Some of the information shared includes the three notable drugs currently being reviewed or those that have been recently approved by the FDA. Also discussed were any interesting industry trends to watch for.
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