Healthcare Industry News: Express2
News Release - February 18, 2009
New England Journal of Medicine Publishes Results from Boston Scientific's Landmark SYNTAX(TM) TrialData show comparable safety for complex patients treated with TAXUS® Express2(TM) Stents and bypass surgery
NATICK, Mass., Feb. 18 (Healthcare Sales & Marketing Network) -- Boston Scientific Corporation (NYSE: BSX ) today welcomed the publication of results from its landmark SYNTAX(TM) trial in this week's issue of the New England Journal of Medicine. In the study, percutaneous coronary intervention (PCI) using the TAXUS® Express2(TM) Paclitaxel-Eluting Coronary Stent System was compared to contemporary coronary artery bypass graft (CABG) surgery in patients with the most complex coronary artery disease (CAD). Trial results at 12 months demonstrated no overall statistically significant differences between PCI and CABG in rates of death or myocardial infarction (heart attack), although PCI patients were more likely to require a repeat revascularization (mostly additional PCI) than were CABG patients.
The SYNTAX trial is the first randomized, controlled clinical trial to compare these two treatments in patients with left main disease and three-vessel disease. These patient groups are typically treated with CABG and represent a population with far more complex anatomy and advanced disease than those studied in prior drug-eluting stent (DES) clinical trials.
"SYNTAX has provided the medical community with critical information on the management of patients with advanced and complex CAD," said Ted Feldman, M.D., F.S.C.A.I., Director of the Cardiac Catheterization Laboratory at NorthShore University HealthSystem in Evanston, Illinois, and a lead investigator of the trial. "While CABG may still be the preferred treatment in many patients with complicated disease, some patients may now be candidates for the less-invasive alternative offered by stents. These data will assist cardiologists in making treatment therapy decisions for these patients."
The SYNTAX trial enrolled 1,800 patients in its randomized arm, using an innovative consecutive enrollment methodology. All patients were assessed by a multidisciplinary team including an interventional cardiologist and a cardiac surgeon. If both the cardiologist and surgeon felt they could offer equivalent complete revascularization, patients were randomized 1:1 into one of the two treatment strategies (PCI or CABG). If either the cardiologist or surgeon felt that one revascularization technique was the preferred treatment, then patients were not randomized, but were entered into the corresponding registry. Accordingly, patients in the PCI registry had been rejected for cardiac surgery, and patients in the CABG registry had been rejected for PCI.
The patients recruited in the SYNTAX trial are a unique study group in the PCI field, given their exceptionally complex anatomy and advanced disease. The average PCI-treated patient enrolled in SYNTAX received 4.6 stents. By contrast, the average number of stents implanted in a PCI patient in everyday practice is 1.5. Further evidence of the complex nature of PCI-treated patients enrolled in SYNTAX include 33 percent of patients with >100 millimeters stented length, 72 percent with bifurcations, 22 percent with total occlusions and 39 percent with left main disease.
The final one-year results published today showed similar safety for the two randomized groups, with a combined rate of all-cause death, stroke and myocardial infarction (MI) of 7.6 percent for PCI and 7.7 percent for CABG (p=0.98). The rate of stroke itself was significantly lower for PCI (0.6 percent for PCI as compared to 2.2 percent for CABG, p=0.003). Overall 12-month MACCE (all-cause death, stroke, MI and repeat revascularization), however, was significantly higher for PCI (17.8 percent versus 12.4 percent, p=0.002), due to more repeat revascularization in the PCI arm (13.5 percent versus 5.9 percent, p=0.001). Most repeat revascularizations in the PCI arm, however, were performed by additional PCI, with only 2.8 percent of PCI patients ultimately requiring CABG.
"Boston Scientific is proud to sponsor the SYNTAX trial, and we are pleased that our robust DES clinical trial program is providing physicians with additional data to determine optimal treatment strategies for patients with challenging coronary artery disease," said Keith Dawkins, M.D., Associate Chief Medical Officer of Boston Scientific.
The SYNTAX trial broke new ground by scientifically defining a new measure for anatomical complexity -- the SYNTAX(TM) Score(TM) -- which characterizes vasculature based on lesion number, complexity and location. In fact, PCI patients in the lower one-third of raw SYNTAX Score results had similar 12-month combined MACCE rates to CABG patients (13.6 percent for PCI and 14.7 percent for CABG, p=0.71).
The TAXUS Express2 Paclitaxel-Eluting Coronary Stent System used in the SYNTAX trial has now been replaced by the Company's second-generation TAXUS® Liberte® Paclitaxel-Eluting Coronary Stent System, which has been approved for use in the United States, Europe and Japan. This stent represents Boston Scientific's latest advance in drug-eluting stent technology, with substantially thinner struts and a more flexible cell geometry for improved deliverability, as well as uniform strut distribution designed specifically for drug elution.
Boston Scientific is a worldwide developer, manufacturer and marketer of medical devices whose products are used in a broad range of interventional medical specialties. For more information, please visit: www.bostonscientific.com.
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Source: Boston Scientific
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