TRITON-TIMI 38 STENT ANALYSIS FAVORS PRASUGREL
CHICAGO, March 29 /PRNewswire/ -- Prasugrel has been shown to block
platelet activity in patients with acute coronary syndromes (ACS) more
effectively than clopidogrel, and to cut by more than half the risk of
thrombosis, or blood clotting, inside the coronary stent. Now a new analysis
of data from the Trial to Assess Improvement in Therapeutic Outcomes by
Optimizing Platelet Inhibition with Prasugrel (TRITON-TIMI 38) reveals that
the investigational drug maintains its edge over clopidogrel regardless of the
type of stent, the amount of time since the stenting procedure, or the way
stent thrombosis is defined.
The results of the TRITON-TIMI 38 analysis are being reported today in a
Late-Breaking Clinical Trials session at the SCAI Annual Scientific Sessions
in Partnership with ACC i2 Summit (SCAI-ACCi2) in Chicago. SCAI-ACCi2 is a
scientific meeting for practicing cardiovascular interventionalists sponsored
by the Society for Cardiovascular Angiography and Interventions (SCAI) in
partnership with the American College of Cardiology (ACC). The study will be
simultaneously published online in The Lancet.
For the main TRITON-TIMI 38 study, researchers recruited 13,608 patients
with ACS who needed stenting from 707 medical centers in 30 countries.
Patients were randomly assigned to anti-platelet therapy consisting of either
a 300-mg loading dose of clopidogrel before the procedure, followed by a
maintenance dose of 75 mg daily for one year, or to a loading dose of 60 mg of
prasugrel, followed by 10 mg daily for one year. Both medications prevent
unwanted blood clotting by inhibiting the ability of platelets to clump
together.
Stephen D. Wiviott, MD, Brigham and Women's Hospital, Boston, led the new
stent analysis. Of the 12,844 patients who ultimately were treated with at
least one coronary stent, 6,461 patients received only bare-metal stents (BMS),
and 5,743 patients received only drug-eluting stents (DES). Overall, prasugrel
reduced both early stent thrombosis -- within 30 days of stenting -- when
compared with clopidogrel (0.64 percent vs. 1.56 percent, hazard ratio 0.41,
p<0.001) -- and late stent thrombosis -- more than 30 days after stenting
(0.49 percent vs. 0.82 percent, hazard ratio 0.60, p=0.035). For bare-metal
stents, the respective rates of stent thrombosis with prasugrel and
clopidogrel were 1.3 percent vs. 2.4 percent, hazard ratio 0.52, p=0.009, and
for drug-eluting stents, 0.8 percent vs. 2.3 percent, hazard ratio 0.36,
p<0.001. Prasugrel's advantage remained highly statistically significant
across a broad array of patient and procedural characteristics.
Dr. Wiviott will present the results of the "Trial to Assess Improvement
in Therapeutic Outcomes by Optimizing Platelet Inhibition with Prasugrel"
(TRITON-TIMI 38) stent substudy on Saturday, March 29 at 9:00 a.m. CDT in the
Grand Ballroom, S100. The study will be simultaneously published online in The
Lancet.
About SCAI
Headquartered in Washington, DC, the Society for Cardiovascular
Angiography and Interventions is a 4,000-member professional organization
representing invasive and interventional cardiologists in over 60 nations.
SCAI's mission is to promote excellence in invasive and interventional
cardiovascular medicine through physician education and representation, and
advancement of quality standards to enhance patient care. SCAI's annual
meeting has become the leading venue for education, discussion, and debate
about the latest developments in this dynamic medical specialty.
About ACC
The American College of Cardiology is leading the way to optimal
cardiovascular care and disease prevention. The College is a 34,000-member
nonprofit medical society and bestows the credential Fellow of the American
College of Cardiology upon physicians who meet its stringent qualifications.
The College is a leader in the formulation of health policy, standards and
guidelines, and is a staunch supporter of cardiovascular research. The ACC
provides professional education and operates national registries for the
measurement and improvement of quality care.
SOURCE SCAI-ACCi2