Date: 2014-11-04
Type of information: Presentation of results at a congress
phase:
Announcement: presentation of results at the Vascular Interventional Advances (VIVA) 2014 conference in Las Vegas, Nev.
Company: Covidien (Ireland)
Product: SilverHawk™ and TurboHawk ™ directional atherectomy systems
Action mechanism:
Disease: peripheral artery disease
Therapeutic area: Cardiovascular diseases
Country:
Trial
details: DEFINITIVE AR, a prospective, multi-center, randomized, pilot study, utilized the Covidien SilverHawk™ and TurboHawk ™ directional atherectomy systems and the Bayer Healthcare peripheral paclitaxel-coated angioplasty catheter with Paccocath™ technology. Ten investigational sites in Europe enrolled 121 patients in this observational investigation, 102 patients were enrolled in the randomized cohort (DAART – 48, DCB alone – 54). The study also included 19 non-randomized DAART registry arm for severely calcified lesions, however calcification was present in all groups. The DEFINITIVE AR trial included adverse event review and adjudication by an independent Clinical Events Committee. The primary outcome was target lesion percent stenosis at one year following initial treatment. Key secondary outcomes included primary patency by Duplex Ultrasound at 12 months following the procedure, primary patency by angiographic assessment at 12 months following the procedure, and assessment of major adverse events at 12 months following the procedure. Clinical follow-up occurred at pre-discharge, 30 days, six months and one year post-procedure. Two-year follow-up is underway. This is the first randomized study involving a drug-coated balloon that included angiographic follow-up at one year to assess patency.
Latest
news: * On November 4, 2014, Covidien announced 12-month results of the DEFINITIVE AR study, the first randomized study designed to identify the clinical benefits of plaque removal using directional atherectomy followed by drug coated balloon. The results were presented by Professor Thomas Zeller of the Universitaets-Herzzentrum, Bad Krozingen, Germany at the Vascular Interventional Advances (VIVA) 2014 conference in Las Vegas, Nev. DEFINITIVE AR results demonstrated higher technical success and lower incidence of vessel injuries known as flow-limiting dissections. Additionally, the study suggests the combination of directional atherectomy and anti-restenosis therapy with drug coated balloons (known as DAART) improves patency in long and severely calcified lesions. Longer lesions have lower patency across all current treatments, and presence of calcification may prohibit drug uptake and lead to less durability and loss of patency. Patency is the ability for the treated artery to remain open. Duplex Ultrasound primary patency rates for the long (≥10 cm) lesion subset at 12 months were 96.8 percent in patients treated with DAART compared to 85.9 percent in patients treated with DCB alone. Primary patency rates at 12 months in severely calcified lesions, per core lab assessment, were 70.4 percent in DAART patients compared to 62.5 percent in DCB alone patients. “Lumen gain, or the amount of plaque removed from the artery with directional atherectomy prior to DCB treatment, may also be a critical factor in contributing to the long-term clinical success of DAART therapy,” said Professor Gunnar Tepe, Klinikum Rosenheim, Germany. “This data suggests when the optimal amount of plaque is removed, that is <30 percent residual stenosis, the patency rate is improved.” Results showed 94.1 percent primary angiographic patency for DAART when more plaque was removed with directional atherectomy (less than 30 percent residual stenosis was achieved) compared to 68.8 percent patency when less plaque was removed (more than 30 percent residual stenosis) prior to treatment with the DCB. Directional atherectomy is unique as it allows for the largest amount of luminal gain while maintaining vessel integrity. The primary endpoint of the study was defined as the percent stenosis (narrowing of the vessel), at one year per Angiographic Core Lab assessment. At 12 months, the percent stenosis in the randomized groups was 33.6 ± 17.7 for the DAART arm compared to 36.4 ± 17.6 for the DCB arm. These results were observational as the study was not powered to detect differences between the groups.
