Four-year results from patient-level meta-analysis confirm safety profile of Philips Stellarex 0.035 low-dose DCB

Sean Lyden takes questions from the panel at VIVA 2020

Royal Philips today announced the results of a patient-level meta-analysis that confirms the safety profile of its Stellarex drug-coated balloon (DCB) at four years. Including data from two major randomised controlled trials (RCTs), the results show no difference in mortality between patients treated with the Stellarex DCB and those treated with percutaneous transluminal angioplasty (PTA), the current standard of care. The meta-analysis was presented at the 2020 Vascular Interventional Advances conference (VIVA 2020; 6–8 November, virtual).

The meta-analysis found that over four years, there was no significant difference in survival among patients treated with the Stellarex DCB (85.7%) compared to those treated with PTA (85.6%). The data includes two Stellarex RCTs: the ILLUMENATE EU RCT and the ILLUMENATE Pivotal RCT, comprised of 589 patients in the USA and Europe followed up to four years with a high compliance on vital status data.

“The meta-analysis reinforces previously presented results from the ILLUMENATE RCTs, demonstrating low mortality rates each year through four years, with no difference in rates between the two patient cohorts,” said Sean Lyden (Cleveland Clinic, Cleveland, USA), who presented the data. Lyden is also co-primary Investigator for the ILLUMENATE Pivotal trial, one of the two RCTs included in the meta-analysis, and a paid consultant to Philips. “This independent, patient-level meta-analysis continues to provide consistent, long-term data for a large group of patients.”

In addition to demonstrating no significant difference in all-cause mortality between patients treated with the Stellarex DCB and those treated with PTA (14.3% vs. 14.4%), the results of the meta-analysis also show no difference in cardiovascular mortality (3.6% vs. 4%) and non-cardiovascular mortality (10.8% vs. 10.9%).

“The results of this study confirm the safety and performance of our unique Stellarex low-dose drug-coated balloon,” said Chris Landon, senior vice president and general manager Image Guided Therapy Devices at Philips. “We are committed to providing healthcare providers with accurate and transparent data in order to help them make an informed decision on the optimal treatment for each patient with peripheral arterial disease. Stellarex, with its low drug dose and unique drug coating composition, is a logical choice for those who require this option.”


Please enter your comment!
Please enter your name here