A randomised trial of sirolimus- versus paclitaxel-coated balloons for de novo coronary lesions
- PMID: 39492703
- PMCID: PMC11522860
- DOI: 10.4244/EIJ-D-23-00868
A randomised trial of sirolimus- versus paclitaxel-coated balloons for de novo coronary lesions
Abstract
Background: Paclitaxel-coated balloons (PCB) are a viable alternative to drug-eluting stents in the treatment of de novo coronary lesions. Whether sirolimus represents an alternative to paclitaxel for drug-coated balloons remains elusive.
Aims: This randomised, controlled, multicentre, non-inferiority trial investigated a novel sirolimus-coated balloon (SCB) with a crystalline coating versus a PCB in de novo coronary lesions.
Methods: To compare a novel SCB with a clinically proven PCB, 70 patients with de novo coronary lesions were enrolled at 4 centres in Germany and Switzerland. The primary endpoint was non-inferiority regarding angiographic late lumen loss (LLL) at 6 months, with a predefined margin of δ=0.35 mm. Secondary endpoints included procedural success, major adverse cardiac events, and individual clinical endpoints.
Results: Quantitative coronary angiography revealed no differences in baseline parameters. At 6 months, in-segment LLL was 0.04±0.39 mm in the PCB group versus 0.11±0.37 mm in the SCB group (non-significant), respectively. The mean difference between SCB and PCB was 0.07 mm (95% confidence interval: -0.12 to 0.26). Non-inferiority at the predefined margin of 0.35 was shown. Clinical event rates up to 12 months were not different between the groups (3 target lesion revascularisations in the PCB group versus 2 in the SCB group, no myocardial infarctions, no deaths).
Conclusions: The novel SCB showed similar angiographic outcomes in the treatment of de novo coronary disease as compared with a clinically proven PCB (ClinicalTrials.gov: NCT03908450).
Conflict of interest statement
B. Scheller is a shareholder of InnoRa GmbH. N. Mangner has received personal fees from Edwards Lifesciences, Medtronic, Biotronik, Novartis, Sanofi Genzyme, AstraZeneca, Pfizer, Bayer, Abbott, Abiomed, and Boston Scientific, outside the submitted work. C. Schwenke is a consultant for InnoRa GmbH, on an honorary basis. R.V. Jeger received grants to the institution from Abbott, Amgen, AstraZeneca, Bayer, Biosense Webster, Biotronik, Boston Scientific, Bristol-Myers Squibb, Cardionovum, Cordis, Daiichi Sankyo, Edwards Lifesciences, GE HealthCare, MCM Medsys, Medtronic, Novartis, Pfizer, Terumo, and Vascular Medical GmbH. F. Mahfoud is supported by Deutsche Gesellschaft für Kardiologie (DGK), Deutsche Forschungsgemeinschaft (SFB TRR219, Project-ID 322900939), and Deutsche Herzstiftung; he has received scientific support from Ablative Solutions, Medtronic, and ReCor Medical; and speaker honoraria/consulting fees from Ablative Solutions, Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Inari, Medtronic, Merck, ReCor Medical, Servier, and Terumo. The other authors have no conflicts of interest to declare with regard to this study.
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