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Paclitaxel-coated balloons and sirolimus-eluting stents in noncomplex coronary bifurcation lesions

Paclitaxel-coated balloons and sirolimus-eluting stents in noncomplex coronary bifurcation lesions
Photo by ClinicalPulse / Seedream 5 Lite
Key Takeaway
Note that DCBs showed a numerically comparable risk for DoCE versus DES in noncomplex bifurcations at 2 years.

This randomized noninferiority trial subgroup analysis, part of the REC-CAGEFREE I trial, included 2,257 participants (99.3% of 2,272 randomized) across 43 sites in China. The study assessed patients with de novo coronary lesions, specifically focusing on noncomplex bifurcation and nonbifurcal lesions.

Participants were randomized to receive either paclitaxel-coated balloons (DCB) or sirolimus-eluting stents (DES). The primary outcome was the device-oriented composite endpoint (DoCE) at 24 months. In the bifurcation group, DoCE occurred in 6.0% of patients (46 of 773) in the DCB group compared to 4.3% in the nonbifurcation group (46 of 773 in bifurcation vs 64 of 1,484 in nonbifurcation), with a hazard ratio of 1.39 (95% CI: 0.87-2.21; P = 0.164). For the bifurcation group specifically, DoCE was 6.7% in the DCB group (26 of 394) versus 5.3% in the DES group (20 of 379), with a hazard ratio of 1.03 (95% CI: 0.53-2.01; P = 0.934).

In the nonbifurcation group, DoCE was 6.3% in the DCB group (46 of 735) compared to 2.4% in the DES group (18 of 749), with a hazard ratio of 2.67 (95% CI: 1.64-4.33; P < 0.001).

Safety and tolerability data, including adverse events and discontinuations, were not reported. Because this was a prespecified subgroup analysis, the results are hypothesis generating. Clinicians should note that DCBs were associated with a numerically comparable risk for DoCE compared with DES in noncomplex bifurcations at 2 years.

Study Details

Study typeRct
Sample sizen = 773
EvidenceLevel 2
Follow-up24.0 mo
PublishedApr 2026
View Original Abstract ↓
BACKGROUND: Drug-coated balloons (DCBs) are attractive for treating de novo coronary lesions, especially when involving bifurcations; however, their efficacy compared with drug-eluting stents (DES) remains uncertain. OBJECTIVES: The aim of this study was to assess the prognosis of DCBs vs DES in patients with noncomplex bifurcation and nonbifurcation lesions. METHODS: This was a prespecified subgroup analysis of the REC-CAGEFREE I (Paclitaxel-Coated Balloon for Treatment of De-Novo Non-Complex Coronary Artery Lesions) trial, which was an investigator-initiated, noninferiority trial conducted at 43 sites in China that randomized 2,272 participants to paclitaxel-coated balloons (the DCB group) or sirolimus-eluting stents (the DES group) for the treatment of de novo lesions, regardless of vessel diameter. The primary outcome was a device-oriented composite endpoint (DoCE) at 24 months. Participants were stratified according to the presence vs absence of bifurcation, and inverse probability of treatment weighting (IPTW) was performed to adjust for between-group imbalances. RESULTS: A total of 2,257 of 2,272 participants (99.3%) with available angiographic results were included. At 24 months, the DoCE had occurred in 46 of 773 patients in the bifurcation group (6.0%) and 64 of 1,484 patients in the nonbifurcation group (4.3%) (HR: 1.39; 95% CI: 0.87-2.21; P = 0.164). Of the 798 bifurcation lesions, 719 (90.1%) had DCB or DES treatment in the main vessel. A significant interaction for the DoCE was observed between bifurcation or nonbifurcation and assigned treatment (P = 0.031). In the nonbifurcation group, the DoCE occurred in 46 of 735 patients with DCBs (6.3%) and 18 of 749 (2.4%) with DES (HR: 2.67; 95% CI: 1.64-4.33; P < 0.001); the in bifurcation group, the DoCE occurred in 26 of 394 patients with DCBs (6.7%) and 20 of 379 (5.3%) with DES (HR: 1.03; 95% CI: 0.53-2.01; P = 0.934). CONCLUSIONS: DCBs were associated with a numerically comparable risk for DoCE compared with DES in noncomplex bifurcations at 2 years. However, these findings should be interpreted as hypothesis generating only. (Paclitaxel-Coated Balloon for Treatment of De-Novo Non-Complex Coronary Artery Lesions; NCT04561739).
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