TY - JOUR
T1 - New-generation drug-eluting stents for left main coronary artery disease according to the EXCEL trial enrollment criteria
T2 - Insights from the all-comers, international, multicenter DELTA-2 registry
AU - DELTA 2 Investigators
AU - Tanaka, Akihito
AU - Giustino, Gennaro
AU - Briede, Ieva
AU - Sawaya, Fadi J.
AU - Daemen, Joost
AU - Kawamoto, Hiroyoshi
AU - Meliga, Emanuele
AU - D'Ascenzo, Fabrizio
AU - Cerrato, Enrico
AU - Stefanini, Giulio G.
AU - Capodanno, Davide
AU - Mangiameli, Andrea
AU - Templin, Christian
AU - Erglis, Andrejs
AU - Morice, Marie Claude
AU - Mehran, Roxana
AU - Van Mieghem, Nicolas M.
AU - Nakamura, Sunao
AU - De Benedictis, Mauro
AU - Pavani, Marco
AU - Varbella, Ferdinando
AU - Pisaniello, Marco
AU - Sharma, Samin K.
AU - Tamburino, Corrado
AU - Tchetche, Didier
AU - Colombo, Antonio
AU - Chieffo, Alaide
N1 - Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2019/4/1
Y1 - 2019/4/1
N2 - Background: Percutaneous coronary intervention (PCI) has been established as an alternative treatment option to coronary artery by-pass graft (CABG) surgery in patients with left main coronary artery disease (LMCAD). Whether the findings of randomized controlled trials are applicable to a real-world patient population is unclear. Methods: We compared the outcomes of PCI with new-generation DES in the all-comer, international, multicenter DELTA-2 registry retrospectively evaluating mid-term clinical outcomes with the historical CABG cohort enrolled in the DELTA-1 registry according to the EXCEL key inclusion or exclusion criteria. The primary endpoint was the composite of death, myocardial infarction, or stroke at the median time of follow-up time of 501 days. The consistency of the effect of DELTA-2 PCI versus DELTA-1 CABG according to the EXCEL enrollment criteria was tested using propensity score-adjusted Cox regression models. Results: Out of 3986 patients enrolled in the DELTA-2 PCI registry, 2418 were EXCEL candidates and 1568 were not EXCEL candidates. The occurrence of the primary endpoint was higher among non-EXCEL candidates compared with EXCEL candidates (15.4% vs. 6.9%; hazard ratio 2.52; 95% confidence interval 2.00–3.16; p < 0.001). Among 901 patients enrolled in the historical DELTA-1 CABG cohort, 471 were EXCEL candidates and 430 were not EXCEL candidates. When comparing the DELTA-2 PCI with the DELTA-1 CABG cohort, the occurrence of the primary endpoint was lower in the PCI group compared with the historical CABG cohort among EXCEL candidates (6.9% vs. 10.7%; adjusted hazard ratio: 0.65; 95% confidence interval: 0.45–0.92), while no significant difference was observed among non-EXCEL candidates (15.4% vs. 12.5%; adjusted hazard ratio: 0.94; 95% confidence interval: 0.67–1.33) with evidence of statistical interaction (adjusted interaction p-value = 0.002). Conclusions: In a real-world population, PCI can be selected more favorably as an alternative to CABG in patients fulfilling the enrollment criteria of the EXCEL trial.
AB - Background: Percutaneous coronary intervention (PCI) has been established as an alternative treatment option to coronary artery by-pass graft (CABG) surgery in patients with left main coronary artery disease (LMCAD). Whether the findings of randomized controlled trials are applicable to a real-world patient population is unclear. Methods: We compared the outcomes of PCI with new-generation DES in the all-comer, international, multicenter DELTA-2 registry retrospectively evaluating mid-term clinical outcomes with the historical CABG cohort enrolled in the DELTA-1 registry according to the EXCEL key inclusion or exclusion criteria. The primary endpoint was the composite of death, myocardial infarction, or stroke at the median time of follow-up time of 501 days. The consistency of the effect of DELTA-2 PCI versus DELTA-1 CABG according to the EXCEL enrollment criteria was tested using propensity score-adjusted Cox regression models. Results: Out of 3986 patients enrolled in the DELTA-2 PCI registry, 2418 were EXCEL candidates and 1568 were not EXCEL candidates. The occurrence of the primary endpoint was higher among non-EXCEL candidates compared with EXCEL candidates (15.4% vs. 6.9%; hazard ratio 2.52; 95% confidence interval 2.00–3.16; p < 0.001). Among 901 patients enrolled in the historical DELTA-1 CABG cohort, 471 were EXCEL candidates and 430 were not EXCEL candidates. When comparing the DELTA-2 PCI with the DELTA-1 CABG cohort, the occurrence of the primary endpoint was lower in the PCI group compared with the historical CABG cohort among EXCEL candidates (6.9% vs. 10.7%; adjusted hazard ratio: 0.65; 95% confidence interval: 0.45–0.92), while no significant difference was observed among non-EXCEL candidates (15.4% vs. 12.5%; adjusted hazard ratio: 0.94; 95% confidence interval: 0.67–1.33) with evidence of statistical interaction (adjusted interaction p-value = 0.002). Conclusions: In a real-world population, PCI can be selected more favorably as an alternative to CABG in patients fulfilling the enrollment criteria of the EXCEL trial.
KW - DELTA-2 registry
KW - Drug-eluting stents
KW - EXCEL trial
KW - Left main coronary artery
UR - http://www.scopus.com/inward/record.url?scp=85059188300&partnerID=8YFLogxK
U2 - 10.1016/j.ijcard.2018.12.003
DO - 10.1016/j.ijcard.2018.12.003
M3 - Article
C2 - 30595357
AN - SCOPUS:85059188300
SN - 0167-5273
VL - 280
SP - 30
EP - 37
JO - International Journal of Cardiology
JF - International Journal of Cardiology
ER -