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Long-term efficacy and safety of moderate-intensity statin with ezetimibe combination therapy versus high-intensity statin monotherapy in patients with atherosclerotic cardiovascular disease (RACING): a randomised, open-label, non-inferiority trial

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dc.contributor.authorKim, Byeong Keuk-
dc.contributor.authorHong, Sung Jin-
dc.contributor.authorLee, Yong Joon-
dc.contributor.authorHong, S.J.-
dc.contributor.authorYun, K.H.-
dc.contributor.authorHong, Bum Kee-
dc.contributor.authorHeo, J.H.-
dc.contributor.authorRha, S.-W.-
dc.contributor.authorCho, Y.-H.-
dc.contributor.authorLee, Seung Jun-
dc.contributor.authorAhn , Chul Min-
dc.contributor.authorKim, Jung Sun-
dc.contributor.authorKo, Young Guk-
dc.contributor.authorChoi, Dong Hoon-
dc.contributor.authorJang, Y.-
dc.contributor.authorHong, Myeong Ki-
dc.date.accessioned2022-12-22T02:48:42Z-
dc.date.available2022-12-22T02:48:42Z-
dc.date.created2023-02-07-
dc.date.issued2022-07-
dc.identifier.issn0140-6736-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/191703-
dc.description.abstractBackground: Drug combinations rather than increasing doses of one drug can achieve greater efficacy and lower risks. Thus, as an alternative to high-intensity statin monotherapy, moderate-intensity statin with ezetimibe combination therapy can lower LDL cholesterol concentrations effectively while reducing adverse effects. However, evidence from randomised trials to compare long-term clinical outcomes is needed. Methods: In this randomised, open-label, non-inferiority trial, patients with atherosclerotic cardiovascular disease (ASCVD) at 26 clinical centres in South Korea were randomly assigned (1:1) to receive either moderate-intensity statin with ezetimibe combination therapy (rosuvastatin 10 mg with ezetimibe 10 mg) or high-intensity statin monotherapy (rosuvastatin 20 mg). The primary endpoint was the 3-year composite of cardiovascular death, major cardiovascular events, or non-fatal stroke, in the intention-to-treat population with a non-inferiority margin of 2·0%. This trial is registered with ClinicalTrials.gov, NCT03044665 and is complete. Findings: Between Feb 14, 2017, and Dec 18, 2018, 3780 patients were enrolled: 1894 patients to the combination therapy group and 1886 to the high-intensity statin monotherapy group. The primary endpoint occurred in 172 patients (9·1%) in the combination therapy group and 186 patients (9·9%) in the high-intensity statin monotherapy group (absolute difference −0·78%; 90% CI −2·39 to 0·83). LDL cholesterol concentrations of less than 70 mg/dL at 1, 2, and 3 years were observed in 73%, 75%, and 72% of patients in the combination therapy group, and 55%, 60%, and 58% of patients in the high-intensity statin monotherapy group (all p<0·0001). Discontinuation or dose reduction of the study drug by intolerance was observed in 88 patients (4·8%) and 150 patients (8·2%), respectively (p<0·0001). Interpretation: Among patients with ASCVD, moderate-intensity statin with ezetimibe combination therapy was non-inferior to high-intensity statin monotherapy for the 3-year composite outcomes with a higher proportion of patients with LDL cholesterol concentrations of less than 70 mg/dL and lower intolerance-related drug discontinuation or dose reduction. Funding: Hanmi Pharmaceutical.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherElsevier-
dc.relation.isPartOfThe Lancet-
dc.relation.isPartOfLANCET-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleLong-term efficacy and safety of moderate-intensity statin with ezetimibe combination therapy versus high-intensity statin monotherapy in patients with atherosclerotic cardiovascular disease (RACING): a randomised, open-label, non-inferiority trial-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorKim, Byeong Keuk-
dc.contributor.googleauthorHong, Sung Jin-
dc.contributor.googleauthorLee, Yong Joon-
dc.contributor.googleauthorHong, S.J.-
dc.contributor.googleauthorYun, K.H.-
dc.contributor.googleauthorHong, Bum Kee-
dc.contributor.googleauthorHeo, J.H.-
dc.contributor.googleauthorRha, S.-W.-
dc.contributor.googleauthorCho, Y.-H.-
dc.contributor.googleauthorLee, Seung Jun-
dc.contributor.googleauthorAhn , Chul Min-
dc.contributor.googleauthorKim, Jung Sun-
dc.contributor.googleauthorKo, Young Guk-
dc.contributor.googleauthorChoi, Dong Hoon-
dc.contributor.googleauthorJang, Y.-
dc.contributor.googleauthorHong, Myeong Ki-
dc.identifier.doi10.1016/S0140-6736(22)00916-3-
dc.relation.journalcodeJ02152-
dc.identifier.eissn1474-547X-
dc.identifier.pmid35863366-
dc.contributor.alternativeNameKo, Young Guk-
dc.contributor.affiliatedAuthorKim, Byeong Keuk-
dc.contributor.affiliatedAuthorHong, Sung Jin-
dc.contributor.affiliatedAuthorLee, Yong Joon-
dc.contributor.affiliatedAuthorHong, Bum Kee-
dc.contributor.affiliatedAuthorLee, Seung Jun-
dc.contributor.affiliatedAuthorAhn , Chul Min-
dc.contributor.affiliatedAuthorKim, Jung Sun-
dc.contributor.affiliatedAuthorKo, Young Guk-
dc.contributor.affiliatedAuthorChoi, Dong Hoon-
dc.contributor.affiliatedAuthorHong, Myeong Ki-
dc.identifier.scopusid2-s2.0-85134939573-
dc.identifier.wosid000923290700023-
dc.citation.volume400-
dc.citation.number10349-
dc.citation.startPage380-
dc.citation.endPage390-
dc.identifier.bibliographicCitationThe Lancet, Vol.400(10349) : 380-390, 2022-07-
dc.identifier.rimsid77488-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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