CBS 2019
CBSMD教育中心
English

科学研究

科研文章

荐读文献

Randomized study of doxorubicin-based chemotherapy regimens, with and without sildenafil, with analysis of intermediate cardiac markers Short-Term Oral Anticoagulation Versus Antiplatelet Therapy Following Transcatheter Left Atrial Appendage Closure Risk of Cardiovascular Diseases Among Older Breast Cancer Survivors in the United States: A Matched Cohort Study 2020 ACC Expert Consensus Decision Pathway on Management of Bleeding in Patients on Oral Anticoagulants: A Report of the American College of Cardiology Solution Set Oversight Committee High Coronary Shear Stress in Patients With Coronary Artery Disease Predicts Myocardial Infarction Mathematical modelling of endovascular drug delivery: balloons versus stents Thirty-Day Outcomes Following Transfemoral Transseptal Transcatheter Mitral Valve Replacement: Intrepid TMVR Early Feasibility Study Results MITRA-FR vs. COAPT: Lessons from two trials with diametrically opposed results Ablation Versus Drug Therapy for Atrial Fibrillation in Heart Failure Results From the CABANA Trial Treatment Effects of Pulmonary Artery Denervation for Pulmonary Arterial Hypertension Stratified by REVEAL Risk Score: Results from PADN-CFDA Trial

Expert Opinion2018 Apr 24;137(17):1763-1766

JOURNAL:Circulation. Article Link

Mortality Differences Associated With Treatment Responses in CANTOS and FOURIER: Insights and Implications

Ridker PM Keywords: atherosclerosis; canakinumab; evolocumab; mortality; prevention and control; randomized controlled trials as topic

ABSTRACT


Similarities and differences in 2 contemporary postrandomization on-treatment analyses from the FOURIER trial (Further Cardiovascular Outcomes Research With PCSK9 Inhibition in Subjects With Elevated Risk) and CANTOS trial (Canakinumab Antiinflammatory Thrombosis Outcome Study) may provide insight into what factors drive reductions in cardiovascular mortality and all-cause mortality among patients with atherosclerosis already treated with high-intensity statins.

In the first article, the FOURIER Investigators elegantly demonstrate that lower is better for low-density lipoprotein cholesterol (LDLC) after adjunctive therapy with the proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor evolocumab. For the FOURIER primary end point (a composite of myocardial infarction, stroke, coronary revascularization, unstable angina, or cardiovascular death), there was a highly significant monotonic relationship between sequentially lower achieved LDLC concentrations and lower cardiovascular risk, extending even to those with on-treatment LDLC <20 mg/dL. This benefit was driven largely by statistically significant reductions in the trial composite end point among those with LDLC levels below the approximate on-treatment median of 50 mg/dL (for which hazard ratios ranged between 0.76 and 0.85). In contrast, marginal and nonsignificant reductions were observed among those in FOURIER with on-treatment LDLC levels >50 mg/dL (for which hazard ratios ranged from 0.94–0.97). These PCSK9 data are important because evolocumab has powerful effects on LDLC but no effect on high-sensitivity C-reactive protein (hs-CRP).

In the second article, the CANTOS Investigators similarly demonstrate that lower is better for inflammation reduction, at least with the interleukin-1β inhibitor canakinumab.2 For the CANTOS primary end point (a composite of myocardial infarction, stroke, or cardiovascular death), there was a highly significant 25% reduction among those with on-treatment hs-CRP levels below the approximate on-treatment median of 2 mg/L. In contrast, marginal and nonsignificant reductions …