Effect of alirocumab dose increase on LDL lowering and lipid goal attainment in patients with dyslipidemia

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Effect of alirocumab dose increase on LDL lowering and lipid goal attainment in patients with dyslipidemia

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Title: Effect of alirocumab dose increase on LDL lowering and lipid goal attainment in patients with dyslipidemia
Author: Kastelein, John J.P.; Kereiakes, Dean J.; Cannon, Christopher P.; Bays, Harold E.; Minini, Pascal; Lee, L. Veronica; Maroni, Jaman; Farnier, Michel

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Citation: Kastelein, John J.P., Dean J. Kereiakes, Christopher P. Cannon, Harold E. Bays, Pascal Minini, L. Veronica Lee, Jaman Maroni, and Michel Farnier. 2017. “Effect of alirocumab dose increase on LDL lowering and lipid goal attainment in patients with dyslipidemia.” Coronary Artery Disease 28 (3): 190-197. doi:10.1097/MCA.0000000000000438. http://dx.doi.org/10.1097/MCA.0000000000000438.
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Abstract: Objectives: The objective of this study is to report the dose response in ODYSSEY phase 3 clinical trials of proprotein convertase subtilisin kexin type 9 inhibition with alirocumab in patients not at prespecified lipid goals who received a per-protocol dose increase from 75 every 2 weeks (Q2W) to 150 mg Q2W. Methods: Patients (n=2181) receiving statins were enrolled in six phase 3 randomized, double-blind, double-dummy trials (24–104 weeks): alirocumab versus placebo or ezetimibe 10 mg/day. The 75 mg subcutaneous Q2W dose was increased to 150 mg at week 12 if week 8 LDL cholesterol (LDL-C) was greater than or equal to 70 mg/dl (>100 mg/dl in OPTIONS studies for patients without previous coronary heart disease, but with other risk factors). LDL-C percentage reductions from baseline (on-treatment data, n=1291) were compared at week 12 versus week 24. Results: Most patients (n=951; 73.7%) with 75 mg Q2W dose plus background statin achieved LDL-C less than 70 or less than 100 mg/dl at week 8. In 340 (26.3%) patients, alirocumab dose was increased to 150 mg Q2W at week 12, and 60.9% of these patients achieved LDL-C goals at week 24, with an additional 14.2% reduction in LDL-C from week 12 to week 24. Adverse event rates were comparable in patients with versus without a dose increase (72.4 vs. 71.8% in placebo-controlled trials; 67.0 vs. 67.6% in ezetimibe-controlled trials). Conclusion: Most patients achieved LDL-C goals with alirocumab 75 mg Q2W plus statins. Of those (26.3%) receiving a dose increase, 60.9% achieved LDL-C goals at week 24 with an additional 14.2% reduction in LDL-C.
Published Version: doi:10.1097/MCA.0000000000000438
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5400401/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:32630480
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