Abstract
LDL-C is the pivotal risk factor for atherosclerotic cardiovascular disease, and the benefit from LDL-C lowering is proportional to the magnitude of reduction. Clinical trials demonstrate that evolocumab reduces LDL-C levels by approximately 60% when measured at the trough of drug effect, which may underestimate cumulative LDL-C reduction. We obtained a time-averaged estimate of LDL-C lowering that included both peaks and troughs. Pooled analysis of 5 phase 2 trials included patients with hypercholesterolemia who received placebo or evolocumab (140 mg every 2 weeks [Q2W] or 420 mg monthly [QM]). Percent changes from baseline LDL-C and free serum PCSK9 were averaged across weeks 9–12. In 372 patients, time-averaged percent reduction from baseline in LDL-C with evolocumab vs placebo was 67.6% (95% CI: 63.9–71.3) with Q2W dosing and 65.0% (95% CI: 60.7–69.3) with QM dosing. The time-averaged measure yielded LDL-C reductions for evolocumab that exceeded measurements at the end of dosing intervals and may provide a better estimate of cardiovascular benefit during long-term therapy.
| Original language | English |
|---|---|
| Pages (from-to) | 538-543 |
| Number of pages | 6 |
| Journal | Journal of Clinical Lipidology |
| Volume | 16 |
| Issue number | 4 |
| DOIs | |
| State | Published - 1 Jul 2022 |
Keywords
- Cardiovascular risk reduction
- Evolocumab
- Hypercholesterolemia
- Lipid lowering
- Methods
- PCSK9 inhibitor