Greater LDL-c reduction by PCSK9i in FH patients in time-averaged analysis
Time-averaged low-density lipoprotein cholesterol lowering with evolocumab: Pooled analysis of phase 2 trials
Literature - Schludi B, Giugliano RP, Sabatine MS, et al. - J Clin Lipidol. 2022 Jun 6;S1933-2874(22)00174-X. doi: 10.1016/j.jacl.2022.05.069.Introduction and methods
Background
In the long term, the PCSK9 inhibitor evolocumab lowers LDL-c concentration by approximately 60%, compared with placebo, according to multiple randomized trials [1-3]. However, in these trials, the effect of evolocumab was evaluated at the end of the dosing interval (i.e., the trough of drug effect), which may underestimate the treatment effect. To more accurately determine the effect of evolocumab, it is better to average the LDL-c concentration over a longer period of time, which includes both peaks and troughs of the drug effect.
Aim of the study
This pooled analysis of data from patients with familial hypercholesterolemia from multiple phase 2 studies examined the LDL-c lowering effect of evolocumab based on time-averaged measurements and compared it with placebo.
Methods
The researchers conducted a pooled analysis of data from 5 phase 2 studies in which patients with familial hypercholesterolemia (n=372) were randomized to evolocumab (140 mg every 2 weeks or 420 mg monthly) or placebo. Patient data were used only if the patient's LDL-c concentration had been measured at baseline and he or she was still being treated with evolocumab or placebo after 8 and 10 weeks (when treated every 2 weeks) or after 8 weeks (when treated monthly). LDL-c concentration was calculated using both the Martin-Hopkins formula and the Friedewald formula. For each patient, the percentage decrease in LDL-c concentration relative to the LDL-c concentration at baseline was averaged over a 4-week period (weeks 9-12). A similar analysis was performed for the serum concentration of free PCSK9.
Outcomes
The researchers were interested in the time-averaged percent reduction in concentrations of LDL-C and free PCSK9 by treatment with evolocumab, compared with placebo.
Main results
- The time-averaged percent reduction in the concentration of LDL-c was 67.6% (95%CI: 63.9-71.3) by treatment with evolocumab 140 mg every 2 weeks and 65.0% (95%CI: 60.7-69.3) by monthly treatment with evolocumab 420 mg, compared with placebo.
- Calculation of LDL-C concentration using the Martin-Hopkins or Friedewald formula yielded similar results.
- The time-averaged percent reduction in the serum concentration of free PCSK9 was 81.9% (95%CI: 76.1-87.8) by treatment with evolocumab 140 mg every 2 weeks and 77.4% (95%CI: 72.5-82.4) by monthly treatment with evolocumab 420 mg, compared with placebo.
Conclusion
This pooled analysis shows that the LDL-c lowering effect of evolocumab is greater when the LDL-c concentration is averaged over a longer period of time rather than measured at the end of the dosing interval. The authors concluded that time-averaged measurements of the LDL-c concentration may better reflect the likely long-term treatment effect of PCSK9 inhibitors.
References
1. Koren MJ, Sabatine MS, Giugliano RP, et al. Long-term efficacy and safety of evolocumab in patients with hypercholesterolemia. J Am Coll Cardiol. 2019;74:2132-2146. doi: 10.1016/j.jacc.2019.08.1024.
2. Sabatine MS, Giugliano RP, Wiviott SD, et al; Open-Label Study of Long-Term Evaluation against LDL Cholesterol (OSLER) Investigators. Efficacy and safety of evolocumab in reducing lipids and cardiovascular events. N Engl J Med . 2015;372:1500-1509. doi: 10.1056/NEJMoa1500858.
3. Blom DJ, Hala T, Bolognese M, et al; DESCARTES Investigators. A 52-week placebo-controlled trial of evolocumab in hyperlipidemia N Engl J Med . 2014;370:1809-1819. doi: 10.1056/NEJMoa1316222