An advance report on the benefits of antidrug antibodies in substantially reducing levels of LDL-cholesterol, from data presented at the American College of Cardiology (ACC) Meeting in Washington DC.
The SPIRE development programme of the humanised PCSK9 inhibitor bococizumab has shown that the development of antidrug antibodies in 15–20% of patients attenuated the substantial reduction in LDL cholesterol (LDL-C) and that in terms of cardiovascular outcomes there was benefit in patients with a baseline LDL-C >100mg/dL but not for a baseline LDL-C <100mg/dL.
The results of the multinational trials were presented the ACC and published simultaneously in the New England Journal of Medicine. The cardiovascular outcomes studies, SPIRE-1 and SPIRE-2 were stopped prematurely in November 2016 after the lipid-lowering trial results led the sponsor to discontinue the drug’s development.
Lipid-lowering results were reported for 4,449 high-risk patients (mean age 61 years, 42% women, LDL-C 122mg/dL) who were treated with maximally tolerated doses of a statin (86% on high-intensity statin) and bococizumab 150mg subcutaneously every two weeks or placebo. The 54.2% reduction in LDL-C seen at 12 weeks with bococizumab was attenuated to 43% at 52 weeks—and in the 16% of patients who developed antibodies this attenuation was greater at 31% The attenuation in LDL-C reduction was greater with higher antibody levels. Further, the reductions in LDL-C were highly variable within patients, regardless of antibody status. In the lipid-lowering studies, there was a similar rate of major adverse cardiovascular events with bococizumab and placebo at 2.5% and 2.7%, respectively.
In the SPIRE-1 outcomes study of 16,817 patients with an LDL-C >70mg/dL, at seven months there was no difference in the primary endpoint of non-fatal myocardial infarction, non-fatal stroke, hospitalisation for unstable angina requiring urgent revascularisation or cardiovascular death. However, in the SPIRE-2 study of 10,621 patients with an LDL-C >100mg/dL, at 12 months there was a 21% reduction in the primary endpoint. Analyses of the combined results for SPIRE-1 and SPIRE-2 revealed that a larger reduction in LDL cholesterol and a longer duration of treatment were both associated with significantly better outcomes.
The investigators stated that the clinical benefits were greater and statistically significant in subgroup analyses in patients who had and sustained greater absolute and proportionate reductions in LDL-C and that this is consistent with the “lower is better for longer” hypothesis. They also state their data support the use of PCSK9 inhibitors on top of aggressive statin therapy in selected patients.