The effect of volanesorsen treatment on the burden associated with familial chylomicronemia syndrome: the results of the ReFOCUS study.

Abstract

BACKGROUND:

Volanesorsen, an investigational inhibitor of apoC-III synthesis, significantly reduced triglyceride levels in clinical trials in patients with familial chylomicronemia syndrome (FCS), a rare genetic disorder characterized by marked chylomicronemia leading to a spectrum of symptoms, including recurrent abdominal pain and episodes of potentially fatal acute pancreatitis (AP).

OBJECTIVE:

To determine the effect of volanesorsen on burden of disease on patients with FCS Methods: ReFOCUS was a retrospective global web-based survey open to patients with FCS who received volanesorsen for ≥3 months in an open-label extension study. The survey included questions about patients' experiences before and after volanesorsen treatment.

RESULTS:

Twenty-two respondents had received volanesorsen for a median of 222 days. Volanesorsen significantly reduced the number of symptoms per patient across physical, emotional, and cognitive domains. Significant reductions from baseline were reported for steatorrhea, pancreatic pain, and constant worry about an attack of pain/AP. Respondents reported that volanesorsen improved overall management of symptoms and reduced interference of FCS with work/school responsibilities. Reductions in the negative impact of FCS on personal, social, and professional life were also reported.

CONCLUSIONS:

Treatment with volanesorsen has the potential to reduce disease burden in patients with FCS through modulation of multiple symptom domains.

• Authors: Marcello Arca, Andrew Hsieh, Handrean Soran, Paul Rosenblit, Louis O'Dea, Michael Stevenson
• Journal: Expert review of cardiovascular therapy (Expert Rev Cardiovasc Ther) Vol. 16 Issue 7 Pg. 537-546 (Jul 2018) ISSN: 1744-8344 [Electronic] England
• PMID: 29889589 (Publication Type: Journal Article)

Chemical References

• Apolipoprotein C-III
• ISIS 304801
• Oligonucleotides

Topics

• Adult
• Aged
• Apolipoprotein C-III (antagonists & inhibitors)
• Female
• Humans
• Hyperlipoproteinemia Type I (drug therapy)
• Male
• Middle Aged
• Oligonucleotides (therapeutic use)
• Retrospective Studies