• Bone Health
  • Immunology
  • Hematology
  • Respiratory
  • Dermatology
  • Diabetes
  • Gastroenterology
  • Neurology
  • Oncology
  • Ophthalmology
  • Rare Disease
  • Rheumatology

Anti-VEGF Drugs Not Associated With Increased Risk of AEs in Eye Diseases

Article

Last week, an overview of systematic reviews and meta-analyses investigating systemic adverse events associated with intravitreal anti-vascular endothelial growth factor (anti-VEGF) treatments was published in JAMA Ophthalmology.

Last week, an overview of systematic reviews and meta-analyses investigating systemic adverse events associated with intravitreal anti-vascular endothelial growth factor (anti-VEGF) treatments was published in JAMA Ophthalmology. The review encompassed adverse events (AEs) in patients with neovascular age-related macular degeneration (AMD), diabetic macular edema (DME), and retinal vein occlusion (RVO) being treated with the intravitreal anti-VEGF agents ranibizumab and bevacizumab.

Researchers analyzed 21 systematic reviews published between January 1, 2011, and June 30, 2016. Of these, 11 analyzed serious AEs as the primary outcome, and the remaining 10 considered serious AEs secondary endpoints. The reviews were screened for quality.

This research found that the studies investigated largely agreed that anti-VEGF treatments were not associated with an increased risk of serious AEs in eye indications; 10 reviews studied patients with AMD that included 2 to 12 randomized controlled trials (RCTs) each, and overlapping comparisons were observed for 7 reviews. Six reviews studied patients with DME, and included 4 to 18 RCTs each, with overlapping comparisons found in 4 reviews. Lastly, 3 reviews analyzed serious AEs as the primary outcome and included patients with all 3 diseases.

In total, 19 serious AEs were reported in the AMD group (among 15,102 patients), 7 were reported in the DME group (among 5357 patients), and 6 were reported in the RVO group (among 1349 patients). Eight were reported in a grouped analysis of patients with AMD, DME, and RVO.

The authors noted some potential limitations of the study: reviews were only included if they reported 95% confidence intervals for serious AEs. In addition, researchers did not re-extract data from original research, which was deemed to be outside the scope of their review. Finally, the risks related to the duration of various treatments as well as AEs related to drug doses were not analyzed due to data not being reported in the included meta-analyses.

The overview of prior reviews and meta-analyses suggests that anti-VEGF treatments do not increase the risk of AEs. However, the authors advise caution in older patients with AMD who may be at a higher risk of hemorrhagic events when taking ranibizumab.

Reference

Thulliez M, Angoulvant D, Pisella PJ, et al. Overview of systematic reviews and meta-analyses on systemic adverse events associated with intravitreal anti-vascular endothelial growth factor medication use. JAMA Opthalmol. Published online March 22, 2018. doi:10.1001/jamaophthalmol.2018.0002.

Recent Videos
Elie Bahou, MD, PhD
Steve Pickette, PharmD
global biosimilars week join the movement
Sophia Humphreys, PharmD
Lakesha Farmer, PharmD
Brian Biehn
GBW 2023 webinar
Stephen Hanauer, MD, professor of medicine, Feinberg School of Medicine, Northwestern University,
Stephen Hanauer, MD, professor of medicine, Feinberg School of Medicine, Northwestern University,
"SEEING EYE TO EYE:  Exploring Different Perspectives on Ophthalmology Biosimilars SEEING EYE TO EYE:  Exploring Different Perspectives on Ophthalmology Biosimilars" with the CfB logo and an image of an eye
Related Content
© 2024 MJH Life Sciences

All rights reserved.