Eylea Bests Avastin, Lucentis in Diabetic Macular Edema With Worse Vision Loss

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Eylea Bests Avastin, Lucentis in Diabetic Macular Edema With Worse Vision Loss
Eylea Bests Avastin, Lucentis in Diabetic Macular Edema With Worse Vision Loss

Aflibercept (Eylea), bevacizumab (Avastin) and ranibizumab (Lucentis) all improved vision in patients with diabetic macular edema, but treatment with aflibercept resulted in greater improvement in those with worse baseline levels of visual acuity, according to data published in the New England Journal of Medicine.

“This comparative effectiveness study will help doctors and patients make informed decisions when choosing treatments for diabetic macular edema,” Paul A Sievivng, MD, PhD, director of the NIH's National Eye Institute (NEI) which sponsored the study, said in a press release.

In the study, the researchers randomly assigned 660 adults (mean age, 61 years) at 89 clinical sites to receive intravitreous aflibercept 2.0 mg (n=224), bevacizumab 1.25 mg (n=218) or ranibizumab 0.3 mg (n=218), administered as often as every 4 weeks according to a protocol-specified algorithm.

All patients had diabetic macular edema involving the macular center. Ninety percent of patients had type 2 diabetes, with a mean duration of diabetes of 17 years. Mean baseline visual-acuity letter score was 64 (Snellen equivalent, 20/50), and mean central subfield thickness was 412 mcm.

Results showed that mean visual-acuity letter score (range, 0 to 100, with higher scores indicating better visual acuity, and a score of 85 being approximately 20/20) improved by 13.3 with aflibercept, 9.7 with bevacizumab and 11.2 with ranibizumab.

Although the researchers observed greater improvement with aflibercept compared with bevacizumab (P<.001) and ranibizumab (P=.03), the difference was not clinically meaningful, as it was primarily driven by eyes with worse baseline visual acuity (P<.001 for interaction).

Specifically, when the initial visual-acuity letter score was less than 69 (Snellen equivalent, 20/50 or worse), the mean improvement was 18.9 with aflibercept, 11.8 with bevacizumab and 14 with ranibizumab, respectively (P<.001 for aflibercept vs. bevacizumab, P=.003 for aflibercept vs. ranibizumab, and P=0.21 for ranibizumab vs. bevacizumab).

However, when visual-acuity letter score was 78 to 69 (equivalent to about 20/32 to 20/40), mean improvement was 8.0 with aflibercept, 7.5 with bevacizumab and 8.3 with ranibizumab (P>.50 for each pairwise comparison), suggesting the drugs were comparable in this patient population, according to the data.

No significant differences in the rates of serious adverse events (P=.40), hospitalization (P=.51), death (P=.072) or major cardiovascular (CV) events (P=.56) were noted.

The researchers also found that all three drugs reduced swelling of the macula, but aflibercept and ranibizumab reduced swelling more than bevacizumab. Further, fewer patients taking aflibercept underwent laser treatment for persistent edema that did not resolve with treatment alone vs. those on bevacizumab or ranibizumab (36% vs. 56% and 46%, respectively).

“Eylea, Avastin and Lucentis yield substantial gains in visual acuity for most people with diabetic macular edema; however, on average, Eylea appears to provide additional benefit for patients who start treatment with moderate or worse vision loss,” John A. Wells, MD, the lead author of the study and a retinal specialist at the Palmetto Retina Center in Columbia, South Carolina, said in the release.

In an accompanying editorial, Daniel F. Martin, MD, of the Cleveland Clinic Cole Eye Institute, and Maureen G. Maguire, PhD, of the University of Pennsylvania in Philadelphia, discussed the findings and addressed the considerations around which of these drugs may be best for various patients.

“Aflibercept should be considered as first-line therapy in [patients with a visual acuity of 20/50 or worse], with bevacizumab as the alternative given the lack of a significant difference in visual outcome between bevacizumab and ranibizumab and the large difference in cost between the two drugs,” the researchers wrote.

“… We believe that all financial incentives and logistic barriers to providing the least expensive drug, among drugs equivalent in safety and efficacy, should be eliminated so that patients may fully benefit from the results of this Diabetic Retinopathy Clinical Research Network trial as well as those from other comparative trials.”

References

  1. The Diabetic Retinopathy Clinical Research Network. N Engl J Med. 2015;doi:10.1056/NEJMoa1414264.
  2. Martin DF, Maguire MG. N Engl J Med. 2015;doi:10.1056/NEJMe1500351.
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