TY - JOUR
T1 - Five-Year Outcomes of Ranibizumab With Prompt or Deferred Laser Versus Laser or Triamcinolone Plus Deferred Ranibizumab for Diabetic Macular Edema
AU - Diabetic Retinopathy Clinical Research Network (DRCR.net)
AU - Bressler, Susan B.
AU - Glassman, Adam R.
AU - Almukhtar, Talat
AU - Bressler, Neil M.
AU - Ferris, Frederick L.
AU - Googe, Joseph M.
AU - Gupta, Shailesh K.
AU - Jampol, Lee M.
AU - Melia, Michele
AU - Wells, John A.
N1 - Funding Information:
Writing Committee financial disclosures: Neil M. Bressler: Grants to investigators at The Johns Hopkins University (Baltimore, MD) are negotiated and administered by the institution (such as the School of Medicine), which receives the grants, typically through the Office of Research Administration. Individual investigators who participate in the sponsored project(s) are not compensated directly by the sponsor, but may receive salary or other support from the institution to support their effort on the projects(s). Dr Bressler is principal investigator of grants at The Johns Hopkins University sponsored by the Bayer (Whippany, NJ), Genentech, Inc (South San Francisco, CA), Novartis Pharma AG (East Hanover, NJ), Regeneron (Tarrytown, NY), and the Emmes Corporation (Rockville, MD) through the Office of Research Administration of the Johns Hopkins University School of Medicine, and has a contract agreement from the American Medical Association to the Johns Hopkins University School of Medicine. A complete list of all DRCR.net investigator financial disclosures can be found at www.drcr.net .
Funding Information:
Funding Support: Supported through cooperative agreements from the National Eye Institute and the National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland (EY14231, EY23207, and EY18817). The funding organization (National Institutes of Health, Bethesda, MD) participated in oversight of the conduct of the study and review of the manuscript, but not directly in the design or conduct of the study; nor in the collection, management, analysis, or interpretation of the data; nor in the preparation of the manuscript. Genentech (South San Francisco, CA) provided the ranibizumab for the study. In addition, Genentech provided funds to DRCR.net to defray the study's clinical site costs. As described in the Diabetic Retinopathy Clinical Research Network ( DRCR.net ) Industry Collaboration Guidelines (available at www.drcr.net ), the DRCR.net had complete control over the design of the protocol, ownership of the data, and all editorial content of presentations and publications related to the protocol. Financial disclosures: Susan B. Bressler: Novartis (East Hanover, NJ), Research to Prevent Blindness (New York, NY), Boehringer-Ingelheim (Ridgefield, CT), Notal Vision (Chantilly, VA), Bayer (Whippany, NJ) (Research Grants, Expert Testimony). Adam R. Glassman: National Eye Institute (Bethesda, MD) (Grants). Neil M. Bressler: Grants to his institution for research agreements for which he is Principal Investigator: Bayer (Whippany, NJ), Genentech/Roche (South San Francisco, CA), Lumenis (San Jose, CA), Novartis (East Hanover, NJ), Optovue (Fremont, CA), Regeneron (Tarrytown, NY). Frederick L. Ferris: Royalties from Bausch and Lomb (Rochester, NY) for AMD nutritional supplements. Michele Melia: National Eye Institute (Bethesda, MD) (Grants, Personal Fees), National Institute on Deafness and Other Communication Disorders (Bethesda, MD) (Personal Fees), Alimera Sciences (Alpharetta, GA) (Personal Fees). John A. Wells III: Consulting fees from Iconic (South San Francisco, CA) and Panoptica (Mount Arlington, NJ), and travel reimbursement from the Jaeb Center (Tampa, FL); investigator in clinical trials for Ampio (Englewood, CO), Emmes (Rockville, MD), Genentech (South San Francisco, CA), Iconic (South San Francisco, CA), Jaeb Center for Health Research (Tampa, FL), Kalvista (Boston, MA), LPath (San Diego, CA), Neurotech (Cumberland, RI), Ophthotech (New York, NY), Panoptica (Mount Arlington, NJ), Regeneron (Tarrytown, NY), and Santen (Emeryville, CA). The following authors have no financial disclosures: Talat Almukhtar, Joseph M. Googe Jr, Shailesh K. Gupta, and Lee M. Jampol.
Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/4
Y1 - 2016/4
N2 - Purpose: To compare long-term vision and anatomic effects of ranibizumab with prompt or deferred laser vs laser or triamcinolone + laser with very deferred ranibizumab in diabetic macular edema (DME). Design: Randomized clinical trial. Methods: Eight hundred and twenty-eight study eyes (558 [67%] completed the 5-year visit), at 52 sites, with visual acuity 20/32 to 20/320 and DME involving the central macula were randomly assigned to intravitreous ranibizumab (0.5 mg) with either (1) prompt or (2) deferred laser; (3) sham injection + prompt laser; or (4) intravitreous triamcinolone (4 mg) + prompt laser. The latter 2 groups could initiate ranibizumab as early as 74 weeks from baseline, for persistent DME with vision impairment. The main outcome measures were visual acuity, optical coherence central subfield thickness, and number of injections through 5 years. Results: At 5 years mean (± standard deviation) change in Early Treatment Diabetic Retinopathy Study visual acuity letter scores from baseline in the ranibizumab + deferred laser (N = 111), ranibizumab + prompt laser (N = 124), laser/very deferred ranibizumab (N = 198), and triamcinolone + laser/very deferred ranibizumab (N = 125) groups were 10 ± 13, 8 ± 13, 5 ± 14, and 7 ± 14, respectively. The difference (95% confidence interval) in mean change between ranibizumab + deferred laser and laser/very deferred ranibizumab and triamcinolone + laser/very deferred ranibizumab was 4.4 (1.2–7.6, P =.001) and 2.8 (−0.9 to 6.5, P =.067), respectively, at 5 years. Conclusions: Recognizing limitations of follow-up available at 5 years, eyes receiving initial ranibizumab therapy for center-involving DME likely have better long-term vision improvements than eyes managed with laser or triamcinolone + laser followed by very deferred ranibizumab for persistent thickening and vision impairment.
AB - Purpose: To compare long-term vision and anatomic effects of ranibizumab with prompt or deferred laser vs laser or triamcinolone + laser with very deferred ranibizumab in diabetic macular edema (DME). Design: Randomized clinical trial. Methods: Eight hundred and twenty-eight study eyes (558 [67%] completed the 5-year visit), at 52 sites, with visual acuity 20/32 to 20/320 and DME involving the central macula were randomly assigned to intravitreous ranibizumab (0.5 mg) with either (1) prompt or (2) deferred laser; (3) sham injection + prompt laser; or (4) intravitreous triamcinolone (4 mg) + prompt laser. The latter 2 groups could initiate ranibizumab as early as 74 weeks from baseline, for persistent DME with vision impairment. The main outcome measures were visual acuity, optical coherence central subfield thickness, and number of injections through 5 years. Results: At 5 years mean (± standard deviation) change in Early Treatment Diabetic Retinopathy Study visual acuity letter scores from baseline in the ranibizumab + deferred laser (N = 111), ranibizumab + prompt laser (N = 124), laser/very deferred ranibizumab (N = 198), and triamcinolone + laser/very deferred ranibizumab (N = 125) groups were 10 ± 13, 8 ± 13, 5 ± 14, and 7 ± 14, respectively. The difference (95% confidence interval) in mean change between ranibizumab + deferred laser and laser/very deferred ranibizumab and triamcinolone + laser/very deferred ranibizumab was 4.4 (1.2–7.6, P =.001) and 2.8 (−0.9 to 6.5, P =.067), respectively, at 5 years. Conclusions: Recognizing limitations of follow-up available at 5 years, eyes receiving initial ranibizumab therapy for center-involving DME likely have better long-term vision improvements than eyes managed with laser or triamcinolone + laser followed by very deferred ranibizumab for persistent thickening and vision impairment.
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U2 - 10.1016/j.ajo.2015.12.025
DO - 10.1016/j.ajo.2015.12.025
M3 - Article
C2 - 26802783
AN - SCOPUS:85017052430
SN - 0002-9394
VL - 164
SP - 57
EP - 68
JO - American journal of ophthalmology
JF - American journal of ophthalmology
ER -