Rationale and Application of the Protocol S Anti–Vascular Endothelial Growth Factor Algorithm for Proliferative Diabetic Retinopathy

To present the rationale, guidelines, and results of ranibizumab treatment for proliferative diabetic retinopathy (PDR) in Diabetic Retinopathy Clinical Research Network (DRCR.net) Protocol S. Post hoc analyses from a randomized clinical trial. Three hundred five participants (394 study eyes) having...

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Published inOphthalmology (Rochester, Minn.) Vol. 126; no. 1; pp. 87 - 95
Main Authors Sun, Jennifer K., Glassman, Adam R., Beaulieu, Wesley T., Stockdale, Cynthia R., Bressler, Neil M., Flaxel, Christina, Gross, Jeffrey G., Shami, Michel, Jampol, Lee M.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.01.2019
Subjects
Online AccessGet full text
ISSN0161-6420
1549-4713
1549-4713
DOI10.1016/j.ophtha.2018.08.001

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Abstract To present the rationale, guidelines, and results of ranibizumab treatment for proliferative diabetic retinopathy (PDR) in Diabetic Retinopathy Clinical Research Network (DRCR.net) Protocol S. Post hoc analyses from a randomized clinical trial. Three hundred five participants (394 study eyes) having PDR without prior panretinal photocoagulation (PRP). Intravitreous ranibizumab (0.5 mg) versus PRP for PDR. Ranbizumab-assigned eyes (n = 191) received monthly injections for 6 months unless resolution was achieved after 4 injections. After 6 months, injections could be deferred if neovascularization was stable over 3 consecutive visits (sustained stability). If neovascularization worsened, monthly treatment resumed. Panretinal photocoagulation could be initiated for failure or futility criteria. Neovascularization status through 2 years. At 1 month, 19% (35 of 188) of ranibizumab-assigned eyes showed complete neovascularization resolution and an additional 60% (113) showed improvement. At 6 months, 52% (80 of 153) showed neovascularization resolution, 3% (4) were improved, 37% (56) were stable, and 8% (13) had worsened since the last visit. Among eyes with versus without resolved neovascularization at 6 months, the median (interquartile range) number of injections between 6 months and 2 years was 4 (1–7; n = 73) versus 7 (4–11; n = 67; P < 0.001). Injections were deferred in 68 of 73 eyes (93%) meeting sustained stability at least once during the study; 62% (42 of 68) resumed injections within 16 weeks after deferral. At 2 years, 43% (66 of 154) showed neovascularization resolution, 5% (7) showed improvement, 23% (36) were stable, and 27% (42) had worsened since the last visit. Only 3 eyes met criteria for failure or futility through 2 years. The DRCR.net treatment algorithm for PDR can provide excellent clinical outcomes through 2 years for patients initiating anti–vascular endothelial growth factor (VEGF) therapy for PDR. When choosing between anti-VEGF and PRP as first-line therapy for PDR, treatment decisions should be guided by consideration of the relative advantages of each therapeutic method and anticipated patient compliance with follow-up and treatment recommendations.
AbstractList To present the rationale, guidelines, and results of ranibizumab treatment for proliferative diabetic retinopathy (PDR) in Diabetic Retinopathy Clinical Research Network (DRCR.net) Protocol S. Post hoc analyses from a randomized clinical trial. Three hundred five participants (394 study eyes) having PDR without prior panretinal photocoagulation (PRP). Intravitreous ranibizumab (0.5 mg) versus PRP for PDR. Ranbizumab-assigned eyes (n = 191) received monthly injections for 6 months unless resolution was achieved after 4 injections. After 6 months, injections could be deferred if neovascularization was stable over 3 consecutive visits (sustained stability). If neovascularization worsened, monthly treatment resumed. Panretinal photocoagulation could be initiated for failure or futility criteria. Neovascularization status through 2 years. At 1 month, 19% (35 of 188) of ranibizumab-assigned eyes showed complete neovascularization resolution and an additional 60% (113) showed improvement. At 6 months, 52% (80 of 153) showed neovascularization resolution, 3% (4) were improved, 37% (56) were stable, and 8% (13) had worsened since the last visit. Among eyes with versus without resolved neovascularization at 6 months, the median (interquartile range) number of injections between 6 months and 2 years was 4 (1-7; n = 73) versus 7 (4-11; n = 67; P < 0.001). Injections were deferred in 68 of 73 eyes (93%) meeting sustained stability at least once during the study; 62% (42 of 68) resumed injections within 16 weeks after deferral. At 2 years, 43% (66 of 154) showed neovascularization resolution, 5% (7) showed improvement, 23% (36) were stable, and 27% (42) had worsened since the last visit. Only 3 eyes met criteria for failure or futility through 2 years. The DRCR.net treatment algorithm for PDR can provide excellent clinical outcomes through 2 years for patients initiating anti-vascular endothelial growth factor (VEGF) therapy for PDR. When choosing between anti-VEGF and PRP as first-line therapy for PDR, treatment decisions should be guided by consideration of the relative advantages of each therapeutic method and anticipated patient compliance with follow-up and treatment recommendations.
Treatment of proliferative diabetic retinopathy with anti-vascular endothelial growth factor following the Diabetic Retinopathy Clinical Research Network treatment algorithm can provide excellent clinical outcomes through two years.
To present the rationale, guidelines, and results of ranibizumab treatment for proliferative diabetic retinopathy (PDR) in Diabetic Retinopathy Clinical Research Network (DRCR.net) Protocol S.PURPOSETo present the rationale, guidelines, and results of ranibizumab treatment for proliferative diabetic retinopathy (PDR) in Diabetic Retinopathy Clinical Research Network (DRCR.net) Protocol S.Post hoc analyses from a randomized clinical trial.DESIGNPost hoc analyses from a randomized clinical trial.Three hundred five participants (394 study eyes) having PDR without prior panretinal photocoagulation (PRP).PARTICIPANTSThree hundred five participants (394 study eyes) having PDR without prior panretinal photocoagulation (PRP).Intravitreous ranibizumab (0.5 mg) versus PRP for PDR. Ranbizumab-assigned eyes (n = 191) received monthly injections for 6 months unless resolution was achieved after 4 injections. After 6 months, injections could be deferred if neovascularization was stable over 3 consecutive visits (sustained stability). If neovascularization worsened, monthly treatment resumed. Panretinal photocoagulation could be initiated for failure or futility criteria.METHODSIntravitreous ranibizumab (0.5 mg) versus PRP for PDR. Ranbizumab-assigned eyes (n = 191) received monthly injections for 6 months unless resolution was achieved after 4 injections. After 6 months, injections could be deferred if neovascularization was stable over 3 consecutive visits (sustained stability). If neovascularization worsened, monthly treatment resumed. Panretinal photocoagulation could be initiated for failure or futility criteria.Neovascularization status through 2 years.MAIN OUTCOME MEASURESNeovascularization status through 2 years.At 1 month, 19% (35 of 188) of ranibizumab-assigned eyes showed complete neovascularization resolution and an additional 60% (113) showed improvement. At 6 months, 52% (80 of 153) showed neovascularization resolution, 3% (4) were improved, 37% (56) were stable, and 8% (13) had worsened since the last visit. Among eyes with versus without resolved neovascularization at 6 months, the median (interquartile range) number of injections between 6 months and 2 years was 4 (1-7; n = 73) versus 7 (4-11; n = 67; P < 0.001). Injections were deferred in 68 of 73 eyes (93%) meeting sustained stability at least once during the study; 62% (42 of 68) resumed injections within 16 weeks after deferral. At 2 years, 43% (66 of 154) showed neovascularization resolution, 5% (7) showed improvement, 23% (36) were stable, and 27% (42) had worsened since the last visit. Only 3 eyes met criteria for failure or futility through 2 years.RESULTSAt 1 month, 19% (35 of 188) of ranibizumab-assigned eyes showed complete neovascularization resolution and an additional 60% (113) showed improvement. At 6 months, 52% (80 of 153) showed neovascularization resolution, 3% (4) were improved, 37% (56) were stable, and 8% (13) had worsened since the last visit. Among eyes with versus without resolved neovascularization at 6 months, the median (interquartile range) number of injections between 6 months and 2 years was 4 (1-7; n = 73) versus 7 (4-11; n = 67; P < 0.001). Injections were deferred in 68 of 73 eyes (93%) meeting sustained stability at least once during the study; 62% (42 of 68) resumed injections within 16 weeks after deferral. At 2 years, 43% (66 of 154) showed neovascularization resolution, 5% (7) showed improvement, 23% (36) were stable, and 27% (42) had worsened since the last visit. Only 3 eyes met criteria for failure or futility through 2 years.The DRCR.net treatment algorithm for PDR can provide excellent clinical outcomes through 2 years for patients initiating anti-vascular endothelial growth factor (VEGF) therapy for PDR. When choosing between anti-VEGF and PRP as first-line therapy for PDR, treatment decisions should be guided by consideration of the relative advantages of each therapeutic method and anticipated patient compliance with follow-up and treatment recommendations.CONCLUSIONSThe DRCR.net treatment algorithm for PDR can provide excellent clinical outcomes through 2 years for patients initiating anti-vascular endothelial growth factor (VEGF) therapy for PDR. When choosing between anti-VEGF and PRP as first-line therapy for PDR, treatment decisions should be guided by consideration of the relative advantages of each therapeutic method and anticipated patient compliance with follow-up and treatment recommendations.
Author Glassman, Adam R.
Stockdale, Cynthia R.
Flaxel, Christina
Jampol, Lee M.
Beaulieu, Wesley T.
Sun, Jennifer K.
Gross, Jeffrey G.
Bressler, Neil M.
Shami, Michel
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  fullname: Jampol, Lee M.
  organization: Feinberg School of Medicine, Northwestern University, Chicago, Illinois
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Keywords DRCR.net
VEGF
CLARITY
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IQR
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PDR
PRP
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Snippet To present the rationale, guidelines, and results of ranibizumab treatment for proliferative diabetic retinopathy (PDR) in Diabetic Retinopathy Clinical...
Treatment of proliferative diabetic retinopathy with anti-vascular endothelial growth factor following the Diabetic Retinopathy Clinical Research Network...
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StartPage 87
SubjectTerms Adult
Algorithms
Angiogenesis Inhibitors - administration & dosage
Angiogenesis Inhibitors - therapeutic use
Clinical Protocols
Diabetic Retinopathy - diagnosis
Diabetic Retinopathy - drug therapy
Diabetic Retinopathy - physiopathology
Female
Follow-Up Studies
Humans
Intravitreal Injections
Laser Coagulation
Male
Middle Aged
Ranibizumab - administration & dosage
Ranibizumab - therapeutic use
Retinal Neovascularization - diagnosis
Retinal Neovascularization - drug therapy
Retinal Neovascularization - physiopathology
Vascular Endothelial Growth Factor A - antagonists & inhibitors
Visual Acuity
Title Rationale and Application of the Protocol S Anti–Vascular Endothelial Growth Factor Algorithm for Proliferative Diabetic Retinopathy
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0161642018314891
https://dx.doi.org/10.1016/j.ophtha.2018.08.001
https://www.ncbi.nlm.nih.gov/pubmed/30096354
https://www.proquest.com/docview/2087594780
https://pubmed.ncbi.nlm.nih.gov/PMC6916649
https://www.ncbi.nlm.nih.gov/pmc/articles/6916649
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