Role of anti-vascular endothelial growth factor in the management of non-proliferative diabetic retinopathy without centre-involving diabetic macular oedema: a meta-analysis of trials

This systematic review and meta-analysis investigated the impact of anti-vascular endothelial growth factor (VEGF) treatment in management of eyes with non-proliferative diabetic retinopathy (NPDR) without centre involving diabetic macular oedema (CI-DMO). We searched multiple databases for all rand...

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Veröffentlicht in:Eye (London) 2023-07, Vol.37 (10), p.1966-1974
Hauptverfasser: Chaudhary, Varun, Sarohia, Gurkaran S., Phillips, Mark R., Park, Daniel, Xie, Jim, Zeraatkar, Dena, Fung, Matthew, Thabane, Lehana, Loewenstein, Anat, Holz, Frank G., Garg, Sunir J., Kaiser, Peter K., Bhandari, Mohit, Guymer, Robyn H., Fraser-Bell, Samantha, Sivaprasad, Sobha, Wykoff, Charles C.
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container_end_page 1974
container_issue 10
container_start_page 1966
container_title Eye (London)
container_volume 37
creator Chaudhary, Varun
Sarohia, Gurkaran S.
Phillips, Mark R.
Park, Daniel
Xie, Jim
Zeraatkar, Dena
Fung, Matthew
Thabane, Lehana
Loewenstein, Anat
Holz, Frank G.
Garg, Sunir J.
Kaiser, Peter K.
Bhandari, Mohit
Guymer, Robyn H.
Fraser-Bell, Samantha
Sivaprasad, Sobha
Wykoff, Charles C.
description This systematic review and meta-analysis investigated the impact of anti-vascular endothelial growth factor (VEGF) treatment in management of eyes with non-proliferative diabetic retinopathy (NPDR) without centre involving diabetic macular oedema (CI-DMO). We searched multiple databases for all randomised clinical trials (RCTs) that evaluated anti-VEGF treatment versus observation in eyes with NPDR without CI-DMO. Data was collected for six outcomes (best corrected visual acuity (BCVA) improvement, diabetic retinopathy severity score (DRSS), central subfield thickness, progression to vision threatening complications (VTCs), ocular adverse events and quality of life measures). Risk of bias was assessed using Cochrane risk-of-bias tool for randomised trials (RoB 2) and certainty of evidence was assessed using Grade of Recommendations, Assessment, Development and Evaluation (GRADE). We identified a total of 2 unique RCTs that compared aflibercept and sham to treat a total of 811 eyes. For BCVA change, there was a small, clinically insignificant benefit for aflibercept treatment at year 2 (MD 0.70, 95% CI 0.02–1.38, GRADE rating: MODERATE). DRSS demonstrated a statistically significant improvement with aflibercept use at year 2 (RR 3.76, 95% CI 2.75–5.13, GRADE rating: MODERATE). VTCs were significantly less in aflibercept arm at year 2 (RR 0.30, 95% CI 0.23–0.40, GRADE rating: MODERATE). In conclusion, aflibercept treatment versus observation in eyes with NPDR without CI-DMO can result in reduced risk of development of VTCs and regression of DRSS score over 2 years. Future trials are needed to increase the precision of the treatment effect and to provide data on quality-of-life metrics. PROSPERO Registration: CRD42021288608.
doi_str_mv 10.1038/s41433-022-02269-y
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DRSS demonstrated a statistically significant improvement with aflibercept use at year 2 (RR 3.76, 95% CI 2.75–5.13, GRADE rating: MODERATE). VTCs were significantly less in aflibercept arm at year 2 (RR 0.30, 95% CI 0.23–0.40, GRADE rating: MODERATE). In conclusion, aflibercept treatment versus observation in eyes with NPDR without CI-DMO can result in reduced risk of development of VTCs and regression of DRSS score over 2 years. Future trials are needed to increase the precision of the treatment effect and to provide data on quality-of-life metrics. 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DRSS demonstrated a statistically significant improvement with aflibercept use at year 2 (RR 3.76, 95% CI 2.75–5.13, GRADE rating: MODERATE). VTCs were significantly less in aflibercept arm at year 2 (RR 0.30, 95% CI 0.23–0.40, GRADE rating: MODERATE). In conclusion, aflibercept treatment versus observation in eyes with NPDR without CI-DMO can result in reduced risk of development of VTCs and regression of DRSS score over 2 years. Future trials are needed to increase the precision of the treatment effect and to provide data on quality-of-life metrics. 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subjects 692/1807/1447
692/699/3161/3175
Acuity
Angiogenesis Inhibitors - therapeutic use
Bevacizumab - therapeutic use
Clinical trials
Diabetes
Diabetes Mellitus
Diabetic retinopathy
Diabetic Retinopathy - complications
Diabetic Retinopathy - drug therapy
Edema
Endothelial Growth Factors - therapeutic use
Eye
Humans
Laboratory Medicine
Laser Coagulation - adverse effects
Macular Edema - etiology
Medicine
Medicine & Public Health
Meta-analysis
Ophthalmology
Pharmaceutical Sciences/Technology
Quality of life
Ranibizumab - therapeutic use
Retinopathy
Review
Review Article
Statistical analysis
Surgery
Surgical Oncology
Vascular endothelial growth factor
Vascular Endothelial Growth Factor A - therapeutic use
title Role of anti-vascular endothelial growth factor in the management of non-proliferative diabetic retinopathy without centre-involving diabetic macular oedema: a meta-analysis of trials
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