Twenty-four–Month Outcomes of the Ranibizumab for Edema of the Macula in Diabetes – Protocol 3 with High Dose (READ-3) Study
To compare 2.0 mg ranibizumab (RBZ) injections with 0.5 mg RBZ for eyes with center-involved diabetic macular edema (DME). Randomized, controlled, double-masked (to the dose), interventional, multicenter clinical trial. A total of 152 patients (152 eyes) with DME. Eligible eyes were randomized in a...
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Published in | Ophthalmology (Rochester, Minn.) Vol. 123; no. 12; pp. 2581 - 2587 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.12.2016
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Online Access | Get full text |
ISSN | 0161-6420 1549-4713 1549-4713 |
DOI | 10.1016/j.ophtha.2016.08.040 |
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Abstract | To compare 2.0 mg ranibizumab (RBZ) injections with 0.5 mg RBZ for eyes with center-involved diabetic macular edema (DME).
Randomized, controlled, double-masked (to the dose), interventional, multicenter clinical trial.
A total of 152 patients (152 eyes) with DME.
Eligible eyes were randomized in a 1:1 ratio to 0.5 mg (n = 77) or 2.0 mg (n = 75) RBZ. Study eyes received 6 monthly mandatory injections followed by as-needed injections until month 24.
The primary efficacy end point of the study was mean change in best-corrected visual acuity (BCVA) and central foveal thickness (CFT) at month 6. Secondary outcomes included the mean change in BCVA and CFT at month 24, and incidence and severity of systemic and ocular adverse events through month 24.
A total of 152 eyes were randomized in the study. At month 24, the mean improvement from baseline BCVA was +11.06 letters in the 0.5 mg RBZ group (n = 59) and +6.78 letters in the 2.0 mg RBZ group (n = 54) (P = 0.02). The mean numbers of RBZ injections through month 24 were 18.4 and 17.3 in the 0.5 mg and 2.0 mg RBZ groups, respectively (P = 0.08). The mean change in CFT was −192.53 μm in the 0.5 mg RBZ group and −170.64 μm in the 2.0 mg RBZ group (P = 0.41). By month 24, 3 deaths had occurred in the 0.5 mg RBZ group and 3 deaths had occurred in the 2.0 mg RBZ group; 5 of these 6 deaths occurred secondary to cardiovascular causes, and 1 death occurred as the result of severe pneumonia. All 5 patients with a cardiovascular cause of death had a history of coronary heart disease.
At month 24, there were significant visual and anatomic improvements in both groups, with subjects in the 0.5 mg RBZ group gaining more vision. Visual and anatomic gains achieved at month 6 were largely maintained through month 24. No new safety events were identified. In this study population, 2.0 mg RBZ does not appear to provide additional benefit over 0.5 mg RBZ. |
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AbstractList | To compare 2.0 mg ranibizumab (RBZ) injections with 0.5 mg RBZ for eyes with center-involved diabetic macular edema (DME).PURPOSETo compare 2.0 mg ranibizumab (RBZ) injections with 0.5 mg RBZ for eyes with center-involved diabetic macular edema (DME).Randomized, controlled, double-masked (to the dose), interventional, multicenter clinical trial.DESIGNRandomized, controlled, double-masked (to the dose), interventional, multicenter clinical trial.A total of 152 patients (152 eyes) with DME.PARTICIPANTSA total of 152 patients (152 eyes) with DME.Eligible eyes were randomized in a 1:1 ratio to 0.5 mg (n = 77) or 2.0 mg (n = 75) RBZ. Study eyes received 6 monthly mandatory injections followed by as-needed injections until month 24.METHODSEligible eyes were randomized in a 1:1 ratio to 0.5 mg (n = 77) or 2.0 mg (n = 75) RBZ. Study eyes received 6 monthly mandatory injections followed by as-needed injections until month 24.The primary efficacy end point of the study was mean change in best-corrected visual acuity (BCVA) and central foveal thickness (CFT) at month 6. Secondary outcomes included the mean change in BCVA and CFT at month 24, and incidence and severity of systemic and ocular adverse events through month 24.MAIN OUTCOME MEASURESThe primary efficacy end point of the study was mean change in best-corrected visual acuity (BCVA) and central foveal thickness (CFT) at month 6. Secondary outcomes included the mean change in BCVA and CFT at month 24, and incidence and severity of systemic and ocular adverse events through month 24.A total of 152 eyes were randomized in the study. At month 24, the mean improvement from baseline BCVA was +11.06 letters in the 0.5 mg RBZ group (n = 59) and +6.78 letters in the 2.0 mg RBZ group (n = 54) (P = 0.02). The mean numbers of RBZ injections through month 24 were 18.4 and 17.3 in the 0.5 mg and 2.0 mg RBZ groups, respectively (P = 0.08). The mean change in CFT was -192.53 μm in the 0.5 mg RBZ group and -170.64 μm in the 2.0 mg RBZ group (P = 0.41). By month 24, 3 deaths had occurred in the 0.5 mg RBZ group and 3 deaths had occurred in the 2.0 mg RBZ group; 5 of these 6 deaths occurred secondary to cardiovascular causes, and 1 death occurred as the result of severe pneumonia. All 5 patients with a cardiovascular cause of death had a history of coronary heart disease.RESULTSA total of 152 eyes were randomized in the study. At month 24, the mean improvement from baseline BCVA was +11.06 letters in the 0.5 mg RBZ group (n = 59) and +6.78 letters in the 2.0 mg RBZ group (n = 54) (P = 0.02). The mean numbers of RBZ injections through month 24 were 18.4 and 17.3 in the 0.5 mg and 2.0 mg RBZ groups, respectively (P = 0.08). The mean change in CFT was -192.53 μm in the 0.5 mg RBZ group and -170.64 μm in the 2.0 mg RBZ group (P = 0.41). By month 24, 3 deaths had occurred in the 0.5 mg RBZ group and 3 deaths had occurred in the 2.0 mg RBZ group; 5 of these 6 deaths occurred secondary to cardiovascular causes, and 1 death occurred as the result of severe pneumonia. All 5 patients with a cardiovascular cause of death had a history of coronary heart disease.At month 24, there were significant visual and anatomic improvements in both groups, with subjects in the 0.5 mg RBZ group gaining more vision. Visual and anatomic gains achieved at month 6 were largely maintained through month 24. No new safety events were identified. In this study population, 2.0 mg RBZ does not appear to provide additional benefit over 0.5 mg RBZ.CONCLUSIONSAt month 24, there were significant visual and anatomic improvements in both groups, with subjects in the 0.5 mg RBZ group gaining more vision. Visual and anatomic gains achieved at month 6 were largely maintained through month 24. No new safety events were identified. In this study population, 2.0 mg RBZ does not appear to provide additional benefit over 0.5 mg RBZ. Purpose To compare 2.0 mg ranibizumab (RBZ) injections with 0.5 mg RBZ for eyes with center-involved diabetic macular edema (DME). Design Randomized, controlled, double-masked (to the dose), interventional, multicenter clinical trial. Participants A total of 152 patients (152 eyes) with DME. Methods Eligible eyes were randomized in a 1:1 ratio to 0.5 mg (n = 77) or 2.0 mg (n = 75) RBZ. Study eyes received 6 monthly mandatory injections followed by as-needed injections until month 24. Main Outcome Measures The primary efficacy end point of the study was mean change in best-corrected visual acuity (BCVA) and central foveal thickness (CFT) at month 6. Secondary outcomes included the mean change in BCVA and CFT at month 24, and incidence and severity of systemic and ocular adverse events through month 24. Results A total of 152 eyes were randomized in the study. At month 24, the mean improvement from baseline BCVA was +11.06 letters in the 0.5 mg RBZ group (n = 59) and +6.78 letters in the 2.0 mg RBZ group (n = 54) ( P = 0.02). The mean numbers of RBZ injections through month 24 were 18.4 and 17.3 in the 0.5 mg and 2.0 mg RBZ groups, respectively ( P = 0.08). The mean change in CFT was −192.53 μm in the 0.5 mg RBZ group and −170.64 μm in the 2.0 mg RBZ group ( P = 0.41). By month 24, 3 deaths had occurred in the 0.5 mg RBZ group and 3 deaths had occurred in the 2.0 mg RBZ group; 5 of these 6 deaths occurred secondary to cardiovascular causes, and 1 death occurred as the result of severe pneumonia. All 5 patients with a cardiovascular cause of death had a history of coronary heart disease. Conclusions At month 24, there were significant visual and anatomic improvements in both groups, with subjects in the 0.5 mg RBZ group gaining more vision. Visual and anatomic gains achieved at month 6 were largely maintained through month 24. No new safety events were identified. In this study population, 2.0 mg RBZ does not appear to provide additional benefit over 0.5 mg RBZ. To compare 2.0 mg ranibizumab (RBZ) injections with 0.5 mg RBZ for eyes with center-involved diabetic macular edema (DME). Randomized, controlled, double-masked (to the dose), interventional, multicenter clinical trial. A total of 152 patients (152 eyes) with DME. Eligible eyes were randomized in a 1:1 ratio to 0.5 mg (n = 77) or 2.0 mg (n = 75) RBZ. Study eyes received 6 monthly mandatory injections followed by as-needed injections until month 24. The primary efficacy end point of the study was mean change in best-corrected visual acuity (BCVA) and central foveal thickness (CFT) at month 6. Secondary outcomes included the mean change in BCVA and CFT at month 24, and incidence and severity of systemic and ocular adverse events through month 24. A total of 152 eyes were randomized in the study. At month 24, the mean improvement from baseline BCVA was +11.06 letters in the 0.5 mg RBZ group (n = 59) and +6.78 letters in the 2.0 mg RBZ group (n = 54) (P = 0.02). The mean numbers of RBZ injections through month 24 were 18.4 and 17.3 in the 0.5 mg and 2.0 mg RBZ groups, respectively (P = 0.08). The mean change in CFT was −192.53 μm in the 0.5 mg RBZ group and −170.64 μm in the 2.0 mg RBZ group (P = 0.41). By month 24, 3 deaths had occurred in the 0.5 mg RBZ group and 3 deaths had occurred in the 2.0 mg RBZ group; 5 of these 6 deaths occurred secondary to cardiovascular causes, and 1 death occurred as the result of severe pneumonia. All 5 patients with a cardiovascular cause of death had a history of coronary heart disease. At month 24, there were significant visual and anatomic improvements in both groups, with subjects in the 0.5 mg RBZ group gaining more vision. Visual and anatomic gains achieved at month 6 were largely maintained through month 24. No new safety events were identified. In this study population, 2.0 mg RBZ does not appear to provide additional benefit over 0.5 mg RBZ. To compare 2.0 mg ranibizumab (RBZ) injections with 0.5 mg RBZ for eyes with center-involved diabetic macular edema (DME). Randomized, controlled, double-masked (to the dose), interventional, multicenter clinical trial. A total of 152 patients (152 eyes) with DME. Eligible eyes were randomized in a 1:1 ratio to 0.5 mg (n = 77) or 2.0 mg (n = 75) RBZ. Study eyes received 6 monthly mandatory injections followed by as-needed injections until month 24. The primary efficacy end point of the study was mean change in best-corrected visual acuity (BCVA) and central foveal thickness (CFT) at month 6. Secondary outcomes included the mean change in BCVA and CFT at month 24, and incidence and severity of systemic and ocular adverse events through month 24. A total of 152 eyes were randomized in the study. At month 24, the mean improvement from baseline BCVA was +11.06 letters in the 0.5 mg RBZ group (n = 59) and +6.78 letters in the 2.0 mg RBZ group (n = 54) (P = 0.02). The mean numbers of RBZ injections through month 24 were 18.4 and 17.3 in the 0.5 mg and 2.0 mg RBZ groups, respectively (P = 0.08). The mean change in CFT was -192.53 μm in the 0.5 mg RBZ group and -170.64 μm in the 2.0 mg RBZ group (P = 0.41). By month 24, 3 deaths had occurred in the 0.5 mg RBZ group and 3 deaths had occurred in the 2.0 mg RBZ group; 5 of these 6 deaths occurred secondary to cardiovascular causes, and 1 death occurred as the result of severe pneumonia. All 5 patients with a cardiovascular cause of death had a history of coronary heart disease. At month 24, there were significant visual and anatomic improvements in both groups, with subjects in the 0.5 mg RBZ group gaining more vision. Visual and anatomic gains achieved at month 6 were largely maintained through month 24. No new safety events were identified. In this study population, 2.0 mg RBZ does not appear to provide additional benefit over 0.5 mg RBZ. |
Author | Hassan, Muhammad Pollack, John Callanan, David G. Afridi, Rubbia Sadiq, Mohammad Ali Halperin, Larry Bennett, Michael Gallemore, Ron Abraham, Prema Sepah, Yasir Jamal Agarwal, Aniruddha Callanan, David Zhang, Kang Wilson, David J. Boyer, David Do, Diana V. Halperin, Lawrence Nguyen, Quan Dong Hanout, Mostafa Lit, Eugene Sepah, Yasir J. Campochiaro, Peter A. Kruger, Erik Marcus, Dennis Symons, Andrew Conway, Brian P. Greer, Lisa |
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ContentType | Journal Article |
Contributor | Hassan, Muhammad Pollack, John Afridi, Rubbia Sadiq, Mohammad Ali Halperin, Larry Bennett, Michael Gallemore, Ron Abraham, Prema Sepah, Yasir Jamal Agarwal, Aniruddha Do, Diana V Conway, Brian P Callanan, David Zhang, Kang Wilson, David J Boyer, David Nguyen, Quan Dong Hanout, Mostafa Lit, Eugene Kruger, Erik Marcus, Dennis Callanan, David G Symons, Andrew Greer, Lisa Campochiaro, Peter A |
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Copyright | 2016 American Academy of Ophthalmology American Academy of Ophthalmology Copyright © 2016 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved. |
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Keywords | OCT SD OCT FDA READ-3 ETDRS VEGF TD-OCT RBZ VA PRN CFT BCVA DME optical coherence tomography ranibizumab pro re nata Food and Drug Administration diabetic macular edema Ranibizumab for Edema of the mAcula in Diabetes – Protocol 3 with High Dose visual acuity spectral-domain optical coherence tomography central foveal thickness time-domain optical coherence tomography Early Treatment Diabetic Retinopathy Study vascular endothelial growth factor best-corrected visual acuity |
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References | Do, Sepah, Boyer (bib7) 2015; 29 Nguyen, Shah, Heier (bib5) 2009; 116 Mitchell, Bandello, Schmidt-Erfurth (bib6) 2011; 118 Bressler, Qin, Beck (bib9) 2012; 130 Elman, Aiello, Beck (bib4) 2010; 117 Nguyen, Tatlipinar, Shah (bib1) 2006; 142 Nguyen, Shah, Khwaja (bib3) 2010; 117 Ho, Busbee, Regillo (bib8) 2014; 121 Nguyen, Brown, Marcus (bib2) 2012; 119 Elman (10.1016/j.ophtha.2016.08.040_bib4) 2010; 117 Nguyen (10.1016/j.ophtha.2016.08.040_bib2) 2012; 119 Mitchell (10.1016/j.ophtha.2016.08.040_bib6) 2011; 118 Ho (10.1016/j.ophtha.2016.08.040_bib8) 2014; 121 Nguyen (10.1016/j.ophtha.2016.08.040_bib1) 2006; 142 Nguyen (10.1016/j.ophtha.2016.08.040_bib3) 2010; 117 Nguyen (10.1016/j.ophtha.2016.08.040_bib5) 2009; 116 Do (10.1016/j.ophtha.2016.08.040_bib7) 2015; 29 Bressler (10.1016/j.ophtha.2016.08.040_bib9) 2012; 130 |
References_xml | – volume: 118 start-page: 615 year: 2011 end-page: 625 ident: bib6 article-title: The RESTORE study: ranibizumab monotherapy or combined with laser versus laser monotherapy for diabetic macular edema publication-title: Ophthalmology – volume: 29 start-page: 1538 year: 2015 end-page: 1544 ident: bib7 article-title: Month-6 primary outcomes of the READ-3 study (Ranibizumab for Edema of the mAcula in Diabetes-Protocol 3 with high dose) publication-title: Eye (Lond) – volume: 142 start-page: 961 year: 2006 end-page: 969 ident: bib1 article-title: Vascular endothelial growth factor is a critical stimulus for diabetic macular edema publication-title: Am J Ophthalmol – volume: 117 start-page: 1064 year: 2010 end-page: 1077.e35 ident: bib4 article-title: Randomized trial evaluating ranibizumab plus prompt or deferred laser or triamcinolone plus prompt laser for diabetic macular edema publication-title: Ophthalmology – volume: 116 start-page: 2175 year: 2009 end-page: 2181.e1 ident: bib5 article-title: Primary end point (six months) results of the Ranibizumab for Edema of the mAcula in diabetes (READ-2) study publication-title: Ophthalmology – volume: 121 start-page: 2181 year: 2014 end-page: 2192 ident: bib8 article-title: Twenty-four-month efficacy and safety of 0.5 mg or 2.0 mg ranibizumab in patients with subfoveal neovascular age-related macular degeneration publication-title: Ophthalmology – volume: 130 start-page: 1153 year: 2012 end-page: 1161 ident: bib9 article-title: Factors associated with changes in visual acuity and central subfield thickness at 1 year after treatment for diabetic macular edema with ranibizumab publication-title: Arch Ophthalmol – volume: 117 start-page: 2146 year: 2010 end-page: 2151 ident: bib3 article-title: Two-year outcomes of the ranibizumab for edema of the mAcula in diabetes (READ-2) study publication-title: Ophthalmology – volume: 119 start-page: 789 year: 2012 end-page: 801 ident: bib2 article-title: Ranibizumab for diabetic macular edema: results from 2 phase III randomized trials: RISE and RIDE publication-title: Ophthalmology – volume: 29 start-page: 1538 year: 2015 ident: 10.1016/j.ophtha.2016.08.040_bib7 article-title: Month-6 primary outcomes of the READ-3 study (Ranibizumab for Edema of the mAcula in Diabetes-Protocol 3 with high dose) publication-title: Eye (Lond) doi: 10.1038/eye.2015.142 – volume: 117 start-page: 2146 year: 2010 ident: 10.1016/j.ophtha.2016.08.040_bib3 article-title: Two-year outcomes of the ranibizumab for edema of the mAcula in diabetes (READ-2) study publication-title: Ophthalmology doi: 10.1016/j.ophtha.2010.08.016 – volume: 118 start-page: 615 year: 2011 ident: 10.1016/j.ophtha.2016.08.040_bib6 article-title: The RESTORE study: ranibizumab monotherapy or combined with laser versus laser monotherapy for diabetic macular edema publication-title: Ophthalmology doi: 10.1016/j.ophtha.2011.01.031 – volume: 142 start-page: 961 year: 2006 ident: 10.1016/j.ophtha.2016.08.040_bib1 article-title: Vascular endothelial growth factor is a critical stimulus for diabetic macular edema publication-title: Am J Ophthalmol doi: 10.1016/j.ajo.2006.06.068 – volume: 117 start-page: 1064 year: 2010 ident: 10.1016/j.ophtha.2016.08.040_bib4 article-title: Randomized trial evaluating ranibizumab plus prompt or deferred laser or triamcinolone plus prompt laser for diabetic macular edema publication-title: Ophthalmology doi: 10.1016/j.ophtha.2010.02.031 – volume: 121 start-page: 2181 year: 2014 ident: 10.1016/j.ophtha.2016.08.040_bib8 article-title: Twenty-four-month efficacy and safety of 0.5 mg or 2.0 mg ranibizumab in patients with subfoveal neovascular age-related macular degeneration publication-title: Ophthalmology doi: 10.1016/j.ophtha.2014.05.009 – volume: 130 start-page: 1153 year: 2012 ident: 10.1016/j.ophtha.2016.08.040_bib9 article-title: Factors associated with changes in visual acuity and central subfield thickness at 1 year after treatment for diabetic macular edema with ranibizumab publication-title: Arch Ophthalmol doi: 10.1001/archophthalmol.2012.1107 – volume: 119 start-page: 789 year: 2012 ident: 10.1016/j.ophtha.2016.08.040_bib2 article-title: Ranibizumab for diabetic macular edema: results from 2 phase III randomized trials: RISE and RIDE publication-title: Ophthalmology doi: 10.1016/j.ophtha.2011.12.039 – volume: 116 start-page: 2175 year: 2009 ident: 10.1016/j.ophtha.2016.08.040_bib5 article-title: Primary end point (six months) results of the Ranibizumab for Edema of the mAcula in diabetes (READ-2) study publication-title: Ophthalmology doi: 10.1016/j.ophtha.2009.04.023 |
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Snippet | To compare 2.0 mg ranibizumab (RBZ) injections with 0.5 mg RBZ for eyes with center-involved diabetic macular edema (DME).
Randomized, controlled,... Purpose To compare 2.0 mg ranibizumab (RBZ) injections with 0.5 mg RBZ for eyes with center-involved diabetic macular edema (DME). Design Randomized,... To compare 2.0 mg ranibizumab (RBZ) injections with 0.5 mg RBZ for eyes with center-involved diabetic macular edema (DME).PURPOSETo compare 2.0 mg ranibizumab... |
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SubjectTerms | Adult Aged Aged, 80 and over Angiogenesis Inhibitors - administration & dosage Angiogenesis Inhibitors - adverse effects Diabetic Retinopathy - drug therapy Diabetic Retinopathy - physiopathology Double-Blind Method Female Follow-Up Studies Humans Intravitreal Injections Macula Lutea - drug effects Macular Edema - drug therapy Macular Edema - physiopathology Male Middle Aged Ophthalmology Ranibizumab - administration & dosage Ranibizumab - adverse effects Retreatment Tomography, Optical Coherence Treatment Outcome Vascular Endothelial Growth Factor A - antagonists & inhibitors Visual Acuity - drug effects Visual Acuity - physiology |
Title | Twenty-four–Month Outcomes of the Ranibizumab for Edema of the Macula in Diabetes – Protocol 3 with High Dose (READ-3) Study |
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