Outcomes following three-line vision loss during treatment of neovascular age-related macular degeneration: subgroup analyses from MARINA and ANCHOR

AimThis study aims to assess the impact of continued ranibizumab treatment for neovascular age-related macular degeneration on patients from the MARINA and ANCHOR randomised clinical studies who lost ≥3 lines of best-corrected visual acuity (BCVA) at any time during the first year of treatment.Metho...

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Veröffentlicht in:British journal of ophthalmology 2011-12, Vol.95 (12), p.1713-1718
Hauptverfasser: Wolf, Sebastian, Holz, Frank G, Korobelnik, Jean-François, Lanzetta, Paolo, Mitchell, Paul, Prünte, Christian, Schmidt-Erfurth, Ursula, Weichselberger, Andreas, Hashad, Yehia
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container_end_page 1718
container_issue 12
container_start_page 1713
container_title British journal of ophthalmology
container_volume 95
creator Wolf, Sebastian
Holz, Frank G
Korobelnik, Jean-François
Lanzetta, Paolo
Mitchell, Paul
Prünte, Christian
Schmidt-Erfurth, Ursula
Weichselberger, Andreas
Hashad, Yehia
description AimThis study aims to assess the impact of continued ranibizumab treatment for neovascular age-related macular degeneration on patients from the MARINA and ANCHOR randomised clinical studies who lost ≥3 lines of best-corrected visual acuity (BCVA) at any time during the first year of treatment.MethodsBaseline characteristics, mean BCVA over time and ocular adverse events (AEs) were evaluated both for patients whose BCVA loss occurred at any post-baseline visit and for patients whose BCVA loss was acute. The visit when the ≥3-line BCVA loss was detected was defined as the new baseline.ResultsContinued monthly ranibizumab treatment led to an improvement in mean BCVA from the new baseline. On average, patients with acute BCVA loss gained 11.9 letters at 3 months after the new baseline, compared with 0.3 letters gained with sham. No strong signals were detected in patient demographics and baseline characteristics for prognostic markers of BCVA loss. Furthermore, there was no pattern in the AE profile of patients with acute BCVA loss to suggest that BCVA recovery could be attributed to spontaneously resolving AEs.ConclusionContinued ranibizumab treatment appears to be beneficial for patients with neovascular age-related macular degeneration who experience a ≥3-line BCVA loss during the first year of treatment.
doi_str_mv 10.1136/bjophthalmol-2011-300471
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The visit when the ≥3-line BCVA loss was detected was defined as the new baseline.ResultsContinued monthly ranibizumab treatment led to an improvement in mean BCVA from the new baseline. On average, patients with acute BCVA loss gained 11.9 letters at 3 months after the new baseline, compared with 0.3 letters gained with sham. No strong signals were detected in patient demographics and baseline characteristics for prognostic markers of BCVA loss. Furthermore, there was no pattern in the AE profile of patients with acute BCVA loss to suggest that BCVA recovery could be attributed to spontaneously resolving AEs.ConclusionContinued ranibizumab treatment appears to be beneficial for patients with neovascular age-related macular degeneration who experience a ≥3-line BCVA loss during the first year of treatment.</description><identifier>ISSN: 0007-1161</identifier><identifier>EISSN: 1468-2079</identifier><identifier>DOI: 10.1136/bjophthalmol-2011-300471</identifier><identifier>PMID: 21951567</identifier><identifier>CODEN: BJOPAL</identifier><language>eng</language><publisher>BMA House, Tavistock Square, London, WC1H 9JR: BMJ Publishing Group Ltd</publisher><subject>Aged ; Angiogenesis Inhibitors - therapeutic use ; angiogenesisretina ; Anti-VEGF ; Antibodies, Monoclonal, Humanized - therapeutic use ; Biological and medical sciences ; choroid ; Choroidal Neovascularization - drug therapy ; Choroidal Neovascularization - physiopathology ; clinical trial ; degeneration ; Double-Blind Method ; epidemiology ; Female ; Humans ; imaging ; maculaneovascularisation ; Macular degeneration ; Macular Degeneration - drug therapy ; Macular Degeneration - physiopathology ; Male ; Marinas ; Medical sciences ; Miscellaneous ; neovascular AMD ; neovascularisation ; Ophthalmology ; pathology ; Patients ; physiologypathology ; Prospective Studies ; public health ; Ranibizumab ; retina ; Retinopathies ; treatment lasers ; treatment medical ; treatment other ; Treatment Outcome ; treatment outcomes ; treatment surgery ; Vision disorders ; Visual Acuity</subject><ispartof>British journal of ophthalmology, 2011-12, Vol.95 (12), p.1713-1718</ispartof><rights>2011, Published by the BMJ Publishing Group Limited. 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The visit when the ≥3-line BCVA loss was detected was defined as the new baseline.ResultsContinued monthly ranibizumab treatment led to an improvement in mean BCVA from the new baseline. On average, patients with acute BCVA loss gained 11.9 letters at 3 months after the new baseline, compared with 0.3 letters gained with sham. No strong signals were detected in patient demographics and baseline characteristics for prognostic markers of BCVA loss. Furthermore, there was no pattern in the AE profile of patients with acute BCVA loss to suggest that BCVA recovery could be attributed to spontaneously resolving AEs.ConclusionContinued ranibizumab treatment appears to be beneficial for patients with neovascular age-related macular degeneration who experience a ≥3-line BCVA loss during the first year of treatment.</description><subject>Aged</subject><subject>Angiogenesis Inhibitors - therapeutic use</subject><subject>angiogenesisretina</subject><subject>Anti-VEGF</subject><subject>Antibodies, Monoclonal, Humanized - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>choroid</subject><subject>Choroidal Neovascularization - drug therapy</subject><subject>Choroidal Neovascularization - physiopathology</subject><subject>clinical trial</subject><subject>degeneration</subject><subject>Double-Blind Method</subject><subject>epidemiology</subject><subject>Female</subject><subject>Humans</subject><subject>imaging</subject><subject>maculaneovascularisation</subject><subject>Macular degeneration</subject><subject>Macular Degeneration - drug therapy</subject><subject>Macular Degeneration - physiopathology</subject><subject>Male</subject><subject>Marinas</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>neovascular AMD</subject><subject>neovascularisation</subject><subject>Ophthalmology</subject><subject>pathology</subject><subject>Patients</subject><subject>physiologypathology</subject><subject>Prospective Studies</subject><subject>public health</subject><subject>Ranibizumab</subject><subject>retina</subject><subject>Retinopathies</subject><subject>treatment lasers</subject><subject>treatment medical</subject><subject>treatment other</subject><subject>Treatment Outcome</subject><subject>treatment outcomes</subject><subject>treatment surgery</subject><subject>Vision disorders</subject><subject>Visual Acuity</subject><issn>0007-1161</issn><issn>1468-2079</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqNkd9u0zAUxiPExMrgFZAlhLgK2Ekc29xVFbBJpdWmwQU31klstylOXGxnsPfggXFJtyGuuLJ8zu_8-74sQwS_IaSs3zY7t9_GLdje2bzAhOQlxhUjj7IZqWqeQkw8zmYYY5YTUpPT7GkIu_QtasKeZKcFEZTQms2yX-sxtq7XARlnrfvRDRsUt17r3HaDRjdd6NyArAsBqdH_yXoNsddDRM6gQbsbCO1owSPY6NxrC1Er1MMUU3qjB-0hpi7vUBibjXfjHsEA9jYchnrXo0_zq4vVPAUVmq8W5-urZ9mJARv08-N7ln3-8P56cZ4v1x8vFvNl3lS0irkomGpJQ4uWgmmYoFBzzUSpag6tAlBEYG4MbUxDS1MLUdaqFaRqSBICMyjPstdT371330cdouy70GprId01Bilw0ohywRL58h9y50afrgiSMMZFRTnBieIT1fokmNdG7n3Xg7-VBMuDcfJv4-TBODkZl0pfHAeMTa_VfeGdUwl4dQSS3mCNh6HtwgNXMV4UWCQun7guRP3zPg_-m0xdGJWrLwv5lYrL8losJU98OfFNv_v_dX8DeALG-g</recordid><startdate>20111201</startdate><enddate>20111201</enddate><creator>Wolf, Sebastian</creator><creator>Holz, Frank G</creator><creator>Korobelnik, Jean-François</creator><creator>Lanzetta, Paolo</creator><creator>Mitchell, Paul</creator><creator>Prünte, Christian</creator><creator>Schmidt-Erfurth, Ursula</creator><creator>Weichselberger, Andreas</creator><creator>Hashad, Yehia</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20111201</creationdate><title>Outcomes following three-line vision loss during treatment of neovascular age-related macular degeneration: subgroup analyses from MARINA and ANCHOR</title><author>Wolf, Sebastian ; 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The visit when the ≥3-line BCVA loss was detected was defined as the new baseline.ResultsContinued monthly ranibizumab treatment led to an improvement in mean BCVA from the new baseline. On average, patients with acute BCVA loss gained 11.9 letters at 3 months after the new baseline, compared with 0.3 letters gained with sham. No strong signals were detected in patient demographics and baseline characteristics for prognostic markers of BCVA loss. Furthermore, there was no pattern in the AE profile of patients with acute BCVA loss to suggest that BCVA recovery could be attributed to spontaneously resolving AEs.ConclusionContinued ranibizumab treatment appears to be beneficial for patients with neovascular age-related macular degeneration who experience a ≥3-line BCVA loss during the first year of treatment.</abstract><cop>BMA House, Tavistock Square, London, WC1H 9JR</cop><pub>BMJ Publishing Group Ltd</pub><pmid>21951567</pmid><doi>10.1136/bjophthalmol-2011-300471</doi><tpages>6</tpages></addata></record>
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subjects Aged
Angiogenesis Inhibitors - therapeutic use
angiogenesisretina
Anti-VEGF
Antibodies, Monoclonal, Humanized - therapeutic use
Biological and medical sciences
choroid
Choroidal Neovascularization - drug therapy
Choroidal Neovascularization - physiopathology
clinical trial
degeneration
Double-Blind Method
epidemiology
Female
Humans
imaging
maculaneovascularisation
Macular degeneration
Macular Degeneration - drug therapy
Macular Degeneration - physiopathology
Male
Marinas
Medical sciences
Miscellaneous
neovascular AMD
neovascularisation
Ophthalmology
pathology
Patients
physiologypathology
Prospective Studies
public health
Ranibizumab
retina
Retinopathies
treatment lasers
treatment medical
treatment other
Treatment Outcome
treatment outcomes
treatment surgery
Vision disorders
Visual Acuity
title Outcomes following three-line vision loss during treatment of neovascular age-related macular degeneration: subgroup analyses from MARINA and ANCHOR
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