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Real-World Outcomes After Switch From Aflibercept to Faricimab in Eyes With Diabetic Macular Edema
To assess the anatomic and functional outcomes in eyes with diabetic macular edema (DME) switched from intravitreal aflibercept to faricimab in a real-world setting. Retrospective, interventional consecutive case series. Patients with DME were switched from aflibercept to faricimab and categorized b...
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Published in: | Investigative ophthalmology & visual science 2024-12, Vol.65 (14), p.46 |
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description | To assess the anatomic and functional outcomes in eyes with diabetic macular edema (DME) switched from intravitreal aflibercept to faricimab in a real-world setting.
Retrospective, interventional consecutive case series. Patients with DME were switched from aflibercept to faricimab and categorized based on central subfield thickness (CST) 4 weeks after last aflibercept injection into responding DME (rDME, CST reduction >20% or CST ≤ 250 µm) and nonresponding DME (nrDME, CST unchanged or increased). Patients received a loading dose of two monthly faricimab injections followed by a treat-and-extend regimen. Differences in response between rDME and nrDME were analyzed based on injection interval, change in CST, and visual acuity (VA) 12 weeks postswitch.
Fifty-two eyes of 40 patients met inclusion criteria (rDME: n = 26, nrDME: n = 26). Baseline and week 12: VA (logMAR) rDME 0.29 ± 0.23 and 0.22 ± 0.28, nrDME 0.42 ± 0.32 and 0.36 ± 0.29; CST (µm) rDME 370 ± 99 and 288 ± 80, nrDME 384 ± 85 and 380 ± 129. After 12 weeks, 54% rDME and 25% nrDME eyes showed a CST decrease of >20% or CST ≤ 250 µm. Forty-six percent rDME and 50% nrDME eyes had a ±20% CST change, 25% of nrDME eyes had a >20% CST increase, and 73% of rDME eyes and 47% of nrDME eyes reached an extended interval of 8 weeks or longer after 12 weeks.
Most DME eyes previously responding or not responding to aflibercept experienced a reduction or stabilization of DME after 12 weeks of faricimab treatment. rDME showed a better anatomic response, and treatment intervals could be extended earlier and longer than nrDME. |
doi_str_mv | 10.1167/iovs.65.14.46 |
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Retrospective, interventional consecutive case series. Patients with DME were switched from aflibercept to faricimab and categorized based on central subfield thickness (CST) 4 weeks after last aflibercept injection into responding DME (rDME, CST reduction >20% or CST ≤ 250 µm) and nonresponding DME (nrDME, CST unchanged or increased). Patients received a loading dose of two monthly faricimab injections followed by a treat-and-extend regimen. Differences in response between rDME and nrDME were analyzed based on injection interval, change in CST, and visual acuity (VA) 12 weeks postswitch.
Fifty-two eyes of 40 patients met inclusion criteria (rDME: n = 26, nrDME: n = 26). Baseline and week 12: VA (logMAR) rDME 0.29 ± 0.23 and 0.22 ± 0.28, nrDME 0.42 ± 0.32 and 0.36 ± 0.29; CST (µm) rDME 370 ± 99 and 288 ± 80, nrDME 384 ± 85 and 380 ± 129. After 12 weeks, 54% rDME and 25% nrDME eyes showed a CST decrease of >20% or CST ≤ 250 µm. Forty-six percent rDME and 50% nrDME eyes had a ±20% CST change, 25% of nrDME eyes had a >20% CST increase, and 73% of rDME eyes and 47% of nrDME eyes reached an extended interval of 8 weeks or longer after 12 weeks.
Most DME eyes previously responding or not responding to aflibercept experienced a reduction or stabilization of DME after 12 weeks of faricimab treatment. rDME showed a better anatomic response, and treatment intervals could be extended earlier and longer than nrDME.</description><identifier>ISSN: 1552-5783</identifier><identifier>ISSN: 0146-0404</identifier><identifier>EISSN: 1552-5783</identifier><identifier>DOI: 10.1167/iovs.65.14.46</identifier><identifier>PMID: 39739347</identifier><language>eng</language><publisher>United States: The Association for Research in Vision and Ophthalmology</publisher><subject>Aged ; Angiogenesis Inhibitors - administration & dosage ; Angiogenesis Inhibitors - therapeutic use ; Diabetic Retinopathy - diagnosis ; Diabetic Retinopathy - drug therapy ; Diabetic Retinopathy - physiopathology ; Drug Substitution ; Female ; Follow-Up Studies ; Humans ; Intravitreal Injections ; Macular Edema - drug therapy ; Macular Edema - physiopathology ; Male ; Middle Aged ; Receptors, Vascular Endothelial Growth Factor - administration & dosage ; Receptors, Vascular Endothelial Growth Factor - therapeutic use ; Recombinant Fusion Proteins - administration & dosage ; Recombinant Fusion Proteins - therapeutic use ; Retina ; Retrospective Studies ; Tomography, Optical Coherence ; Treatment Outcome ; Vascular Endothelial Growth Factor A - antagonists & inhibitors ; Visual Acuity - physiology</subject><ispartof>Investigative ophthalmology & visual science, 2024-12, Vol.65 (14), p.46</ispartof><rights>Copyright 2024 The Authors 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1865-5d7dd72eca4f7bdd44fe95115013baace13fd92c72fc66bb25e3eb68d02cc34b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11687153/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11687153/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39739347$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huber, Kim Lien</creatorcontrib><creatorcontrib>Stino, Heiko</creatorcontrib><creatorcontrib>Steiner, Irene</creatorcontrib><creatorcontrib>Fuchs, Philipp</creatorcontrib><creatorcontrib>Goldbach, Felix</creatorcontrib><creatorcontrib>Mai, Julia</creatorcontrib><creatorcontrib>Gerendas, Bianca S</creatorcontrib><creatorcontrib>Kriechbaum, Katharina</creatorcontrib><creatorcontrib>Schmidt-Erfurth, Ursula</creatorcontrib><creatorcontrib>Pollreisz, Andreas</creatorcontrib><title>Real-World Outcomes After Switch From Aflibercept to Faricimab in Eyes With Diabetic Macular Edema</title><title>Investigative ophthalmology & visual science</title><addtitle>Invest Ophthalmol Vis Sci</addtitle><description>To assess the anatomic and functional outcomes in eyes with diabetic macular edema (DME) switched from intravitreal aflibercept to faricimab in a real-world setting.
Retrospective, interventional consecutive case series. Patients with DME were switched from aflibercept to faricimab and categorized based on central subfield thickness (CST) 4 weeks after last aflibercept injection into responding DME (rDME, CST reduction >20% or CST ≤ 250 µm) and nonresponding DME (nrDME, CST unchanged or increased). Patients received a loading dose of two monthly faricimab injections followed by a treat-and-extend regimen. Differences in response between rDME and nrDME were analyzed based on injection interval, change in CST, and visual acuity (VA) 12 weeks postswitch.
Fifty-two eyes of 40 patients met inclusion criteria (rDME: n = 26, nrDME: n = 26). Baseline and week 12: VA (logMAR) rDME 0.29 ± 0.23 and 0.22 ± 0.28, nrDME 0.42 ± 0.32 and 0.36 ± 0.29; CST (µm) rDME 370 ± 99 and 288 ± 80, nrDME 384 ± 85 and 380 ± 129. After 12 weeks, 54% rDME and 25% nrDME eyes showed a CST decrease of >20% or CST ≤ 250 µm. Forty-six percent rDME and 50% nrDME eyes had a ±20% CST change, 25% of nrDME eyes had a >20% CST increase, and 73% of rDME eyes and 47% of nrDME eyes reached an extended interval of 8 weeks or longer after 12 weeks.
Most DME eyes previously responding or not responding to aflibercept experienced a reduction or stabilization of DME after 12 weeks of faricimab treatment. rDME showed a better anatomic response, and treatment intervals could be extended earlier and longer than nrDME.</description><subject>Aged</subject><subject>Angiogenesis Inhibitors - administration & dosage</subject><subject>Angiogenesis Inhibitors - therapeutic use</subject><subject>Diabetic Retinopathy - diagnosis</subject><subject>Diabetic Retinopathy - drug therapy</subject><subject>Diabetic Retinopathy - physiopathology</subject><subject>Drug Substitution</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Intravitreal Injections</subject><subject>Macular Edema - drug therapy</subject><subject>Macular Edema - physiopathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Receptors, Vascular Endothelial Growth Factor - administration & dosage</subject><subject>Receptors, Vascular Endothelial Growth Factor - therapeutic use</subject><subject>Recombinant Fusion Proteins - administration & dosage</subject><subject>Recombinant Fusion Proteins - therapeutic use</subject><subject>Retina</subject><subject>Retrospective Studies</subject><subject>Tomography, Optical Coherence</subject><subject>Treatment Outcome</subject><subject>Vascular Endothelial Growth Factor A - antagonists & inhibitors</subject><subject>Visual Acuity - physiology</subject><issn>1552-5783</issn><issn>0146-0404</issn><issn>1552-5783</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpVUU1PGzEQtaoiApRjr5WPvWyw11_JqUI0ASQQElDlaPljtnG1G6e2l4p_jxFpBKcZzbx58_QeQl8pmVIq1VmIT3kqxZTyKZef0BEVom2EmrHP7_oJOs75DyEtpS05RBM2V2zOuDpC9h5M36xi6j2-G4uLA2R83hVI-OFfKG6NlykOddIHC8nBtuAS8dKk4MJgLA4bvHiuJ6tQ1vhnMBZKcPjWuLE3CS88DOYLOuhMn-F0V0_Qr-Xi8eKqubm7vL44v2kcnUnRCK-8Vy04wztlvee8g7mgVBDKrDEOKOv8vHWq7ZyU1rYCGFg586R1jnHLTtCPN97taAfwDjYlmV5vUxWannU0QX_cbMJa_45Puvo4U1SwyvB9x5Di3xFy0UPIDvrebCCOWbMqRlQPCanQ5g3qUsw5Qbf_Q8krodKvwWgpNOWay4r_9l7cHv0_CfYCX0GLyw</recordid><startdate>20241231</startdate><enddate>20241231</enddate><creator>Huber, Kim Lien</creator><creator>Stino, Heiko</creator><creator>Steiner, Irene</creator><creator>Fuchs, Philipp</creator><creator>Goldbach, Felix</creator><creator>Mai, Julia</creator><creator>Gerendas, Bianca S</creator><creator>Kriechbaum, Katharina</creator><creator>Schmidt-Erfurth, Ursula</creator><creator>Pollreisz, Andreas</creator><general>The Association for Research in Vision and Ophthalmology</general><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20241231</creationdate><title>Real-World Outcomes After Switch From Aflibercept to Faricimab in Eyes With Diabetic Macular Edema</title><author>Huber, Kim Lien ; Stino, Heiko ; Steiner, Irene ; Fuchs, Philipp ; Goldbach, Felix ; Mai, Julia ; Gerendas, Bianca S ; Kriechbaum, Katharina ; Schmidt-Erfurth, Ursula ; Pollreisz, Andreas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1865-5d7dd72eca4f7bdd44fe95115013baace13fd92c72fc66bb25e3eb68d02cc34b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aged</topic><topic>Angiogenesis Inhibitors - administration & dosage</topic><topic>Angiogenesis Inhibitors - therapeutic use</topic><topic>Diabetic Retinopathy - diagnosis</topic><topic>Diabetic Retinopathy - drug therapy</topic><topic>Diabetic Retinopathy - physiopathology</topic><topic>Drug Substitution</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Intravitreal Injections</topic><topic>Macular Edema - drug therapy</topic><topic>Macular Edema - physiopathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Receptors, Vascular Endothelial Growth Factor - administration & dosage</topic><topic>Receptors, Vascular Endothelial Growth Factor - therapeutic use</topic><topic>Recombinant Fusion Proteins - administration & dosage</topic><topic>Recombinant Fusion Proteins - therapeutic use</topic><topic>Retina</topic><topic>Retrospective Studies</topic><topic>Tomography, Optical Coherence</topic><topic>Treatment Outcome</topic><topic>Vascular Endothelial Growth Factor A - antagonists & inhibitors</topic><topic>Visual Acuity - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huber, Kim Lien</creatorcontrib><creatorcontrib>Stino, Heiko</creatorcontrib><creatorcontrib>Steiner, Irene</creatorcontrib><creatorcontrib>Fuchs, Philipp</creatorcontrib><creatorcontrib>Goldbach, Felix</creatorcontrib><creatorcontrib>Mai, Julia</creatorcontrib><creatorcontrib>Gerendas, Bianca S</creatorcontrib><creatorcontrib>Kriechbaum, Katharina</creatorcontrib><creatorcontrib>Schmidt-Erfurth, Ursula</creatorcontrib><creatorcontrib>Pollreisz, Andreas</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Investigative ophthalmology & visual science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huber, Kim Lien</au><au>Stino, Heiko</au><au>Steiner, Irene</au><au>Fuchs, Philipp</au><au>Goldbach, Felix</au><au>Mai, Julia</au><au>Gerendas, Bianca S</au><au>Kriechbaum, Katharina</au><au>Schmidt-Erfurth, Ursula</au><au>Pollreisz, Andreas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Real-World Outcomes After Switch From Aflibercept to Faricimab in Eyes With Diabetic Macular Edema</atitle><jtitle>Investigative ophthalmology & visual science</jtitle><addtitle>Invest Ophthalmol Vis Sci</addtitle><date>2024-12-31</date><risdate>2024</risdate><volume>65</volume><issue>14</issue><spage>46</spage><pages>46-</pages><issn>1552-5783</issn><issn>0146-0404</issn><eissn>1552-5783</eissn><abstract>To assess the anatomic and functional outcomes in eyes with diabetic macular edema (DME) switched from intravitreal aflibercept to faricimab in a real-world setting.
Retrospective, interventional consecutive case series. Patients with DME were switched from aflibercept to faricimab and categorized based on central subfield thickness (CST) 4 weeks after last aflibercept injection into responding DME (rDME, CST reduction >20% or CST ≤ 250 µm) and nonresponding DME (nrDME, CST unchanged or increased). Patients received a loading dose of two monthly faricimab injections followed by a treat-and-extend regimen. Differences in response between rDME and nrDME were analyzed based on injection interval, change in CST, and visual acuity (VA) 12 weeks postswitch.
Fifty-two eyes of 40 patients met inclusion criteria (rDME: n = 26, nrDME: n = 26). Baseline and week 12: VA (logMAR) rDME 0.29 ± 0.23 and 0.22 ± 0.28, nrDME 0.42 ± 0.32 and 0.36 ± 0.29; CST (µm) rDME 370 ± 99 and 288 ± 80, nrDME 384 ± 85 and 380 ± 129. After 12 weeks, 54% rDME and 25% nrDME eyes showed a CST decrease of >20% or CST ≤ 250 µm. Forty-six percent rDME and 50% nrDME eyes had a ±20% CST change, 25% of nrDME eyes had a >20% CST increase, and 73% of rDME eyes and 47% of nrDME eyes reached an extended interval of 8 weeks or longer after 12 weeks.
Most DME eyes previously responding or not responding to aflibercept experienced a reduction or stabilization of DME after 12 weeks of faricimab treatment. rDME showed a better anatomic response, and treatment intervals could be extended earlier and longer than nrDME.</abstract><cop>United States</cop><pub>The Association for Research in Vision and Ophthalmology</pub><pmid>39739347</pmid><doi>10.1167/iovs.65.14.46</doi><oa>free_for_read</oa></addata></record> |
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subjects | Aged Angiogenesis Inhibitors - administration & dosage Angiogenesis Inhibitors - therapeutic use Diabetic Retinopathy - diagnosis Diabetic Retinopathy - drug therapy Diabetic Retinopathy - physiopathology Drug Substitution Female Follow-Up Studies Humans Intravitreal Injections Macular Edema - drug therapy Macular Edema - physiopathology Male Middle Aged Receptors, Vascular Endothelial Growth Factor - administration & dosage Receptors, Vascular Endothelial Growth Factor - therapeutic use Recombinant Fusion Proteins - administration & dosage Recombinant Fusion Proteins - therapeutic use Retina Retrospective Studies Tomography, Optical Coherence Treatment Outcome Vascular Endothelial Growth Factor A - antagonists & inhibitors Visual Acuity - physiology |
title | Real-World Outcomes After Switch From Aflibercept to Faricimab in Eyes With Diabetic Macular Edema |
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