Short-Term Clinical Outcomes of Patients with Diabetic Macular Edema Following a Therapy Switch to Faricimab

被引:7
作者
Wolfrum, Peter [1 ]
Boehm, Elsa Wilma [1 ]
Lorenz, Katrin [1 ]
Stoffelns, Bernhard [1 ]
Pfeiffer, Norbert [1 ]
Korb, Christina A. [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Ophthalmol, Langenbeckstr 1, D-55131 Mainz, Germany
关键词
diabetic retinopathy; diabetic macular edema; diabetes; anti-VEGF; retina; DME; faricimab; CONTROL-CARDIOVASCULAR-RISK; GROWTH-FACTOR THERAPY; REAL-WORLD; RETINOPATHY; PROGRESSION;
D O I
10.3390/jcm13154508
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: With this study, we investigate the short-term clinical outcomes of patients affected by diabetic macular edema (DME) after switching to intravitreal Faricimab (IVF) in a real-world setting. Methods: We conducted a retrospective chart review on all patients treated for DME with IVF who showed insufficient responses to prior anti-VEGF therapy. Data collected included baseline patient demographics, medical history, best-corrected visual acuity (BCVA), central retinal thickness (CRT) and central retinal volume (CRV). We analyzed functional and structural measures before and after IVF, compared baseline demographics and treatment factors between Faricimab-responders and reduced-responders and assessed influencing factors of the follow-up BCVA and CRT. Results: This study included 25 eyes from 16 patients. After switching to IVF, the mean BCVA showed no significant improvement, changing from 59.4 +/- 13.4 Early Treatment of Diabetic Retinopathy Study (ETDRS) letters at baseline to 61.4 +/- 12.8 ETDRS letters at follow-up (p = 0.26). CRT significantly reduced from 414.4 +/- 126.3 mu m to 353.3 +/- 131.1 mu m (p < 0.011), and the 3 mm CRV significantly decreased from 2.8 +/- 0.5 mm(3) to 2.6 +/- 0.6 mm(3) (p < 0.012). Seven patients met the responder criteria, exhibiting an improvement of at least 5 ETDRS letters and a simultaneous CRT reduction of at least 30 mu m. Further analysis showed that higher BCVA at baseline (p < 0.001) was associated with better BCVA following IVF, while higher baseline CRT (p < 0.003), a higher number of prior anti-VEGF agents (p < 0.034) and prior corticosteroid injections (p < 0.019) were associated with greater CRT at follow-up. Conclusions: Following the initial IVF injection series, we observed a clear improvement of anatomical measures. No functional improvement was observed, although visual acuity remained stable. Higher baseline BCVA was associated with better post-IVF BCVA, while higher baseline CRT, a greater number of prior anti-VEGF agents and prior corticosteroid injections were linked to higher CRT post-IVF.
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页数:11
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共 36 条
[1]  
[Anonymous], 1991, OPHTHALMOLOGY, V98, P741
[2]  
Beaser Richard S, 2018, Diabetes Spectr, V31, P65, DOI [10.2337/ds16-0043, 10.2337/ds16-0043]
[3]   A computerized method of visual acuity testing: Adaptation of the early treatment of diabetic retinopathy study testing protocol [J].
Beck, RW ;
Moke, PS ;
Turpin, AH ;
Ferris, FL ;
Sangiovanni, JP ;
Johnson, CA ;
Birch, EE ;
Chandler, DL ;
Cox, TA ;
Blair, RC ;
Kraker, RT .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 2003, 135 (02) :194-205
[4]   Delineating effects of angiopoietin-2 inhibition on vascular permeability and inflammation in models of retinal neovascularization and ischemia/reperfusion [J].
Canonica, Jeremie ;
Foxton, Richard ;
Garrido, Marina Garcia ;
Lin, Cheng-Mao ;
Uhles, Sabine ;
Shanmugam, Sumathi ;
Antonetti, David A. ;
Abcouwer, Steven F. ;
Westenskow, Peter D. .
FRONTIERS IN CELLULAR NEUROSCIENCE, 2023, 17
[5]   Persistent Effects of Intensive Glycemic Control on Retinopathy in Type 2 Diabetes in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) Follow-On Study [J].
Chew, Emily Y. ;
Lovato, James F. ;
Davis, Matthew D. ;
Gerstein, Hertzel C. ;
Danis, Ronald P. ;
Ismail-Beigi, Faramarz ;
Genuth, Saul ;
Greven, Craig M. ;
Perdue, Letitia H. ;
Cushman, William C. ;
Elam, Marshall B. ;
Bigger, J. Thomas ;
Ginsberg, Henry N. ;
Goff, David C., Jr. ;
Ambrosius, Walter T. .
DIABETES CARE, 2016, 39 (07) :1089-1100
[6]   The Effects of Medical Management on the Progression of Diabetic Retinopathy in Persons with Type 2 Diabetes The Action to Control Cardiovascular Risk in Diabetes (ACCORD) Eye Study [J].
Chew, Emily Y. ;
Davis, Matthew D. ;
Danis, Ronald P. ;
Lovato, James F. ;
Perdue, Letitia H. ;
Greven, Craig ;
Genuth, Saul ;
Goff, David C. ;
Leiter, Lawrence A. ;
Ismail-Beigi, Faramarz ;
Ambrosius, Walter T. .
OPHTHALMOLOGY, 2014, 121 (12) :2443-2451
[7]   Effects of Medical Therapies on Retinopathy Progression in Type 2 Diabetes. [J].
Chew, Emily Y. ;
Ambrosius, Walter T. ;
Davis, Matthew D. ;
Danis, Ronald P. ;
Gangaputra, Sapna ;
Greven, Craig M. ;
Hubbard, Larry ;
Esser, Barbara A. ;
Lovato, James F. ;
Perdue, Letitia H. ;
Goff, David C., Jr. ;
Cushman, William C. ;
Ginsberg, Henry N. ;
Elam, Marshall B. ;
Genuth, Saul ;
Gerstein, Hertzel C. ;
Schubart, Ulrich ;
Fine, Lawrence J. .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (03) :233-244
[8]   Real-world Outcomes of Anti-Vascular Endothelial Growth Factor Therapy in Diabetic Macular Edema in the United States [J].
Ciulla, Thomas A. ;
Bracha, Peter ;
Pollack, John ;
Williams, David F. .
OPHTHALMOLOGY RETINA, 2018, 2 (12) :1179-1187
[9]   Functional outcomes of sustained improvement on Diabetic Retinopathy Severity Scale with intravitreal aflibercept in the VISTA and VIVID trials [J].
Dhoot, Dilsher S. ;
Moini, Hadi ;
Reed, Kimberly ;
Du, Weiming ;
Vitti, Robert ;
Berliner, Alyson J. ;
Singh, Rishi P. .
EYE, 2023, 37 (10) :2020-2025
[10]   Angiopoietin-2 differentially regulates angiogenesis through TIE2 and integrin signaling [J].
Felcht, Moritz ;
Luck, Robert ;
Schering, Alexander ;
Seidel, Philipp ;
Srivastava, Kshitij ;
Hu, Junhao ;
Bartol, Arne ;
Kienast, Yvonne ;
Vettel, Christiane ;
Loos, Elias K. ;
Kutschera, Simone ;
Bartels, Susanne ;
Appak, Sila ;
Besemfelder, Eva ;
Terhardt, Dorothee ;
Chavakis, Emmanouil ;
Wieland, Thomas ;
Klein, Christian ;
Thomas, Markus ;
Uemura, Akiyoshi ;
Goerdt, Sergij ;
Augustin, Hellmut G. .
JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (06) :1991-2005