TY - JOUR
T1 - Anti-vascular endothelial growth factor treatment in diabetic macular edema
T2 - Results from a large single-center cohort with bevacizumab as first-line therapy
AU - Zur, Dinah
AU - Hod, Keren
AU - Trivizki, Omer
AU - Rabinovitch, David
AU - Schwartz, Shulamit
AU - Shulman, Shiri
N1 - Publisher Copyright:
© by Ophthalmic Communications Society, Inc.
PY - 2024/8/1
Y1 - 2024/8/1
N2 - Purpose:To explore visual acuity (VA) outcomes of anti-vascular endothelial growth factor (VEGF) intravitreal injections in treatment-naive eyes with diabetic macular edema (DME), with bevacizumab as first-line treatment.Methods:Retrospective single-center cohort study over a three-year follow-up. Overall, 1765 eyes from 1179 patients treated with intravitreal injections were evaluated. The cohort was divided according to the treatment given: (1) bevacizumab monotherapy, (2) eyes switched to a second-line agent, and (3) eyes switched to a third-line agent.Results:In total, 644 eyes of 444 patients met inclusion criteria. The mean age at presentation was 64.0 ± 11.1 years. The mean follow-up period was 24.6 ± 12.4 months. Furthermore, 67.1% of eyes were treated with bevacizumab monotherapy, 25.45% switched to a second-line agent, and 7.45% were switched to a third-line agent. The mean number of injections decreased significantly during each treatment year in the total cohort and within each treatment group (P < 0.001). Mean VA for the total cohort and within each treatment group improved significantly throughout follow-up (P < 0.001). No significant difference in VA was found between the groups (P = 0.373).Conclusion:This real-world study demonstrates robust and consistent VA gains over long-term follow-up in eyes with DME treated with either bevacizumab monotherapy or switching to alternative anti-VEGF agents in cases of suboptimal response.
AB - Purpose:To explore visual acuity (VA) outcomes of anti-vascular endothelial growth factor (VEGF) intravitreal injections in treatment-naive eyes with diabetic macular edema (DME), with bevacizumab as first-line treatment.Methods:Retrospective single-center cohort study over a three-year follow-up. Overall, 1765 eyes from 1179 patients treated with intravitreal injections were evaluated. The cohort was divided according to the treatment given: (1) bevacizumab monotherapy, (2) eyes switched to a second-line agent, and (3) eyes switched to a third-line agent.Results:In total, 644 eyes of 444 patients met inclusion criteria. The mean age at presentation was 64.0 ± 11.1 years. The mean follow-up period was 24.6 ± 12.4 months. Furthermore, 67.1% of eyes were treated with bevacizumab monotherapy, 25.45% switched to a second-line agent, and 7.45% were switched to a third-line agent. The mean number of injections decreased significantly during each treatment year in the total cohort and within each treatment group (P < 0.001). Mean VA for the total cohort and within each treatment group improved significantly throughout follow-up (P < 0.001). No significant difference in VA was found between the groups (P = 0.373).Conclusion:This real-world study demonstrates robust and consistent VA gains over long-term follow-up in eyes with DME treated with either bevacizumab monotherapy or switching to alternative anti-VEGF agents in cases of suboptimal response.
KW - anti-VEGF
KW - bevacizumab
KW - DME
KW - visual acuity
UR - http://www.scopus.com/inward/record.url?scp=85199680493&partnerID=8YFLogxK
U2 - 10.1097/IAE.0000000000004096
DO - 10.1097/IAE.0000000000004096
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C2 - 38471038
AN - SCOPUS:85199680493
SN - 0275-004X
VL - 44
SP - 1305
EP - 1313
JO - Retina
JF - Retina
IS - 8
ER -