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Updated: Apr 18, 2026

Author Spotlight: Overcoming Anti-VEGF Resistance Through Advanced Vascular Morphology Assessment in Choroidal Neovascularization
Published on: August 11, 2023
Changes of choroidal neovascularization in indocyanine green angiography after intravitreal ranibizumab injection
Ji Eun Lee1, Hyun Woong Kim, Sang Joon Lee
1*Department of Ophthalmology, School of Medicine, Pusan National University, Yangsan, Korea; †Medical Institute, Pusan National University Hospital, Busan, Korea; ‡College of Medicine, Inje University, Busan, Korea; §Department of Ophthalmology, Busan Paik Hospital, Busan, Korea; ¶Department of Ophthalmology, Gospel Hospital, College of Medicine, Kosin University, Busan, Korea; and **Department of Ophthalmology, Haeundae Paik Hospital, Busan, Korea.
Purpose:
To investigate vascular structural changes of choroidal neovascularization (CNV) followed by intravitreal ranibizumab injections using indocyanine green angiography.
Methods:
A total of 31 patients with exudative age-related macular degeneration and CNV whose structures were identifiable in indocyanine green angiography were included. Ranibizumab was injected into the vitreous cavity once a month for 3 months and then as needed for the next 3 months prospectively. Indocyanine green angiography was performed at baseline, 3, and 6 months. Early to midphase images of the indocyanine green angiography in the details of vascular structure of the CNV were discerned the best were used in the image analysis. Vascular structures of CNV were described as arteriovenular and capillary components, and structural changes were assessed.
Results:
Arteriovenular components were observed in 29 eyes (94%). Regression of the capillary components was observed in most cases. Although regression of arteriovenular component was noted in 14 eyes (48%), complete resolution was not observed. The eyes were categorized into 3 groups according to CNV structural changes: the regressed (Group R, 10 eyes, 31%), the matured (Group M, 7 eyes, 23%), and the growing (Group G, 14 eyes, 45%). In Group R, there was no regrowth of CNV found at 6 months. In Group M, distinct vascular structures were observed at 3 months and persisted without apparent changes at 6 months. In Group G, growth or reperfusion of capillary components from the persisting arteriovenular components was noted at 6 months.
Conclusion:
Both capillary and arteriovenular components were regressed during monthly ranibizumab injections. However, CNV regrowth was observed in a group of patients during the as-needed treatment phase.
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