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Early Peripapillary and Macular Microvascular Changes Following Ruthenium-106 Plaque Brachytherapy For Uveal
Mai A Abdelkader1, Shaymaa H Salah1, Salma F Al-Etr1
1From the Cairo University Ocular Oncology Service, Department of Ophthalmology, Kasr Al-Ainy School of Medicine, Cairo University, Cairo, Egypt.
American Journal of Ophthalmology
|January 6, 2026
Summary
Ruthenium-106 brachytherapy for uveal melanoma causes early, subclinical microvascular damage detectable by OCTA. Radial peripapillary capillary changes correlate with radiation dose and vision loss.
Area of Science:
- Ophthalmology
- Radiation Oncology
- Medical Imaging
Background:
- Uveal melanoma is the most common primary intraocular malignancy.
- Ruthenium-106 (Ru-106) episcleral plaque brachytherapy is a standard treatment for uveal melanoma.
- Assessing treatment-induced microvascular changes is crucial for understanding visual outcomes.
Purpose of the Study:
- To evaluate early peripapillary and macular microvascular changes after Ru-106 brachytherapy for uveal melanoma.
- To assess the utility of optical coherence tomography angiography (OCTA) in detecting these changes.
- To correlate microvascular changes with radiation dose and visual acuity.
Main Methods:
- Prospective case series of 24 patients with uveal melanoma treated with Ru-106 brachytherapy.
- Ophthalmic evaluation and OCTA imaging performed at baseline, 3 months, and 6 months post-treatment.
- Quantitative OCTA parameters (vessel density in superficial, deep, and radial peripapillary capillary plexuses; foveal avascular zone area) were analyzed.
Main Results:
- Best-corrected visual acuity declined significantly at 6 months (p=0.028).
- Radial peripapillary capillary density showed early significant reduction (p<0.001), correlating with optic nerve radiation dose and visual decline.
- Deep capillary plexus density declined progressively, with significant foveal avascular zone enlargement (p<0.001).
- Tumor location influenced vascular response patterns.
Conclusions:
- Ru-106 brachytherapy induces early, subclinical microvascular injury detectable by OCTA.
- OCTA can identify distinct patterns of vascular damage (RPC, SCP, DCP) related to radiation dose and tumor location.
- OCTA serves as a potential noninvasive biomarker for early detection and risk stratification of radiation-induced microvascular injury.

