Early detection and management of radiation maculopathy after plaque brachytherapy for uveal melanoma: a multimodal imaging narrative review
- 1Department of Ophthalmology, University Hospital and Faculty of Medicine, Autonomous University of Nuevo Leon
- 2Department of Ophthalmology, Universidad Maimonides
Abstract
Background: Radiation retinopathy is a dose- and time-dependent neurovascular complication of ocular radiotherapy. Radiation maculopathy denotes macular involvement and may present with early retinal thickening or edema, progressive nonperfusion, or late atrophy. Its biology is not a single linear sequence: endothelial, inflammatory, permeability, ischemic, and neuronal changes overlap.
Objective: To critically review terminology, classification, plaque-related dosimetry, multimodal imaging biomarkers, and preventive and therapeutic evidence for radiation maculopathy after plaque brachytherapy for uveal melanoma.
Methods: PubMed/MEDLINE was searched from January 2000 through 24 September 2026 using combinations of uveal melanoma, radiation retinopathy, radiation maculopathy, plaque brachytherapy, iodine-125, ruthenium-106, palladium-103, cesium-131, OCT, OCT angiography, fluorescein angiography, laser speckle flowgraphy, anti-VEGF, bevacizumab, ranibizumab, aflibercept, corticosteroid, and laser. Seminal pre-2000 studies and additional records identified from reference lists were retained when they defined classification, natural history, or treatment. Original clinical studies were prioritized for efficacy and imaging claims; reviews were used for context and evidence synthesis.
Results: Structural OCT can reveal macular edema before ophthalmoscopic radiation retinopathy, but thickness changes also reflect neuronal swelling and late atrophy. OCTA detects capillary-density loss and foveal avascular zone change, yet measurements depend on signal quality and segmentation and are especially vulnerable to cystoid edema. Fluorescein angiography remains important for leakage and wide-field ischemic burden, while laser speckle flowgraphy is an investigational perfusion measure. Anti-VEGF therapy is the best-supported treatment for established radiation-related macular edema and generally requires sustained dosing. Prophylactic anti-VEGF cohorts show lower rates of edema and some radiation complications, but long-term visual superiority is not consistently demonstrated and randomized plaque-specific evidence is lacking. Corticosteroids and laser have selective roles.
Conclusions: Surveillance should be multimodal and individualized according to tumor location, patient-specific dosimetry, visual potential, and serial structural and perfusion findings. OCTA complements rather than replaces structural OCT and angiography. No validated OCTA threshold currently justifies treatment in an otherwise unaffected eye; prospective studies must define reproducible biomarkers and treatment triggers.
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BibTeX
@article{gonzalezcortes2026early,
title = {{Early detection and management of radiation maculopathy after plaque brachytherapy for uveal melanoma: a multimodal imaging narrative review}},
author = {Jesus Hernan Gonzalez-Cortes and Jesus Emiliano Gonzalez-Cantu and Anibal Martin Folgar and David Pelayes and Jesus Mohamed-Hamsho},
journal = {Frontiers in Oncology},
year = {2026},
month = oct,
doi = {10.3389/fonc.2026.1926816},
url = {https://www.frontiersin.org/articles/10.3389/fonc.2026.1926816/full},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Early detection and management of radiation maculopathy after plaque brachytherapy for uveal melanoma: a multimodal imaging narrative review
AU - Jesus Hernan Gonzalez-Cortes
AU - Jesus Emiliano Gonzalez-Cantu
AU - Anibal Martin Folgar
AU - David Pelayes
AU - Jesus Mohamed-Hamsho
PY - 2026
DA - 2026/10/29
JO - Frontiers in Oncology
DO - 10.3389/fonc.2026.1926816
UR - https://www.frontiersin.org/articles/10.3389/fonc.2026.1926816/full
AB - Background: Radiation retinopathy is a dose- and time-dependent neurovascular complication of ocular radiotherapy. Radiation maculopathy denotes macular involvement and may present with early retinal thickening or edema, progressive nonperfusion, or late atrophy. Its biology is not a single linear sequence: endothelial, inflammatory, permeability, ischemic, and neuronal changes overlap. Objective: To critically review terminology, classification, plaque-related dosimetry, multimodal imaging biomarkers, and preventive and therapeutic evidence for radiation maculopathy after plaque brachytherapy for uveal melanoma. Methods: PubMed/MEDLINE was searched from January 2000 through 24 September 2026 using combinations of uveal melanoma, radiation retinopathy, radiation maculopathy, plaque brachytherapy, iodine-125, ruthenium-106, palladium-103, cesium-131, OCT, OCT angiography, fluorescein angiography, laser speckle flowgraphy, anti-VEGF, bevacizumab, ranibizumab, aflibercept, corticosteroid, and laser. Seminal pre-2000 studies and additional records identified from reference lists were retained when they defined classification, natural history, or treatment. Original clinical studies were prioritized for efficacy and imaging claims; reviews were used for context and evidence synthesis. Results: Structural OCT can reveal macular edema before ophthalmoscopic radiation retinopathy, but thickness changes also reflect neuronal swelling and late atrophy. OCTA detects capillary-density loss and foveal avascular zone change, yet measurements depend on signal quality and segmentation and are especially vulnerable to cystoid edema. Fluorescein angiography remains important for leakage and wide-field ischemic burden, while laser speckle flowgraphy is an investigational perfusion measure. Anti-VEGF therapy is the best-supported treatment for established radiation-related macular edema and generally requires sustained dosing. Prophylactic anti-VEGF cohorts show lower rates of edema and some radiation complications, but long-term visual superiority is not consistently demonstrated and randomized plaque-specific evidence is lacking. Corticosteroids and laser have selective roles. Conclusions: Surveillance should be multimodal and individualized according to tumor location, patient-specific dosimetry, visual potential, and serial structural and perfusion findings. OCTA complements rather than replaces structural OCT and angiography. No validated OCTA threshold currently justifies treatment in an otherwise unaffected eye; prospective studies must define reproducible biomarkers and treatment triggers.
SN - 2234-943X
ER -