# Outcomes and Predictive Factors of I-125 Plaque Therapy for Refractory Retinoblastoma

**Authors:** Yacoub A. Yousef, Farah Halawa, Mona Mohammad, Lama Al-Fahoum, Rama Soudi, Mustafa Mehyar, Reem AlJabari, Hadeel Halalsheh, Ibrahim AlNawaiseh, Imad Jaradat

PMC · DOI: 10.3390/jcm14051778 · Journal of Clinical Medicine · 2025-03-06

## TL;DR

I-125 radioactive plaque therapy helps control 70% of hard-to-treat retinoblastoma cases but has a 30% recurrence rate, suggesting the need for better treatment strategies.

## Contribution

The study identifies predictive factors for eye salvage and tumor recurrence in refractory retinoblastoma treated with I-125 plaque therapy.

## Key findings

- I-125 plaque therapy achieved tumor control and eye salvage in 70% of refractory retinoblastoma cases.
- Recurrence occurred in 30% of cases within 6 months on average, with factors like Group D disease and active vitreous seeds linked to poor outcomes.
- Complications included cataracts, tumor hemorrhage, and retinal detachment, but most patients remained metastasis-free.

## Abstract

Objective: This study aimed to evaluate the outcomes and predictive factors of I-125 radioactive plaque therapy for recurrent and refractory retinoblastoma (Rb) cases that failed primary systemic chemotherapy and focal therapies. Methods: A retrospective study of 20 eyes with intraocular Rb treated with I-125 radioactive plaque therapy (Apex dose 45 Gy) from 2013 to 2023 was conducted. Data on tumor characteristics, treatments, and outcomes were collected over a follow-up period of at least one year. Results: There were 11 (55%) males and 8 (40%) patients who had bilateral disease. All 20 treated eyes (100%) showed initial tumor regression, while long-term tumor control and eye salvage were achieved in 14 eyes (70%). Six eyes (30%) experienced uncontrollable tumor recurrence after a mean of 6 months (range: 3–12 months) after plaque therapy. Recurrence included main tumor activity in six eyes and additional resistant vitreous seeds in two of them. Poor predictive factors for eye salvage included Group D at diagnosis (p = 0.044), active vitreous seeds at the time of plaque therapy ((p = 0.045), tumor thickness >5.0 mm (p = 0.045), and tumor base dimension >12 mm (p = 0.023). Post-plaque complications included cataracts in seven eyes (35%), tumor hemorrhage in six eyes (30%), retinal detachment in four eyes (20%), radiation retinopathy in three eyes (15%), and neovascular glaucoma in one eye (5%). Five (83%) of those with tumor hemorrhage had plaque surgery performed within less than 6 months of the last cycle of systemic chemotherapy. At a mean follow-up of 36 months (range: 12–96 months), five eyes (25%) were enucleated, and high-risk pathological features were identified in three eyes, including post-laminar optic nerve infiltration (one eye) and massive choroidal invasion (two eyes). All patients were alive and free of metastasis except one patient (5%) whose parents refused enucleation and came back with extra-scleral extension and bone marrow metastasis and eventually passed away. Conclusions: I-125 radioactive plaque therapy is a valuable salvage treatment for recurrent and refractory retinoblastoma, achieving tumor control and eye salvage in 70% of cases with an acceptable safety profile. However, the observed recurrence rate (30%) at an apex dose of 45 Gy suggests a need for dose optimization and individualized treatment strategies. Identifying high-risk features, such as Group D disease, active vitreous seeds, and larger tumors, is crucial for patient selection and outcome prediction. Future research should explore alternative dosing strategies, combination therapies, and improved predictive models to enhance long-term tumor control while minimizing complications.

## Linked entities

- **Diseases:** retinoblastoma (MONDO:0008380)

## Full-text entities

- **Diseases:** D (MESH:D014808), bone marrow metastasis (MESH:D001855), cataracts (MESH:D002386), radiation retinopathy (MESH:D011832), neovascular glaucoma (MESH:D015355), metastasis (MESH:D009362), Rb (MESH:D012175), tumor (MESH:D009369), retinal detachment (MESH:D012163)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC11901221/full.md

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Source: https://tomesphere.com/paper/PMC11901221