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Updated: Jul 1, 2026

Reconstruct Human Retinoblastoma In Vitro
Published on: October 11, 2022
[Radiotherapy in the treatment of retinoblastoma: about 40 cases]
1Unité de recherche, radiothérapie oculaire et cervico-faciale, service de radiothérapie, institut Salah-Azaiz-Bab-Saadoun, boulevard du 9-Avril, 1006 Tunis, Tunisie. hatem.frikha@rns.tn
Insights
Radiotherapy for retinoblastoma offers functional eye conservation but carries risks. Newer techniques aim to reduce these complications, leading to more restricted use of traditional radiotherapy.
Area of Science:
- Ophthalmology
- Pediatric Oncology
- Radiation Oncology
Context:
- Retinoblastoma is a pediatric eye cancer.
- Radiotherapy has been a treatment modality for retinoblastoma.
- Assessing radiotherapy outcomes and complications is crucial for treatment planning.
Purpose:
- To analyze the results and complications of radiotherapy in retinoblastoma treatment.
- To evaluate the efficacy and safety of radiotherapy in a cohort of pediatric patients.
- To understand the long-term outcomes and side effects of radiotherapy for retinoblastoma.
Summary:
- Forty children with retinoblastoma received radiotherapy between 1994 and 2004.
- External beam radiotherapy was the primary method, with some cases receiving brachytherapy.
- Radiotherapy was administered conservatively in 20 eyes and postoperatively in 36 orbital cavities, often combined with chemotherapy.
Impact:
- Radiotherapy demonstrated functional eye conservation in 18 of 20 conservatively treated eyes.
- The major complication observed was facial bone growth defects, with one case of secondary bone sarcoma.
- While effective for local control, radiotherapy's use is increasingly limited due to iatrogenic risks, favoring newer methods like chemotherapy and advanced radiotherapy techniques.
Purpose:
The aim of this study is to analyze the results and the complications of radiotherapy in the treatment of retinoblastoma.
Patients And Methods:
Between 1994 and 2004, 40 children received radiotherapy for a retinoblastoma in Salah Azaiz Institute. The average age of the patients was 36 months (four to 132 months). There were 16 girls and 24 boys. Sixteen children presented a bilateral disease and 24 children a unilateral disease. Twenty eyes and thirty-six orbital cavities in 40 children with retinoblastoma were treated by radiotherapy. One child with a unilateral anterior retinoblastoma was treated with 106 ruthenium brachytherapy. External radiotherapy has been used to treat the 39 patients. In 20 cases the irradiation was conservative and in 36 cases postoperatively. The latter (n=36) presented at least one risk factor of relapses noted in the histological examination. The average dose was 44 Gy (1.8 to 2 Gy per fraction, five fractions weekly). This radiotherapy was associated with chemotherapy in 24 cases.
Results:
Thirty-five children were followed with an average follow-up of 53 months (3-108 months). The average delay of relapses was of 10 months (two to 26 months). We found four orbital relapses and seven metastasis in nine children. The conservation of the eye with a useful visual field was noted in 18 cases among the 20 conservative irradiated eyes. The major therapeutic complication was the growth defect of the bones face. A femoral bone sarcoma was noted five years after the end of the irradiation and chemotherapy in one case.
Conclusion:
If the radiotherapy offers the advantage of the functional conservation and the improvement of the local control, its indications are more and more restricted in favor of the other therapeutic methods (chemotherapy, thermochemotherapy) and this considering the iatrogene risk. The development of new techniques of brachytherapy and the progresses of the conformational radiotherapy appear to reduce considerably this risk.
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