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Ocular Toxicity in GD-2 Antibody Therapy: A Case Study.
1Division of Pediatric Hematology/Oncology, Department of Pediatrics, Center for Children's Cancer and Blood Disorders, SUNY Upstate Medical University, Syracuse, NY, USA.
Journal of Pediatric Hematology/Oncology Nursing
|April 18, 2025
Summary
Ocular toxicities like pupillary palsy are rare side effects of dinutuximab therapy in children with neuroblastoma. Early recognition and reporting by care providers are crucial for managing these visual adverse events.
Area of Science:
- Pediatric Oncology
- Ophthalmology
- Pharmacology
Background:
- Neuroblastoma treatment with GD-2 antibodies, such as dinutuximab, can rarely cause ocular toxicities.
- Ocular adverse events, including pupillary palsy, visual acuity changes, and photophobia, require careful monitoring.
Purpose of the Study:
- To present the clinical presentation and management of two cases of ocular toxicity in children undergoing dinutuximab therapy.
- To emphasize the importance of healthcare providers in recognizing and reporting ocular adverse effects.
Main Methods:
- A case study of a 6-year-old boy with high-risk neuroblastoma treated with dinutuximab.
- Ophthalmological evaluation and symptomatic treatment with pilocarpine drops and sunglasses.
Main Results:
- The patient experienced bilateral mydriasis, decreased visual acuity, and photophobia after dinutuximab therapy.
- Pilocarpine provided some relief from photophobia and improved pupillary response, though visual acuity did not fully recover.
- Lack of baseline visual screening hindered precise toxicity assessment, and treatment was continued due to greater risks associated with dose modification.
Conclusions:
- Baseline ophthalmological screening is essential before initiating GD-2 antibody therapy to accurately assess visual changes.
- Less common ocular toxicities associated with dinutuximab therapy may be underreported, necessitating improved recognition and management strategies for healthcare providers.

