# Prolonged overall survival in a child with multimetastatic retinoblastoma treated with anti-GD2 monoclonal antibody dinutuximab beta: a case report

**Authors:** Valentina Di Ruscio, Alessia Carboni, Giada Del Baldo, Maria Debora De Pasquale, Paola Valente, Angela Di Giannatale, Annalisa Serra, Rita De Vito, Angela Mastronuzzi, Concetta Quintarelli, Biagio De Angelis, Giuseppe Maria Milano, Ida Russo

PMC · DOI: 10.3389/fonc.2025.1665968 · 2025-10-17

## TL;DR

A 2-year-old child with advanced retinoblastoma achieved long-term remission using anti-GD2 monoclonal antibody therapy as part of their treatment.

## Contribution

This case report demonstrates the potential of anti-GD2 immunotherapy as a consolidation treatment for advanced retinoblastoma.

## Key findings

- The patient achieved complete remission after treatment with anti-GD2 monoclonal antibody Dinutuximab beta.
- The child remained disease-free for six years following the initial diagnosis.
- The treatment may reduce the toxicity of standard therapies for retinoblastoma.

## Abstract

High-dose chemotherapy with autologous stem cell rescue has improved outcomes in patients with metastatic retinoblastoma (RB). However, significant short- and long-term toxicities—especially in very young children with a constitutional RB1 gene mutation—highlight the need for alternative therapeutic strategies. Monoclonal antibodies targeting tumor-associated antigens such as GD2 have emerged as promising agents in this setting. We report the case of a 2-year-old child diagnosed with extensive left-eye retinoblastoma and massive extraocular dissemination at presentation. The patient was treated with systemic conventional and high-dose chemotherapy combined with intrathecal Topotecan. As consolidation therapy, the child received three courses of the anti-GD2 monoclonal antibody Dinutuximab beta over a 10-day schedule. The patient achieved complete remission and remains disease-free six years after the initial diagnosis. This case suggests that anti-GD2 immunotherapy, used as consolidation treatment, may improve the prognosis of patients with advanced retinoblastoma and potentially reduce the toxicity associated with standard therapies. Further clinical investigation is warranted to validate these findings.

## Linked entities

- **Genes:** RB1 (RB transcriptional corepressor 1) [NCBI Gene 5925]
- **Chemicals:** Topotecan (PubChem CID 60700)
- **Diseases:** retinoblastoma (MONDO:0008380)

## Full-text entities

- **Genes:** RB1 (RB transcriptional corepressor 1) [NCBI Gene 5925] {aka OSRC, PPP1R130, RB, p105-Rb, p110-RB1, pRb}
- **Diseases:** RB (MESH:D012175), tumor (MESH:D009369), toxicities (MESH:D064420)
- **Chemicals:** Dinutuximab beta (MESH:C112746), Topotecan (MESH:D019772)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12575136/full.md

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Source: https://tomesphere.com/paper/PMC12575136