Interleukin-2 was part of the original immunotherapy package but a large European trial showed it adds toxicity and no benefit, so it has been dropped.
Interleukin-2 was part of the original anti-GD2 immunotherapy package for high-risk neuroblastoma, and this caution pairing records why it has been dropped. In the R2 randomised comparison of the SIOPEN HR-NBL1 trial, adding subcutaneous IL-2 to dinutuximab beta produced no meaningful improvement in event-free survival but far more severe toxicity. The rationale is that IL-2 expands regulatory T cells and causes capillary leak, whereas the NK-cell-mediated antibody-dependent cytotoxicity that the anti-GD2 antibody relies on is sufficiently supported by GM-CSF. European protocols omit IL-2 and the Children's Oncology Group has since removed it as well in ANBL1531, so the combination now stands as a warning example within the broader cytokine therapy record.
Shares Dinutuximab (ch14.18) / dinutuximab beta, High-risk neuroblastoma, Neuroblastoma (paediatric).
Shares SIOPEN HR-NBL1, High-risk neuroblastoma.
Shares SIOPEN HR-NBL1, Neuroblastoma (paediatric).
Shares Dinutuximab (ch14.18) / dinutuximab beta, High-risk neuroblastoma, Neuroblastoma (paediatric).
Shares Dinutuximab (ch14.18) / dinutuximab beta, High-risk neuroblastoma, Neuroblastoma (paediatric).
Shares Dinutuximab (ch14.18) / dinutuximab beta, High-risk neuroblastoma, Neuroblastoma (paediatric).
Shares Dinutuximab (ch14.18) / dinutuximab beta, High-risk neuroblastoma, Neuroblastoma (paediatric).
Shares Dinutuximab (ch14.18) / dinutuximab beta, High-risk neuroblastoma, Neuroblastoma (paediatric).