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A review of the clinical use of the humanized mAb Hu3F8, the efficacy of which has been demonstrated in clinical trials and which has been demonstrated in clinical trials.
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Despite the use of multimodal therapy in patients with high-risk neuroblastoma (NB), the prognosis in high-risk patients remains unfavorable. Immunotherapy with monoclonal antibodies (mAb) in the post-consolidation period of treatment of high-risk NB has marked significant progress in improving the prognosis for patients who have achieved a good response to first-line therapy. Currently, the US Food and Drug Administration has approved three mAb drugs for the treatment of patients with high-risk NB: dinutuximab (Ch14.18), dinutuximab beta (Ch14.18/CHO), and naxitamab (Hu3F8). This publication is devoted to a review of the clinical use of the humanized mAb Hu3F8, the efficacy of which has been demonstrated in clinical trials.
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@article{Sagoyan2026Treatment,
title = {Treatment of patients with high-risk neuroblastoma using a humanized monoclonal antibody},
author = {G. B. Sagoyan and А. M. Suleymanova and M. V. Rubanskaya and К. И. Киргизов and С. Р. Варфоломеева},
journal = {Russian Journal of Pediatric Hematology and Oncology},
year = {2026},
doi = {10.21682/2311-1267-2026-13-2-98-107},
url = {https://doi.org/10.21682/2311-1267-2026-13-2-98-107}
}
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