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High-Risk Neuroblastoma Challenges and Opportunities for Antibody-Based Cellular Immunotherapy
Natasha V Persaud1, Jeong A Park2, Nai Kong V Cheung1
1Department of Pediatrics Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Journal of Clinical Medicine
|August 29, 2024
Summary
Immunotherapy offers a promising avenue for high-risk neuroblastoma (NB). This review explores immune strategies, including novel T cell-based therapies targeting GD2, to improve outcomes for NB patients.
Area of Science:
- Oncology
- Immunology
- Cancer Therapeutics
Background:
- Neuroblastoma (NB) is a heterogeneous cancer of the sympathetic nervous system with approximately 50% cure rates despite intensive treatment.
- Relapsed or refractory high-risk neuroblastoma (HRNB) presents significant therapeutic challenges.
- Risk stratification and stage-adapted therapies have improved outcomes but curative challenges persist.
Purpose of the Study:
- To review current immune approaches for neuroblastoma (NB).
- To discuss the tumor microenvironment (TME) in the context of NB immunotherapy.
- To propose a novel T cell-based therapeutic strategy for HRNB.
Main Methods:
- Review of existing literature on immunotherapy for neuroblastoma.
- Analysis of immune strategies including monoclonal antibodies, vaccines, and adoptive cell therapy.
- Exploration of the tumor microenvironment (TME) and its role in NB pathogenesis and treatment.
Main Results:
- Immunotherapy, including targeted agents like monoclonal antibodies, is an attractive option for relapsed/refractory HRNB.
- Adoptive cellular therapies and their combinations show potential but face toxicity concerns.
- Leveraging tumor surface antigens like ganglioside GD2 is a key strategy.
Conclusions:
- Novel T cell-based immunotherapies hold promise for improving cure rates in high-risk neuroblastoma.
- Integrating advancements in adoptive cell therapy with antibody-based approaches may overcome current limitations.
- Further research into TME modulation is crucial for optimizing NB immunotherapy.
Keywords:
adoptive cellular therapyex vivo armed T cell with bispecific antibody (EAT)high-risk neuroblastomaMore Related Videos
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