Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Dec:105 Suppl 1:S68-S79.
doi: 10.1016/S0007-4551(18)30392-8.

Nouvelles perspectives dans l’immunothérapie des cancers pédiatriques

[Article in French]
Affiliations
Review

Nouvelles perspectives dans l’immunothérapie des cancers pédiatriques

[Article in French]
Claudia Pasqualini et al. Bull Cancer. 2018 Dec.

Abstract

New therapeutic paradigms are needed to improve the survival of children and adolescents with high-risk malignancies, and to reduce the sequelae associated with treatment. Immunotherapies, targeting tumor cells and/or the immune system to enhance existing anti-tumor immunity or induce novel anti-tumor immune responses, are becoming increasingly successful in adult oncology. Based on the results obtained with anti-ganglioside2 antibodies in neuroblastoma, rituximab in mature B malignancies, immune checkpoint inhibitors in lymphoma and especially in Hodgkin lymphoma, blinatumomab and CAR-T CD19 cells for B-cell acute lymphoblastic leukemia, immunotherapy has demonstrated irrefutable benefits in pediatric patients. However, these results are currently limited to a minority of patients and histologies. Current and ongoing trials tend to focus on a single type of immunotherapy, but it is likely that combinations of immunotherapies with different mechanisms of action or combination with other classes of anti-cancer treatments will be additives or even synergistic. The development of this new class of drugs in the treatment of pediatric cancers has multiple challenges: to better evaluate the response to treatment, to define the optimal doses and schedules, to manage immuno-mediated toxicities, to identify its specific sequelae, and, finally, to better understand the strategies of immune evasion of pediatric cancers in order to develop efficient immunotherapies.

Keywords: Anticorps; CAR T-cells; Cancer; Child; Enfant; Immune checkpoint; Immunotherapy; Immunothérapie; Inhibiteurs des; Monoclonal antibody; immunitaires; inhibitors; monoclonaux; points de contrôle.

PubMed Disclaimer

MeSH terms

LinkOut - more resources