Antidrug Antibodies Against Immune Checkpoint Blockers: Impairment of Drug Efficacy or Indication of Immune Activation?


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
15 02 2020
Historique:
received: 18 07 2019
revised: 07 10 2019
accepted: 14 11 2019
pubmed: 24 11 2019
medline: 18 11 2020
entrez: 24 11 2019
Statut: ppublish

Résumé

The generation of antibodies following exposure to therapeutic drugs has been widely studied, however in oncology, data in relation to their clinical relevance are limited. Antidrug antibodies (ADAs) can cause a decrease in the amount of drug available, resulting in some cases in decreased antitumor activity and a consequent impact on clinical outcomes. Several immunologic factors can influence the development of ADAs, and in addition, the sensitivity of the different testing methods used in different studies can vary, representing an additional potential confounding factor. The reported frequency of ADA-positive patients following treatment with immune checkpoint inhibitors varies from as low as 1.5% for pembrolizumab to 54% for atezolizumab. This latter drug is the only immune checkpoint inhibitor to have undergone an expanded analysis of the clinical implications of ADAs, but with discordant results. Given that immune checkpoint inhibitors can modify the immune response and potentially impact ADA formation, data from published as well as prospective trials need to be evaluated for a better understanding of the clinical implications of ADAs in this setting.

Identifiants

pubmed: 31757876
pii: 1078-0432.CCR-19-2337
doi: 10.1158/1078-0432.CCR-19-2337
doi:

Substances chimiques

Antibodies 0
Antibodies, Monoclonal 0
Antineoplastic Agents, Immunological 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

787-792

Informations de copyright

©2019 American Association for Cancer Research.

Auteurs

Diego Enrico (D)

Gustave Roussy Cancer Campus, Villejuif, France.
Medical Oncology Department, Gustave Roussy Cancer Center, Villejuif, France.

Angelo Paci (A)

Gustave Roussy Cancer Campus, Villejuif, France.
Faculty of Pharmacy, University Paris-Saclay, Chatenay-Malabry, France.
Laboratory of Pharmacology and Drug Analysis, Gustave Roussy Cancer Center, Villejuif, France.

Nathalie Chaput (N)

Gustave Roussy Cancer Campus, Villejuif, France.
Faculty of Pharmacy, University Paris-Saclay, Chatenay-Malabry, France.
Laboratory for Immunomonitoring in Oncology, UMS 3655 CNRS/US 23 INSERM, Gustave Roussy Cancer Campus, Villejuif, France.

Eleni Karamouza (E)

Gustave Roussy Cancer Campus, Villejuif, France.
Ligue Nationale Contre le Cancer Meta-Analysis Platform, Biostatistics and Epidemiology Unit, INSERM U1018, CESP, Villejuif, France.

Benjamin Besse (B)

Gustave Roussy Cancer Campus, Villejuif, France. benjamin.besse@gustaveroussy.fr.
Medical Oncology Department, Gustave Roussy Cancer Center, Villejuif, France.
Faculty of Medicine, University Paris-Saclay, Le Kremlin-Bicêtre, France.

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Classifications MeSH