| Literature DB >> 30361681 |
Stéphane Champiat1,2, Roberto Ferrara3, Christophe Massard1, Benjamin Besse2, Aurélien Marabelle1,4, Jean-Charles Soria5,6, Charles Ferté7.
Abstract
Anti-PD-1/PD-L1 monoclonal antibodies have substantially improved the overall survival of a subset of patients across multiple solid tumour types, but other patients can have a deterioration of their disease as a result of such therapies. This paradoxical phenomenon is defined as hyperprogression. In this Review, we present the available evidence of hyperprogressive disease following immune-checkpoint inhibition, the pathophysiological hypotheses that might explain hyperprogressive disease and the current challenges for patient management in routine clinical settings. Finally, we also discuss how the risk of hyperprogressive disease should be taken into account in clinical decisions involving immune-checkpoint inhibition.Entities:
Mesh:
Substances:
Year: 2018 PMID: 30361681 DOI: 10.1038/s41571-018-0111-2
Source DB: PubMed Journal: Nat Rev Clin Oncol ISSN: 1759-4774 Impact factor: 66.675