TY - JOUR
T1 - Hyperprogressive disease
T2 - recognizing a novel pattern to improve patient management
AU - Champiat, Stéphane
AU - Ferrara, Roberto
AU - Massard, Christophe
AU - Besse, Benjamin
AU - Marabelle, Aurélien
AU - Soria, Jean Charles
AU - Ferté, Charles
N1 - Publisher Copyright:
© 2018, Springer Nature Limited.
PY - 2018/12/1
Y1 - 2018/12/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85055478281&partnerID=8YFLogxK
U2 - 10.1038/s41571-018-0111-2
DO - 10.1038/s41571-018-0111-2
M3 - Review article
C2 - 30361681
AN - SCOPUS:85055478281
SN - 1759-4774
VL - 15
SP - 748
EP - 762
JO - Nature Reviews Clinical Oncology
JF - Nature Reviews Clinical Oncology
IS - 12
ER -