Hyperprogression under Immunotherapy.

hyperprogression immunotherapy new patterns of response pseudoprogression treatment beyond progression

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
30 May 2019
Historique:
received: 30 04 2019
revised: 27 05 2019
accepted: 28 05 2019
entrez: 2 6 2019
pubmed: 4 6 2019
medline: 26 11 2019
Statut: epublish

Résumé

Immunotherapy is now widely prescribed in oncology, leading to the observation of new types of responses, including rapid disease progression sometimes reported as hyperprogression. However, only a few studies have assessed the question of hyperprogression and there is no consensual definition of this phenomenon. We reviewed existing data on hyperprogression in published studies, focusing on reported definitions, predictive factors, and potential biological mechanisms. Seven studies retrospectively assessed hyperprogression incidence, using various definitions, some based on the tumoral burden variation across time with repeated computed-tomography (CT) scan, others based on an association of radiological and clinical criteria. Reported hyperprogression incidence varied between 4% and 29% of all responses, mostly in multi-tumor cohorts and with patients receiving immune checkpoint inhibitors. Hyperprogression correlated with worse chances of survival than standard progression in two studies. However, no strong predictive factors of hyperprogression were identified, and none were consistent across studies. In total, hyperprogression is a frequent pattern of response under immunotherapy, with a strong impact on patient outcome. There is a need for a consensual definition of hyperprogression. Immunotherapy should be stopped early in cases where there is suspicion of hyperprogression.

Identifiants

pubmed: 31151303
pii: ijms20112674
doi: 10.3390/ijms20112674
pmc: PMC6600249
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Déclaration de conflit d'intérêts

C.L.T. has participated in advisory boards from MSD, BMS, Merck Serono, Astra Zeneca, Roche, Novartis, Amgen, Nanobiotix. The other authors declared no conflicts of interest.

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Auteurs

Maxime Frelaut (M)

Department of Drug Development and Innovation (D3i), Institut Curie, Paris & Saint-Cloud, France. maxime.frelaut@curie.fr.

Christophe Le Tourneau (C)

Department of Drug Development and Innovation (D3i), Institut Curie, Paris & Saint-Cloud, France. christophe.letourneau@curie.fr.
INSERM U900 Research unit, Saint-Cloud, France. christophe.letourneau@curie.fr.
Paris-Saclay University, Paris, France. christophe.letourneau@curie.fr.

Edith Borcoman (E)

Department of Drug Development and Innovation (D3i), Institut Curie, Paris & Saint-Cloud, France. edith.borcoman@curie.fr.

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