Assessment of interferon-γ in pleural fluid as a prognostic factor of survival in malignant pleural mesothelioma.


Journal

Cancer immunology, immunotherapy : CII
ISSN: 1432-0851
Titre abrégé: Cancer Immunol Immunother
Pays: Germany
ID NLM: 8605732

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 01 07 2020
accepted: 09 05 2021
pubmed: 19 5 2021
medline: 16 10 2021
entrez: 18 5 2021
Statut: ppublish

Résumé

Literature reports suggest that the host immune system may control Malignant Pleural Mesothelioma (MPM) growth, although its activity is limited by regulatory mechanisms. In this retrospective study, we analyzed the levels of pro-inflammatory (IL-1, IL-6, TNF), immune-regulatory (IL-10) and Th1/CTL-related cytokines (IL-12p70, IFN-γ) in the pleural exudate and their relationship with overall survival (OS) in MPM. Cytokines were quantified by multiplexed immunoassay. Concentrations were dichotomized with respect to the median value. Correlation between cytokine level and OS was assessed using univariate (Kaplan-Meier curves) and multivariate (Cox regression) analyses. Regarding outcome, tumor histology, therapies undergone and IFN-γ were independent prognostic factors of OS in a 72 MPM training cohort. Notably, high concentrations of IFN-γ halved death probability (HR of high vs low IFN-γ concentration = 0.491, 95%CI 0.3-0.8, p = 0.007). Also in patients with epithelioid histology and those receiving at least one line of therapy, high IFN-γ level was an independent factor predictive of OS (HR of high vs low IFN-γ concentration were 0.497, p = 0.007 and 0.324, p = 0.006, respectively). However, these data were not confirmed in a 77 MPM validation cohort, possibly due to the low IFN-γ levels encountered in this population, and the heterogeneous distribution of disease stages between the training and the validation cohorts. None of the other cytokines showed any effect on survival. High level of IFN-γ in pleural effusion may be associated with better survival in MPM patients and potentially serve as a prognostic biomarker. Larger prospective studies are needed to ascertain this hypothesis.

Identifiants

pubmed: 34003301
doi: 10.1007/s00262-021-02965-w
pii: 10.1007/s00262-021-02965-w
doi:

Substances chimiques

Cytokines 0
Interferon-gamma 82115-62-6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3349-3355

Subventions

Organisme : Italian Ministry of Health
ID : GR-2013-02356568
Organisme : Italian Ministry of Health
ID : 5x1000 Funds 2015
Organisme : Italian Ministry of Health
ID : Ricerca Corrente

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Références

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Auteurs

Beatrice Dozin (B)

Clinical Epidemiology Unit, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Grazia Carbotti (G)

Biotherapies Unit, IRCCS Ospedale Policlinico San Martino, Largo Benzi 10, 16132, Genoa, Italy.

Silvio Roncella (S)

Histopathology and Cytopathology Division, Azienda Sanitaria Locale N. 5 , La Spezia, Italy.

Paola Ferro (P)

Histopathology and Cytopathology Division, Azienda Sanitaria Locale N. 5 , La Spezia, Italy.

Paolo Dessanti (P)

Histopathology and Cytopathology Division, Azienda Sanitaria Locale N. 5 , La Spezia, Italy.

Pier Aldo Canessa (PA)

Pneumology Division, Azienda Sanitaria Locale N. 5 , La Spezia, Italy.

Silvano Ferrini (S)

Biotherapies Unit, IRCCS Ospedale Policlinico San Martino, Largo Benzi 10, 16132, Genoa, Italy.

Marina Fabbi (M)

Biotherapies Unit, IRCCS Ospedale Policlinico San Martino, Largo Benzi 10, 16132, Genoa, Italy. marina.fabbi@hsanmartino.it.

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