Cytotoxic Natural Killer Subpopulations as a Prognostic Factor of Malignant Pleural Effusion.


Journal

Lung
ISSN: 1432-1750
Titre abrégé: Lung
Pays: United States
ID NLM: 7701875

Informations de publication

Date de publication:
02 2019
Historique:
received: 11 04 2018
accepted: 29 11 2018
pubmed: 14 12 2018
medline: 16 1 2020
entrez: 8 12 2018
Statut: ppublish

Résumé

Malignant pleural effusion (MPE) is a sign of advanced disease of poor prognosis. As natural killer (NK) cells are involved in the first line of tumour defence, we aimed to validate a new diagnostic and prognostic indicator for MPE based on NK subpopulations of pleural fluid (PF) and peripheral blood (PB). NK subpopulations were determined in PF and PB in 71 patients with malignant, paramalignant or benign pleural effusion. The receiver operating characteristic (ROC) curves, Kaplan-Meier, multivariable Cox model and decision trees created with the CHAID (Chi-square automatic interaction detector) methodology were employed. We demonstrated that the PF/PB ratios of the CD56 bright CD16- and CD56 dim CD16- NK subpopulations were higher (p = 0.013 and p = 0.003, respectively) in MPEs and paramalignant pleural effusions (PPEs) than in benign ones, with an AUC of 0.757 and 0.741, respectively. The PF/PB ratio of CD16+ NK and CD57+ NK obtained a higher hazard ratio (HR) in the crude Cox's regression analysis. In the adjusted Cox's regression analysis, the PF/PB ratio of CD16+ NK gave the highest HR (HR 6.1 [1.76-21.1]) (p = 0.004). In the decision tree created for the MPE prognosis, we observed that the main predictor variable among the studied clinical, radiological, and analytical variables was lung mass, and that 92.9% of the patients who survived had a PF/PB ratio of the CD56 dim CD16+ NK subpopulation ≤ 0.43. Our data suggest that both the PF/PB ratios of cytotoxic subpopulations CD57+ NK and CD16+ NK are useful as a prognostic factor of MPE. Other subpopulations (CD56 bright CD16- and CD56 dim CD16- NK) could help to diagnose MPE.

Sections du résumé

BACKGROUND
Malignant pleural effusion (MPE) is a sign of advanced disease of poor prognosis. As natural killer (NK) cells are involved in the first line of tumour defence, we aimed to validate a new diagnostic and prognostic indicator for MPE based on NK subpopulations of pleural fluid (PF) and peripheral blood (PB).
METHODS
NK subpopulations were determined in PF and PB in 71 patients with malignant, paramalignant or benign pleural effusion. The receiver operating characteristic (ROC) curves, Kaplan-Meier, multivariable Cox model and decision trees created with the CHAID (Chi-square automatic interaction detector) methodology were employed.
RESULTS
We demonstrated that the PF/PB ratios of the CD56 bright CD16- and CD56 dim CD16- NK subpopulations were higher (p = 0.013 and p = 0.003, respectively) in MPEs and paramalignant pleural effusions (PPEs) than in benign ones, with an AUC of 0.757 and 0.741, respectively. The PF/PB ratio of CD16+ NK and CD57+ NK obtained a higher hazard ratio (HR) in the crude Cox's regression analysis. In the adjusted Cox's regression analysis, the PF/PB ratio of CD16+ NK gave the highest HR (HR 6.1 [1.76-21.1]) (p = 0.004). In the decision tree created for the MPE prognosis, we observed that the main predictor variable among the studied clinical, radiological, and analytical variables was lung mass, and that 92.9% of the patients who survived had a PF/PB ratio of the CD56 dim CD16+ NK subpopulation ≤ 0.43.
CONCLUSIONS
Our data suggest that both the PF/PB ratios of cytotoxic subpopulations CD57+ NK and CD16+ NK are useful as a prognostic factor of MPE. Other subpopulations (CD56 bright CD16- and CD56 dim CD16- NK) could help to diagnose MPE.

Identifiants

pubmed: 30523401
doi: 10.1007/s00408-018-0186-7
pii: 10.1007/s00408-018-0186-7
doi:

Substances chimiques

Biomarkers 0
CD56 Antigen 0
CD57 Antigens 0
FCGR3B protein, human 0
GPI-Linked Proteins 0
NCAM1 protein, human 0
Receptors, IgG 0

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

53-60

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Auteurs

Susana Herrera Lara (S)

Pulmonology Department, Dr Peset University Hospital, Avenue Gaspar Aguilar, 90, 46017, Valencia, Spain. susancord5@hotmail.com.

Estrella Fernández-Fabrellas (E)

Pulmonology Department, General University Consorci Hospital, Valencia, Spain.

Gustavo Juan Samper (G)

Pulmonology Department, General University Consorci Hospital, Valencia, Spain.

Josefa Marco Buades (J)

Hematology Department, Dr Peset University Hospital, Valencia, Spain.

Rafael Andreu Lapiedra (R)

Hematology Department, La Fe University and Polytechnic Hospital, Valencia, Spain.

Amparo Pinilla Moreno (A)

Hematology Department, Dr Peset University Hospital, Valencia, Spain.

María Morales Suárez-Varela (M)

Unit of Public Health and Environmental Care, Department of Preventive Medicine, University of Valencia, Valencia, Spain.
Biomedical Research Centre Network on Epidemiology and Public Health (CIBERESP), Institute of Health Carlos III, Madrid, Spain.

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Classifications MeSH