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External Validation of a Breath-Based Prediction Model for Malignant Pleural Mesothelioma.
Janssens, Eline; Schillebeeckx, Eline; Zwijsen, Kathleen; Raskin, Jo; Van Cleemput, Joris; Surmont, Veerle F; Nackaerts, Kristiaan; Marcq, Elly; van Meerbeeck, Jan P; Lamote, Kevin.
Afiliação
  • Janssens E; Laboratory of Experimental Medicine and Pediatrics, Infla-Med Center of Excellence, University of Antwerp, 2610 Antwerp, Belgium.
  • Schillebeeckx E; Laboratory of Experimental Medicine and Pediatrics, Infla-Med Center of Excellence, University of Antwerp, 2610 Antwerp, Belgium.
  • Zwijsen K; VIB-UGent Center for Medical Biotechnology, 9000 Ghent, Belgium.
  • Raskin J; Laboratory of Experimental Medicine and Pediatrics, Infla-Med Center of Excellence, University of Antwerp, 2610 Antwerp, Belgium.
  • Van Cleemput J; Department of Pulmonology & Thoracic Oncology, Antwerp University Hospital, 2650 Edegem, Belgium.
  • Surmont VF; Occupational Health Service, Eternit N.V., 1880 Kapelle-op-den-Bos, Belgium.
  • Nackaerts K; Department of Respiratory Medicine, Ghent University Hospital, 9000 Ghent, Belgium.
  • Marcq E; Department of Respiratory Medicine, University Hospital Gasthuisberg, 3000 Leuven, Belgium.
  • van Meerbeeck JP; Center for Oncological Research (CORE), Integrated Personalized and Precision Oncology Network (IPPON), University of Antwerp, 2610 Antwerp, Belgium.
  • Lamote K; Laboratory of Experimental Medicine and Pediatrics, Infla-Med Center of Excellence, University of Antwerp, 2610 Antwerp, Belgium.
Cancers (Basel) ; 14(13)2022 Jun 29.
Article em En | MEDLINE | ID: mdl-35804954
ABSTRACT
During the past decade, volatile organic compounds (VOCs) in exhaled breath have emerged as promising biomarkers for malignant pleural mesothelioma (MPM). However, as these biomarkers lack external validation, no breath test for MPM has been implemented in clinical practice. To address this issue, we performed the first external validation of a VOC-based prediction model for MPM. The external validation cohort was prospectively recruited, consisting of 47 MPM patients and 76 asbestos-exposed (AEx) controls. The predictive performance of the previously developed model was assessed by determining the degree of agreement between the predicted and actual outcome of the participants (patient/control). Additionally, to optimise the performance, the model was updated by refitting it to the validation cohort. External validation revealed a poor performance of the original model as the accuracy was estimated at only 41%, indicating poor generalisability. However, subsequent updating of the model improved the differentiation between MPM patients and AEx controls significantly (73% accuracy, 92% sensitivity, and 92% negative predictive value), substantiating the validity of the original predictors. This updated model will be more generalisable to the target population and exhibits key characteristics of a potential screening test for MPM, which could significantly impact MPM management.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article