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The highlights of the 15th international conference of the international mesothelioma interest group - Do molecular concepts challenge the traditional approach to pathological mesothelioma diagnosis?
Klebe, Sonja; Galateau Salle, Francoise; Bruno, Rossella; Brcic, Luka; I Chen-Yost, Heather; Jaurand, Marie-Claude.
Afiliação
  • Klebe S; Department of Anatomical Pathology, SA Pathology at Flinders Medical Centre, Adelaide, South Australia, Australia; Flinders University, Adelaide, South Australia, Australia.
  • Galateau Salle F; MESOPATH College, MESONAT, MESOBANK, Department of BioPathology Centre Léon Bérard, 28 Rue Laennec, 69008 Lyon, France; Department of Biopathology, Unit of Molecular Pathology and Cancer Research Center of Lyon, INSERM U1052-CNRS5286, 69008 Lyon, France.
  • Bruno R; Unit of Pathological Anatomy, University Hospital of Pisa, Via Roma 67, 56126 Pisa, Italy.
  • Brcic L; Diagnostic and Research Institute of Pathology, Medical University of Graz, Neue Stiftingtalstrasse 6, 8010 Graz, Austria.
  • I Chen-Yost H; The University of Chicago Hospitals, Chicago, IL, United States.
  • Jaurand MC; Centre de Recherche des Cordeliers, Inserm, Sorbonne Université, Université de Paris, Functional Genomics of Solid Tumors, Paris, France. Electronic address: marie-claude.jaurand@inserm.fr.
Lung Cancer ; 163: 1-6, 2022 01.
Article em En | MEDLINE | ID: mdl-34864334
ABSTRACT
Pathology plays an important role in diagnosing mesothelioma since radiological and clinical findings alone cannot distinguish mesothelioma reliably from its many mimics. The long-held gold standard for pathological diagnosis requires a tissue biopsy that, in addition to mesothelial phenotype, demonstrates invasion, but this is challenged by the WHO recognition of mesothelioma in situ (MIS) and concurrent acknowledgement of all mesotheliomas as malignant. Tumor sampling and ancillary techniques are of paramount importance for diagnosis of MIS. Standardisation of these techniques, cut-off points and terminology, and an updated staging system are urgently required. These clinically relevant issues and the impact of new developments were illustrated at the pathology session of 15th meeting of the International Mesothelioma Interest Group. It was reported that combination of losses in p16 nuclear expression, with cut-off ≤ 1%, and cytoplasmic MTAP with cut-off ≥ 30% demonstrated increased specificity (96%) and high sensitivity (86%) for CDKN2A HD detection. Otherwise, the combination of p16 IHC and CDKN2A HD may improve prognosis. The potential usefulness of pleural effusions for early diagnosis was demonstrated in a retrospective study investigating pleural effusions had been diagnosed as benign prior to mesothelioma diagnosis. Alterations of BAP1 (IHC) and CDKN2A (FISH) were detectable 2 or more years prior diagnosis. Moreover, analysis of gene expression profiles in cytology samples by principal component analysis discriminated reactive hyperpasia from epitheliod mesothelioma. Early diagnosis, including cytology diagnosis, is being acyively investigated. Since no treatment recommendations exist for MIS, pathologists recognise the need for international collaborations to fully characterise this rare entity. Clear communication with the clinical teams is required to ensure optimum patient care. The data reported in this meeting are encouraging and open avenues for further work that will allow even earlier diagnosis and better characterisation of mesothelioma progression, based on changes in gene expression, including epigenetic changes.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pleurais / Neoplasias Pulmonares / Mesotelioma Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pleurais / Neoplasias Pulmonares / Mesotelioma Idioma: En Ano de publicação: 2022 Tipo de documento: Article