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ERS/ESTS/EACTS/ESTRO guidelines for the management of malignant pleural mesothelioma.

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BORIS DOI
10.7892/boris.144503
Date of Publication
May 25, 2020
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Author
Opitz, Isabelle
Scherpereel, Arnaud
Berghmans, Thierry
Psallidas, Ioannis
Glatzer, Markus
Universitätsklinik für Radio-Onkologie
Rigau, David
Astoul, Philippe
Bölükbas, Servet
Boyd, Jeanette
Coolen, Johan
De Bondt, Charlotte
De Ruysscher, Dirk
Durieux, Valerie
Faivre-Finn, Corinne
Fennell, Dean A
Galateau-Salle, Francoise
Greillier, Laurent
Hoda, Mir Ali
Klepetko, Walter
Lacourt, Aude
McElnay, Phil
Maskell, Nick A
Mutti, Luciano
Pairon, Jean-Claude
Van Schil, Paul
van Meerbeeck, Jan P
Waller, David
Weder, Walter
Putora, Paul Martin
Universitätsklinik für Radio-Onkologie
Cardillo, Giuseppe
Subject(s)

600 - Technology::610...

Series
European journal of cardio-thoracic surgery
ISSN or ISBN (if monograph)
1873-734X
Publisher
Oxford University Press
Language
English
Publisher DOI
10.1093/ejcts/ezaa158
PubMed ID
32448904
Uncontrolled Keywords

Chemotherapy Guidelin...

Description
The European Respiratory Society (ERS)/European Society of Thoracic Surgeons (ESTS)/European Association for Cardio-Thoracic Surgery (EACTS)/European Society for Radiotherapy and Oncology (ESTRO) task force brought together experts to update previous 2009 ERS/ESTS guidelines on management of malignant pleural mesothelioma (MPM), a rare cancer with globally poor outcome, after a systematic review of the 2009-2018 literature. The evidence was appraised using the Grading of Recommendations, Assessment, Development and Evaluation approach. The evidence syntheses were discussed and recommendations formulated by this multidisciplinary group of experts. Diagnosis: pleural biopsies remain the gold standard to confirm the diagnosis, usually obtained by thoracoscopy but occasionally via image-guided percutaneous needle biopsy in cases of pleural symphysis or poor performance status. Pathology: standard staining procedures are insufficient in ∼10% of cases, justifying the use of specific markers, including BAP-1 and CDKN2A (p16) for the separation of atypical mesothelial proliferation from MPM. Staging: in the absence of a uniform, robust and validated staging system, we advise using the most recent 2016 8th TNM (tumour, node, metastasis) classification, with an algorithm for pretherapeutic assessment. Monitoring: patient's performance status, histological subtype and tumour volume are the main prognostic factors of clinical importance in routine MPM management. Other potential parameters should be recorded at baseline and reported in clinical trials. Treatment: (chemo)therapy has limited efficacy in MPM patients and only selected patients are candidates for radical surgery. New promising targeted therapies, immunotherapies and strategies have been reviewed. Because of limited data on the best combination treatment, we emphasize that patients who are considered candidates for a multimodal approach, including radical surgery, should be treated as part of clinical trials in MPM-dedicated centres.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/36148
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