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Implantation and Monitoring by PET/CT of an Orthotopic Model of Human Pleural Mesothelioma in Athymic Mice
Published on: December 21, 2019
[Malignant pleural mesothelioma: diagnosis and treatment]
J Delourme1, X Dhalluin, A B Cortot
1Service de pneumologie et d'oncologie thoracique, hôpital Calmette, CHRU de Lille, boulevard Professeur-Jules-Leclercq, 59037 Lille cedex, France.
Abstract:
Malignant pleural mesothelioma (MPM) is a rare and aggressive tumor issued from the mesothelial surface of the pleural space. A previous exposure to asbestos is the main risk factor of mesothelioma. Clinical signs are most of the time late and unspecific. Chest CT-scan, a key imaging procedure, usually shows a (unilateral) pleurisy associated with pleural nodular thickening. PET-scan associated with CT-scan may help to differenciate MPM from pleural benign tumors but it is not recommended for the diagnosis of MPM, as well as chest resonance magnetic imaging and blood or pleural fluid biomarkers, including soluble mesothelin still under investigation. The diagnosis of MPM is based on histology using essentially immunohistochemistry on pleural biopsies best obtained by thoracoscopy. The treatment of MPM relies mostly on chemotherapy. Surgery, pleurectomy/decortication or extrapleural pneumonectomy, is not recommended outside a clinical trial, as well as adjuvant chest radiotherapy. Prophylactic irradiation of chest scars and drains, validated by the French guidelines in 2005, is however highly discussed at the international level. Finally, numerous research studies presently assess the value of targeted therapies and biomarkers in MPM, opening new perspectives in the management of this cancer.
Insights
Malignant pleural mesothelioma (MPM) is a rare cancer linked to asbestos exposure. Diagnosis relies on histology, with chemotherapy being the primary treatment, while surgery and radiotherapy are generally not recommended outside clinical trials.
Area of Science:
- Oncology
- Pulmonology
- Pathology
Context:
- Malignant pleural mesothelioma (MPM) is a rare, aggressive tumor arising from the pleural space.
- Asbestos exposure is the primary risk factor, with late and unspecific clinical signs.
- Current diagnostic and treatment strategies for MPM are limited.
Purpose:
- To provide a comprehensive overview of malignant pleural mesothelioma.
- To discuss current diagnostic methods, including imaging and histology.
- To outline established and emerging treatment modalities for MPM.
Summary:
- MPM diagnosis is primarily based on immunohistochemistry on pleural biopsies obtained via thoracoscopy.
- Chest CT-scan is key for imaging, while PET-scan, MRI, and biomarkers have limited diagnostic roles.
- Chemotherapy is the mainstay treatment; surgery and radiotherapy are generally reserved for clinical trials.
Impact:
- Highlights the diagnostic challenges and limitations in current MPM management.
- Emphasizes the importance of histological confirmation and the role of chemotherapy.
- Points to ongoing research in targeted therapies and biomarkers for future MPM treatment strategies.
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