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您所在的位置:首頁 > 呼吸科診療指南 > 2010歐洲呼吸學會和歐洲胸外科醫(yī)師學會惡性胸膜間皮瘤診療指南

2010歐洲呼吸學會和歐洲胸外科醫(yī)師學會惡性胸膜間皮瘤診療指南

2013-11-11 16:09 閱讀:4589 來源:愛愛醫(yī)資源網(wǎng) 責任編輯:李思杰
[導讀] 《2010歐洲呼吸學會和歐洲胸外科醫(yī)師學會惡性胸膜間皮瘤診療指南》內(nèi)容預覽 ABSTRACT: Malignant pleural mesothelioma (MPM) is a rare tumour but with increasingincidence and a poor prognosis. In 2008, the European Respiratory Society/European So

《2010歐洲呼吸學會和歐洲胸外科醫(yī)師學會惡性胸膜間皮瘤診療指南》內(nèi)容預覽

ABSTRACT: Malignant pleural mesothelioma (MPM) is a rare tumour but with increasingincidence and a poor prognosis. In 2008, the European Respiratory Society/European Society ofThoracic Surgeons Task Force brought together experts to propose practical and up-to-datedguidelines on the management of MPM.

To obtain an earlier and reliable diagnosis of MPM, the experts recommend performingthoracoscopy, except in cases of pre-operative contraindication or pleural symphysis. Thestandard staining procedures are insufficient in ,10% of cases. Therefore, we propose usingspecific immunohistochemistry markers on pleural biopsies. In the absence of a uniform, robustand validated staging system, we advice use of the most recent TNM based classification, andpropose a three step pre-treatment assessment. Patient’s performance status and histologicalsubtype are currently the only prognostic factors of clinical importance in the management ofMPM. Other potential parameters should be recorded at baseline and reported in clinical trials.MPM exhibits a high resistance to chemotherapy and only a few patients are candidates forradical surgery. New therapies and strategies have been reviewed.

Because of limited data on the best combination treatment, we emphasise that patients who areconsidered candidates for a multimodal approach should be included in a prospective trial at aspecialised centre.

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