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Recent progress in treatment of malignant pleural mesothelioma

机译:恶性胸膜间皮瘤治疗的最新进展

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Incidence of malignant pleural mesothelioma will rise until 2030-2040 because the elapsed time between exposure and diagnostic is up to several decades. Prognosis remains very poor with median survival less than one year and five-year survival not exceeding 5%. As compared to 1999, standart treatment adds chemotherapy with cisplatin and pemetrexed to local radiotherapy for prevention of local seeding after invasive diagnostic procedures. Despite various growth factors and their receptors are involved in malignant mesothelioma, first clinical trials of targeted therapies reported poor results. Multimodality therapy with extrapleural pneumonectomy and radiation therapy (+/-chemotherapy) can be of benefit in subgroups of patients but it cannot be recommended in a routine approach. As compared to bronchial carcinoma, inclusion of patients in clinical trials (using intensity-modulated radiation therapy) is the only way to somewhat improve results.
机译:直到2030年至2040年,恶性胸膜间皮瘤的发病率将上升,因为暴露和诊断之间的间隔时间长达数十年。预后仍然很差,中位生存期少于一年,五年生存期不超过5%。与1999年相比,标准治疗方法在局部放射治疗后增加了顺铂和培美曲塞的化疗,以防止侵入性诊断程序后发生局部播种。尽管各种生长因子及其受体参与了恶性间皮瘤,但针对靶向疗法的第一项临床试验报道了不良的结果。伴有胸膜外肺切除术和放射疗法(+/-化学疗法)的多模态治疗可能对亚组患者有益,但在常规治疗方法中不建议使用。与支气管癌相比,将患者纳入临床试验(使用强度调制放射疗法)是在某种程度上改善结果的唯一方法。

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