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Advances in the diagnosis, evaluation, and management of malignant pleural mesothelioma.

机译:恶性胸膜间皮瘤的诊断,评估和管理进展。

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Advances in the diagnosis, evaluation, and management of malignant pleural mesothelioma STERMAN DH, ALBELDA SM. Respirology 2005; 10: 266-283 Abstract: Malignant mesothelioma is an insidious neoplasm arising from the mesothelial surfaces of the pleural and peritoneal cavities, the pericardium, or the tunica vaginalis. A total of 80% of all cases are pleural in origin. The predominant cause of malignant mesothelioma is inhalational exposure to asbestos, although evidence is increasing to support the hypothesis that simian virus-40 virus plays a role in cocarcinogenesis. Immunohistochemical markers such as calretinin, WT-1, and cytokeratin 5/6 are becoming established diagnostic markers. Preliminary data suggests that a soluble form of mesothelin could serve as a serum marker for established and early cases of mesothelioma. Positron emission tomography with 18-fluorodeoxyglucose in conjunction with computed tomograhy scanning has improved preoperative imaging and staging. Prognostic factors have been identified and verified. Negative indicators include thrombocytosis, high leukocyte counts, poor performance status, and nonepithelial histology. For the first time, there is now evidence that some treatments are increasing the quality and quantity of life for patients with mesothelioma. Chemotherapy, with the new multitargeted antifolate drug Pemetrexed, combined with cisplatin, has shown superior survival rates in a large phase III trial when compared to cisplatin alone. High-dose intensity-modulated radiotherapy when administered after extrapleural pneumonectomy has resulted in excellent local control. Multimodality treatment programs that combine surgical cytoreduction with novel forms of radiation therapy and more effective chemotherapy combinations may offer significant increases in survival for certain subgroups of mesothelioma patients. Innovative palliative approaches have proved successful in alleviation of the significant symptoms experienced by many mesothelioma patients. Experimental treatments such as immunotherapy and gene therapy present a window of hope for all mesothelioma patients, and in the future, may be combined with 'standard therapy' in multimodality protocols. Patients with adequate performance status should be enrolled into clinical trials where possible. Over the past decade, significant advances have been made on several fronts that have improved the ability to diagnose a stage, define prognosis, and treat malignant pleural mesothelioma.
机译:恶性胸膜间皮瘤STERMAN DH,ALBELDA SM的诊断,评估和管理进展。呼吸科学2005; 10:266-283摘要:恶性间皮瘤是一种隐匿性肿瘤,起源于胸膜和腹膜腔,心包膜或阴道膜的间皮表面。共有80%的病例起源于胸膜。恶性间皮瘤的主要病因是吸入石棉,尽管有越来越多的证据支持猿猴病毒-40病毒在致癌性中起作用的假说。免疫组织化学标记物(例如钙调蛋白,WT-1和细胞角蛋白5/6)已成为公认的诊断标记物。初步数据表明,间皮素的可溶形式可作为间皮瘤确诊和早期病例的血清标志物。正电子发射断层扫描与18氟脱氧葡萄糖结合计算机断层扫描已改善了术前成像和分期。预后因素已经确定和证实。阴性指标包括血小板增多,白细胞计数高,表现状态差和上皮无组织学。现在,有史以来第一次有证据表明,某些治疗方法可以提高间皮瘤患者的生活质量和数量。化学疗法与新的多靶点抗叶酸药物Pemetrexed联合顺铂在大型III期试验中显示出比单独使用顺铂更高的生存率。胸膜外肺切除术后给予大剂量强度调节放疗可实现出色的局部控制。将外科细胞减少与新颖形式的放射疗法和更有效的化学疗法相结合的多模态治疗计划可能会为间皮瘤患者的某些亚组提供显着的生存率增加。实践证明,创新的姑息治疗方法可以缓解许多间皮瘤患者的明显症状。免疫疗法和基因疗法等实验性疗法为所有间皮瘤患者带来了希望之窗,并且将来可能与多模式方案中的“标准疗法”结合使用。有足够表现状态的患者应尽可能参加临床试验。在过去的十年中,在多个方面已经取得了重大进展,这些方面已经提高了诊断阶段,确定预后和治疗恶性胸膜间皮瘤的能力。

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