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A European project on incidence, treatment, and outcome of sarcoma

机译:关于肉瘤的发病率,治疗和结果的欧洲项目

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Background Sarcomas are rare tumors (1-2% of all cancers) of mesenchymal origin that may develop in soft tissues and viscera. Since the International Classification of Disease (ICD) attributes visceral sarcomas (VS) to the organ of origin, the incidence of sarcoma is grossly underestimated. The rarity of the disease and the variety of histological types (more than 70) or locations account for the difficulty in acquiring sufficient personal experience. In view of the above the European Commission funded the project called Connective Tissues Cancers Network (CONTICANET), to improve the prognosis of sarcoma patients by increasing the level of standardization of diagnostic and therapeutic procedures through a multicentre collaboration. Methods/Design Two protocols of epidemiological researches are here presented. The first investigation aims to build the population-based incidence of sarcoma in a two-year period, using the new 2002 WHO classification and the "second opinion" given by an expert regional pathologist on the initial diagnosis by a local pathologist. A three to five year survival rate will also be determined. Pathology reports and clinical records will be the sources of information. The second study aims to compare the effects on survival or relapse-free period - allowing for histological subtypes, clinical stage, primary site, age and gender - when the disease was treated or not according to the clinical practice guidelines (CPGs). Discussion Within CONTICANET, each group was asked to design a particular study on a specific objective, the partners of the network being free to accept or not the proposed protocol. The first protocol was accepted by the other researchers, therefore the incidence of sarcoma will be assessed in three European regions, Rhone-Alpes and Aquitaine (France) and Veneto (Italy), where the geographic distribution of sarcoma will be compared after taking into account age and gender. The conformity of the clinical practice with the recommended guidelines will be investigated in a French (Rhone Alps) and Italian (Veneto) region since the CPGs were similar in both areas.
机译:背景肉瘤是间充质起源的罕见肿瘤(占所有癌症的1-2%),可能在软组织和内脏中发展。由于国际疾病分类(ICD)将内脏肉瘤(VS)归因于起源器官,因此肉瘤的发生率被严重低估了。这种疾病的稀有性和多种组织学类型(超过70种)或位置,导致难以获得足够的个人经验。鉴于上述情况,欧洲委员会资助了名为结缔组织癌症网络(CONTICANET)的项目,以通过多中心协作提高诊断和治疗程序的标准化水平来改善肉瘤患者的预后。方法/设计这里介绍了两种流行病学研究方案。首次调查的目的是利用2002年WHO新分类以及专家区域病理学家对当地病理学家的初步诊断得出的“第二种意见”,建立两年内以人群为基础的肉瘤发病率。还将确定三到五年的生存率。病理报告和临床记录将成为信息来源。第二项研究旨在比较根据临床实践指南(CPG)治疗或不治疗疾病时对生存或无复发期的影响-包括组织学亚型,临床分期,主要部位,年龄和性别。讨论在CONTICANET中,要求每个小组针对特定目标设计一项特定的研究,网络的合作伙伴可以自由接受或不接受提议的协议。第一个方案被其他研究人员接受,因此将在三个欧洲地区(法国的罗纳-阿尔卑斯和阿基坦和意大利的威尼托)评估肉瘤的发生率,在考虑到肉瘤的地理分布后,年龄和性别。由于在两个地区的CPG都相似,因此将在法国(罗纳阿尔卑斯山)和意大利(威尼托)地区研究临床实践与推荐指南的符合性。

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