意大利软组织肉瘤和骨肉瘤的流行病学:来自15个基于人群的癌症登记处的数据分析

Q2 Medicine Sarcoma Pub Date : 2020-09-01 DOI:10.1155/2020/6142613
Sabrina Fabiano, P. Contiero, Giulio Barigelletti, Anna D’Agostino, A. Tittarelli, L. Mangone, I. Bisceglia, Salvatore Bongiorno, Lucia Elena De Lorenzis, G. Mazzoleni, M. Castaing, T. Intrieri, A. Puppo, G. Carrozzi, G. Sini, llaria Fontanili, L. Boschetti, R. Tumino, F. Bella, A. Fanetti, Maurizio Castelli, A. Ardizzone, F. Vittadello, S. Sciacca, G. Manneschi, C. Casella, C. Cirilli, F. Pala, M. Michiara, S. Migliazza, F. Ferrari, E. Spata, Y. Dinaro, I. Cometti, A. Maghini, G. Tagliabue
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引用次数: 12

摘要

肉瘤是一组罕见的间充质癌。在这项研究中,我们提供了意大利恶性软组织肉瘤(ICD-O-3地形代码C47–C49)和骨肉瘤(C40,C41)的最新世界年龄标准发病率(ASR)和欧洲年龄标准患病率,按地区(北部、中部和南部)和癌症登记。我们还评估了与部位和面积相关的形态学,并在诊断时评估了转移。我们分析了意大利癌症注册协会(AIRTUM)下属的15个癌症注册中心(CR)提供的1112例2009-2012年发病率的病例。总的来说,软组织肉瘤的ASR为1.7/1000000/年,骨肉瘤的ASR为0.7。意大利中部软组织肉瘤的ASR最高(2.4),意大利南部软组织肉瘤ASR最低(1.6)。意大利中部骨肉瘤ASR最高(1.1),意大利北部骨肉瘤ASR最低(0.7)。根据CR,软组织肉瘤的ASRs为1.1至2.6,骨肉瘤的ASRs为0至1.4。最常见的软组织肉瘤是未另行说明的肉瘤(NOS)(29.4%)和脂肪肉瘤(22.2%);骨肉瘤以软骨肉瘤最常见(37.6%),软组织肉瘤以下肢结缔组织最常见(35.6%);骨肉瘤主要发生在长骨(68.8%)。在不同位置出现的形态频率因意大利地区而异;例如,在意大利南部,20%的血管瘤发生在头颈部,17%发生在该部位,6%发生在北部。对于软组织肉瘤,2.6和2.4的最高ASR与1.1和1.3的最低ASR形成对比,这表明高风险热点值得进一步调查。形态学分布随部位和地理位置的显著变化表明危险因素的地理差异也可能值得进一步研究,特别是因为对肉瘤病因的了解很少。
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Epidemiology of Soft Tissue Sarcoma and Bone Sarcoma inItaly: Analysis of Data from 15 Population-Based Cancer Registries
Sarcomas are a heterogeneous group of rare cancers of mesenchymal origin. In this study, we provide updated, world age-standardised incidence rate (ASR) and European age-standardised incidence rate for malignant soft tissue sarcoma (ICD-O-3 topographic code C47–C49) and bone sarcoma (C40, C41) in Italy, by area (north, centre, and south) and by cancer registry. We also assess morphology in relation to site and area and assess metastases at diagnosis. We analysed 1,112 cases, with incidence 2009–2012, provided by 15 cancer registries (CRs) affiliated to the Association of Italian Cancer Registries (AIRTUM). Overall, ASR was 1.7/100,000/year for soft tissue sarcoma and 0.7 for bone sarcoma. Central Italy had the highest (2.4) ASR and south Italy had the lowest (1.6) ASR for soft tissue sarcoma. Central Italy had the highest (1.1) ASR and north Italy had the lowest (0.7) ASR for bone sarcoma. By CR, ASRs ranged from 1.1 to 2.6 for soft tissue sarcoma and from 0 to 1.4 for bone sarcoma. The most frequent soft tissue sarcomas were sarcoma not otherwise specified (NOS) (29.4%) and liposarcoma (22.2%); the most common bone sarcoma was chondrosarcoma (37.6%). Soft tissue sarcomas occurred most frequently (35.6%) in lower limb connective tissue; bone sarcomas arose mainly (68.8%) in long bones. The frequencies of morphologies arising at different sites varied considerably by Italian area; for example, 20% of hemangiosarcomas occurred in the head and neck in south Italy with 17% at this site in the centre and 6% in the north. For soft tissue sarcoma, the highest ASRs of 2.6 and 2.4 contrast with the lowest ASRs 1.1 and 1.3, suggesting high-risk hot spots that deserve further investigation. The marked variations in morphology distribution with site and geography suggest geographic variation in risk factors that may also repay further investigation particularly since sarcoma etiology is poorly understood.
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来源期刊
Sarcoma
Sarcoma Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
5.00
自引率
0.00%
发文量
15
审稿时长
14 weeks
期刊介绍: Sarcoma is dedicated to publishing papers covering all aspects of connective tissue oncology research. It brings together work from scientists and clinicians carrying out a broad range of research in this field, including the basic sciences, molecular biology and pathology and the clinical sciences of epidemiology, surgery, radiotherapy and chemotherapy. High-quality papers concerning the entire range of bone and soft tissue sarcomas in both adults and children, including Kaposi"s sarcoma, are published as well as preclinical and animal studies. This journal provides a central forum for the description of advances in diagnosis, assessment and treatment of this rarely seen, but often mismanaged, group of patients.
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