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欧洲诊断为髓系恶性肿瘤患者的生存情况:HAEMACARE 研究。

Survival of European patients diagnosed with myeloid malignancies: a HAEMACARE study.

机构信息

Registre des Hémopathies Malignes de Côte d’Or, EA 4184, Université de Bourgogne; Service d’Hématologie Biologique, CHU de Dijon, France.

出版信息

Haematologica. 2013 Feb;98(2):230-8. doi: 10.3324/haematol.2012.064014. Epub 2012 Sep 14.

Abstract

Population-based information on the survival of patients with myeloid malignancies is rare mainly because some entities were not recognized as malignant until the publication of the third revision of the International Classification of Diseases for Oncology and World Health Organization classification in 2000. In this study we report the survival of patients with myeloid malignancies, classified by updated criteria, in Europe. We analyzed 58,800 cases incident between 1995 to 2002 in 48 population-based cancer registries from 20 European countries, classified into HAEMACARE myeloid malignancy groupings. The period approach was used to estimate 5-year relative survival in 2000-2002. The relative overall survival rate was 37%, but varied significantly between the major groups: being 17% for acute myeloid leukemia, 20% for myelodysplastic/myeloproliferative neoplasms, 31% for myelodysplastic syndromes and 63% for myeloproliferative neoplasms. Survival of patients with individual disease entities ranged from 90% for those with essential thrombocythemia to 4% for those with acute myeloid leukemia with multilineage dysplasia. Regional European variations in survival were conspicuous for myeloproliferative neoplasms, with survival rates being lowest in Eastern Europe. This is the first paper to present large-scale, European survival data for patients with myeloid malignancies using prognosis-based groupings of entities defined by the third revision of the International Classification of Diseases for Oncology/World Health Organization classifications. Poor survival in some parts of Europe, particularly for treatable diseases such as chronic myeloid leukemia, is of concern for hematologists and public health authorities.

摘要

人群中关于髓系恶性肿瘤患者生存的信息很少,主要是因为直到 2000 年国际肿瘤学疾病分类和世界卫生组织分类的第三次修订版出版,一些实体才被认为是恶性的。在这项研究中,我们报告了欧洲更新标准分类的髓系恶性肿瘤患者的生存情况。我们分析了 1995 年至 2002 年期间在欧洲 20 个国家的 48 个基于人群的癌症登记处登记的 58800 例病例,这些病例被归入 HAEMACARE 髓系恶性肿瘤分组。使用时期法估计 2000-2002 年的 5 年相对生存率。整体相对生存率为 37%,但在主要分组之间差异显著:急性髓系白血病为 17%,骨髓增生异常/骨髓增殖性肿瘤为 20%,骨髓增生异常综合征为 31%,骨髓增殖性肿瘤为 63%。个体疾病实体的患者生存率从原发性血小板增多症的 90%到多谱系发育不良的急性髓系白血病的 4%不等。欧洲不同地区的生存差异在骨髓增殖性肿瘤中尤为明显,东欧的生存率最低。这是第一篇使用国际肿瘤学疾病分类/世界卫生组织分类第三次修订版定义的基于预后的实体分组,为欧洲髓系恶性肿瘤患者提供大规模生存数据的论文。欧洲部分地区的生存状况较差,特别是对可治疗疾病(如慢性髓系白血病),这引起了血液学家和公共卫生当局的关注。

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