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首页> 外文期刊>The lancet oncology >Survival for haematological malignancies in Europe between 1997 and 2008 by region and age: Results of EUROCARE-5, a population-based study
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Survival for haematological malignancies in Europe between 1997 and 2008 by region and age: Results of EUROCARE-5, a population-based study

机译:1997年至2008年欧洲按地区和年龄划分的血液系统恶性肿瘤生存率:基于人群的研究EUROCARE-5的结果

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Background: More effective treatments have become available for haematological malignancies from the early 2000s, but few large-scale population-based studies have investigated their effect on survival. Using EUROCARE data, and HAEMACARE morphological groupings, we aimed to estimate time trends in population-based survival for 11 lymphoid and myeloid malignancies in 20 European countries, by region and age. Methods: In this retrospective observational study, we included patients (aged 15 years and older) diagnosed with haematological malignancies, diagnosed up to Dec 31, 2007, and followed up to Dec 31, 2008. We used data from the 30 cancer registries (across 20 countries) that provided continuous incidence and good quality data from 1992 to 2007. We used a hybrid approach to estimate age-standardised and age-specific 5-year relative survival, for each malignancy, overall and for five regions (UK, and northern, central, southern, and eastern Europe), and four 3-year periods (1997-99, 2000-02, 2003-05, 2006-08). For each malignancy, we also estimated the relative excess risk of death during the 5 years after diagnosis, by period, age, and region. Findings: We analysed 560 444 cases. From 1997-99 to 2006-08 survival increased for most malignancies: the largest increases were for diffuse large B-cell lymphoma (42·0% [95% CI 40·7-43·4] to 55·4% [54·6-56·2], p<0·0001), follicular lymphoma (58·9% [57·3-60·6] to 74·3% [72·9-75·5], p<0·0001), chronic myeloid leukaemia (32·3% [30·6-33·9] to 54·4% [52·5-56·2], p<0·0001), and acute promyelocytic leukaemia (50·1% [43·7-56·2] to 61·9% [57·0-66·4], p=0·0038, estimate not age-standardised). Other survival increases were seen for Hodgkin's lymphoma (75·1% [74·1-76·0] to 79·3% [78·4-80·1], p<0·0001), chronic lymphocytic leukaemia/small lymphocytic lymphoma (66·1% [65·1-67·1] to 69·0% [68·1-69·8], p<0·0001), multiple myeloma/plasmacytoma (29·8% [29·0-30·6] to 39·6% [38·8-40·3], p<0·0001), precursor lymphoblastic leukaemia/lymphoma (29·8% [27·7-32·0] to 41·1% [39·0-43·1], p<0·0001), acute myeloid leukaemia (excluding acute promyelocytic leukaemia, 12·6% [11·9-13·3] to 14·8% [14·2-15·4], p<0·0001), and other myeloproliferative neoplasms (excluding chronic myeloid leukaemia, 70·3% [68·7-71·8] to 74·9% [73·8-75·9], p<0·0001). Survival increased slightly in southern Europe, more in the UK, and conspicuously in northern, central, and eastern Europe. However, eastern European survival was lower than that for other regions. Survival decreased with advancing age, and increased with time only slightly in patients aged 75 years or older, although a 10% increase in survival occurred in elderly patients with follicular lymphoma, diffuse large B-cell lymphoma, and chronic myeloid leukaemia. Interpretation: These trends are encouraging. Widespread use of new and more effective treatment probably explains much of the increased survival. However, the persistent differences in survival across Europe suggest variations in the quality of care and availability of the new treatments. High-resolution studies that collect data about stage at diagnosis and treatments for representative samples of cases could provide further evidence of treatment effectiveness and explain geographic variations in survival.
机译:背景:从2000年代初期开始,针对血液恶性肿瘤的更有效治疗方法已经可用,但是很少有大规模的基于人群的研究调查其对生存的影响。利用EUROCARE数据和HAEMACARE形态学分组,我们旨在按地区和年龄来估算20个欧洲国家/地区11种淋巴和髓样恶性肿瘤基于人群生存的时间趋势。方法:在这项回顾性观察性研究中,我们纳入了被诊断为血液系统恶性肿瘤的患者(年龄在15岁及以上),诊断时间截至2007年12月31日,随后随访至2008年12月31日。我们使用了来自30个癌症登记处( 20个国家/地区提供了1992年至2007年的连续发病率和高质量的数据。我们使用混合方法来估算每个恶性肿瘤,总体和五个地区(英国和北部)的年龄标准化和特定年龄的5年相对生存率,中欧,南欧和东欧)和四个三年期(1997-99、2000-02、2003-05、2006-08)。对于每种恶性肿瘤,我们还按时期,年龄和地区来估计诊断后5年内相对过高的死亡风险。调查结果:我们分析了560444例。从1997-99年到2006-08年,大多数恶性肿瘤的生存率都有所提高:最大的增长是弥漫性大B细胞淋巴瘤(从42·0%[95%CI 40·7-43·4]到55·4%[54· 6-56·2],p <0·0001),滤泡性淋巴瘤(58·9%[57·3-60·6]至74·3%[72·9-75·5],p <0·0001 ),慢性粒细胞白血病(32·3%[30·6-33·9]至54·4%[52·5-56·2],p <0·0001)和急性早幼粒细胞白血病(50·1% [43·7-56·2]到61·9%[57·0-66·4],p = 0·0038,估计值未按年龄标准化)。霍奇金淋巴瘤(75·1%[74·1-76·0]至79·3%[78·4-80·1],p <0·0001),慢性淋巴细胞性白血病/小淋巴细胞的其他存活率增加淋巴瘤(66·1%[65·1-67·1]至69·0%[68·1-69·8],p <0·0001),多发性骨髓瘤/浆细胞瘤(29·8%[29·0 -30·6]至39·6%[38·8-40·3],p <0·0001),前体淋巴母细胞白血病/淋巴瘤(29·8%[27·7-32·0]至41·1 %[39·0-43·1],p <0·0001),急性髓细胞性白血病(不包括急性早幼粒细胞白血病,从12·6%[11·9-13·3]到14·8%[14·2- 15·4],p <0·0001)和其他骨髓增生性肿瘤(不包括慢性粒细胞白血病)从70·3%[68·7-71·8]到74·9%[73·8-75·9], p <0·0001)。在南欧,英国的生存率略有提高,在北欧,中欧和东欧的生存率则明显提高。但是,东欧的生存率低于其他地区。存活率随年龄的增长而降低,而在75岁或75岁以上的患者中存活率仅随时间略有增加,尽管在滤泡性淋巴瘤,弥漫性大B细胞淋巴瘤和慢性粒细胞白血病的老年患者中存活率增加了10%。解释:这些趋势令人鼓舞。广泛使用新的更有效的治疗方法可能可以解释许多增加的生存率。但是,欧洲各地生存率的持续差异表明,护理质量和新疗法的可用性存在差异。为代表病例样本收集有关诊断和治疗阶段的数据的高分辨率研究可以提供治疗有效性的进一步证据,并解释生存的地理差异。

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