Mounier Morgane, Bossard Nadine, Remontet Laurent, Belot Aurélien, Minicozzi Pamela, De Angelis Roberta, Capocaccia Riccardo, Iwaz Jean, Monnereau Alain, Troussard Xavier, Sant Milena, Maynadié Marc, Giorgi Roch
Registre des Hémopathies Malignes de Côte d'Or, Université de Bourgogne Franche-Comté, Dijon, France; Université de Lyon, Lyon, France; Université Lyon 1, Villeurbanne, France; Centre national de la recherche scientifique unités mixtes de recherche 5558, Laboratoire de Biométrie et Biologie Evolutive, Equipe Biostatistique Santé, Villeurbanne, France; Institut national de la santé et de la recherche médicale unités mixtes de recherche S 912 Sciences Economiques et Sociales de la Santé et Traitement de l'Information Médicale, Faculté de Médecine, Marseille, France; Aix Marseille Université unités mixtes de recherche S 912 Institut de recherche pour le développement, Marseille, France.
Université de Lyon, Lyon, France; Université Lyon 1, Villeurbanne, France; Centre national de la recherche scientifique unités mixtes de recherche 5558, Laboratoire de Biométrie et Biologie Evolutive, Equipe Biostatistique Santé, Villeurbanne, France; Service de Biostatistique, Hospices Civils de Lyon, Lyon, France.
Lancet Haematol. 2015 Nov;2(11):e481-91. doi: 10.1016/S2352-3026(15)00155-6. Epub 2015 Oct 23.
Since 2001, the World Health Organization classification of tumours of haematopoietic and lymphoid tissues and the International Classification of Diseases for Oncology (third edition) have improved data collection for lymphoma subtypes in most European cancer registries and allowed reporting on the major non-Hodgkin lymphoma subtypes. Treatment of non-Hodgkin lymphoma has changed profoundly, benefiting patients with follicular lymphoma or diffuse large B-cell lymphoma. We aimed to compare dynamics of cancer mortality in patients with follicular lymphoma or diffuse large B-cell lymphoma in five large European areas using data for survival from the largest number of collaborative European population-based cancer registries (EUROCARE).
We considered follicular lymphoma and diffuse large B-cell lymphoma cases in patients aged older than 15 years diagnosed between Jan 1, 1996, and Dec 31, 2004, and recorded in 43 cancer registries in five areas: Scotland and Wales, and northern, central, eastern, and southern Europe. We excluded cases incidentally diagnosed at autopsy or known from death certificates only. The vital status could be updated on Dec 31, 2008, in all registries but the French ones (Dec 31, 2007). We obtained changes in net survival with the Pohar-Perme estimator and excess mortality rate with a flexible parametric model according to age and year of diagnosis.
We identified 13,988 follicular lymphoma and 25,320 diffuse large B-cell lymphoma cases. We noted improvements in 5-year net survival for all ages between the 1999-2001 and 2002-04 periods for both cancers (except for follicular lymphoma in Scotland and Wales and diffuse large B-cell lymphoma in eastern Europe). For follicular lymphoma, 5-year net survival in northern Europe was 64% (95% CI 58-71) in 1999-2001 versus 75% (69-80) for 2002-04, for Scotland and Wales, it was 71% (66-76) versus 68% (64-72), for central Europe, it was 64% (61-67) versus 72% (70-75), for southern Europe, it was 67% (63-70) versus 73% (70-76), and for eastern Europe, it was 50% (43-57) versus 61% (54-69). For diffuse large B-cell lymphoma, 5-year net survival in northern Europe was 41% (35-49) versus 58% (54-62), in Scotland and Wales, it was 44% (41-48) versus 52% (49-54), in central Europe, it was 46% (44-47) versus 50% (48-51), in southern Europe, it was 44% (42-47) versus 50% (48-52), and in eastern Europe, it was 47% (41-54) versus 46% (43-50). We noted the largest area disparity during the 2002-04 period between eastern and northern Europe. We noted a significant effect of the year of diagnosis on the excess mortality rate for all ages in all areas, except for diffuse large B-cell lymphoma in eastern Europe. The excess mortality rate was not constant during the follow-up period: we noted a high rate early for both lymphomas, except for follicular lymphoma in northern Europe.
Although survival for follicular lymphoma and diffuse large B-cell lymphoma is improving, the results from this study should foster the search for more and better means of improvement of access to adequate care than that at present, as there remains variation in survival between European regions. Study of the dynamics of the excess mortality rate seems to be a useful clinical indicator to help the practitioner's choice of optimum management of patients.
Compagnia di San Paolo, Fondazione Cariplo Italy, Italian Ministry of Health, European Commission, Registre des Hémopathies Malignes de Côte d'Or, and French Agence Nationale de la Recherche.
自2001年以来,世界卫生组织造血与淋巴组织肿瘤分类以及国际肿瘤疾病分类(第三版)改进了大多数欧洲癌症登记处淋巴瘤亚型的数据收集工作,并允许报告主要的非霍奇金淋巴瘤亚型。非霍奇金淋巴瘤的治疗发生了深刻变化,使滤泡性淋巴瘤或弥漫性大B细胞淋巴瘤患者受益。我们旨在利用来自数量最多的欧洲协作性基于人群的癌症登记处(EUROCARE)的生存数据,比较欧洲五个大区域中滤泡性淋巴瘤或弥漫性大B细胞淋巴瘤患者的癌症死亡率动态变化。
我们纳入了1996年1月1日至2004年12月31日期间确诊的15岁以上滤泡性淋巴瘤和弥漫性大B细胞淋巴瘤患者,并记录在五个区域的43个癌症登记处:苏格兰和威尔士,以及北欧、中欧、东欧和南欧。我们排除了尸检时偶然诊断或仅从死亡证明得知的病例。除法国登记处(截至2007年12月31日)外,所有登记处的生命状态均可在2008年12月31日更新。我们使用Pohar-Perme估计量获得净生存变化,并使用灵活的参数模型根据诊断年龄和年份获得超额死亡率。
我们识别出13988例滤泡性淋巴瘤和25320例弥漫性大B细胞淋巴瘤病例。我们注意到,在1999 - 2001年和2002 - 2004年期间,两种癌症各年龄段的5年净生存均有所改善(苏格兰和威尔士的滤泡性淋巴瘤以及东欧的弥漫性大B细胞淋巴瘤除外)。对于滤泡性淋巴瘤,1999 - 2001年北欧的5年净生存为64%(95%CI 58 - 71),2002 - 2004年为75%(69 - 80);苏格兰和威尔士分别为71%(66 - 76)和68%(64 - 72);中欧分别为64%(61 - 67)和72%(70 - 75);南欧分别为67%(63 - 70)和73%(70 - 76);东欧分别为50%(43 - 57)和61%(54 - 69)。对于弥漫性大B细胞淋巴瘤,1999 - 2001年北欧的5年净生存为41%(35 - 49),2002 - 2004年为58%(54 - 62);苏格兰和威尔士分别为44%(41 - 48)和52%(