Alexander F E, Boyle P, Carli P M, Coebergh J W, Draper G J, Ekbom A, Levi F, McKinney P A, McWhirter W, Magnani C, Michaelis J, Olsen J H, Peris-Bonet R, Petridou E, Pukkala E, Vatten L
Department of Public Health Sciences, The University of Edinburgh, Medical School, UK.
Br J Cancer. 1998 Mar;77(5):812-7. doi: 10.1038/bjc.1998.132.
The EUROCLUS project included information on residence at diagnosis for 13351 cases of childhood leukaemia diagnosed in the period 1980-89 in defined geographical regions in 17 countries. A formal algorithm permits identification of small census areas as containing case excesses. The present analysis examines spatial-temporal patterns of the cases (n = 970) within these clustered areas. The objectives were, first, to compare these results with those from an analysis conducted for UK data for the period 1966-83, and, second, to extend them to consider infant leukaemias. A modification of the Knox test investigates, within the small areas, temporal overlap between cases in a subgroup of interest at a putative critical time and all other cases at any time between birth and diagnosis. Critical times were specified in advance as follows: for cases of acute lymphoblastic leukaemia aged 2-4 years, the 18-month period preceding diagnosis; for cases of total leukaemia aged 5-14 years, 1 year before to 1 year after birth; and for infant cases (diagnosed < 1 year), 1 year before to 6 months after birth. Each of the analyses found evidence of excess space-time overlap compared with that expected; these were 10% (P = 0.005), 15% (P= 0.0002) and 26% (P= 0.03) respectively. The results are interpreted in terms of an infectious origin of childhood leukaemia.
EUROCLUS项目包含了1980年至1989年期间在17个国家特定地理区域诊断出的13351例儿童白血病病例的诊断时居住地信息。一种正式算法能够识别出存在病例超额的小普查区域。本分析研究了这些聚集区域内病例(n = 970)的时空模式。目标一是将这些结果与针对1966年至1983年英国数据进行的分析结果相比较,目标二是扩展这些结果以纳入婴儿白血病病例。对诺克斯检验进行了修改,在小区域内研究感兴趣亚组病例在假定关键时间与出生至诊断期间任何时间的所有其他病例之间的时间重叠情况。关键时间预先设定如下:对于2至4岁的急性淋巴细胞白血病病例,为诊断前18个月期间;对于5至14岁的所有白血病病例,为出生前1年至出生后1年;对于婴儿病例(诊断时年龄<1岁),为出生前1年至出生后6个月。每项分析均发现与预期相比存在超额时空重叠的证据;这些超额分别为10%(P = 0.005)、15%(P = 0.0002)和26%(P = 0.03)。这些结果从儿童白血病的感染源角度进行了解释。