Congenital abnormalities and childhood cancer - A cohort record-linkage study

被引:76
作者
Agha, MM
Williams, JI
Marrett, L
To, T
Zipursky, A
Dodds, L
机构
[1] SUNY Hlth Sci Ctr, Ontario & Clin Epidemiol Unit, Inst Clin Evaluat Sci, Toronto, ON M4N 3M5, Canada
[2] Univ Toronto, Dept Publ Hlth Sci, Toronto, ON, Canada
[3] Toronto Rehab Inst, Toronto, ON, Canada
[4] Canc Care Ontario, Toronto, ON, Canada
[5] Hosp Sick Children, Populat Hlth Sci Res Inst, Toronto, ON, Canada
[6] Hosp Sick Children, Toronto, ON, Canada
[7] Dalhousie Univ, Dept Obstet & Gynecol, Halifax, NS B3H 3J5, Canada
[8] Dalhousie Univ, Dept Pediat, Halifax, NS B3H 3J5, Canada
关键词
genetic susceptibility; children; neoplasm; congenital abnormalities; cohort studies; proportional hazards models; medical record linkage;
D O I
10.1002/cncr.20985
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The examination of specific characteristics of neoplasms diagnosed in children have suggested that a significant proportion can be attributed to a genetic mutation or genetic predisposition. Although the study of a genetic predisposition to cancer in children remains in the early stages, congenital abnormalities could provide essential information for mapping predisposing lesions in children with cancer. METHODS. in the current study, 2 large cohorts of children with and without congenital abnormalities were followed for the occurrence of cancer and death up to 18 years. Through this study, the risk of developing cancer by age at diagnosis, effects of birth characteristics on cancer risk, and possible associations between specific anomalies and tumor types were examined. RESULTS. Based on the follow-up of 90,400 children, the risk of developing cancer during the first year of life was found to be nearly 6 times higher in children with anomalies (rate ratio [RR] of 5.8; 95% confidence interval [95% CI], 3.7-9.1). Children with birth defects were found to be at a higher risk for developing leukemia (RR of 2.7; 95% CI, 2.1-3.6), tumors of the central nervous system (RR of 2.5; 95% CI, 1.8-3.4), sympathetic nervous system tumors (RR of 2.2; 95% CI, 1.4-3.4), and soft tissue sarcomas (RR of 1.9; 95% CI, 1.0-3.5). Among children with birth defects, children with Down syndrome, nervous system anomalies, and anomalies of the urinary system had the highest incidence rates of cancer. In the presence of birth defects, other factors such as birth weight, gestational age, age of the mother, and birth order were not found to be associated significantly with the risk of cancer. CONCLUSIONS. The significant relative risks found in the current study provided evidence of links between the presence of abnormalities and the development of cancer. Some "cancer- prone" abnormalities were identified in the current study. Such anomalies may he markers of other exposures or processes that increase the risk of developing cancer. (c) 2005 American Cancer Society.
引用
收藏
页码:1939 / 1948
页数:10
相关论文
共 26 条
[1]   Associations between congenital malformations and childhood cancer. A register based case-control study [J].
Altmann, AE ;
Halliday, JL ;
Giles, GG .
BRITISH JOURNAL OF CANCER, 1998, 78 (09) :1244-1249
[2]  
[Anonymous], 1996, THIS BATTLE WHICH I
[3]   THE AGE DISTRIBUTION OF CANCER AND A MULTI-STAGE THEORY OF CARCINOGENESIS [J].
ARMITAGE, P ;
DOLL, R .
BRITISH JOURNAL OF CANCER, 1954, 8 (01) :1-12
[4]   Genes and cancer [J].
Birch, JM .
ARCHIVES OF DISEASE IN CHILDHOOD, 1999, 80 (01) :1-3
[5]   Delay in the diagnosis of paediatric brain tumours [J].
Dobrovoljac, M ;
Hengartner, H ;
Boltshauser, E ;
Grotzer, MA .
EUROPEAN JOURNAL OF PEDIATRICS, 2002, 161 (12) :663-667
[6]   DOWNS-SYNDROME AND LEUKEMIA - EPIDEMIOLOGY, GENETICS, CYTOGENETICS AND MECHANISMS OF LEUKEMOGENESIS [J].
FONG, C ;
BRODEUR, GM .
CANCER GENETICS AND CYTOGENETICS, 1987, 28 (01) :55-76
[7]  
Foulkes WD, 1997, MED PEDIATR ONCOL, V29, P272, DOI 10.1002/(SICI)1096-911X(199710)29:4<272::AID-MPO7>3.0.CO
[8]  
2-J
[9]   Delay in diagnosis of children with cancer: A retrospective study of 315 children [J].
Haimi, M ;
Nahum, MP ;
Ben Arush, MW .
PEDIATRIC HEMATOLOGY AND ONCOLOGY, 2004, 21 (01) :37-48
[10]   PROBABILISTIC LINKAGE OF LARGE PUBLIC-HEALTH DATA FILES [J].
JARO, MA .
STATISTICS IN MEDICINE, 1995, 14 (5-7) :491-498