TY - JOUR
T1 - Bayesian methods for early detection of changes in childhood cancer incidence
T2 - Trends for acute lymphoblastic leukaemia are consistent with an infectious aetiology
AU - Maule, Milena Maria
AU - Zuccolo, Luisa
AU - Magnani, Corrado
AU - Pastore, Guido
AU - Dalmasso, Paola
AU - Pearce, Neil
AU - Merletti, Franco
AU - Gregori, Dario
N1 - Funding Information:
The CCRP is supported by the Piedmont Region. This project was partly supported by the ‘Oncology Special Project’, Compagnia di San Paolo FIRMS, the Italian Association for Cancer Research (AIRC) and the special programme ‘Ricerca Sanitaria Finalizzata’ of the Piedmont Region. This work was also supported by the Progetto Lagrange, Fondazione CRT/ISI, the Master of Epidemiology (University of Turin), and the Health Research Council of New Zealand.
PY - 2006/1
Y1 - 2006/1
N2 - Published data on time trends in the incidence of childhood leukaemia show inconsistent patterns, with some studies showing increases and others showing relatively stable incidence rates. Data on time trends in childhood cancer incidence from the Childhood Cancer Registry of Piedmont, Italy were analysed using two different approaches: standard Poisson regression and a Bayesian regression approach including an autoregressive component. Our focus was on acute lymphoblastic leukaemia (ALL), since this is hypothesised to have an infectious aetiology, but for purposes of comparison we also conducted similar analyses for selected other childhood cancer sites (acute non-lymphoblastic leukaemia (AnLL), central nervous system (CNS) tumours and neuroblastoma (NB)). The two models fitted the data equally well, but led to different interpretations of the time trends. The first produced ever-increasing rates, while the latter produced non-monotonic patterns, particularly for ALL, which showed evidence of a cyclical pattern. The Bayesian analysis produced findings that are consistent with the hypothesis of an infectious aetiology for ALL, but not for AnLL or for solid tumours (CNS and NB). Although sudden changes in time trends should be interpreted with caution, the results of the Bayesian approach are consistent with current knowledge of the natural history of childhood ALL, including a short latency time and the postulated infectious aetiology of the disease.
AB - Published data on time trends in the incidence of childhood leukaemia show inconsistent patterns, with some studies showing increases and others showing relatively stable incidence rates. Data on time trends in childhood cancer incidence from the Childhood Cancer Registry of Piedmont, Italy were analysed using two different approaches: standard Poisson regression and a Bayesian regression approach including an autoregressive component. Our focus was on acute lymphoblastic leukaemia (ALL), since this is hypothesised to have an infectious aetiology, but for purposes of comparison we also conducted similar analyses for selected other childhood cancer sites (acute non-lymphoblastic leukaemia (AnLL), central nervous system (CNS) tumours and neuroblastoma (NB)). The two models fitted the data equally well, but led to different interpretations of the time trends. The first produced ever-increasing rates, while the latter produced non-monotonic patterns, particularly for ALL, which showed evidence of a cyclical pattern. The Bayesian analysis produced findings that are consistent with the hypothesis of an infectious aetiology for ALL, but not for AnLL or for solid tumours (CNS and NB). Although sudden changes in time trends should be interpreted with caution, the results of the Bayesian approach are consistent with current knowledge of the natural history of childhood ALL, including a short latency time and the postulated infectious aetiology of the disease.
KW - Bayesian methods
KW - Childhood leukaemia
KW - Incidence
KW - Trend
UR - https://www.scopus.com/pages/publications/29144472646
U2 - 10.1016/j.ejca.2005.07.028
DO - 10.1016/j.ejca.2005.07.028
M3 - Article
SN - 0959-8049
VL - 42
SP - 78
EP - 83
JO - European Journal of Cancer
JF - European Journal of Cancer
IS - 1
ER -