Rm. Merrill et al., Cancer prevalence estimates based on tumour registry data in the Surveillance, Epidemiology, and End Results (SEER) Program, INT J EPID, 29(2), 2000, pp. 197-207
Citations number
25
Categorie Soggetti
Envirnomentale Medicine & Public Health","Medical Research General Topics
Background The Connecticut Tumor Registry (CTR) has collected cancer data f
or a sufficiently long period of time to capture essentially all prevalent
cases of cancer, and to provide unbiased estimates of cancer prevalence. Ho
wever, prevalence proportions estimated from Connecticut data may not be re
presentative of the total US, particularly for racial/ethnic subgroups. The
purpose of this study is to apply the modelling approach developed by Capo
caccia and De Angelis to cancer data from the Surveillance, Epidemiology, a
nd End Results (SEER) Program of the National Cancer Institute to obtain mo
re representative US site-specific cancer prevalence proportion estimates f
or white and black patients.
Methods Incidence and relative survival were modelled and used to obtain es
timated completeness indices of SEER prevalence proportions for ail cancer
sites combined, stomach, cervix uteri, skin melanomas, non-Hodgkin's lympho
mas, lung and bronchus, colon/rectum, female breast, and prostate. For vali
dation purposes, modelled completeness indices were computed for Connecticu
t and compared with empirical completeness indices (the ratio of Connecticu
t based prevalence proportion estimates using 1973-1993 data to 1940-1993 d
ata). The SEER-based modelled completeness indices were used to adjust SEER
prevalence proportion estimates for white and black patients.
Results Model validation showed that the adjusted SEER cancer prevalence pr
oportions provided reasonably unbiased prevalence proportion estimates in g
eneral, although more complex modelling of the completeness indices is nece
ssary for female cancers of the colon, melanoma, breast, cervix, and all ca
ncers combined. The SEER-based cancer prevalence proportions are incomplete
for most cancer sites, more so for women, whites, and at older ages. For a
ll cancers combined, prevalence proportions tended to he higher for whites
than blacks. For the site-specific cancers this was true for stomach, prost
ate, cervix uteri, and lung and bronchus (men only). For colon/rectal cance
rs the prevalence proportions were higher for blacks through ages 59 (men)
and 64 (women), and then for the remaining ages they were higher for whites
. Prevalence proportions were lowest for stomach cancer and highest for pro
state and female breast cancers. Men experienced higher prevalence proporti
ons than women for skin melanomas, non-Hodgkin's lymphomas, lung and bronch
us, and colon/rectal cancers.
Conclusion The modelling approach applied to SEER data generally provided r
easonable estimates of cancer prevalence. These estimates are useful becaus
e they are more representative of cancer prevalence than previously obtaine
d and reported in the US.