Phenacetin-based analgesics have been linked to the development of renal pe
lvis cancer and renal cell carcinoma (RCC); The relationship between non-ph
enacetin types of analgesics and kidney cancer is less clear, although labo
ratory evidence suggests that these drugs possess carcinogenic potential. A
population-based case-control study involving 1204 non-Asian RCC patients
aged 25-74 and an equal number of sex-, age- and race-matched neighbourhood
controls was conducted in Los Angeles, California, to investigate the rela
tionship between sustained use of analgesics and risk of RCC according to m
ajor formulation categories. Detailed information on medical and medication
histories, and other lifestyle factors was collected through in-person int
erviews. Regular use of analgesics was a significant risk factor for RCC in
both men and women (odds ratio (OR) = 1.6, 95% confidence interval (CI) =
1.4-1.9 for both sexes combined). Risks were elevated across all four major
classes of analgesics (aspirin, non-steroidal anti-inflammatory agents oth
er than aspirin, acetaminophen and phenacetin). Within each class of analge
sics, there was statistically significant increasing risk with increasing l
evel of exposure. Although there was some minor variability by major class
of formulation, in general individuals in the highest exposure categories e
xhibited approximately 2.5-fold increase in risk relative to non- or irregu
lar users of analgesics. Subjects who took one regular-strength (i.e. 325 m
g) aspirin a day or less for cardiovascular disease prevention were not at
an increased risk of RCC (OR = 0.9, 95% CI = 0.0-1.4). (C) 1999 Cancer Rese
arch Campaign.