There has been concern about the role of analgesics in the development
of renal-cell cancer, although a few studies have reported moderately
elevated risks with regular or long-term use. In a large internationa
l case-control study of renal-cell cancer we examined, among other hyp
otheses, the effect of phenacetin-containing and of other types of ana
lgesics: paracetamol (acetaminophen), salicylates (mainly aspirin) and
pyrazolones (e.g., antipyrine or phenazone). Relative risks, adjusted
for the effects of age, sex, body-mass index, tobacco smoking and stu
dy centre, were not significantly increased with intake of phenacetin,
either when lifetime consumption was categorized at the level of grea
ter than or equal to 0.1 kg or when subjects were subdivided further b
y amount. Nor were paracetamol, salicylates or pyrazolones linked with
renal-cell cancer. No consistently increasing risks with consumption
level was found. The lack of association was not altered by restrictin
g analgesic use to that which occurred 5 or IO years before the define
d ''cut-off'' date or when analysis was restricted to exclusive users
of a particular type of analgesic. Neither was the risk influenced by
the rate of consumption or whether the consumption had occurred at a y
oung age. Our study provides clear evidence that aspirin is unrelated
to renal-cell cancer risk, and our findings do not support the hypothe
sis that analgesics containing phenacetin or paracetamol increase the
risk, although the number of ''regular'' users and the amount of these
types of analgesic consumed were too small to confidently rule out a
minor carcinogenic effect of phenacetin and paracetamol. (C) 1995 Wile
y-Liss, Inc.