Cancer risk in persons receiving prescriptions for paracetamol: A Danish cohort study

Citation
S. Friis et al., Cancer risk in persons receiving prescriptions for paracetamol: A Danish cohort study, INT J CANC, 97(1), 2002, pp. 96-101
Citations number
36
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
INTERNATIONAL JOURNAL OF CANCER
ISSN journal
00207136 → ACNP
Volume
97
Issue
1
Year of publication
2002
Pages
96 - 101
Database
ISI
SICI code
0020-7136(20020101)97:1<96:CRIPRP>2.0.ZU;2-W
Abstract
The use of paracetamol has been associated with increased risks for urinary tract cancers and decreased risk for ovarian cancer, although results have been inconsistent. We conducted a population-based cohort study using data from the Prescription Database of North Jutland County and the Danish Canc er Registry. Cancer incidence among 39,946 individuals receiving prescripti ons for paracetamol was compared with expected incidence based on the North Jutland population who did not receive paracetamol prescriptions, during a 9-year follow-up period. Standardized incidence ratios (SIRs) with corresp onding 95% confidence intervals (95% Cis) were calculated for cancers overa ll and at selected sites. Overall, 2,173 cancers were observed with 1,973 e xpected, yielding a SIR of 1.10 (95% Cl, 1.06-1.15). Significantly elevated SIRs were found for cancers of the esophagus (1.9; 95% Cl, 1.3-2.8) and lu ng (1.6; 95% Cl, 1.4-1.7). Nonsignificantly increased SIRs were observed fo r cancers of the liver (1.5; 95% Cl, 0.96-2.2), renal parenchyma (1.3; 95% Cl, 0.9-1.7) and renal pelvis/ureter (1.6; 95% Cl, 0.96-2.6), whereas the S IR for cancer of the urinary bladder was close to unity (1. 1; 95% Cl, 0.9- 1.4). For ovarian cancer, the SIR was close to expectation (0.9; 95% Cl, 0. 6-1.2) with no evidence of trends with duration of follow-up or number of p rescriptions. A similar risk pattern was observed after exclusion of person -time experience following prescription for aspirin or other nonsteroidal a ntiinflammatory drugs in the study cohort and reference population. Our res ults do not support a major role for paracetamol in the development of canc ers of the urinary tract, and we found little evidence of a protective effe ct of paracetamol against ovarian cancer. The elevated risks for cancers of the esophagus, lung and liver are most likely a result of confounding vari ables, but may warrant further investigation. (C) 2002 Wiley-Liss, Inc.