Epidemiologic evaluation of pharmaceuticals with limited evidence of carcinogenicity
β Scribed by Gary D. Friedman; Sheng-Fang Jiang; Natalia Udaltsova; Charles P. Quesenberry Jr.; James Chan; Laurel A. Habel
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- French
- Weight
- 82 KB
- Volume
- 125
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Thorough review by the International Agency for Research on Cancer (IARC) has resulted in classifying many substances, including pharmaceuticals, as probably or possibly carcinogenic to humans, based on experiments on animals or limited data on humans. We evaluated 9 such pharmaceuticals for evidence of carcinogenicity in patients receiving them in a large medical care program with automated pharmacy records and a cancer registry. Nested caseβcontrol analyses were performed in a cohort of 6.5 million subscribers with up to 12 years of followβup, focusing on cancer sites suggested by previous evidence and other sites with odds ratio of at least 1.50, p < 0.01 and some evidence of doseβresponse. Unmeasured confounding was estimated in sensitivity analyses. We found some supportive evidence for carcinogenicity of griseofulvin, metronidazole and phenytoin and for the known carcinogen, cyclophosphamide, which was added for validation of our data and analyses. Findings for chloramphenicol, ironβdextran complex, phenoxybenzamine and phenobarbital were essentially nonβcontributory. Confounding by cigarette smoking and prior thyroid disease could account, respectively, for associations of oxazepam with lung cancer and propylthiouracil with thyroid cancer. Although not definitive, these findings should be considered in the evaluations of these pharmaceuticals. Β© 2009 UICC
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