Screening pharmaceuticals for possible carcinogenic effects: initial positive results for drugs not previously screened

ObjectiveTo screen commonly used prescription drugs for possible carcinogenic effects.MethodsIn a large health care program we identified 105 commonly used drugs, not previously screened. Recipients were followed for up to 12½ years for incident cancer. Nested case–control analyses of 55 cancer sites and all combined included up to ten matched controls per case, with lag of at least 2 years between drug dispensing and cancer. Positive associations entailed a relative risk of 1.50, with p ≤ 0.01 and higher risk for three or more, than for one prescription. Evaluation included further analyses, searches of the literature, and clinical judgment.ResultsThere were 101 associations of interest for 61 drugs. Sixty-six associations were judged to have involved substantial confounding. We found evidence that of the remaining 35, the following associations may not be due to chance: sulindac with gallbladder cancer and leukemia, hyoscyamine with nonHodgkin lymphoma, nortriptyline with esophageal and hepatic cancer, oxazepam with lung cancer, both fluoxetine and paroxetine with testicular cancer, hydrochlorothiazide with renal and lip cancer, and nifedipine with lip cancer.ConclusionsThese preliminary findings suggest that further studies are indicated regarding sulindac, hyoscyamine, nortriptyline, oxazepam, fluoxetine, paroxetine, hydrochlorothiazide, and nifedipine.

[1]  D. Winn,et al.  Cancers of the Oral Cavity and Pharynx , 2009 .

[2]  D. Mellor,et al.  Cohort study of COX-1 and COX-2 expression in canine rectal and bladder tumours. , 2006, The Journal of small animal practice.

[3]  L. Fishbein,et al.  A Toxicological Review of Beta-Adrenergic Blockers , 1986 .

[4]  Patrick Neven,et al.  Endometrial cancer. , 2005, Lancet.

[5]  D. Lawlor,et al.  Systematic review of the epidemiologic and trial evidence of an association between antidepressant medication and breast cancer. , 2003, Journal of clinical epidemiology.

[6]  J. Martínez,et al.  SULINDAC-INDUCED BONE MARROW TOXICITY , 1980, The Lancet.

[7]  F. Wojnarowska,et al.  Photo‐damage in Northern European renal transplant recipients is associated with use of calcium channel blockers , 2003, Clinical and experimental dermatology.

[8]  J. Vauthey,et al.  Biliary tract cancer , 1995 .

[9]  W. Elliott Antihypertensive medication and their impact on cancer incidence: a mixed treatment comparison meta-analysis of randomized controlled trials , 2009 .

[10]  M. Majchrowicz,et al.  [Anal cancer]. , 1996, SIDAhora : un proyecto del Departamento de Publicaciones del PWA Coalition, NY.

[11]  Peter D Siersema,et al.  Esophageal cancer. , 2008, Gastroenterology clinics of North America.

[12]  D. Petitti,et al.  Breast cancer risk in a large cohort of female antidepressant medication users. , 2005, Cancer letters.

[13]  H. Ury,et al.  Screening for possible drug carcinogenicity: second report of findings. , 1983, Journal of the National Cancer Institute.

[14]  R. Haden The leukemias. , 1988, Pediatric clinics of North America.

[15]  D. Argyle,et al.  The in vitro effects of piroxicam and meloxicam on canine cell lines. , 2006, The Journal of small animal practice.

[16]  S. K. Van Den Eeden,et al.  Prescription drug screening for subsequent carcinogenicity , 1995 .

[17]  X. Shu,et al.  Prescription medication use during pregnancy and risk of infant leukemia (United States) , 2003, Cancer Causes & Control.

[18]  P. Coogan Review of the epidemiological literature on antidepressant use and breast cancer risk , 2006, Expert review of neurotherapeutics.

[19]  A. Kamat,et al.  Atorvastatin: a potential chemopreventive agent in bladder cancer. , 2005, Urology.

[20]  S. Orsulic,et al.  Ovarian Cancer , 1993, British Journal of Cancer.

[21]  J. Fraumeni,et al.  Cancer epidemiology and prevention. , 2006 .

[22]  M. Cotterchio,et al.  Do antidepressants cause, promote, or inhibit cancers? , 1995, Journal of clinical epidemiology.

[23]  L. A. Dostal,et al.  Fertility and general reproduction studies in rats with the HMG-CoA reductase inhibitor, atorvastatin. , 1996, Fundamental and applied toxicology : official journal of the Society of Toxicology.

[24]  D. Silverman,et al.  Cancer of the Pancreas , 2009 .

[25]  H. Ury,et al.  Initial screening for carcinogenicity of commonly used drugs. , 1980, Journal of the National Cancer Institute.

[26]  J. Baron,et al.  Psychotropic medication use and risk of epithelial ovarian cancer. , 1998, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[27]  Gardiner Pa Letter: care of children's eyes. , 1973 .

[28]  P DESAIVE,et al.  [Thyroid cancer]. , 1951, Revue medicale de Liege.

[29]  C. la Vecchia,et al.  Calcium channel blockers, verapamil and cancer risk. , 2003, European journal of cancer.

[30]  N. Krieger Overcoming the absence of socioeconomic data in medical records: validation and application of a census-based methodology. , 1992, American journal of public health.

[31]  J. Miller Marrow aplasia and sulindac. , 1980, Annals of internal medicine.

[32]  G. Friedman AN EDITOR COMMENTS , 1992 .

[33]  A. Zuckerman,et al.  IARC Monographs on the Evaluation of Carcinogenic Risks to Humans , 1995, IARC monographs on the evaluation of carcinogenic risks to humans.

[34]  L. A. Dostal,et al.  Repeated analysis of semen parameters in beagle dogs during a 2-year study with the HMG-CoA reductase inhibitor, atorvastatin. , 2001, Toxicological sciences : an official journal of the Society of Toxicology.

[35]  Michael J Thun,et al.  Nonsteroidal anti-inflammatory drugs as anticancer agents: mechanistic, pharmacologic, and clinical issues. , 2002, Journal of the National Cancer Institute.

[36]  A. Hofman,et al.  Verapamil is associated with an increased risk of cancer in the elderly: the Rotterdam study. , 2003, European journal of cancer.

[37]  G. Friedman,et al.  Screening prescription drugs for possible carcinogenicity: eleven to fifteen years of follow-up. , 1989, Cancer research.

[38]  D. Frisbie,et al.  Nonsteroidal antiinflammatory drugs. , 1981, Delaware medical journal.

[39]  I. Bairati,et al.  Antihypertensive Drug Use and The Risk of Prostate Cancer (Canada) , 2004, Cancer Causes & Control.

[40]  H. Sørensen,et al.  Use of photosensitising diuretics and risk of skin cancer: a population-based case–control study , 2008, British Journal of Cancer.

[41]  Y. Muto,et al.  Drug-associated cholelithiasis: a case of sulindac stone formation and the incorporation of sulindac metabolites into the gallstones , 1999, American Journal of Gastroenterology.

[42]  J. Williamson,et al.  A review of cancer chemopreventive agents. , 2001, Current medicinal chemistry.

[43]  G. Friedman,et al.  Pharmaceuticals Other Than Hormones , 2006 .

[44]  M. Dobrinska,et al.  Enterohepatic circulation of sulindac and metabolites , 1983, Clinical pharmacology and therapeutics.

[45]  V. Ooi,et al.  Cytostatic and cytotoxic effects of cyclooxygenase inhibitors and their synergy with docosahexaenoic acid on the growth of human skin melanoma A-375 cells. , 2005, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

[46]  G. Friedman,et al.  Screening statins for possible carcinogenic risk: up to 9 years of follow‐up of 361 859 recipients , 2008, Pharmacoepidemiology and drug safety.