Markers of inflammation and risk of ovarian cancer in Los Angeles County

Factors that increase inflammation have been suggested to influence the development of ovarian cancer, but these factors have not been well studied. To further investigate this question, we studied the role of talc use, history of endometrioisis and use of non‐steroidal anti‐inflammatory drugs (NSAIDs) and risk of ovarian cancer in a population‐based case‐control study in Los Angeles County involving 609 women with newly diagnosed epithelial ovarian cancer and 688 population‐based control women. Risk of ovarian cancer increased significantly with increasing frequency and duration of talc use; compared to never users risk was highest among long‐duration (20+ years), frequent (at least daily) talc users (adjusted relative risk (RR) = 2.08, 95% confidence interval (CI) = 1.34–3.23). A history of physician‐diagnosed endometriosis was statistically significantly associated with risk (RR = 1.66, 95% CI = 1.01–2.75). Women who were talc users and had a history of endometriosis showed a 3‐fold increased risk (RR = 3.12, 95% CI = 1.36–7.22). Contrary to the hypothesis that risk of ovarian cancer may be reduced by use of NSAIDs; risk increased with increasing frequency (per 7 times/week, RR = 1.27, 95% CI = 1.14–1.43) and years of NSAID use (per 5 years of use, RR = 1.25, 95% CI = 1.10–1.42); this was consistent across types of NSAIDs. We conclude that risk of ovarian cancer is significantly associated with talc use and with a history of endometriosis, as has been found in previous studies. The NSAID finding was unexpected and suggests that factors associated with inflammation are associated with ovarian cancer risk. This result needs confirmation with careful attention to the reasons for NSAID use. © 2008 Wiley‐Liss, Inc.

[1]  R. Shore,et al.  Aspirin and epithelial ovarian cancer. , 2001, Preventive medicine.

[2]  C. la Vecchia,et al.  Aspirin and ovarian cancer: an Italian case-control study. , 2000, Annals of oncology : official journal of the European Society for Medical Oncology.

[3]  M. Piver,et al.  Perineal talc exposure and subsequent epithelial ovarian cancer: a case-control study. , 1999, Obstetrics and gynecology.

[4]  M. Yu,et al.  Regular use of analgesics is a risk factor for renal cell carcinoma , 1999, British Journal of Cancer.

[5]  M. Piver,et al.  Regular use of analgesic drugs and ovarian cancer risk. , 2001, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[6]  J. Cerhan,et al.  Postmenopausal cancer risk after self‐reported endometriosis diagnosis in the Iowa Women's Health Study , 2002, Cancer.

[7]  M. Rossing,et al.  Analgesic drug use and risk of epithelial ovarian cancer. , 2008, American journal of epidemiology.

[8]  H T Sørensen,et al.  Risk of cancer in a large cohort of nonaspirin NSAID users: a population-based study , 2003, British Journal of Cancer.

[9]  A. Berchuck,et al.  Analgesic Drug Use and Risk of Ovarian Cancer , 2006, Epidemiology.

[10]  H. Jick,et al.  Association Between Acetaminophen or Nonsteroidal Antiinflammatory Drugs and Risk of Developing Ovarian, Breast, or Colon Cancer , 2002, Pharmacotherapy.

[11]  S. Bonovas,et al.  Do nonsteroidal anti-inflammatory drugs affect the risk of developing ovarian cancer? A meta-analysis. , 2005, British journal of clinical pharmacology.

[12]  M. Thun,et al.  Paracetamol and risk of ovarian cancer mortality in a prospective study of women in the USA , 1998, The Lancet.

[13]  R. Cress,et al.  Perineal talc exposure and epithelial ovarian cancer risk in the Central Valley of California , 2004, International journal of cancer.

[14]  J. Baron,et al.  Genital talc exposure and risk of ovarian cancer , 1999, International journal of cancer.

[15]  Kurt Straif,et al.  Carcinogenicity of carbon black, titanium dioxide, and talc. , 2006, The Lancet Oncology.

[16]  A. Green,et al.  Talcum powder, chronic pelvic inflammation and NSAIDs in relation to risk of epithelial ovarian cancer , 2008, International journal of cancer.

[17]  M. Pike,et al.  Estrogen-progestin replacement therapy and endometrial cancer. , 1998, Journal of the National Cancer Institute.

[18]  P. Hartge,et al.  Medication use and risk of ovarian carcinoma: A prospective study , 2004, International journal of cancer.

[19]  Kathleen M. Fairfield,et al.  Aspirin, other NSAIDs, and ovarian cancer risk (United States) , 2002, Cancer Causes & Control.

[20]  S. Shapiro,et al.  A case-control study of analgesic use and ovarian cancer. , 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[21]  A. Trentham-Dietz,et al.  Inverse association of NSAID use and ovarian cancer in relation to oral contraceptive use and parity , 2008, British Journal of Cancer.

[22]  J. Olsen,et al.  Relationship of Benign Gynecologic Diseases to Subsequent Risk of Ovarian and Uterine Tumors , 2005, Cancer Epidemiology Biomarkers & Prevention.

[23]  R. Ness,et al.  Possible role of ovarian epithelial inflammation in ovarian cancer. , 1999, Journal of the National Cancer Institute.

[24]  M. Goodman,et al.  Oral contraceptive use, reproductive history, and risk of epithelial ovarian cancer in women with and without endometriosis. , 2004, American journal of obstetrics and gynecology.

[25]  D. Cramer,et al.  Over-the-counter analgesics and risk of ovarian cancer , 1998, The Lancet.

[26]  N. Weiss,et al.  Perineal powder exposure and the risk of ovarian cancer. , 1997, American journal of epidemiology.

[27]  D. Cramer,et al.  Perineal Exposure to Talc and Ovarian Cancer Risk , 1992, Obstetrics and gynecology.

[28]  M. Morgan,et al.  Factors related to inflammation of the ovarian epithelium and risk of ovarian cancer. , 2000, Epidemiology.

[29]  J. Olsen,et al.  A population-based cohort study of the risk of colorectal and other cancers among users of low-dose aspirin , 2003, British Journal of Cancer.