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Exposure to cyclooxygenase-2 inhibitors and risk of cancer: nested case-control studies
Y Vinogradova1, C Coupland, J Hippisley-Cox
1Division of Primary Care, 13th Floor, Tower Building, University Park, University of Nottingham, Nottingham, NG7 2RD, UK. yana.vinogradova@nottingham.ac.uk
Background:
Selective cyclooxygenase-2 (COX2) inhibitors are widely used as analgesics and it is unclear whether its long-term use affects cancer risk.
Methods:
A series of nested case-control studies using the QResearch primary care database. Associations of COX2 inhibitor use with risk of all cancers and 10 common site-specific cancers were estimated using conditional logistic regression adjusted for comorbidities, smoking status, socioeconomic status, and use of non-steroidal anti-inflammatory drugs, aspirin and statins.
Results:
A total of 88,125 cancers, diagnosed between 1998 and 2008, matched with up to five controls, were analysed. Use of COX2 inhibitors for more than a year was associated with a significantly increased risk of breast cancer (odds ratio (OR) 1.24, 95% confidence interval (CI) 1.08-1.42) and haematological malignancies (OR 1.38, 95% CI 1.12-1.69) and a decreased risk of colorectal cancer (OR 0.76, 95% CI 0.63-0.92). There were no other significant associations.
Conclusion:
Prolonged use of COX2 inhibitors was associated with an increased risk of breast and haematological cancers and decreased risk of colorectal cancer. These findings need to be confirmed using other data sources.
Insights
Long-term use of selective cyclooxygenase-2 (COX2) inhibitors is linked to increased breast and hematological cancer risks. However, prolonged COX2 inhibitor use may decrease colorectal cancer risk.
Area of Science:
- Oncology
- Pharmacology
- Epidemiology
Background:
- Selective cyclooxygenase-2 (COX2) inhibitors are common analgesics.
- The long-term impact of COX2 inhibitors on cancer risk remains uncertain.
Purpose of the Study:
- To investigate the association between COX2 inhibitor use and the risk of developing various cancers.
- To determine if prolonged use of COX2 inhibitors influences the risk of specific cancer types.
Main Methods:
- A nested case-control study design was employed using the QResearch primary care database.
- Conditional logistic regression analysis was used to estimate associations, adjusting for multiple confounding factors.
Main Results:
- Prolonged COX2 inhibitor use was associated with a significantly increased risk of breast cancer (OR 1.24) and hematological malignancies (OR 1.38).
- A decreased risk of colorectal cancer was observed with prolonged COX2 inhibitor use (OR 0.76).
- No other significant associations were found for other common cancers.
Conclusions:
- Prolonged use of COX2 inhibitors is associated with differential risks for specific cancers.
- Findings suggest an increased risk for breast and hematological cancers and a decreased risk for colorectal cancer.
- Further validation using diverse data sources is recommended.
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