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Epidemiology
Tamoxifen and toremifene treatment of breast cancer and risk of subsequent endometrial cancer: A population-based case-control study
Article first published online: 24 MAY 2002
DOI: 10.1002/ijc.10454
Copyright © 2002 Wiley-Liss, Inc.
Additional Information
How to Cite
Pukkala, E., Kyyrönen, P., Sankila, R. and Holli, K. (2002), Tamoxifen and toremifene treatment of breast cancer and risk of subsequent endometrial cancer: A population-based case-control study. International Journal of Cancer, 100: 337–341. doi: 10.1002/ijc.10454
Publication History
- Issue published online: 27 JUN 2002
- Article first published online: 24 MAY 2002
- Manuscript Accepted: 26 MAR 2002
- Manuscript Revised: 25 MAR 2002
- Manuscript Received: 26 NOV 2001
Funded by
- Orion Pharma
- Abstract
- Article
- References
- Cited By
Keywords:
- antiestrogen;
- hormonal treatment;
- breast cancer;
- endometrial cancer;
- tamoxifen;
- toremifene
Abstract
A population-based case-control study was performed to evaluate the risk of endometrial cancer related to tamoxifen or toremifene treatment. All patients with breast cancer diagnosis since 1980 in Finland who subsequently developed an endometrial cancer by the end of 1995 and 3 matched controls were identified among the 38,000 breast cancer patients of the Finnish Cancer Registry database. Detailed information on treatment of breast cancer and potential confounders was collected from hospital records. The OR for tamoxifen treatment (59 cases), adjusted for significant cofactors (increased risk associated with obesity, low parity and PR positivity) was 2.9 (95% CI 1.8–4.7). The OR for toremifene (3 cases) was 0.9 (95% CI 0.3–3.9). The OR related to adjuvant tamoxifen treatment reached its maximum 2–5 years after the beginning of treatment (OR 5.1, 95% CI 2.1–13), while the OR for tamoxifen used for palliative treatment of advanced breast cancer was especially high after a lag of over 5 years (OR 9.5, 95% CI 2.5–36). The risk increase due to tamoxifen was slightly higher if the age at initiation was below 55, and risk was more pronounced among patients with well-differentiated endometrial cancer than patients with cancers of clinical grades 2 or 3. According to our results, treatment with tamoxifen increases the risk of endometrial cancer. Due to the rare use of toremifene up to the mid-1990s, the risk assessment concerning it was inconclusive. © 2002 Wiley-Liss, Inc.

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