Incidence of new primary cancers after adjuvant tamoxifen therapy and radiotherapy for early breast cancer
- PMID: 2072407
- DOI: 10.1093/jnci/83.14.1013
Incidence of new primary cancers after adjuvant tamoxifen therapy and radiotherapy for early breast cancer
Abstract
The incidence of new primary cancers was evaluated in 3538 postmenopausal patients who had received surgical treatment for primary breast cancer. Of these patients, 1828 with a low risk of recurrence received no further treatment. High-risk patients were randomly assigned to one of two groups. The first group (n = 846) received postoperative radiotherapy, while the second group (n = 864) received radiotherapy plus tamoxifen at a dose of 30 mg given daily for 48 weeks. The median observation time was 7.9 years. In comparison with the number of new cancers in the general population, the number of new cancers in the three groups was elevated mostly due to a high number of cancers of the contralateral breast and of colorectal cancers in the high-risk groups. The cumulative risk of nonlymphatic leukemia was increased among patients who received postoperative radiotherapy (P = .04). Cancer incidence in the high-risk tamoxifen-treated group relative to that in the high-risk group not treated with tamoxifen was not significant (1.3). No protective effect of tamoxifen on the opposite breast was seen (rate ratio for breast cancer = 1.1), but a tendency to an elevated risk of endometrial cancer was observed (rate ratio = 3.3; 95% confidence interval = 0.6-32.4). Continued and careful follow-up of women treated with tamoxifen is necessary to clarify the potential cancer-suppressive or cancer-promoting effects of this drug.
Similar articles
-
Carcinogenic effects of adjuvant tamoxifen treatment and radiotherapy for early breast cancer.Acta Oncol. 1992;31(2):259-63. doi: 10.3109/02841869209088912. Acta Oncol. 1992. PMID: 1622643 Clinical Trial.
-
Cardiac and thromboembolic morbidity among postmenopausal women with early-stage breast cancer in a randomized trial of adjuvant tamoxifen. The Stockholm Breast Cancer Study Group.J Natl Cancer Inst. 1993 Sep 1;85(17):1398-406. doi: 10.1093/jnci/85.17.1398. J Natl Cancer Inst. 1993. PMID: 8350363 Clinical Trial.
-
Endometrial cancer in tamoxifen-treated breast cancer patients: findings from the National Surgical Adjuvant Breast and Bowel Project (NSABP) B-14.J Natl Cancer Inst. 1994 Apr 6;86(7):527-37. doi: 10.1093/jnci/86.7.527. J Natl Cancer Inst. 1994. PMID: 8133536 Clinical Trial.
-
Reducing the risk for breast cancer recurrence after completion of tamoxifen treatment in postmenopausal women.Clin Ther. 2007 Aug;29(8):1535-47. doi: 10.1016/j.clinthera.2007.08.013. Clin Ther. 2007. PMID: 17919537 Review.
-
[Adjuvant therapy of breast cancer with tamoxifen and endometrial carcinoma].Bull Cancer. 1992;79(10):969-77. Bull Cancer. 1992. PMID: 1292764 Review. French.
Cited by
-
Meta-analysis of vascular and neoplastic events associated with tamoxifen.J Gen Intern Med. 2003 Nov;18(11):937-47. doi: 10.1046/j.1525-1497.2003.20724.x. J Gen Intern Med. 2003. PMID: 14687281 Free PMC article.
-
The effects of intermittent progesterone upon tamoxifen inhibition of tumor growth in the 7,12-dimethylbenzanthracene rat mammary tumor model.Breast Cancer Res Treat. 1993 Sep;27(3):283-7. doi: 10.1007/BF00665699. Breast Cancer Res Treat. 1993. PMID: 8312587
-
The occurrence of invasive cancers following a diagnosis of breast carcinoma in situ.Br J Cancer. 2008 Aug 19;99(4):611-5. doi: 10.1038/sj.bjc.6604524. Epub 2008 Jul 29. Br J Cancer. 2008. PMID: 18665169 Free PMC article.
-
Tamoxifen stimulates in vivo growth of drug-resistant estrogen receptor-negative breast cancer.Cancer Chemother Pharmacol. 1993;32(5):396-8. doi: 10.1007/BF00735926. Cancer Chemother Pharmacol. 1993. PMID: 8339392
-
Bioactivation of the cancer chemopreventive agent tamoxifen to quinone methides by cytochrome P4502B6 and identification of the modified residue on the apoprotein.Drug Metab Dispos. 2012 Dec;40(12):2280-8. doi: 10.1124/dmd.112.047266. Epub 2012 Aug 31. Drug Metab Dispos. 2012. PMID: 22942317 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical