Literature DB >> 2072407

Incidence of new primary cancers after adjuvant tamoxifen therapy and radiotherapy for early breast cancer.

M Andersson1, H H Storm, H T Mouridsen.   

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.

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Year:  1991        PMID: 2072407     DOI: 10.1093/jnci/83.14.1013

Source DB:  PubMed          Journal:  J Natl Cancer Inst        ISSN: 0027-8874            Impact factor:   13.506


  25 in total

Review 1.  Management of early breast cancer.

Authors:  R D Rubens
Journal:  BMJ       Date:  1992-05-23

2.  The effects of intermittent progesterone upon tamoxifen inhibition of tumor growth in the 7,12-dimethylbenzanthracene rat mammary tumor model.

Authors:  D F Gibson; D A Johnson; S M Langan-Fahey; M K Lababidi; W H Wolberg; V C Jordan
Journal:  Breast Cancer Res Treat       Date:  1993-09       Impact factor: 4.872

3.  Tamoxifen and cancer of the endometrium.

Authors:  G O'Connell; A Arnold
Journal:  CMAJ       Date:  1993-06-15       Impact factor: 8.262

Review 4.  Comparative tolerability of first-generation selective estrogen receptor modulators in breast cancer treatment and prevention.

Authors:  M G Curtis
Journal:  Drug Saf       Date:  2001       Impact factor: 5.606

Review 5.  Tamoxifen and secondary tumours. An update.

Authors:  N Wilking; E Isaksson; E von Schoultz
Journal:  Drug Saf       Date:  1997-02       Impact factor: 5.606

6.  Radiotherapy for ductal carcinoma in situ and risk of second non-breast cancers.

Authors:  Diana R Withrow; Lindsay M Morton; Rochelle E Curtis; Sara J Schonfeld; Amy Berrington de González
Journal:  Breast Cancer Res Treat       Date:  2017-07-25       Impact factor: 4.872

7.  Meta-analysis of vascular and neoplastic events associated with tamoxifen.

Authors:  R Scott Braithwaite; Rowan T Chlebowski; Joseph Lau; Suzanne George; Rachel Hess; Nananda F Col
Journal:  J Gen Intern Med       Date:  2003-11       Impact factor: 5.128

8.  Tamoxifen stimulates in vivo growth of drug-resistant estrogen receptor-negative breast cancer.

Authors:  J Maenpaa; V Wiebe; S Koester; G Wurz; V Emshoff; R Seymour; P Sipila; M DeGregorio
Journal:  Cancer Chemother Pharmacol       Date:  1993       Impact factor: 3.333

Review 9.  Gynaecologic effects of tamoxifen.

Authors:  D Y Kuo; C D Runowicz
Journal:  Med Oncol       Date:  1995-06       Impact factor: 3.064

Review 10.  What do we know and what don't we know about tamoxifen in the human uterus.

Authors:  A Friedl; V C Jordan
Journal:  Breast Cancer Res Treat       Date:  1994       Impact factor: 4.872

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