Immunohistochemical Phenotype of Breast Cancer during 25-Year Follow-up of the Royal Marsden Tamoxifen Prevention Trial.
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Embargo End Date
ICR Authors
Authors
Detre, SI
Ashley, S
Mohammed, K
Smith, IE
Powles, TJ
Dowsett, M
Ashley, S
Mohammed, K
Smith, IE
Powles, TJ
Dowsett, M
Document Type
Journal Article
Date
2017-03
Date Accepted
2016-12-19
Abstract
The randomized, double-blinded Royal Marsden Tamoxifen Breast Cancer Prevention Trial in healthy high-risk women started in 1986 and is still blinded. Eligible participants (<i>n</i> = 2,471) were randomly assigned to tamoxifen (20 mg/d) or placebo for 8 years. Analysis in 2006 showed a 30% risk reduction of estrogen receptor (ER)-positive invasive breast cancer mostly in the posttreatment period. Biomarker analysis in this population may identify any subgroup-specific preventive effects tamoxifen. After a median follow-up of 18.4 years, 242 patients had developed invasive cancer, 134 on placebo and 108 on tamoxifen. From these, 180 tissue blocks were available and ER, progesterone receptor (PgR), Ki67, HER2, and EGFR were immunohistochemically analyzed. A 32% reduction in ER<sup>+</sup> and PgR<sup>+</sup> invasive cancers resulted after 8 years of treatment. Quantitative levels of ER and PgR were lower in the tamoxifen-treated group, significantly so for ER (<i>P</i> = 0.001). These lower ER levels were restricted to the posttreatment period (<i>P</i> = 0.018). Among the ER<sup>+</sup> group, there was a similar proportional decrease in PgR<sup>+</sup> and PgR<sup>-</sup> tumors by tamoxifen. The median levels of Ki67 were similar in both arms. The numbers of HER2-positive and EGFR-positive cancers were higher in the tamoxifen arm but not significantly so. In conclusion, the preventive effects of tamoxifen result in reduced ER-positive but not ER-negative tumors and reduced ER expression in the ER-positive cases largely confined to the posttreatment period. Overall reductions in PgR expression are explained by lower frequency of ER-positive cases. Impact on Ki67, HER2, and EGFR was modest. <i>Cancer Prev Res; 10(3); 171-6. ©2017 AACR</i>.
Citation
Cancer prevention research (Philadelphia, Pa.), 2017, 10 (3), pp. 171 - 176
Source Title
Publisher
ISSN
1940-6207
eISSN
1940-6215
Research Team
Medicine (RMH Smith Cunningham)
Endocrinology
Endocrinology