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2013
DOI: 10.1093/annonc/mdt244
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A phase-III prevention trial of low-dose tamoxifen in postmenopausal hormone replacement therapy users: the HOT study

Abstract: The addition of low-dose tamoxifen to HRT did not significantly reduce breast cancer risk and increased climacteric symptoms in recently postmenopausal women. However, we noted beneficial trends in some subgroups which may deserve a larger study.

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Cited by 30 publications
(35 citation statements)
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“…Tamoxifen showed a significant trend in luminal‐A tumors (RR, 0.32; 95% CI 0.12–0.86). No differences in serious adverse events were observed compared to placebo (Decensi et al., 2013).…”
Section: Selective Estrogen Receptor Modulators (Serms)mentioning
confidence: 93%
“…Tamoxifen showed a significant trend in luminal‐A tumors (RR, 0.32; 95% CI 0.12–0.86). No differences in serious adverse events were observed compared to placebo (Decensi et al., 2013).…”
Section: Selective Estrogen Receptor Modulators (Serms)mentioning
confidence: 93%
“…Menopausal symptoms such as hot flashes, fatigue, sweating, insomnia, and arthralgia were more common in those taking exemestane IBIS-II [16] No significant differences in any of the cognitive tasks more women in the anastrozole group complained of hot flushes HOT [18] Serious adverse events did not differ between placebo and Tamoxifen Coronary heart syndrome (6 vs. 4), cerebrovascular events (2 vs. 5), VTE (2 vs. 5) and uterine cancers (3 vs. 1).…”
Section: Possible Additional Toxicity Due To Chemopreventionmentioning
confidence: 97%
“…Low‐dose tamoxifen at 5 mg/day has been evaluated in the randomized prospective HRT Opposed to Low‐dose Tamoxifen trial . There was a trend for reduced breast cancer incidence, but this was not statistically significant, and climacteric symptoms were significantly increased.…”
Section: Chemopreventionmentioning
confidence: 99%