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©The Author(s) 2022.
World J Clin Oncol. Feb 24, 2022; 13(2): 71-100
Published online Feb 24, 2022. doi: 10.5306/wjco.v13.i2.71
Table 2 Systemic hormonal treatments in breast cancer survivors: summary of studies and their outcomes
Ref.
Yr
n1
Design
Treatment
Conclusion
Holmberg et al[147,149]2004 2008221 vs 221 Randomized, non-placebo-controlled noninferiority trialOral estradiol hemihydrate and Norethisterone (cyclic or continuous) vs controlIn BCSs, an increased risk of new breast cancer events and adverse events were observed after 2 yr of therapy (HR = 2.4)
von Schoultz et al[150]2005188 vs 190Randomized, non-placebo-controlled noninferiority trial2 mg estradiol for 21 d with addition of 10 mg medroxyprogesterone acetate for last 10 d; or 2 mg estradiol for 84 d with 20 mg medroxyprogesterone acetate for last 10 d; or 2 mg estradiol valerate dailyNo increased risk of breast cancer recurrence; trial was closed early. So, HT doses of estrogen and progestogen and treatment regimens for menopausal hormone therapy may be associated with the recurrence of breast cancer
Kenemans et al[153]20091556 vs 1542Prospective randomized placebo controlledTibolone 2.5 mg daily or placeboTrial was closed early. Tibolone had a significantly increased risk of breast cancer recurrence
Cai et al[168]20201728 vs 3456Retrospective matched cohort studyIncidence rate in ospemifene users vs untreated patientsNo differences were observed in the BC incidence and recurrence rates in ospemifene users compared with matched controls


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