New Australian paper below.
It's not clear to me why this paper wasn't written ten years ago.
"Recently it has become apparent that many of the biological actions attributed to androgens in men are in fact not direct, but mediated by estradiol. Available evidence supports a primary role for estradiol in vasomotor stability, skeletal maturation ..."
"Potential role for estradiol could be ... as low dose add-back treatment while continuing androgen deprivation therapy."
-Patrick
ncbi.nlm.nih.gov/pubmed/286...
Endocr Relat Cancer. 2017 Jun 30. pii: ERC-17-0153. doi: 10.1530/ERC-17-0153. [Epub ahead of print]
Estradiol for the mitigation of adverse effects of androgen deprivation therapy.
Russell N1, Cheung AS2, Grossmann M3.
Author information
1
N Russell, Endocrine Department, Austin Health, Heidelberg, 3084, Australia nicholas.russell@austin.org.au.
2
A Cheung, Medicine, The University of Melbourne, Heidelberg West, 3081, Australia.
3
M Grossmann, Medicine, University of Melbourne, Heidelberg, 3084, Australia.
Abstract
Prostate cancer is the second most commonly diagnosed cancer in men. Conventional endocrine treatment for prostate cancer leads to global sex steroid deprivation. The ensuing severe hypogonadism is associated with well-documented adverse effects. Recently it has become apparent that many of the biological actions attributed to androgens in men are in fact not direct, but mediated by estradiol. Available evidence supports a primary role for estradiol in vasomotor stability, skeletal maturation and maintenance, and prevention of fat accumulation. Hence there has been interest in revisiting estradiol as a treatment for prostate cancer. Potential roles for estradiol could be in lieu of conventional androgen deprivation therapy or as low dose add-back treatment while continuing androgen deprivation therapy. These strategies may limit some of the side effects associated with conventional androgen deprivation therapy. However, although available data are reassuring, the potential for cardiovascular risk and pro-carcinogenic effects on prostate cancer via estrogen receptor signalling must be considered.
PMID: 28667081 DOI: 10.1530/ERC-17-0153