Austin Health

Title
Management of bone and metabolic effects of androgen deprivation therapy.
Publication Date
2021
Author(s)
Russell, Nicholas
Grossmann, Mathis
Subject
25(OH)D
25-hydroxy vitamin D
ADT
AR
ARKO
Androgen deprivation therapy
BMD
BP
CRPC
CaP
DBP
DXA
Diabetes
GnRH
HDL-C
HR-PQCT
LBM
LDL-C
Osteoporosis
Prostate cancer
RCT
SBP
TC
TG
androgen deprivation therapy
androgen receptor
androgen receptor knockout
blood pressure
bone mineral density
castrate-resistant Prostate cancer
diastolic blood pressure
dual energy X-ray absorptiometry
gonadotrophin-releasing hormone
high density lipoprotein cholesterol
high resolution-peripheral quantitative computed tomography
lean body mass
low density lipoprotein cholesterol
Prostate cancer
randomized controlled trial
systolic blood pressure
total cholesterol
triglycerides
Type of document
Journal Article
OrcId
0000-0001-8261-3457
#PLACEHOLDER_PARENT_METADATA_VALUE#
DOI
10.1016/j.urolonc.2018.10.007
Abstract
Androgen deprivation therapy (ADT) is commonly given to men with prostate cancer. Both its benefits as well as its adverse effects are a direct consequence of sex steroid withdrawal. While ADT improves oncologic outcomes in appropriately selected men, it is associated with adverse effects, including accelerated bone loss leading to increased fracture risk, and with metabolically unfavorable body composition changes that predispose to diabetes and may increase cardiovascular risk. In this review, we will describe the pathophysiology behind these ADT-associated adverse effects, and discuss the clinical evidence guiding clinical assessment and management. A proactive approach is important to minimize ADT-associated adverse sequelae, so that the benefit-risk ratio of this treatment is optimized.
Link
Citation
Urologic Oncology 2021; 39(10): 704-712
Jornal Title
Urologic Oncology

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