2017
DOI: 10.1016/s1470-2045(17)30426-6
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Health-related quality of life for immediate versus delayed androgen-deprivation therapy in patients with asymptomatic, non-curable prostate cancer (TROG 03.06 and VCOG PR 01-03 [TOAD]): a randomised, multicentre, non-blinded, phase 3 trial

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Cited by 48 publications
(13 citation statements)
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“…Side effects of ADT include hot flashes, decreased libido, fatigue, osteoporosis, weight gain, sarcopenia, and increased risk of cardiovascular disease. In general, side effects from ADT increase with the length of treatment duration ( 11 , 12 ). Intermittent ADT (I-ADT) is a treatment option for men with biochemically recurrent prostate cancer with the aim of decreasing long term side effects from ADT ( 9 , 13 ).…”
Section: Intermittent Androgen Deprivation Therapymentioning
confidence: 99%
“…Side effects of ADT include hot flashes, decreased libido, fatigue, osteoporosis, weight gain, sarcopenia, and increased risk of cardiovascular disease. In general, side effects from ADT increase with the length of treatment duration ( 11 , 12 ). Intermittent ADT (I-ADT) is a treatment option for men with biochemically recurrent prostate cancer with the aim of decreasing long term side effects from ADT ( 9 , 13 ).…”
Section: Intermittent Androgen Deprivation Therapymentioning
confidence: 99%
“…The timing and duration of ADT in the setting of biochemical failure have been investigated to reduce side effects in these patients who have a relatively long life expectancy and are asymptomatic from their local/biochemical recurrence. Two phase III trials, Timing of Androgen Deprivation (TOAD) ( 20 ) and Early vs. Late Androgen Ablation Trial (ELAAT) (NCT00439751) have explored the timing of ADT. The TOAD trial randomized 293 patients between immediate or delayed ADT.…”
Section: Adtmentioning
confidence: 99%
“…Moul et al report that initiating hormone therapy after biochemical recurrence will delay the onset of clinical metastasis, especially in those with high‐risk features on their initial pathology . Another trial randomized men who had a prostate‐specific antigen relapse to receive either immediate or delayed ADT and reported that 5‐year overall survival (OS) was higher in those who received immediate therapy …”
Section: Prostate Cancermentioning
confidence: 99%