Table 6.
Clinical setting | Is androgen deprivation therapy recommended? | LE* | Ref |
---|---|---|---|
ADT alone compared with local standard of care | |||
Compared with observation | No | 1b | [7–9] |
Compared with radiotherapy | No | 1a | [10,11] |
Compared with surgery | No | 3a | [13–16] |
RT plus ADT compared with RT alone | |||
Low risk | No | 1b | [22,27,28] |
Intermediate risk | Yes: 4–6 mo of ADT should be combined to RT | 1b | [22,29] |
High risk | Yes: 24–36 mo of ADT should be combined to RT | 1a | [17,18,20,21, 23,25,30,32] |
ADT adjuvant after a local therapy | |||
N+ | Yes: patients with multiple LN metastases should receive LHRH-A | 1b | [39,40] |
Local–regional disease | Consider ADT only in patients at high risk for developing distant metastases (GS ≥8, PSA DT <12 mo) |
1b | [44] |
PSA failure | Consider ADT only in patients at high risk for developing distant metastases (GS ≥8, PSA DT <12 mo) |
3b | [46,47] |
ADT in metastatic disease | |||
Start at diagnosis | Yes: surgical or chemical castration with continous LHRH-A | – | |
Disease flare prevention with AA | Yes in all patients, 2–7 d before LHRH-A start | 1b | [57,63] |
Abiraterone acetate | Yes in docetaxel-treated patients with CRPC | 1b | [81] |
AA = antiandrogens; ADT = androgen deprivation therapy; CRPC = castration-resistant prostate cancer; GS = Gleason score; LHRH-A = luteinizing hormone – releasing hormone agonist; LE = level of evidence; LN = lymph node; PSA = prostate-specific antigen; PSA DT = prostate-specific antigen doubling time; Ref = reference; RT = radiation therapy.
LE is defined according to the Oxford Centre for Evidence-Based Medicine [104].