Table 5.
Author | Year | Study design | Total patients | Clinical risk | Eligibility criteria | Neoadjuvant therapy | Undetectable PSA (%) | Stage pT0 (%) | Stage pT4 (%) | Stage pN1 (%) | PSM (%) | BCR (%) | 10-year OS |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Pan | 2019 | Retrospective study | 177 | Very high risk or locally advanced | >cT3a disease or primary Gleason pattern 5 or ≥5 cores with Gleason sum 8-10 or PSA ≥50 ng/mL or with pelvic metastatic lymph node involvement | 4-6 cycles of goserelin acetate/bicalutamide/docetaxel every 3 weeks (nCHT) versus goserelin acetate/bicalutamide (nADT) versus immediate RP | RP 48 nADT 73 nCHT 81 | RP 0 nADT 9 nCHT 17 | RP 30 nADT 14 nCHT 19 | RP 30 nADT 14 nCHT 19 | RP 32 nADT 22 nCHT 17 | RP 81 nADT 47 nCHT 14 | - |
Narita | 2019 | Retrospective propensity matched | 56 matched pairs | High-risk | cT3 disease or PSA ≥15 ng/mL, or any Gleason pattern 5 | Complete androgen blockage, 6 cycles docetaxel and entramustine versus immediate RP | - | - | - | - | - | RP 45 (approx.) nCHT 70 (approx.) | - |
Eastham | 2009 | Randomized Trial | 391 nCHT versus 297 immediate RP | High-risk | Stage T3-T4 disease or Gleason score ≥8, or PSA >20 ng/mL | Neoadjuvant ADT and docetaxel versus immediate RP | - | - | - | - | - | - | RP 74% nCHT 80% |
ADT=Androgen deprivation therapy, PSA=Prostate specific antigen, nCHT=Neoadjuvant chemohormonal therapy, nADT=Neoadjuvant ADT, RP=Radical prostatectomy,