| Primary goal |
Immediate removal of prostate and seminal vesicles; potential pelvic lymph node dissection (PLND). |
Deliver curative dose to prostate ± seminal vesicles; sometimes elective pelvic node radiation. Often combined with ADT for intermediate/high risk. |
| Oncologic control |
Definitive cytoreduction. Enables direct negative margin pursuit; adjuvant/salvage radiation can be added if pathology indicates. |
Excellent control in selected patients with modern dosing and planning; benefit may rely on appropriate ADT duration in higher-risk disease. |
| Staging accuracy |
Gold standard pathology: exact Grade Group, margins, EPE, SV invasion, node status. |
Clinical (imaging-based) staging; no full pathologic specimen. Biologic risk inferred from PSA/MRI/biopsy and imaging. |
| Plan B (salvage) |
Radiation remains available if PSA rises (adjuvant or salvage). Salvage RT generally well-tolerated. |
Salvage prostatectomy after XRT is feasible but technically demanding with higher risks (incontinence, strictures, fistula) vs primary surgery. |
| PSA kinetics |
PSA should fall to undetectable; biochemical recurrence is highly specific for disease. |
PSA “nadir then bounce” patterns; interpretation depends on Phoenix criteria (nadir + 2 ng/mL). |
| Hospital course |
Typically 1 night (sometimes outpatient); catheter ~5–10 days; return to desk work ~2–3 weeks. |
Outpatient fractions over ~4–8 weeks (IMRT) or 5 fractions (SBRT), or brachytherapy implant; no catheter typically. |
| Urinary function |
Early stress incontinence common, usually improves with time/pelvic floor therapy; long-term pad-free rates high with experienced teams. |
Lower early incontinence risk; potential late irritative/obstructive symptoms, urgency/frequency, or hematuria due to radiation cystitis in a minority. |
| Erectile function |
Nerve-sparing possible; potency recovery varies by age, baseline function, and extent of disease. |
ED risk accumulates over time post-radiation; ADT adds libido/erection suppression during therapy. |
| Bowel effects |
Minimal bowel toxicity with surgery. |
Possible proctitis/rectal urgency/bleeding (modern techniques reduce risk but don’t eliminate it). |
| ADT side effects |
Not routine unless high-risk features post-op. |
Commonly used for 6–36 months depending on risk: hot flashes, fatigue, weight gain, metabolic effects, mood changes, sexual dysfunction, bone loss. |
| Second primary risks |
No radiation exposure. |
Small long-term risk of secondary malignancies in pelvis with radiation (rare; decades-scale). |
| Future options |
Radiation, systemic therapy, clinical trials remain accessible if needed. |
Local surgical salvage harder; systemic options remain. |