What is prostate cancer?
Prostate cancer develops when cells in the prostate gland grow abnormally and uncontrollably. The prostate is a walnut-sized gland that sits below the bladder and produces the fluid that nourishes sperm. Prostate cancer most commonly develops in the outer zone of the gland — which is why it typically causes no urinary symptoms in its early stages.
Prostate cancer varies enormously in behaviour. Some tumours are slow-growing, low-grade, and unlikely to cause harm in a man's lifetime. Others are aggressive and require prompt treatment. The critical question — and the reason for thorough investigation — is identifying which type you have.
Symptoms of prostate cancer
Early prostate cancer typically causes no symptoms at all. This is why PSA testing is the primary method of early detection — and why men with no symptoms should still consider a PSA discussion with their GP.
When symptoms do appear, they are often related to urinary function — but these same symptoms overlap completely with benign enlargement (BPH):
- Difficulty starting urination or a weak urine stream
- Needing to urinate more frequently, especially at night
- A feeling that the bladder hasn't emptied fully
- Blood in the urine (haematuria) or semen (haematospermia)
Advanced prostate cancer — which has spread beyond the gland — can cause bone pain (particularly in the lower back, hips or pelvis), unexplained weight loss, or fatigue. If you have these symptoms alongside urinary changes, seek an urgent urology review.
How prostate cancer is diagnosed
Understanding your Gleason score and Grade Group
The Gleason score describes how the cancer cells appear under a microscope — specifically, how different they look from normal prostate cells. The score is the sum of the two most common patterns seen in the biopsy, each graded 1–5. Modern practice uses Grade Groups (1–5), which map to Gleason scores:
Treatment options for prostate cancer
The main curative treatments for localised prostate cancer are robotic radical prostatectomy and radiotherapy. Active surveillance is appropriate for low-risk disease. The right choice depends on your Grade Group, PSA, staging, age, overall health, and personal priorities.
Frequently asked questions
Early prostate cancer usually causes no symptoms. When symptoms do occur, they typically involve urinary flow — difficulty starting, weak stream, frequent urination at night, or blood in urine or semen. Advanced cancer can cause bone pain in the back or hips. Because these symptoms overlap with benign prostate conditions, only investigation (PSA and MRI) can differentiate. Many men are diagnosed through a routine PSA test with no symptoms at all.
Yes — having a first-degree relative (father or brother) with prostate cancer approximately doubles your lifetime risk. Men with BRCA2 gene mutations have a significantly higher risk of aggressive prostate cancer. Men of Black African or Caribbean ethnicity have approximately double the population risk, independent of family history. If you have a family history of prostate cancer, BRCA status, or relevant ethnicity, earlier PSA testing (from age 40–45) should be discussed with your GP or a urologist.
Cancer control outcomes are equivalent between robotic prostatectomy and radiotherapy for localised prostate cancer — neither is clearly superior. The choice comes down to side effect profiles, personal preference, and practical considerations. Surgery offers the clearest post-treatment monitoring (PSA should be undetectable); radiotherapy avoids surgery and general anaesthetic. Both affect sexual function, though differently and with different timescales. A multidisciplinary discussion — including both a urologist and an oncologist's perspectives — is the best approach for anyone facing this decision.
Prostate cancer has an excellent prognosis when caught early. 5-year survival for stage 1–2 is approximately 98–100%. For stage 3 (locally advanced), 5-year survival is around 95%. Even stage 4 (metastatic) disease is increasingly manageable with modern systemic therapies — many men live well for many years. Survival has improved dramatically over the past 30 years due to earlier detection and better treatments.
Yes — biochemical recurrence (a detectable or rising PSA after primary treatment) occurs in approximately 20–30% of men after prostatectomy and a similar proportion after radiotherapy. This does not necessarily mean the cancer has spread. After surgery, salvage radiotherapy to the prostate bed is highly effective. After radiotherapy, further treatment options include hormone therapy and focal salvage treatments. Recurrence is detected early through regular PSA monitoring — which is why lifelong follow-up matters.