Last reviewed: 28 May 2026
Last reviewed: 28 May 2026
The PSA test is a blood test that measures the amount of prostate-specific antigen (PSA), a protein made by cells in the prostate gland. It’s normal for all people with a prostate - including men, trans women and some non-binary people - to have some PSA in their blood.
A raised PSA may indicate prostate cancer, but can also be caused by other factors such as:
Age
Benign prostate enlargement
Infection (UTI)
Recent ejaculation or exercise
A normal PSA does not exclude cancer and prostate cancer could also be present without increased PSA levels.
Before offering a PSA test to patients, the potential benefits and harms should always be discussed so they can make an informed choice.
A PSA test is the first-line investigation for people with possible symptoms of prostate cancer. Guidelines suggest considering a PSA test and DRE in men and people with a prostate who have:
Lower urinary tract symptoms
Erectile dysfunction
Visible haematuria
Haematospermia
Consider delaying the PSA test for the following:
Active UTI or prostatitis (wait ≥6 weeks)
Recent biopsy or urological procedure (≥6 weeks)
Ejaculation or vigorous exercise (last 48 hours)
Below are the age-specific PSA thresholds for an urgent suspected cancer referral according to national guidelines.
Age (years) | PSA level (micrograms/litre) |
Below 40 | Use clinical judgement |
40 to 49 | > 2.5 |
50 to 59 | > 3.5 |
60 to 69 | > 4.5 |
70 to 79 | > 6.5 |
Over 79 | Use clinical judgement. AoMRC advise more than 20 or more than 7.5 and symptoms suggestive of metastatic disease (bone pain and/or fatigue and/or unintended weight loss) |
NICaN recommends making an urgent suspected cancer referral if PSA levels are above the age-based thresholds at both initial testing and when repeated 2-4 weeks later, or based on a single result if the level is >20 µg /L.
For more detail, refer to the following:
NICE NG12(2021_ and clinical knowledge summary (March 2026)
England and Wales GP guide to managing suspected prostate cancer(PDF, 348 KB) (November 2025)
Northern Ireland Referral Guidance for Suspected Cancer(NICaN) (2022)
Northern Ireland GP guide to managing suspected prostate cancer(PDF, 358 KB) (November 2025)
Age (years) | PSA level (micrograms/litre) |
Below 70 | ≥ 3 |
70 to 79 | ≥ 5 |
80 and over | ≥ 20 - find further guidance below |
SRG recommend PSA testing in men aged 80 or over only in the following scenarios:
The patient has clinical features suggestive of metastatic prostate cancer (e.g. new significant bone pain, unexplained weight loss or unexplained anaemia)
The patient wants a PSA test after shared decision-making. See the benefits and harms of PSA testing for points to discuss.
For more detail, refer to the following:
Scottish Referral Guidelines (SRG) (2025)
Scotland GP guide to managing suspected prostate cancer(PDF, 385 KB) (November 2025)
Population-level PSA testing to screen for prostate cancer is not recommended in the UK, as harms are likely to outweigh benefits. However, in May 2026, the UK National Screening Committee (UK NSC) recommended PSA-based screening for men with a BRCA2 pathogenic variant and relevant family history(see targeted prostate cancer screening).
Despite this, men may request a PSA test. In this scenario, it’s important to:
Support informed decision-making by discussing the potential benefits and harms before testing
Provide clear patient information on PSA testing – you can signpost our ‘screening for prostate cancer’ webpage
Document the discussion
May detect prostate cancer at an earlier stage, when treatment can be more effective and associated with less severe side effects.
False positive results. Around 72-80% of people with a raised PSA do not have prostate cancer. This may lead to unnecessary and potentially invasive investigations, usually an MRI* or prostate biopsy, which carry their own risks.
False negative results. Around 7-15% of people with a normal PSA may have prostate cancer, which means it can miss aggressive and fast-growing cancers that need treatment.
Overdiagnosis and overtreatment. PSA testing can lead to the detection of slow-growing tumours that may
never cause harm, leading to unnecessary diagnosis (overdiagnosis), anxiety and treatment. Treatment can have significant long-term effects. For example:
Overdiagnosis and overtreatment. PSA testing can lead to the detection of slow-growing tumours that may never cause harm, leading to unnecessary diagnosis (overdiagnosis), anxiety and treatment. Treatment can have significant long-term effects. For example:
For men who have surgery, almost 50% experience erectile problems, and almost 20% experience leaking
urine after 5 years.
For men who have radiotherapy, almost 40% experience erectile problems and around 5% experience bowel problems.
There are also psychological harms associated with treatment and an overall impact on quality of life.
*Multiparametric MRI (mpMRI) is used across most of the UK to help decide whether a prostate biopsy is needed. It may improve detection of clinically significant cancers, but its impact on reducing overdiagnosis and overtreatment is still uncertain. Research to optimise the diagnostic pathway is ongoing.
The UK NSC recommends targeted prostate cancer screening every 2 years for men aged 45-61 with a BRCA2 pathogenic variant and a family history of pancreatic, prostate, breast or ovarian cancer.
This recommendation reflects strong evidence that this group is at higher risk of aggressive prostate cancer, meaning the benefits of screening are more likely to outweigh the harms.
For further information and commentary, read our latest cancer news article: UK NSC recommends targeted prostate cancer screening (May 2026).
This recommendation is yet to be implemented. GPs should continue to follow existing guidance for men with BRCA2 pathogenic variants as follows:
The UK Cancer Genetics Group recommends that men with a confirmed BRCA2 pathogenic variant are offered annual PSA tests from age 40 and referred onwards if PSA >3ng/mL.
For men who are concerned that they may be carriers of BRCA2 pathogenic variants, refer to existing guidance to assess eligibility for referral onto specialist clinical genomics services:
NG241 and CG164 cover referral criteria based on family history of breast or ovarian cancer.
The NHS England National Genomics Education Programme provides example clinical scenarios for managing patients with a family history of prostate cancer.
Refer to regional genetics services guidance.
Refer to Belfast Health and Social Care Trust guidance.
Once someone is referred, specialist clinical genomics services will assess detailed family history alongside clinical factors to guide testing and/or management.
If unsure, consider seeking specialist advice (e.g. Advice and Guidance services). Further national guidance is expected as progress is made on targeted screening.
The UK NSC’s review of the current evidence also confirmed that there is currently insufficient evidence to support prostate cancer screening for:
black men
men with a relevant family history of cancer without BRCA2 pathogenic variants
men with pathogenic variants in BRCA1
Although these groups have a higher incidence of prostate cancer, evidence is not yet clear whether they are at greater risk of aggressive disease. The committee concluded that, based on the available evidence, the potential harms of PSA-based screening for these groups of men are likely to outweigh the benefits.
Research and innovation are ongoing to develop more accurate approaches to diagnosing prostate cancer. Emerging areas include new blood, urine and genetic tests aimed at improving early detection. Current research is exploring:
Screening for prostate cancer using newer diagnostic technology (eg TRANSFORM trial)
How to optimise the PSA test. For example, by combining it with other patient factors or test results like free PSA or PSA volume (eg PROSCREEN, GOTEBORG-2 and ReIMAGINE trials)
The role of risk prediction models, including genetic risk scores to inform how likely a person is to develop prostate cancer (eg TRANSFORM, BARCODE-1 and Stockholm-3 trials)
The use of AI to support current diagnostics
The potential of urinary biomarkers (eg ExoDx and MyProstateScore trials)
To read more about the latest and emerging evidence for prostate cancer and across the pathway, read our cancer news article: “Detecting prostate cancer: why we need more research (April 2025)” or download our Technical summary of earlier detection and diagnosis of prostate cancer(PDF, 578 KB) (May 2026).
England and Wales GP guide to managing suspected prostate cancer(PDF, 348 KB)
Scotland GP guide to managing suspected prostate cancer(PDF, 385 KB)
Northern Ireland GP guide to managing suspected prostate cancer(PDF, 358 KB)
UK NSC recommends targeted prostate cancer screening (May 2026)
Earlier detection and diagnosis of prostate cancer: A technical summary of the challenges and evidence(PDF, 535 KB) (November 2025)
GatewayC ‘The role of genomics in primary care’ course (England and Wales only) (February 2025)
NICE. How should I assess a person with suspected prostate cancer. Accessed January 2025.
Thompson IM, Pauler DK, Goodman PJ, et al. Prevalence of prostate cancer among men with a prostate-specific antigen level < or =4.0 ng per milliliter N Engl J Med. 2004.
Merriel SWD, Pocock L, Gilbert E, et al. Systematic review and meta-analysis of the diagnostic accuracy of prostate-specific antigen (PSA) for the detection of prostate cancer in symptomatic patients. BMC medicine. 2022.
NICE. Suspected cancer: recognition and referral NICE guideline NG12. Accessed January 2025.
NICaN Northern Ireland Referral Guidance for Suspected Cancer – Red Flag Criteria. Accessed January 2025.
NHS Scotland Scottish Referral Guidelines for Suspected Cancer, Urological cancer. Accessed August 2025.
UK National Screening Committee. Prostate cancer screening recommendation. Accessed May 2026.
Donovan JL, Hamdy FC, Lane JA, Young GJ, Metcalfe C, Walsh EI, et al. Patient-Reported Outcomes 12 Years after Localized Prostate Cancer Treatment. NEJM Evidence. 2023.
Hamdy FC, Donovan JL, Lane JA, Metcalfe C, Davis M, Turner EL, et al. Fifteen-Year Outcomes after Monitoring, Surgery, or Radiotherapy for Prostate Cancer. N Engl J Med. 2023.
Fanshawe JB, Wai-Shun Chan V, Asif A, et al. Decision Regret in Patients with Localised Prostate Cancer: A Systematic Review and Meta-analysis. Eur Urol Oncol. 2023.
Ahmed HU, El-Shater Bosaily A, Brown LC, et al. Diagnostic accuracy of multi-parametric MRI and TRUS biopsy in prostate cancer (PROMIS): a paired validating confirmatory study. Lancet. 2017.