A laboratory technician in gloves holds a blood sample tube beside a microscope, with a rack of blood sample tubes on the bench
Health & Medicine

Prostate screening cut deaths 13 percent over 23 years, and the trade-off keeps improving

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The largest trial of PSA testing ever run followed 162,236 men across eight European countries for a median of 23 years. Deaths from prostate cancer were 13 percent lower among the men offered screening, and the number who had to be invited to prevent one death fell to 456, down from 628 at 16 years.

Peer-reviewed Checked 27 October 2026
Key numbers
13%
Fewer prostate cancer deaths among men offered screening
rate ratio 0.87 after a median 23 years of follow-up
456
Men invited to screening to prevent one death
down from 628 at 16 years
12
Men diagnosed for each death averted
down from 18 at 16 years
162,236
Men aged 55 to 69 randomised across eight countries
recruited from 1993

In 1993, researchers in eight European countries began splitting men aged 55 to 69 at random into two groups. One group was offered repeated blood tests for prostate-specific antigen, or PSA, a protein the prostate makes that leaks into the blood in larger amounts when the gland is enlarged, inflamed or cancerous. The other group carried on with ordinary care. By the time the trial closed its books, 162,236 men had been followed for a median of 23 years, half for longer and half for less, and those offered screening were 13 percent less likely to have died of prostate cancer. The gap did not fade with time. It grew: at 16 years, 628 men had to be invited for screening to prevent one death; at 23 years, 456.

How we know

The figures come from the European Randomized Study of Screening for Prostate Cancer, known as ERSPC, whose 23-year analysis appeared in the New England Journal of Medicine on 29 October 2025. Because men were assigned to the two groups by chance, the design of a randomised controlled trial, the only systematic difference between them was the invitation to screening, so the difference in deaths can be laid at its door. Prostate cancer mortality in the screening group was 0.87 times that of the control group, a rate ratio whose 95 percent confidence interval ran from 0.80 to 0.95. The 13 percent is a relative reduction; in absolute terms it was 0.22 percentage points. The trial counted the cost as carefully as the gain. Men offered screening were diagnosed with prostate cancer 30 percent more often, a rate ratio of 1.30, and many of those extra cancers were slow-growing tumours that would never have caused symptoms: overdiagnosis, the detection of a disease that would not have harmed the person in their lifetime. That ratio of harm to benefit improved as the years passed. At 16 years, 18 men were diagnosed for every death averted. At 23 years, 12. In the Finnish arm, which supplied nearly half the men, 16 percent had a raised PSA at their first tests, and a biopsy, in which a sample of prostate tissue is removed and examined, confirmed cancer in 24 percent of those. Screening found more low-risk cancers and fewer advanced ones.

Why it matters

Prostate cancer is the most common cancer in men, and the ERSPC authors expect deaths from it to rise worldwide as populations grow and live longer. For three decades the case against screening every man has been that a PSA test finds too many harmless cancers for too few lives saved, and the 23-year figures do not dissolve that argument so much as rebalance it: fewer men invited per death prevented, fewer men diagnosed per death prevented, with the overdiagnosis still real. The protection is also not permanent. Anssi Auvinen, who led the Finnish arm at Tampere University, said the effect starts to wane once screening stops and largely disappears within nine years. The authors' answer is not blanket testing but risk-based screening, which concentrates testing on the men most likely to carry a dangerous cancer and uses MRI scans to sort harmless tumours from ones that need treating. Finland, which supplied nearly half the men in the trial, still has no national screening programme. Whether countries build one, and how carefully they aim it, is now the question these 23 years leave open.

What is not solved yet

The absolute gain is small: 0.22 percentage points, or one death prevented for every 456 men invited over 23 years. Screening also found 30 percent more cancers, many of them slow-growing tumours that would never have caused harm, so 12 men were diagnosed for every death averted. The protection fades within about nine years of stopping, and the authors call for risk-based screening with MRI rather than blanket PSA testing.

Common questions
What is PSA screening?

PSA, or prostate-specific antigen, is a protein made by the prostate, and a blood test measures how much of it is circulating. A raised level prompts further checks, usually a biopsy, to see whether cancer is present. In the trial the men offered screening were given repeated PSA tests, while the control group was not invited.

Why is a 13 percent reduction described as small?

The 13 percent is a relative figure: the screening group's death rate was 0.87 times the control group's. In absolute terms it comes to 0.22 percentage points, or one death prevented for every 456 men invited over 23 years, because dying of prostate cancer is uncommon even without screening.

What is overdiagnosis and why does it matter here?

Overdiagnosis is finding a cancer that would never have caused harm in the person's lifetime. Men offered screening were diagnosed 30 percent more often than the control group, and many of those extra cancers were slow-growing tumours, so those men faced tests and treatment they did not need. The ratio improved from 18 to 12 men diagnosed per death averted, and the authors want risk-based screening and MRI to reduce it further.

Does the benefit last after screening stops?

Not indefinitely. Anssi Auvinen, who led the Finnish arm, said the effect starts to wane once screening is discontinued and largely disappears within nine years. The protection therefore depends on continuing to screen, which is one reason the authors favour targeted programmes over a one-off test.