Finding a cancer that would never have caused symptoms or death in a person's lifetime, so that the diagnosis and treatment bring harm without benefit. It is the main downside of screening.
Overdiagnosis is invisible to the individual: a screen-detected cancer is treated and the person is cured of a disease that would not have hurt them. It is measured at population level as the excess incidence in a screened group that is never matched by a deficit later. Estimates are around 10-20% of screen-detected breast cancers in most reviews (the UK Independent Breast Screening Review put it at about 19%), a large share of PSA-detected low-grade prostate cancers before MRI-first pathways, and much of the rise in thyroid cancer and thin melanoma incidence. Remedies include raising thresholds (MRI-first prostate screening, Lung-RADS), renaming indolent lesions, and active surveillance rather than treatment. Multi-cancer blood tests raise the same question for cancers with no screening today.
Showing the technology this term belongs to: PSA and MRI-first prostate cancer screening.
This is the polyp pathway UK radiologists and surgeons follow (a UK author, Foley, leads it). It is a surveillance-and-surgery guideline built on low to moderate quality evidence, and the Kaiser Permanente cohort published two years earlier questions whether following small polyps finds cancer at all.
The document that defines who is offered a scan in the United States, and therefore the document any argument about the screening eligibility gap has to engage with. Eligibility is still defined by pack-years and years since quitting rather than by an individual risk estimate.
The largest natural history study of gallbladder polyps undermines the surveillance half of the 2022 European guideline: small polyps grow as a matter of course and almost never become cancer, while size at first scan carries most of the risk.
Size is a blunt tool: a 10 mm cut-off sends many people with cholesterol polyps to surgery and misses some neoplastic polyps below it. Better imaging (contrast-enhanced or endoscopic ultrasound) or a risk score is the research need the 2022 guideline itself acknowledges.
The clearest evidence that radical treatment of localised prostate cancer saves lives when the cancer was found clinically rather than by a blood test, and the clearest single statement of what grade does: a Gleason score above 7 carried ten times the risk of death of a score of 6 or lower in the same trial.
The current shape of the screening question in the United States, and the best short statement of the trade-off in numbers a man can weigh. The three-to-one ratio between metastatic cases prevented and deaths prevented is also the argument for using metastatic presentation, not mortality, to judge a screening programme sooner.
The trial that made observation a defensible choice for low-risk prostate cancer found by a blood test, and that supplied the number a man needs when weighing surgery: the progression it prevents is mostly progression on a scan or a blood test, and the harms it causes are felt every day.
The honest state of the overdiagnosis question. Prostate cancer is common in the prostates of men who die of something else, screening finds a proportion of it, and how much of that is harm depends on what is done next. The fix is not a better estimate but fewer treatments for the cancers that do not need them.
Shares The benefits and harms of breast cancer screening: an independent review, Outcomes of Gallbladder Polyps and Their Association With Gallbladder Cancer in a 20-Year Cohort, Screening by chest radiograph and lung cancer mortality: the Prostate, Lung, Colorectal, and Ovarian (PLCO) randomized trial, Risk-targeted ultrasound screening in high-incidence regions, tested against usual care.
Shares ERSPC (European Randomized Study of Screening for Prostate Cancer), USPSTF 2012: screening for prostate cancer, recommendation statement (grade D), Prostate cancer diagnosis and treatment after the introduction of prostate-specific antigen screening, 1986 to 2005, Lead time and overdiagnosis in prostate-specific antigen screening: importance of methods and context.
Shares Screening by chest radiograph and lung cancer mortality: the Prostate, Lung, Colorectal, and Ovarian (PLCO) randomized trial, USPSTF 2012: screening for prostate cancer, recommendation statement (grade D), Lead time, and lead-time bias, Number needed to screen (and number needed to diagnose).
Shares GÖTEBORG-2 (MRI-based prostate cancer screening), Polygenic risk score (PRS), Number needed to screen (and number needed to diagnose), ERSPC: screening and prostate cancer mortality in a randomised European study.
Shares ERSPC (European Randomized Study of Screening for Prostate Cancer), SPCG-4: radical prostatectomy or watchful waiting in prostate cancer, 29-year follow-up, PIVOT: follow-up of prostatectomy versus observation for early prostate cancer, Template mapping biopsy (transperineal template prostate mapping).
Shares Lead time and overdiagnosis in prostate-specific antigen screening: importance of methods and context, Number needed to screen (and number needed to diagnose), ERSPC: screening and prostate cancer mortality in a randomised European study, PSA and MRI-first prostate cancer screening.
Shares Lead time, and lead-time bias, Number needed to screen (and number needed to diagnose), ERSPC: screening and prostate cancer mortality in a randomised European study, PSA (prostate-specific antigen).
Shares SPCG-4: radical prostatectomy or watchful waiting in prostate cancer, 29-year follow-up, PIVOT: follow-up of prostatectomy versus observation for early prostate cancer, USPSTF 2018: screening for prostate cancer, recommendation statement (grade C at 55 to 69, grade D at 70 and over), Overtreatment.