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. 2020 Jul 16;147(12):3305–3312. doi: 10.1002/ijc.33178

TABLE 1.

Criteria for screening for various cancers (based on Wilson and Jungner's classic screening criteria)

Cervix Vulva Vagina Ovary Breast Oral (mouth) a Anal a Colorectal a Melanoma Lung a Prostate Thyroid a
Men Women Men Women
Incidence b ++ c ++ + ++ + +++ ++ + +++ +++ ++ +++ +++ c ++
Survival b ++ ++ +++ +++ ++ + +++ ++ ++ + + +++ + +
Natural history of condition adequately understood ++ ++ + + +/− ++ ++ ++ ++ ++ ++ + ++ +/−
Recognizable latent or early symptomatic stage exists ++ ++ ++ + +/− ++ ++ ++ ++ + + ++ ++ +/−
Suitable test or examination available d ++ ++ ++ +/− ++ ++ ++ ++ ++ ++ ++ ++ ++ ++
Test acceptable to population d ++ ++ ++ ++ + ++ ++ ++ ++ ++ ++ ++ ++ ++
Accepted treatment for disease exists Yes (conditional on availability of secondary and tertiary care facilities)
Facilities for diagnosis and treatment available e
Agreed policy on whom to treat as patients ++ ++ ++ + + ++ ++ ++ ++ ++ ++ ++ + +
Potential harms of undergoing screening f Yes
Cost‐effectiveness g ++ +/− +/− +/− +/− ++ +/− + ++ ++ ++ + +/− +/−
Case‐finding a continuing process Yes (conditional on risk group or antecedents)
a

Estimates for men and women were collapsed because of comparability in incidence and survival statistics.

b

Incidence and survival data were used to reflect Wilson and Jungner's first criterion (ie, whether the disease at hand is an important health problem). For incidence: +: <10, ++: >10, <100, +++: >100 per 100 000. For survival: +: >75%, ++: <75%, >50%, +++: <50%.

c

Incidence directly affected by screening (downwards for cervix and upwards for prostate).

d

Includes only tests that have been in widespread use and/or have clinical application in specific circumstances. Diagnostic work‐up procedures not considered.

e

Includes management decisions and diagnostic work‐up.

f

Considers psychological harms and potential morbidity and risks during the entire screening process, including diagnostic work‐up and treatment.

g

Cancers for which organized, guideline‐driven screening programs currently exist were considered highly cost‐effective (ie, ++). Cancers for which screening guidelines exist for high‐risk subgroups only, or in opportunistic settings were considered moderately cost‐effective (ie, +). Uncertainty regarding the cost‐effectiveness of screening was considered equivocally cost‐effective (ie, +/−).