A mammography screening programme reports better 5-year survival among screen-detected breast cancers than among clinically detected cancers. Critics note that screening disproportionately picks up slow-growing tumours that remain in the detectable pre-clinical phase for a long time, inflating apparent survival without reducing deaths. This criticism describes:
- A Length bias ✓
- B Lead time bias
- C Neyman's bias
- D Berkson's bias
Explanation
Length bias arises because indolent, slowly progressing tumours spend longer in the detectable pre-clinical phase and are therefore more likely to be caught by periodic screening, whereas aggressive fast-growing cancers surface clinically between screening rounds. Screen-detected cases are thus enriched for better-prognosis tumours, improving survival statistics without lowering mortality. Lead time bias is different: it merely shifts the diagnosis date earlier, lengthening measured survival without changing the course of disease.
Reference: Park's Textbook of Preventive and Social Medicine, 27th ed.
High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP
Written and medically reviewed by the StethoPrep medical team.