A simple way to measure the burden of interval cancers in breast cancer screening

Sune Bangsbøll Andersen, Sven Törnberg, Elsebeth Lynge, My Von Euler-Chelpin, Sisse Helle Njor

8 Citations (Scopus)

Abstract

Background: The sensitivity of a mammography program is normally evaluated by comparing the interval cancer rate to the expected breast cancer incidence without screening, i.e. the proportional interval cancer rate (PICR). The expected breast cancer incidence in absence of screening is, however, difficult to estimate when a program has been running for some time. As an alternative to the PICR we propose the interval cancer ratio (inline-equation). We validated this simple measure by comparing it with the traditionally used PICR. Method: We undertook a systematic review and included studies: 1) covering a service screening program, 2) women aged 50-69 years, 3) observed data, 4) interval cancers, women screened, or interval cancer rate, screen detected cases, or screen detection rate, and 5) estimated breast cancer incidence rate of background population. This resulted in 5 papers describing 12 mammography screening programs. Results: Covering initial screens only, the ICR varied from 0.10 to 0.28 while the PICR varied from 0.22 to 0.51. For subsequent screens only, the ICR varied from 0.22 to 0.37 and the PICR from 0.28 to 0.51. There was a strong positive correlation between the ICR and the PICR for initial screens (r = 0.81), but less so for subsequent screens (r = 0.65). Conclusion: This alternate measure seems to capture the burden of interval cancers just as well as the traditional PICR, without need for the increasingly difficult estimation of background incidence, making it a more accessible tool when evaluating mammography screening program performance.

Original languageEnglish
Article number782
JournalB M C Cancer
Volume14
Pages (from-to)1-8
Number of pages8
ISSN1471-2407
DOIs
Publication statusPublished - 2014

Fingerprint

Dive into the research topics of 'A simple way to measure the burden of interval cancers in breast cancer screening'. Together they form a unique fingerprint.

Cite this