Evidence map›Paper›PMID 41781728›Full record

ArticleEuropean radiology2026

Finding the optimal recall rate in breast cancer screening: results from the ROCS study.

Daniëlle van der Waal, Craig K Abbey, Eric Tetteroo, Tanya D Geertse, Maartje J A Smid-Geirnaerdt, Ioannis Sechopoulos, Mireille J M Broeders

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Article in European radiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Daniëlle van der Waal *Dutch Expert Centre for Screening (LRCB), Nijmegen, The Netherlands. Danielle.vanderWaal@radboudumc.nl.ORCID http://orcid.org/0000-0002-5850-8814
Craig K Abbey *Department of Psychological and Brain Sciences, University of California-Santa Barbara, Santa Barbara, CA, USA.
Eric TetterooDutch Expert Centre for Screening (LRCB), Nijmegen, The Netherlands.
Tanya D GeertseDutch Expert Centre for Screening (LRCB), Nijmegen, The Netherlands.
Maartje J A Smid-GeirnaerdtDutch Expert Centre for Screening (LRCB), Nijmegen, The Netherlands.
Ioannis SechopoulosDutch Expert Centre for Screening (LRCB), Nijmegen, The Netherlands.
Mireille J M BroedersDutch Expert Centre for Screening (LRCB), Nijmegen, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesIn breast cancer screening, determining the optimal balance between the number of screen-detected cancer cases and false-positive recalls is essential. This study explored the relationship between these indicators for the Dutch Digital Mammography Screening Program and aimed to determine the optimal recall rate. MATERIALS AND

methodsFrom March to June 2019, 21 screening radiologists provided continuous Probability-of-Malignancy (PoM) scores during their standard reading sessions. Scores ranged from 'no suspicion' (PoM = -100) to 'highest suspicion' (PoM = 100). Follow-up data were obtained in June 2024 and included recall decisions after double reading, outcomes of further assessments (false positive or screen-detected cancer), and interval cancer diagnoses. Recall-detection and receiver operating characteristic (ROC) curves were constructed for each reader and averaged to obtain summary curves, with error bars computed from hierarchical bootstrapping of cases within readers (1000 resamples). The overall screening performance was quantified using the area under the ROC curve (AUC).

resultsThe final dataset comprised 40,829 screening records with 315 cancer cases. The overall recall rate was 2.33%, and the cancer detection rate after double reading was 6.4 per 1000 screens. Radiologist performance was high (AUC = 0.91). Moving the operating point results in either substantially lower cancer detection or relatively little gain.

conclusionThis prospective study identified the trade-off between unconditional recall and detection rates, as well as conditional sensitivity and specificity. We found that Dutch screening radiologists perform at a high level and operate at a point that seems to optimize the false-positive recall and cancer detection rate trade-off. KEY POINTS: Question Breast cancer screening requires a good balance between detection and false-positive rate. However, the interrelationship between these rates, and thus the optimal recall, is unknown. Findings Overall, the Dutch screening radiologists performed with high accuracy, and the current operating point optimizes the trade-off between cancer detection and false-positive recalls. Clinical relevance ROCS provides an efficient method to evaluate performance and determine target values based on data from screening practice. This method applies to various screening programs. Screening evaluation is essential for achieving and maintaining a positive benefit-to-harm ratio for participants.

Indexed as

Breast NeoplasmsEarly Detection of CancerMammographyAgedFalse Positive ReactionsFemaleHumansMiddle AgedNetherlandsROC CurveSensitivity and SpecificityBreastBreast cancerMammographyScreening

Identifiers

PMID41781728
PMCPMC13282243

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.