Evidence map›Paper›PMID 38332187›Full record

ArticleInsights into imaging2024

Digital breast tomosynthesis in mammographic screening: false negative cancer cases in the To-Be 1 trial.

Nataliia Moshina, Axel Gräwingholt, Kristina Lång, Ritse Mann, Tone Hovda, Solveig Roth Hoff, Per Skaane, Christoph I Lee, Hildegunn S Aase, Aslak B Aslaksen and 1 more

Open access · goldAbstract read
In one paragraph

Article in Insights into imaging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 9 institutions in 5 countries.

Nataliia MoshinaSection for Breast Cancer Screening, Cancer Registry of Norway, Oslo, Norway.
Axel GräwingholtMammographiescreening-Zentrum Paderborn, Breast Cancer Screening, Paderborn, NRW, Germany.
Kristina LångDepartment of Translational Medicine, Lund University, Lund, Sweden.
Ritse MannDepartment of Medical Imaging, Radboud University Medical Center, Nijmegen, the Netherlands.
Tone HovdaDepartment of Radiology, Vestre Viken Hospital Trust, Drammen, Norway.
Solveig Roth HoffDepartment of Radiology, Ålesund Hospital, Møre Og Romsdal Hospital Trust, Ålesund, Norway.
Per SkaaneDepartment of Radiology, Oslo University Hospital, University of Oslo, Oslo, Norway.
Christoph I LeeDepartment of Radiology, University of Washington School of Medicine, Seattle, WA, USA.
Hildegunn S AaseDepartment of Radiology, Haukeland University Hospital, Bergen, Norway.
Aslak B AslaksenDepartment of Radiology, Haukeland University Hospital, Bergen, Norway.
Solveig HofvindSection for Breast Cancer Screening, Cancer Registry of Norway, Oslo, Norway. sshh@kreftregisteret.no.ORCID http://orcid.org/0000-0003-0178-8939
Cancer Registry of Norway · NOHaukeland University Hospital · NOLund University · SENorwegian University of Science and Technology · NOOslo University Hospital · NOPaderborn University · DERadboud University Nijmegen · NLUniversity of Washington · USVestre Viken Hospital Trust · NO

Funding

Kreftforeningen no number
6 · The paper itself

Abstract

objectivesThe randomized controlled trial comparing digital breast tomosynthesis and synthetic 2D mammograms (DBT + SM) versus digital mammography (DM) (the To-Be 1 trial), 2016-2017, did not result in higher cancer detection for DBT + SM. We aimed to determine if negative cases prior to interval and consecutive screen-detected cancers from DBT + SM were due to interpretive error.

methodsFive external breast radiologists performed the individual blinded review of 239 screening examinations (90 true negative, 39 false positive, 19 prior to interval cancer, and 91 prior to consecutive screen-detected cancer) and the informed consensus review of examinations prior to interval and screen-detected cancers (n = 110). The reviewers marked suspicious findings with a score of 1-5 (probability of malignancy). A case was false negative if ≥ 2 radiologists assigned the cancer site with a score of ≥ 2 in the blinded review and if the case was assigned as false negative by a consensus in the informed review.

resultsIn the informed review, 5.3% of examinations prior to interval cancer and 18.7% prior to consecutive round screen-detected cancer were considered false negative. In the blinded review, 10.6% of examinations prior to interval cancer and 42.9% prior to consecutive round screen-detected cancer were scored ≥ 2. A score of ≥ 2 was assigned to 47.8% of negative and 89.7% of false positive examinations.

conclusionsThe false negative rates were consistent with those of prior DM reviews, indicating that the lack of higher cancer detection for DBT + SM versus DM in the To-Be 1 trial is complex and not due to interpretive error alone. CRITICAL RELEVANCE STATEMENT: The randomized controlled trial on digital breast tomosynthesis and synthetic 2D mammograms (DBT) and digital mammography (DM), 2016-2017, showed no difference in cancer detection for the two techniques. The rates of false negative screening examinations prior to interval and consecutive screen-detected cancer for DBT were consistent with the rates in prior DM reviews, indicating that the non-superior DBT performance in the trial might not be due to interpretive error alone. KEY POINTS: • Screening with digital breast tomosynthesis (DBT) did not result in a higher breast cancer detection rate compared to screening with digital mammography (DM) in the To-Be 1 trial. • The false negative rates for examinations prior to interval and consecutive screen-detected cancer for DBT were determined in the trial to test if the lack of differences was due to interpretive error. • The false negative rates were consistent with those of prior DM reviews, indicating that the lack of higher cancer detection for DBT versus DM was complex and not due to interpretive error alone.

Indexed as

Breast cancerDigital breast tomosynthesisInterval cancerMammographic screeningScreen-detected cancer

Identifiers

PMID38332187
PMCPMC10853101
OpenAlexW4391656724

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.