Evidence map›Paper›PMID 38168198›Full record

ArticleResearch square2023

Artificial intelligence-based morphometric signature to identify ductal carcinoma in situ with low risk of progression to invasive breast cancer.

Marcelo Sobral-Leite, Simon Castillo, Shiva Vonk, Xenia Melillo, Noomie Lam, Brandi de Bruijn, Yeman Hagos, Joyce Sanders, Mathilde Almekinders, Lindy Visser and 9 more

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 3 institutions in 3 countries.

Marcelo Sobral-LeiteNetherlands Cancer Institute.ORCID https://orcid.org/0000-0002-4275-8050
Simon CastilloThe University of Texas MD Anderson Cancer Center.ORCID https://orcid.org/0000-0002-0606-2160
Shiva VonkNetherlands Cancer Institute.
Xenia MelilloNetherlands Cancer Institute.
Noomie LamNetherlands Cancer Institute.
Brandi de BruijnNetherlands Cancer Institute.
Yeman HagosThe Institute of Cancer Research.
Joyce SandersNetherlands Cancer Institute.
Mathilde AlmekindersNetherlands Cancer Institute.
Lindy VisserNetherlands Cancer Institute.ORCID https://orcid.org/0000-0001-7856-1981
Emma GroenNetherlands Cancer Institute.
Petra KristelNetherlands Cancer Institute.
Caner ErcanThe University of Texas MD Anderson Cancer Center.ORCID https://orcid.org/0000-0002-5611-2699
Leyla AzarangNetherlands Cancer Institute.
Yinyin YuanThe Institute of Cancer Research, London.
Grand Challenge PRECISION Consortium
Renee MenezesNetherlands Cancer Institute.
Esther LipsNetherlands Cancer Institute.
Jelle WesselingNetherlands Cancer Institute.
The Netherlands Cancer Institute · NLInstitute of Cancer Research · CAThe University of Texas MD Anderson Cancer Center · US

Funding

(PQC3) Genomic Diversity and Microenvironment as Drivers of Metastasis in DCISR01CA185138 · NCI · DUKE UNIVERSITY · PI HWANG, E.SHELLEY, MALEY, CARLO · 2014 to 2017
$2.0M
NCI NIH HHS R01 CA185138
6 · The paper itself

Abstract

Ductal carcinoma in situ (DCIS) may progress to ipsilateral invasive breast cancer (iIBC), but often never will. Because DCIS is treated as early breast cancer, many women with harmless DCIS face overtreatment. To identify these women that may forego treatment, we hypothesized that DCIS morphometric features relate to the risk of subsequent iIBC. We developed an artificial intelligence-based DCIS morphometric analysis pipeline (AIDmap) to detect DCIS as a pathologist and measure morphological structures in hematoxylin-eosin-stained (H&E) tissue sections. These were from a case-control study of patients diagnosed with primary DCIS, treated by breast-conserving surgery without radiotherapy. We analyzed 689 WSIs of DCIS of which 226 were diagnosed with subsequent iIBC (cases) and 463 were not (controls). The distribution of 15 duct morphological measurements in each H&E was summarized in 55 morphometric variables. A ridge regression classifier with cross validation predicted 5-years-free of iIBC with an area-under the curve of 0.65 (95% CI 0.55-0.76). A morphometric signature based on the 30 variables most associated with outcome, identified lesions containing small-sized ducts, low number of cells and low DCIS/stroma area ratio. This signature was associated with lower iIBC risk in a multivariate regression model including grade, ER, HER2 and COX-2 expression (HR = 0.56; 95% CI 0.28-0.78). AIDmap has potential to identify harmless DCIS that may not need treatment.

Indexed as

artificial intelligencebiomarkersDCISdigital pathology

Identifiers

PMID38168198
PMCPMC10760295
OpenAlexW4389666230

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.