Evidence map›Paper›PMID 39920303›Full record

ArticleEuropean radiology2025

Predicting axillary residual disease after neoadjuvant therapy in breast cancer using baseline MRI and ultrasound.

Caroline Malhaire, Ozgun Umay, Vincent Cockenpot, Fatine Selhane, Toulsie Ramtohul, Fabien Reyal, Jean-Yves Pierga, Emanuella Romano, Anne Vincent-Salomon, Youlia Kirova and 3 more

Abstract read
In one paragraph

Article in European radiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Methodological considerations in predicting axillary residual disease using imaging features.Translational breast cancer research : a journal focusing on translational research in breast cancer · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Caroline Malhaire *Institut Curie, Department of Medical Imaging, PSL Research University, 26 rue d'Ulm, 75005, Paris, France. caroline.malhaire@curie.fr.ORCID http://orcid.org/0000-0002-9235-9816
Ozgun Umay *Institut Curie, Department of Medical Imaging, PSL Research University, 26 rue d'Ulm, 75005, Paris, France.
Vincent CockenpotInstitut Curie, Department of Pathology, 26 rue d'Ulm, 75005, Paris, France.
Fatine SelhaneGustave Roussy, Department of Imaging, 94800, Villejuif, France.
Toulsie RamtohulInstitut Curie, Department of Medical Imaging, PSL Research University, 26 rue d'Ulm, 75005, Paris, France.
Fabien ReyalInstitut Curie, Surgical Oncology Department, 26 rue d'Ulm, 75005, Paris, France.
Jean-Yves PiergaInstitut Curie, Medical Oncology, 26 rue d'Ulm, 75005, Paris, France.
Emanuella RomanoInstitut Curie, Medical Oncology, 26 rue d'Ulm, 75005, Paris, France.
Anne Vincent-SalomonInstitut Curie, Department of Pathology, 26 rue d'Ulm, 75005, Paris, France.
Youlia KirovaInstitut Curie, Department of Radiotherapy, University Versailles St Quentin, 26 rue d'Ulm, 75005, Paris, France.
Enora LaasInstitut Curie, Surgical Oncology Department, 26 rue d'Ulm, 75005, Paris, France.
Hervé J BrisseInstitut Curie, Department of Medical Imaging, PSL Research University, 26 rue d'Ulm, 75005, Paris, France.
Frédérique FrouinInstitut Curie, LITO Laboratory, INSERM U1288, Paris-Saclay University, 91401, Orsay, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo predict axillary node residual disease in women treated for node-positive breast cancer (BC) by neoadjuvant therapy (NAT), using breast BI-RADS MRI features and axillary ultrasound at baseline. MATERIAL AND

methodsIn this single-center, retrospective study, women with node-positive BC who underwent NAT between 2016 and 2021 were included. Pre-treatment axillary US and breast MRIs were evaluated using the BI-RADS lexicon and T2 features, including Breast Edema Score. Univariate and multivariate logistic regression analyses were conducted for the prediction of axillary residual disease (ARD). A multivariable model based on logistic regression was trained and evaluated on randomly split train and test sets (7:3 ratio).

resultsOut of the 141 women, 41% had post-NAT ARD. Axillary metastasis was independently associated with luminal subtype (odds ratio (OR), 25.5; p < 0.001), anterior tumor location (OR, 14.1; p = 0.008), and cortical thickening ≥ 7 mm (OR, 6.09; p = 0.002). Intratumoral T2 high signal intensity was protective (OR, 0.16; p = 0.006), while Ki67 had a marginal association (p = 0.064). In the training and test sets, the model, which is available online, achieved AUCs of 0.860 (95% CI: 0.783-0.936) and 0.843 (95% CI: 0.714-0.971), respectively. Anterior depth location and cortical thickening greater than 7 mm were also independently associated with post-NAT axillary burden.

conclusionAdjusting for BC subtype and KI-67 index, the anterior third location of BC, a cortical thickness greater than 7 mm, and the absence of intratumoral T2 hyperintensity is predictive of ARD after NAT. KEY POINTS: Question What baseline imaging-based predictive models can identify patients at risk of persistent nodal disease after neoadjuvant therapy? Findings Baseline US cortical thickness superior to 7 mm, anterior tumor location, and absence of an intratumoral high signal on T2-weighted MRI predict residual axillary disease. Clinical relevance Our predictive model, available online at: litoic.shinyapps.io/LNPred_Apps , including breast cancer subtype, Ki-67 index level, breast cancer location, intratumoral signal intensity on T2WI, and initial lymph node thickness, could guide post-NAT axillary management.

Indexed as

Breast NeoplasmsLymphatic MetastasisMagnetic Resonance ImagingNeoadjuvant TherapyUltrasonography, MammaryAdultAgedAxillaFemaleHumansMiddle AgedNeoplasm, ResidualPredictive Value of TestsRetrospective StudiesUltrasonographyBreast neoplasmsLymph nodesModels, StatisticalNeoadjuvant therapyTumour burden

Identifiers

PMID39920303
PMCPMC12226675

What OpenQuestion holds

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Registered trials

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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.