Evidence map›Paper›PMID 40997111›Full record

ArticlePloS one2025

Latent representation of H&E images retains biological information in a breast cancer cohort.

Chloé Benmussa, Esther Sanfeliu, Anabel Martínez-Romero, Blanca González-Farré, Tomás Pascual, Joaquín Gavilá, Alona Levy-Jurgenson, Ariel Shamir, Fara Brasó-Maristany, Aleix Prat and 1 more

Abstract read
In one paragraph

Article in PloS one, 2025. 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.

No citing paper in PubMed yet.

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.

Chloé BenmussaSchool of Computer Science, Reichman University IDC, Herzliya, Israel.ORCID https://orcid.org/0000-0003-4293-8606
Esther SanfeliuTranslational Genomics and Targeted Therapies in Solid Tumors Group, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
Anabel Martínez-RomeroTranslational Genomics and Targeted Therapies in Solid Tumors Group, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.ORCID https://orcid.org/0000-0001-5626-6674
Blanca González-FarréTranslational Genomics and Targeted Therapies in Solid Tumors Group, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
Tomás PascualTranslational Genomics and Targeted Therapies in Solid Tumors Group, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
Joaquín GaviláSOLTI Breast Cancer Research Group, Barcelona, Spain.
Alona Levy-JurgensonSchool of Computer Science, Reichman University IDC, Herzliya, Israel.
Ariel ShamirSchool of Computer Science, Reichman University IDC, Herzliya, Israel.
Fara Brasó-MaristanyTranslational Genomics and Targeted Therapies in Solid Tumors Group, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
Aleix PratTranslational Genomics and Targeted Therapies in Solid Tumors Group, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
Zohar YakhiniSchool of Computer Science, Reichman University IDC, Herzliya, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Imaging technologies and staining based pathology are important components of common practice cancer care. Specifically, H&E imaging is standard for almost all cancer patients. Traditionally, H&E images can serve, when used by experienced trained pathologists, to infer important biological properties of the samples. Recent work demonstrated that machine learning and machine vision analysis of H&E images can further expand the scope of the inference. However, H&E images are high-resolution, making them difficult to analyze and possibly noisy. In this work, we propose an autoencoder-based pipeline that greatly reduces the dimension of the data representation while maintaining valuable properties. In particular, we investigate how different latent space dimensions affect bulk label predictions from H&E. We use autoencoders applied to image tiles as a tool in this investigation and also examine other information that may be inferred from image tiles. For example, we show classification results for tiles, such as Luminal A versus Luminal B, with an F1 score larger than 0.85. We also show that Ki67 levels can be inferred from H&E tiles, as shown before on other cohorts, and that inference is still possible when working with lower dimensional latent representations. The two main contributions of this paper are as follows. First, demonstrating that the use of image tiles can be informative, both at the global classification level, and, more importantly, to support the assessment of heterogeneity. Second, reasonably accurate inference can be performed with lower dimensional latent representations of the H&E images.

Indexed as

Breast NeoplasmsImage Processing, Computer-AssistedCohort StudiesFemaleHematoxylinHumansKi-67 AntigenMachine LearningHematoxylinKi-67 Antigen

Identifiers

PMID40997111
PMCPMC12463230

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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.