Evidence map›Paper›PMID 42557566›Full record

SynthesisBMC medicine2026

Assessment of Trophoblast cell surface antigen 2 (Trop-2) expression and its clinical significance in breast cancer: a multi-level analysis of protein and gene expression.

Maria Angeliki Toli, Michail Sarafidis, Panagiotis Filis, Evangelos Tzoras, Nikolaos Tsiknakis, Emmanouil Sifakis, Efstathia Liatsou, Georgios Rassidakis, Jonas Bergh, Alexios Matikas and 2 more

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in BMC medicine, 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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0cells of the map it votes in
0citing papers in PubMed
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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

12 authors.

Maria Angeliki ToliDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden. maria.angeliki.toli@ki.se.
Michail SarafidisDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Panagiotis FilisDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Evangelos TzorasDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Nikolaos TsiknakisDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Emmanouil SifakisDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Efstathia LiatsouDepartment of Surgery, Sahlgrenska University Hospital, Gothenburg, Sweden.
Georgios RassidakisDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Jonas BerghDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Alexios MatikasDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Ioannis ZerdesDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Theodoros FoukakisDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrophoblast cell surface antigen 2 (Trop-2) is a targetable transmembrane glycoprotein commonly overexpressed in breast cancer (BC). This study combines a systematic review and meta-analysis with a retrospective analysis of an independent early BC patient cohort, aiming to investigate the expression patterns of Trop-2 and their clinical significance in BC.

methodsA systematic literature search was conducted up to October 2025 to identify studies evaluating Trop-2 protein expression levels and clinical outcomes in patients with BC receiving Trop-2-directed antibody-drug conjugates (ADCs) or chemotherapy. Random-effects meta-analyses were performed to estimate pooled Trop-2 positivity rates and to assess progression-free (PFS) and overall survival (OS) across Trop-2 expression levels. Additionally, an association analysis between Trop-2 protein and gene expression was performed in an early BC patient cohort (n = 564) using immunohistochemistry and gene expression data. Trop-2 protein expression was assessed using both conventional observer-based methods and digital quantitative image analysis.

resultsA total of 41 studies fulfilled the inclusion criteria. The overall pooled Trop-2 protein positivity rate was 72% [95% Confidence Interval (CI), 67-77%; 41 studies, n = 9170]. Trop-2-directed ADCs improved PFS versus chemotherapy across different H-score groups, with the greatest benefit in tumours with high H-score [3 studies; n = 575; Hazard Ratio (HR) = 0.33, 95% CI 0.20-0.56, p < 0.0001]. For OS, the benefit was observed in the low H-score group (2 studies; n = 272; HR = 0.75, 95% CI 0.57-0.98, p = 0.034). In the study cohort, Trop-2 protein by observer-read assessment was detected in 396/454 patients (87.22%). Digital pathology identified 54 (11.90%) tumours with low, 326 (71.80%) with medium, and 74 (16.30%) with high H-scores. Observer-read and digital assessments were significantly associated (Pearson's chi-square test, p < 0.001). Higher Trop-2 protein and gene expression were associated with worse distant recurrence-free interval (HR

conclusionsTrop-2 was detectable across all BC subtypes, exhibiting a wide range of expression levels. Our study suggests that Trop-2 may have a potential prognostic significance in early BC.

Indexed as

Antigens, NeoplasmBiomarkers, TumorBreast NeoplasmsCell Adhesion MoleculesFemaleGene Expression Regulation, NeoplasticHumansRetrospective StudiesAntigens, NeoplasmBiomarkers, TumorCell Adhesion MoleculesTACSTD2 protein, humanAntibody-drug conjugatesBiomarkersBreast cancerMolecular targetPrognosisTherapeutic targetTrop-2

Identifiers

PMID42557566
PMCPMC13445770

What Socratic holds

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LicenceCC BY
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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 Socratic graph.