Evidence map›Paper›PMID 41390750›Full record

ArticleNPJ breast cancer2025

Clinical outcome and proportion of hereditary cancer genes gPV in TNBC: the HEaRTBeat study.

Martina Rotolo, Claudia Piombino, Marta Venturelli, Elena Tenedini, Angela Toss, Elena Barbieri, Elisa Gasparini, Isabella Marchi, Federica Domati, Monica Civallero and 5 more

Abstract read
In one paragraph

Article in NPJ breast cancer, 2025. 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

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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

15 authors.

Martina RotoloDepartment of Medical and surgical Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Claudia PiombinoDepartment of Oncology and Hematology, Azianda Ospedaliero - Universitaria di Modena, Modena, Italy.
Marta VenturelliDepartment of Oncology and Hematology, Azianda Ospedaliero - Universitaria di Modena, Modena, Italy.
Elena TenediniDepartment of Laboratory Medicine and Pathology, Diagnostic Hematology and Clinical Genomics Unit, University of Modena and Reggio Emilia, Modena, Italy.
Angela TossDepartment of Medical and surgical Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Elena BarbieriDepartment of Oncology and Hematology, Azianda Ospedaliero - Universitaria di Modena, Modena, Italy.
Elisa GaspariniMedical Oncology, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Isabella MarchiDepartment of Oncology and Hematology, Azianda Ospedaliero - Universitaria di Modena, Modena, Italy.
Federica DomatiDepartment of Medical and surgical Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Monica CivalleroDepartment of Medical and surgical Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Luigi MarcheselliFondazione Italiana Linfomi, Modena, Italy.
Elisabetta RazzaboniHospital Psychology Service, Azienda Ospedaliero Universitaria di Modena, Modena, Italy.
Enrico TagliaficoDepartment of Laboratory Medicine and Pathology, Diagnostic Hematology and Clinical Genomics Unit, University of Modena and Reggio Emilia, Modena, Italy.
Massimo DominiciDepartment of Medical and surgical Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Laura CortesiDepartment of Medical and surgical Sciences, University of Modena and Reggio Emilia, Modena, Italy. hbc@unimore.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to study the proportion of germline pathogenic variants (gPV) in hereditary cancer genes and the clinical-pathological characteristics, local and systemic treatments, pathological complete response (pCR) rate to neoadjuvant therapy, invasive breast cancer-free survival (IBCFS), and overall survival (OS) in triple-negative breast cancer (TNBC) patients, consecutively tested between 2017 and 2024 at Modena and Reggio Emilia University Hospital, Italy. A total of 387 early-stage patients were included in the study. Eighty-seven patients (22%) showed gPV in hereditary predisposing genes, mostly BRCA1/2 (11%), PALB2 (5%), RAD51C/D (2%), MUTYH (2%), ATM (1%), and others (1%). The proliferation index was high in all, whereas the most frequent stage was stage I/II, except in MUTYH gPV carriers. More mastectomies, also contralateral, were performed in gPV than in non-carriers. Finally, 64% gPV achieved pCR compared to 39% non-carriers (p < 0.001), although no differences were observed between the two groups in IBCFS or OS.

Identifiers

PMID41390750
PMCPMC12804956

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