Evidence map›Paper›PMID 37676829›Full record

ArticleJournal of the National Cancer Institute2024

Metastatic site patterns by intrinsic subtype and HER2DX in early HER2-positive breast cancer.

Maria Vittoria Dieci, PierFranco Conte, Giancarlo Bisagni, Stefania Bartolini, Antonio Frassoldati, Daniele Generali, Federico Piacentini, Gaia Griguolo, Enrico Tagliafico, Fara Brasó Maristany and 8 more

Abstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Trial
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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

18 authors.

Maria Vittoria DieciDepartment of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.ORCID 0000-0002-3967-9861
PierFranco ConteVeneto Oncology Network, Padova, Italy.ORCID 0000-0002-5210-5344
Giancarlo BisagniDepartment of Oncology and Advanced Technologies, Oncology Unit, Azienda Unità Sanitaria Locale-Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Reggio Emilia, Italy.ORCID 0000-0003-1042-3771
Stefania BartoliniNervous System Medical Oncology Department, IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.ORCID 0000-0003-1255-0109
Antonio FrassoldatiClinical Oncology, Department of Translational Medicine and for Romagna, S. Anna University Hospital, Ferrara, Italy.ORCID 0000-0003-3487-3259
Daniele GeneraliDepartment of Medicine, Surgery and Health Sciences, University of Trieste, Trieste, Italy.ORCID 0000-0003-2480-3855
Federico PiacentiniDepartment of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Modena, Italy.ORCID 0000-0001-8969-638X
Gaia GriguoloDepartment of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.ORCID 0000-0002-8782-4509
Enrico TagliaficoCenter for Genome Research, University of Modena and Reggio Emilia, Modena, Italy.ORCID 0000-0003-0981-2542
Fara Brasó MaristanyTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.ORCID 0000-0001-5440-9643
Nuria ChicTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.ORCID 0000-0001-9736-6276
Laia ParéReveal Genomics, Barcelona, Spain.ORCID 0000-0002-4904-558X
Federica MigliettaDepartment of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.ORCID 0000-0001-6203-874X
Roberto ViciniDepartment of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Modena, Italy.ORCID 0000-0002-1799-6567
Roberto D'AmicoDepartment of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Modena, Italy.ORCID 0000-0002-3211-6687
Sara BalduzziDepartment of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Modena, Italy.ORCID 0000-0003-1205-1895
Aleix PratTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.ORCID 0000-0003-2377-540X
Valentina GuarneriDepartment of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy.ORCID 0000-0002-2375-8397

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEven with contemporary treatment strategies, more than 10% of HER2-positive early stage breast cancer patients may experience distant metastasis as first event during follow-up. Tools for predicting unique patterns of metastatic spread are needed to plan personalized surveillance. We evaluated how molecular heterogeneity affects the pattern of distant relapse in HER2-positive breast cancer.

methodsA total of 677 HER2-positive stage I-III breast cancer patients from ShortHER trial, Cher-LOB trial, and 2 institutional cohorts were included. PAM50 molecular subtypes and research-based HER2DX scores were evaluated. The cumulative incidence of distant relapse as the first event (any site and site specific) was evaluated using competing risk analysis. Median follow-up was 8.4 years. Tests of statistical significance are 2-sided.

resultsStage III and high HER2DX risk score identified patients at the highest risk of distant relapse as first event (10-year incidence 24.5% and 19.7%, respectively). Intrinsic molecular subtypes were associated with specific patterns of metastatic spread: compared with other subtypes, HER2-enriched tumors were more prone to develop brain metastases (10-year incidence 3.8% vs 0.6%, P = .005), basal-like tumors were associated with an increased risk of lung metastases (10-year incidence 11.1% vs 2.6%, P = .001), and luminal tumors developed more frequently bone-only metastases (10-year incidence 5.1% vs 2.0%, P = .042). When added to stage or HER2DX risk score in competing risk regression models, intrinsic subtype maintained an independent association with site-specific metastases.

conclusionsThe integration of intrinsic molecular subtypes with stage or HER2DX risk score predicts site-specific metastatic risk in HER2-positive breast cancer, with potential implications for personalized surveillance and clinical trials aimed at preventing site-specific recurrence.

Indexed as

Bone NeoplasmsBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesFemaleHumansNeoplasm Recurrence, LocalPrognosisRecurrenceRisk AssessmentRisk FactorsErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID37676829
PMCPMC10777675

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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.