Evidence map›Paper›PMID 40348907›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2025

Predictive factors for pCR and relapse following neoadjuvant dual HER2-blockade in HER2+ breast cancer: an international cohort study.

Paulo Luz, Raquel Lopes-Brás, Inês Soares de Pinho, Vanessa Patel, Miguel Esperança-Martins, Lisa Gonçalves, Joana Gonçalves, Rita Freitas, Diana Simão, Maria Roldán Galnares and 9 more

Abstract readMulticenter Study
In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

19 authors.

Paulo LuzCBIOS - Universidade Lusófona's Research Center for Biosciences & Health Technologies, Lisbon, Portugal.
Raquel Lopes-BrásMedical Oncology Department, Unidade Local de Saúde de Santa Maria, Lisbon, Portugal.
Inês Soares de PinhoMedical Oncology Department, Unidade Local de Saúde de Santa Maria, Lisbon, Portugal.
Vanessa PatelMedical Oncology Department, Unidade Local de Saúde de Santa Maria, Lisbon, Portugal.
Miguel Esperança-MartinsMedical Oncology Department, Unidade Local de Saúde de Santa Maria, Lisbon, Portugal.
Lisa GonçalvesMedical Oncology Department, Unidade Local de Saúde de Santa Maria, Lisbon, Portugal.
Joana GonçalvesMedical Oncology Department, Unidade Local de Saúde do Arco Ribeirinho, Barreiro, Portugal.
Rita FreitasMedical Oncology Department, Unidade Local de Saúde de Amadora/Sintra, Amadora, Portugal.
Diana SimãoMedical Oncology Department, Unidade Local de Saúde de São José, Lisbon, Portugal.
Maria Roldán GalnaresPharmacy Departament, Hospital Virgen de Valme, Seville, Spain.
Silvia Artacho CriadoPharmacy Departament, Hospital Virgen de Valme, Seville, Spain.
Amanda NobreMedical Oncology Department, Unidade Local de Saúde de Entre Douro e Vouga, Santa Maria da Feira, Portugal.
Elias A Gracia MedinaNational Institute of Oncology and Radiobiology, La Habana, Cuba.
Isabel M Saffie VegaReconstructive and Oncological Breast Surgery Unit, Arturo López Pérez Foundation, Providencia, Chile.
Rita Teixeira de SousaMedical Oncology Department, Unidade Local de Saúde de Santa Maria, Lisbon, Portugal.
Luís CostaMedical Oncology Department, Unidade Local de Saúde de Santa Maria, Lisbon, Portugal.
João GregórioCBIOS - Universidade Lusófona's Research Center for Biosciences & Health Technologies, Lisbon, Portugal.
João G CostaCBIOS - Universidade Lusófona's Research Center for Biosciences & Health Technologies, Lisbon, Portugal.
Ana S FernandesCBIOS - Universidade Lusófona's Research Center for Biosciences & Health Technologies, Lisbon, Portugal. ana.fernandes@ulusofona.pt.ORCID http://orcid.org/0000-0001-6350-0641

Funding

Fundação para a Ciência e a Tecnologia CEEC/CBIOS/EPH/2018Fundação para a Ciência e a Tecnologia DOI 10.54499/UIDB/04567/2020Fundação para a Ciência e a Tecnologia DOI 10.54499/UIDP/04567/2020
6 · The paper itself

Abstract

purposeNeoadjuvant systemic therapy with dual HER2-blockade, trastuzumab and pertuzumab, combined with chemotherapy has become a standard approach in patients with HER2-positive (HER2+) breast cancer (BC). However, the variability in treatment outcomes, such as pathological complete response (pCR) or relapse rates, underscores the need to identify predictive factors to optimize therapeutic strategies. This study aims to explore the relationship between clinicopathological factors and both pCR and disease-free survival (DFS) in an international cohort of patients with HER2+ BC, contributing to defining personalized treatment strategies.

methodsAn international, multicenter, retrospective cohort study was conducted, including 517 patients with HER2+ BC who received neoadjuvant therapy comprising trastuzumab, pertuzumab, and chemotherapy. Data were collected between January 2016 and December 2023. The relationship between clinicopathological factors and treatment outcomes was analyzed using univariate tests, logistic regression for pCR, and Cox proportional hazards regression for DFS. Kaplan-Meier survival curves with log-rank tests and hazard ratios were used to compare DFS across subgroups.

resultsMultivariable analysis revealed that hormonal receptor (HR) expression and nodal status significantly predicted the achievement of pCR in this cohort. Factors such as age, HR status, tumor grade, Ki-67 index, nodal status, and pathological response were associated with relapse risk.

conclusionOur real-world data demonstrates that a comprehensive approach considering pCR, age, HR status, and nodal involvement is essential for personalized treatment strategies. These factors should be taken into account when deciding whether to escalate or de-escalate treatment, contributing to improved HER2+ BC patient outcomes.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesNeoadjuvant TherapyNeoplasm Recurrence, LocalAdultAgedAntibodies, Monoclonal, HumanizedCohort StudiesDisease-Free SurvivalFemaleHumansMiddle AgedRetrospective StudiesTrastuzumabAntibodies, Monoclonal, HumanizedERBB2 protein, humanErb-b2 Receptor Tyrosine KinasespertuzumabTrastuzumabAnti-HER2 neoadjuvant therapyHER2 positive breast cancerPathological complete responseReal-world evidence

Identifiers

PMID40348907
PMCPMC12559113

What OpenQuestion 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 OpenQuestion graph.