Evidence map›Paper›PMID 31829264›Full record

ArticleBreast cancer research : BCR2019

Human leucocyte antigen class I in hormone receptor-positive, HER2-negative breast cancer: association with response and survival after neoadjuvant chemotherapy.

Bruno Valentin Sinn, Karsten E Weber, Wolfgang Daniel Schmitt, Peter A Fasching, William Fraser Symmans, Jens-Uwe Blohmer, Thomas Karn, Eliane Tabea Taube, Frederick Klauschen, Frederik Marmé and 8 more

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% of its field
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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
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  4. The immunology of human breast cancer.Nature reviews. Immunology · 2026
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  11. Vaccines targetingHuman vaccines & immunotherapeutics · 2024
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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 at 12 institutions in 2 countries.

Bruno Valentin SinnDepartment of Pathology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt - Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany. bruno.sinn@charite.de.ORCID 0000-0002-1257-9799
Karsten E WeberGerman Breast Group Forschungs GmbH, Neu-Isenburg, Germany.
Wolfgang Daniel SchmittDepartment of Pathology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt - Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
Peter A FaschingDepartment of Gynecology, University Hospital Erlangen, Erlangen, Germany.
William Fraser SymmansDepartment of Translational Molecular Pathology, The University of Texas - MD Anderson Cancer Center, Houston, TX, USA.
Jens-Uwe BlohmerDepartment of Gynecology with Breast Cancer, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt - Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
Thomas KarnDepartment of Gynecology and Obstetrics, University Hospital Frankfurt, Frankfurt, Germany.
Eliane Tabea TaubeDepartment of Pathology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt - Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
Frederick KlauschenDepartment of Pathology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt - Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
Frederik MarméDepartment of Gynecology and Obstetrics, University Hospital Heidelberg, Heidelberg, Germany.
Christian SchemDepartment of Gynecology and Obstetrics, University Hospital Schleswig-Holstein, Kiel, Germany.
Elmar StickelerDepartment of Gynecology and Obstetrics, RWTH Aachen, Aachen, Germany.
Beyhan AtasevenDepartment of Gynecology and Gynecologic Oncology, Kliniken Essen Mitte, Essen, Germany.
Jens HuoberDepartment of Gynecology and Breast Medical Oncology, Universitätsklinikum Ulm, Ulm, Germany.
Gunter von MinckwitzGerman Breast Group Forschungs GmbH, Neu-Isenburg, Germany.
Barbara SeligerInstitute of Medical Immunology, Martin Luther University Halle-Wittenberg, Halle, Germany.
Carsten DenkertDepartment of Pathology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt - Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
Sibylle LoiblGerman Breast Group Forschungs GmbH, Neu-Isenburg, Germany.
Humboldt-Universität zu Berlin · DEGerman Breast group · DEGoethe University Frankfurt · DEHeidelberg University · DELMU Klinikum · DEMartin Luther University Halle-Wittenberg · DEPhilipps University of Marburg · DERWTH Aachen University · DEThe University of Texas MD Anderson Cancer Center · USUniversitätsklinikum Erlangen · DEUniversity Hospital Schleswig-Holstein · DEUniversity Hospital Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClinical application of cancer immunotherapy requires a better understanding of tumor immunogenicity and the tumor microenvironment. HLA class I molecules present antigens to CD8

methodsWe evaluated HLA class I heavy chain expression by immunohistochemistry in 863 biopsies (GeparTrio trial). Patients received neoadjuvant chemotherapy and adjuvant endocrine treatment if tumors were hormone receptor-positive (HR+). In parallel, the expression of HLA-A was analyzed using a microarray cohort of 320 breast cancer patients from the MD Anderson Cancer Center. We evaluated its association with clinical outcome, tumor-infiltrating lymphocytes (TILs), and immune cell metagenes.

resultsIn HR+/HER2- breast cancer, HLA class I heavy chain expression was associated with increased TILs and better response to chemotherapy (7% vs. 14% pCR rate, P = 0.029), but worse disease-free survival (hazard ratio (HR) 1.6 (1.1-2.4); P = 0.024). The effect was significant in a multivariate model adjusted for clinical and pathological variables (HR 1.7 (1.1-2.6); P = 0.016) and was confirmed by analysis of HLA-A in a microarray cohort. HLA-A was correlated to most immune cell metagenes. There was no association with response or survival in triple-negative or HER2+ disease.

conclusionsThe study confirms the negative prognostic role of lymphocytes in HR+ breast cancer and points at a complex interaction between chemotherapy, endocrine treatment, and tumor immunogenicity. The results point at a subtype-specific and potentially treatment-specific role of tumor-immunological processes in breast cancer with different implications in triple-negative and hormone receptor-positive disease.

Indexed as

Biomarkers, TumorAntineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesFemaleGene ExpressionHistocompatibility Antigens Class IHumansImmunohistochemistryLymphocytes, Tumor-InfiltratingNeoadjuvant TherapyNeoplasm StagingPrognosisProportional Hazards ModelsReceptors, EstrogenReceptors, ProgesteroneBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesHistocompatibility Antigens Class IReceptors, EstrogenReceptors, ProgesteroneBreast cancerHLATumor-infiltrating lymphocytes

Identifiers

PMID31829264
PMCPMC6907189
OpenAlexW2996721496

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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.