Evidence map›Paper›PMID 33397968›Full record

ArticleNPJ breast cancer2021

Clinical, pathological, and PAM50 gene expression features of HER2-low breast cancer.

Francesco Schettini, Nuria Chic, Fara Brasó-Maristany, Laia Paré, Tomás Pascual, Benedetta Conte, Olga Martínez-Sáez, Barbara Adamo, Maria Vidal, Esther Barnadas and 17 more

Erratum issued 2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in NPJ breast cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 2 registered trials, which are not on this map. Cited by 373 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
373citing papers in PubMed, 8 pooled it
47.7field-weighted citation impact, top 1% 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.

NCT00130533 phase3completednot on this map

Multicenter, Open-label, Randomized Phase III to Evaluate Efficacy of Maintenance Treatment With Capecitabine Following Standard Adjuvant Chemotherapy in Operable Triple Negative Breast Cancer Patients

TypeinterventionalSponsorSpanish Breast Cancer Research GroupRan2006 to 2017Enrolled876ConditionsBreast CancerArmsCapecitabine
NCT07561346 completednot on this map

Clinico-pathological and Genomic Features of HER2-low Early Breast Cancer (eBC). Results of Retrospective Analysis of Seven Adjuvant Trials by the Hellenic Cooperative Oncology Group (HeCOG)

TypeobservationalSponsorHellenic Cooperative Oncology GroupRan1996 to 2026Enrolled3,648ConditionsHER2-zero, HER2-low and HER2-positive Tumors Distribution Across HR Expression Categories
3 · Its place in the literature

Who cites it

373 citing papers in PubMed, 8 syntheses or guidelines pooled it, 669 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Pooled it
  4. SEOM-GEICAM-SOLTI clinical guidelines in advanced breast cancer (UPDATE 2025).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Guideline
  5. Pooled it
  6. Guideline
  7. Guideline
  8. Pooled it
  9. Trial
  10. Trial
  11. Trial
  12. Trial
  13. Trial
  14. Trial
  15. Trial
  16. Trial
  17. Trial
  18. Trial
  19. Article
  20. Article

313 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 13 institutions in 4 countries.

Francesco SchettiniDepartment of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.ORCID http://orcid.org/0000-0001-6561-1919
Nuria ChicTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
Fara Brasó-MaristanyTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
Laia ParéSOLTI Breast Cancer Research Group, Barcelona, Spain.ORCID http://orcid.org/0000-0002-4904-558X
Tomás PascualTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.ORCID http://orcid.org/0000-0001-8431-3183
Benedetta ConteTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
Olga Martínez-SáezTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
Barbara AdamoTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
Maria VidalTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.ORCID http://orcid.org/0000-0003-1992-5727
Esther BarnadasTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
Aranzazu Fernández-MartinezDepartment of Genetics, University of North Carolina, Chapel Hill, NC, USA.
Blanca González-FarreTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
Esther SanfeliuTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
Juan Miguel CejalvoINCLIVA Biomedical Research Institute, Hospital Clínico Universitario Valencia, University of Valencia, Valencia, Spain.
Giuseppe PerronePathology Department, Campus Bio-Medico University, Rome, Italy.
Giovanna SabaresePathology Department, Campus Bio-Medico University, Rome, Italy.
Francesca ZalfaPathology Department, Campus Bio-Medico University, Rome, Italy.
Vicente PegVall d´Hebron University Hospital, Barcelona, Spain.
Roberta FasaniVall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
Patricia VillagrasaSOLTI Breast Cancer Research Group, Barcelona, Spain.
Joaquín GaviláSOLTI Breast Cancer Research Group, Barcelona, Spain.
Carlos H BarriosCentro de Pesquisa Clínica Hospital São Lucas da PUCRS, Porto Alegre, Brazil.ORCID http://orcid.org/0000-0001-6021-667X
Ana LluchGEICAM, Grupo Español de Investigación en Cáncer de Mama, Madrid, Spain.ORCID http://orcid.org/0000-0003-2766-407X
Miguel MartínGEICAM, Grupo Español de Investigación en Cáncer de Mama, Madrid, Spain.
Mariavittoria LocciDepartment of Neuroscience, Reproductive Sciences and Dentistry, University of Naples Federico II, Naples, Italy.
Sabino De PlacidoDepartment of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.
Aleix PratTranslational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain. alprat@clinic.cat.ORCID http://orcid.org/0000-0003-2377-540X
Hospital Clínic de Barcelona · ESUniversità Campus Bio-Medico · ITUniversity of Naples Federico II · ITUniversity of North Carolina at Chapel Hill · USBreast Cancer Research Foundation · USFundación Instituto Valenciano de Oncología · ESHospital Clínico Universitario de Valencia · ESHospital General Universitario Gregorio Marañón · ESHospital São Lucas da PUCRS · BROspedale Policlinico San Martino · ITUniversitat de València · ESVall d'Hebron Hospital Universitari · ESVall d'Hebron Institute of Oncology · ES

Funding

Breast Cancer Now 2018NOVPCC1294Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) PI16/00904
6 · The paper itself

Abstract

Novel antibody-drug conjugates against HER2 are showing high activity in HER2-negative breast cancer (BC) with low HER2 expression (i.e., 1+ or 2+ and lack of ERBB2 amplification). However, the clinical and molecular features of HER2-low BC are yet to be elucidated. Here, we collected retrospective clinicopathological and PAM50 data from 3,689 patients with HER2-negative disease and made the following observations. First, the proportion of HER2-low was higher in HR-positive disease (65.4%) than triple-negative BC (TNBC, 36.6%). Second, within HR-positive disease, ERBB2 and luminal-related genes were more expressed in HER2-low than HER2 0. In contrast, no gene was found differentially expressed in TNBC according to HER2 expression. Third, within HER2-low, ERBB2 levels were higher in HR-positive disease than TNBC. Fourth, HER2-low was not associated with overall survival in HR-positive disease and TNBC. Finally, the reproducibility of HER2-low among pathologists was suboptimal. This study emphasizes the large biological heterogeneity of HER2-low BC, and the need to implement reproducible and sensitive assays to measure low HER2 expression.

Identifiers

PMID33397968
PMCPMC7782714
OpenAlexW3119128530

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.