Evidence map›Paper›PMID 35595761›Full record

ArticleNPJ breast cancer2022

HER2-low-positive breast cancer: evolution from primary tumor to residual disease after neoadjuvant treatment.

Federica Miglietta, Gaia Griguolo, Michele Bottosso, Tommaso Giarratano, Marcello Lo Mele, Matteo Fassan, Matilde Cacciatore, Elisa Genovesi, Debora De Bartolo, Grazia Vernaci and 5 more

Open access · goldAbstract read
In one paragraph

Article in NPJ breast cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 3 pooled it
9.7field-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.

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

58 citing papers in PubMed, 3 syntheses or guidelines pooled it, 93 citations in OpenAlex.

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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

15 authors at 3 institutions in 1 country.

Federica MigliettaDepartment of Surgery, Oncology and Gastroenterology (DISCOG), University of Padova, 35128, Padova, Italy.
Gaia GriguoloDepartment of Surgery, Oncology and Gastroenterology (DISCOG), University of Padova, 35128, Padova, Italy.ORCID http://orcid.org/0000-0002-8782-4509
Michele BottossoDepartment of Surgery, Oncology and Gastroenterology (DISCOG), University of Padova, 35128, Padova, Italy.ORCID http://orcid.org/0000-0002-8098-1819
Tommaso GiarratanoMedical Oncology 2, Istituto Oncologico Veneto IOV-IRCCS, 35128, Padova, Italy.
Marcello Lo MeleSurgical Pathology Unit, University Hospital of Padua, 35121, Padua, Italy.
Matteo FassanDepartment of Medicine (DIMED), Surgical Pathology & Cytopathology Unit, University of Padua, 35121, Padua, Italy.ORCID http://orcid.org/0000-0001-6515-5482
Matilde CacciatoreDepartment of Pathology and Molecular Genetics, Treviso General Hospital, Treviso, Italy.
Elisa GenovesiDepartment of Surgery, Oncology and Gastroenterology (DISCOG), University of Padova, 35128, Padova, Italy.
Debora De BartoloDepartment of Medicine (DIMED), Surgical Pathology & Cytopathology Unit, University of Padua, 35121, Padua, Italy.
Grazia VernaciDepartment of Surgery, Oncology and Gastroenterology (DISCOG), University of Padova, 35128, Padova, Italy.ORCID http://orcid.org/0000-0003-4401-7579
Ottavia AmatoDepartment of Surgery, Oncology and Gastroenterology (DISCOG), University of Padova, 35128, Padova, Italy.ORCID http://orcid.org/0000-0002-3690-8542
Francesca PorraDepartment of Surgery, Oncology and Gastroenterology (DISCOG), University of Padova, 35128, Padova, Italy.
PierFranco ConteDepartment of Surgery, Oncology and Gastroenterology (DISCOG), University of Padova, 35128, Padova, Italy.
Valentina GuarneriDepartment of Surgery, Oncology and Gastroenterology (DISCOG), University of Padova, 35128, Padova, Italy. valentina.guarneri@unipd.it.ORCID http://orcid.org/0000-0002-2375-8397
Maria Vittoria DieciDepartment of Surgery, Oncology and Gastroenterology (DISCOG), University of Padova, 35128, Padova, Italy.ORCID http://orcid.org/0000-0002-3967-9861
University of Padua · ITCa' Foncello Hospital · ITIstituto Oncologico Veneto · IT

Funding

Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) 5 per mille ID. 22759 programUniversità degli Studi di Padova (University of Padova) BIRD 2019Università degli Studi di Padova (University of Padova) BIRD-2019Università degli Studi di Padova (University of Padova) BIRD 2020Università degli Studi di Padova (University of Padova) DOR-2194859/21
6 · The paper itself

Abstract

Approximately a half of breast tumors classified as HER2-negative exhibit HER2-low-positive expression. We recently described a high instability of HER2-low-positive expression from primary breast cancer (BC) to relapse. Previous studies reporting discordance in HER2 status between baseline biopsy and residual disease (RD) in patients undergoing neoadjuvant treatment did not include the HER2-low-positive category. The aim of this study is to track the evolution of HER2-low-positive expression from primary BC to RD after neoadjuvant treatment. Patients undergoing neoadjuvant treatment with available baseline tumor tissue and matched samples of RD (in case of no pCR) were included. HER2-negative cases were sub-classified as HER2-0 or HER2-low-positive (IHC 1+ or 2+ and ISH negative). Four-hundred forty-six patients were included. Primary BC phenotype was: HR-positive/HER2-negative 23.5%, triple-negative (TN) 35%, HER2-positive 41.5%. HER2-low-positive cases were 55.6% of the HER2-negative cohort and were significantly enriched in the HR-positive/HER2-negative vs. TN subgroup (68.6% vs. 46.8%, p = 0.001 χ

Identifiers

PMID35595761
PMCPMC9122970
OpenAlexW4280492346

What OpenQuestion holds

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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.