Evidence map›Paper›PMID 38942987›Full record

ArticleBritish journal of cancer2024

A population-based study on trajectories of HER2 status during neoadjuvant chemotherapy for early breast cancer and metastatic progression.

Caroline Boman, Xingrong Liu, Louise Eriksson Bergman, Wenwen Sun, Christian Tranchell, Maria Angeliki Toli, Balazs Acs, Jonas Bergh, Theodoros Foukakis, Alexios Matikas

Abstract read
In one paragraph

Article in British journal of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
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

10 authors.

Caroline Boman *Karolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden.
Xingrong Liu *Karolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden.
Louise Eriksson BergmanKarolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden.
Wenwen SunKarolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden.
Christian TranchellBreast Center, Karolinska Comprehensive Cancer Center, Stockholm, Sweden.
Maria Angeliki ToliKarolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden.
Balazs AcsKarolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-0972-4633
Jonas BerghKarolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden.ORCID http://orcid.org/0000-0001-5526-1847
Theodoros FoukakisKarolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden.ORCID http://orcid.org/0000-0001-8952-9987
Alexios MatikasKarolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden. alexios.matikas@ki.se.ORCID http://orcid.org/0000-0002-4122-9624

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to investigate the distribution and changes of HER2 status in untreated tumours, in residual disease and in metastasis, and their long-term prognostic implications.

methodsThis is a population-based cohort study of patients treated with neoadjuvant chemotherapy for breast cancer during 2007-2020 in the Stockholm-Gotland region which comprises 25% of the entire Swedish population. Information was extracted from the National Breast Cancer Registry and electronic patient charts to minimize data missingness and misclassification.

resultsIn total, 2494 patients received neoadjuvant chemotherapy, of which 2309 had available pretreatment HER2 status. Discordance rates were 29.9% between primary and residual disease (kappa = 0.534), 31.2% between primary tumour and metastasis (kappa = 0.512) and 33.3% between residual disease to metastasis (kappa = 0.483). Adjusted survival curves differed between primary HER2 0 and HER2-low disease (p < 0.001), with the former exhibiting an early peak in risk for death which eventually declined below the risk of HER2-low. Across all disease settings, increasing the number of biopsies increased the likelihood of detecting HER2-low status.

conclusionHER2 status changes during neoadjuvant chemotherapy and metastatic progression, and the long-term behaviours of HER2 0 and HER2-low disease differ, underscoring the need for obtaining tissue biopsies and for extended follow-up in breast cancer studies.

Indexed as

Breast NeoplasmsDisease ProgressionErb-b2 Receptor Tyrosine KinasesNeoadjuvant TherapyAdultAgedChemotherapy, AdjuvantCohort StudiesFemaleHumansMiddle AgedNeoplasm MetastasisNeoplasm, ResidualPrognosisSwedenERBB2 protein, humanErb-b2 Receptor Tyrosine Kinasesbreast cancerHER2 changeHER2-lowneoadjuvant chemotherapyprognosis

Identifiers

PMID38942987
PMCPMC11333620

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.