Evidence map›Paper›PMID 41422117›Full record

ArticleOncogene2026

Chromosome centromere copy number amplification associated with exceptional response in HER2-positive metastatic breast cancer patients.

Charlotte Andrieu, Jojanneke Stoof, Dalal AlSultan, Laura Ivers, Jose Javier Berenguer Pina, Darko Skrobo, Jo Ballot, Debbie O'Reilly, Denis M Collins, Alex J Eustace and 5 more

Abstract read
In one paragraph

Article in Oncogene, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

15 authors.

Charlotte AndrieuLife Sciences Institute, School of Biotechnology, Dublin City University (DCU), Dublin, Ireland.
Jojanneke StoofLife Sciences Institute, School of Biotechnology, Dublin City University (DCU), Dublin, Ireland.ORCID http://orcid.org/0000-0002-8331-1597
Dalal AlSultanLife Sciences Institute, School of Biotechnology, Dublin City University (DCU), Dublin, Ireland.
Laura IversLife Sciences Institute, School of Biotechnology, Dublin City University (DCU), Dublin, Ireland.
Jose Javier Berenguer PinaDepartment of Medical Oncology, St Vincent's University Hospital, Dublin, Ireland.
Darko SkroboDepartment of Histopathology, Galway University Hospital, Galway, Ireland.
Jo BallotDepartment of Medical Oncology, St Vincent's University Hospital, Dublin, Ireland.
Debbie O'ReillyLife Sciences Institute, School of Biotechnology, Dublin City University (DCU), Dublin, Ireland.
Denis M CollinsLife Sciences Institute, School of Biotechnology, Dublin City University (DCU), Dublin, Ireland.
Alex J EustaceLife Sciences Institute, School of Biotechnology, Dublin City University (DCU), Dublin, Ireland.ORCID http://orcid.org/0000-0002-4092-1360
Cecily QuinnDepartment of Pathology, St Vincent's University Hospital, Dublin, Ireland.
Janice M WalsheDepartment of Medical Oncology, St Vincent's University Hospital, Dublin, Ireland.
Giuseppe GulloDepartment of Medical Oncology, St Vincent's University Hospital, Dublin, Ireland.
Naomi WalshLife Sciences Institute, School of Biotechnology, Dublin City University (DCU), Dublin, Ireland. naomi.walsh@dcu.ie.ORCID http://orcid.org/0000-0002-2178-3564
John CrownDepartment of Medical Oncology, St Vincent's University Hospital, Dublin, Ireland. john.crown@ccrt.ie.

Funding

Health Research Board (HRB) EIA-2019-013
6 · The paper itself

Abstract

Metastatic breast cancer (MBC) is generally an incurable neoplasm. A small cohort of patients with HER2-positive MBC, however, achieve such prolonged remission without relapse following anti-HER2 therapy and chemotherapy, that it is speculated they might be cured. The genomes of these patients might provide insights into the underlying mechanisms for their successful treatment. Here, a total of 243 HER2-positive patients diagnosed with MBC between 2000 and 2015 were studied. Of these, 29 patients were identified as exceptional responders (ExR) with an overall survival (OS) > 60 months and no evidence of relapse, 54 patients with an OS > 60 months but who relapsed or developed progressive disease were defined as exceptional survivors (ExS), and 160 patients with an OS < 60 months were identified as short-term responders (STR). Whole-Genome Sequencing and centromere copy number (CCN) analysis was performed on 27 patients (12 ExR; 4 ExS; 11 STR). A significant amplification was observed in the centromeric regions of ExR, exhibiting higher CCN compared to the ExS and STR. Digital PCR validation of chromosome 4 centromere region D4Z1 copy number was not associated with ExR OS. Our results suggest that the amplification of centromere regions are associated with very prolonged remission and survival in patients with HER2-positive MBC.

Indexed as

Breast NeoplasmsCentromereDNA Copy Number VariationsErb-b2 Receptor Tyrosine KinasesAdultAgedFemaleGene AmplificationHumansMiddle AgedNeoplasm MetastasisERBB2 protein, humanErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID41422117
PMCPMC12815647

What Socratic 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 Socratic graph.