Evidence map›Paper›PMID 36831640›Full record

ReviewCancers2023

Clinical Utility of Genomic Tests Evaluating Homologous Recombination Repair Deficiency (HRD) for Treatment Decisions in Early and Metastatic Breast Cancer.

Loïck Galland, Nicolas Roussot, Isabelle Desmoulins, Didier Mayeur, Courèche Kaderbhai, Silvia Ilie, Audrey Hennequin, Manon Reda, Juliette Albuisson, Laurent Arnould and 4 more

Abstract readReview
In one paragraph

Review in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Ki-67 correlations in breast cancer.Journal of medicine and life · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Biomarkers in breast cancer 2024: an updated consensus statement by the Spanish Society of Medical Oncology and the Spanish Society of Pathology.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. 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

14 authors.

Loïck GallandDepartment of Medical Oncology, Georges-François Leclerc Center, 21000 Dijon, France.
Nicolas RoussotDepartment of Medical Oncology, Georges-François Leclerc Center, 21000 Dijon, France.ORCID 0000-0002-6562-6827
Isabelle DesmoulinsDepartment of Medical Oncology, Georges-François Leclerc Center, 21000 Dijon, France.
Didier MayeurDepartment of Medical Oncology, Georges-François Leclerc Center, 21000 Dijon, France.
Courèche KaderbhaiDepartment of Medical Oncology, Georges-François Leclerc Center, 21000 Dijon, France.
Silvia IlieDepartment of Medical Oncology, Georges-François Leclerc Center, 21000 Dijon, France.
Audrey HennequinDepartment of Medical Oncology, Georges-François Leclerc Center, 21000 Dijon, France.
Manon RedaDepartment of Medical Oncology, Georges-François Leclerc Center, 21000 Dijon, France.ORCID 0000-0003-3144-3990
Juliette AlbuissonDepartment of Pathology and Tumor Biology, Georges-François Leclerc Center, 21000 Dijon, France.ORCID 0000-0002-8947-6499
Laurent ArnouldDepartment of Pathology and Tumor Biology, Georges-François Leclerc Center, 21000 Dijon, France.
Romain BoidotDepartment of Pathology and Tumor Biology, Georges-François Leclerc Center, 21000 Dijon, France.ORCID 0000-0001-9956-1737
Caroline TruntzerPlatform of Transfer in Biological Oncology, Georges-François Leclerc Cancer Center, 21000 Dijon, France.ORCID 0000-0003-0895-4813
François GhiringhelliDepartment of Medical Oncology, Georges-François Leclerc Center, 21000 Dijon, France.ORCID 0000-0002-5465-8305
Sylvain LadoireDepartment of Medical Oncology, Georges-François Leclerc Center, 21000 Dijon, France.ORCID 0000-0002-0331-9194

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is the most frequently occurring cancer worldwide. With its increasing incidence, it is a major public health problem, with many therapeutic challenges such as precision medicine for personalized treatment. Thanks to next-generation sequencing (NGS), progress in biomedical technologies, and the use of bioinformatics, it is now possible to identify specific molecular alterations in tumor cells-such as homologous recombination deficiencies (HRD)-enabling us to consider using DNA-damaging agents such as platinum salts or PARP inhibitors. Different approaches currently exist to analyze impairment of the homologous recombination pathway, e.g., the search for specific mutations in homologous recombination repair (HRR) genes, such as

Indexed as

BRCAbreast cancerearly breast cancerhomologous recombination deficiencyHRD scoremetastatic breast cancermutational signatureNGSPARPiplatinum salts

Identifiers

PMID36831640
PMCPMC9954086

What OpenQuestion holds

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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.