Evidence map›Paper›PMID 20956982›Full record

ReviewNature reviews. Clinical oncology2010

BRCA mutations in the management of breast cancer: the state of the art.

Steven A Narod

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Clinical oncology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04014283 (Prevention of Females Malignancies in Families With Hereditary Breast Cancer by Personalized Optimization of Se Levels in the Organism.), which is not on this map. Cited by 71 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 1 pooled it
8.1field-weighted citation impact, top 2% 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.

NCT04014283 naunknown statusnot on this mapstarted 2014, after this paper: background citation

Prevention of Females Malignancies in Families With Hereditary Breast Cancer by Personalized Optimization of Se Levels in the Organism.

TypeinterventionalSponsorRead-Gene S.A.Ran2014 to 2023Enrolled7,000ConditionsBreast NeoplasmsArmsSelenium supplementation or placebo treatment, Diet modification, Selenium supplementation or placebo treatment and diet modification
3 · Its place in the literature

Who cites it

71 citing papers in PubMed, 1 synthesis or guideline pooled it, 159 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  5. Review
  6. Review
  7. Review
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  10. Epigenome editing and epigenetic gene regulation in disease phenotypes.The Korean journal of chemical engineering · 2022
    Article
  11. Preventive medicine reports · 2022
    Article
  12. PARP Inhibition and Beyond in BRCA-Associated Breast Cancer in Women: A State-Of-The-Art Summary of Preclinical Research on Risk Reduction and Clinical Benefits.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2022
    Review
  13. BRCA1: An Endocrine and Metabolic Regulator.Frontiers in endocrinology · 2022
    Review
  14. Article
  15. Article
  16. Article
  17. Article
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  19. Review
  20. Article

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

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

1 author at 1 institution in 1 country.

Steven A NarodWomens College Research Institute, 790 Bay Street, Toronto, ON M5G 1N8, Canada. steven.narod@wchospital.ca
Women's College Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic testing for BRCA1 and BRCA2 mutations is gaining acceptance in clinical oncology worldwide and may help target unaffected high-risk women for prevention and for close surveillance. Annual screening with MRI seems to be an effective surveillance strategy, but the long term follow-up of women with small MRI-detected breast cancers is necessary to establish its ultimate value. Women with cancer and a BRCA mutation may benefit from tailored treatments, such as cisplatin or olaparib. The treatment goals for a woman with a BRCA-associated breast cancer should be to prevent recurrence of the initial cancer and to prevent second primary breast and ovarian cancers. Mutations in BRCA1 and BRCA2 are presented throughout the world and it is important that the benefits of genetic testing and of targeted therapies be extended to women who live outside of North America and Western Europe.

Indexed as

Genes, BRCA1Genes, BRCA2MutationAdultAntineoplastic AgentsAntineoplastic Agents, HormonalBreast NeoplasmsCisplatinEstrogen AntagonistsEthnicityFemaleFounder EffectGenetic Predisposition to DiseaseGenetic TestingHumansMagnetic Resonance ImagingAntineoplastic AgentsAntineoplastic Agents, HormonalCisplatinEstrogen AntagonistsolaparibPhthalazinesPiperazinesPoly(ADP-ribose) Polymerase InhibitorsTamoxifen

Identifiers

PMID20956982
OpenAlexW2012946235

What OpenQuestion holds

Textmetadata
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.