Evidence map›Paper›PMID 34981296›Full record

ArticleFamilial cancer2022

BRCA1 Norway: comparison of classification for BRCA1 germline variants detected in families with suspected hereditary breast and ovarian cancer between different laboratories.

Henrikke N Hovland, Rafal Al-Adhami, Sarah Louise Ariansen, Marijke Van Ghelue, Wenche Sjursen, Sigrid Lima, Marte Bolstad, Amund H Berger, Hildegunn Høberg-Vetti, Per Knappskog and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Familial cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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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

13 authors at 5 institutions in 1 country.

Henrikke N HovlandWestern Norway Familial Cancer Center, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0002-0955-6465
Rafal Al-AdhamiWestern Norway Familial Cancer Center, Haukeland University Hospital, Bergen, Norway.
Sarah Louise AriansenDepartment of Medical Genetics, Oslo University Hospital, Oslo, Norway.
Marijke Van GhelueDepartment of Medical Genetics, University Hospital of North Norway, Tromsø, Norway.
Wenche SjursenDepartment of Medical Genetics, St. Olavs University Hospital, Trondheim, Norway.
Sigrid LimaDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Marte BolstadDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Amund H BergerDepartment of Medical Genetics, Haukeland University Hospital, Bergen, Norway.
Hildegunn Høberg-VettiWestern Norway Familial Cancer Center, Haukeland University Hospital, Bergen, Norway.
Per KnappskogDepartment of Medical Genetics, Haukeland University Hospital, Bergen, Norway.
Bjørn Ivar HaukanesDepartment of Medical Genetics, Haukeland University Hospital, Bergen, Norway.
Ingvild AukrustDepartment of Medical Genetics, Haukeland University Hospital, Bergen, Norway.
Elisabet OgnedalWestern Norway Familial Cancer Center, Haukeland University Hospital, Bergen, Norway. elisabet.ognedal@helse-bergen.no.ORCID 0000-0003-4775-0661
Haukeland University Hospital · NOUniversity of Bergen · NOOslo University Hospital · NOSt Olav's University Hospital · NOUniversity Hospital of North Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathogenic germline variants in Breast cancer susceptibility gene 1 (BRCA1) predispose carriers to hereditary breast and ovarian cancer (HBOC). Through genetic testing of patients with suspected HBOC an increasing number of novel BRCA1 variants are discovered. This creates a growing need to determine the clinical significance of these variants through correct classification (class 1-5) according to established guidelines. Here we present a joint collection of all BRCA1 variants of class 2-5 detected in the four diagnostic genetic laboratories in Norway. The overall objective of the study was to generate an overview of all BRCA1 variants in Norway and unveil potential discrepancies in variant interpretation between the hospitals, serving as a quality control at the national level. For a subset of variants, we also assessed the change in classification over a ten-year period with increasing information available. In total, 463 unique BRCA1 variants were detected. Of the 126 variants found in more than one hospital, 70% were interpreted identically, while 30% were not. The differences in interpretation were mainly by one class (class 2/3 or 4/5), except for one larger discrepancy (class 3/5) which could affect the clinical management of patients. After a series of digital meetings between the participating laboratories to disclose the cause of disagreement for all conflicting variants, the discrepancy rate was reduced to 10%. This illustrates that variant interpretation needs to be updated regularly, and that data sharing and improved national inter-laboratory collaboration greatly improves the variant classification and hence increases the accuracy of cancer risk assessment.

Indexed as

Breast NeoplasmsOvarian NeoplasmsBRCA1 ProteinBRCA2 ProteinCarcinoma, Ovarian EpithelialFemaleGenes, BRCA1Genetic Predisposition to DiseaseGenetic TestingGerm CellsGerm-Line MutationHumansLaboratoriesBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA1Breast and ovarian cancerVariant classificationVariants of uncertain significance

Identifiers

PMID34981296
PMCPMC9636114
OpenAlexW4205756385

What OpenQuestion holds

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LicenceCC BY
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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.