Evidence map›Paper›PMID 34807276›Full record

ReviewDer Pathologe2022

[Detection of BRAF V600E mutation in metastatic colorectal carcinoma : A QuIP round robin test].

Korinna Jöhrens, Josephine Fischer, Markus Möbs, Klaus Junker, Jutta Kirfel, Sven Perner, Silke Laßmann, Martin Werner, Vanessa Borgmann, Hendrik Bläker and 1 more

Open access · greenAbstract readReview
In one paragraph

Review in Der Pathologe, 2022. 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, top 79% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Review
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

11 authors at 7 institutions in 1 country.

Korinna JöhrensInstitut für Pathologie, Universitätsklinikum Carl Gustav Carus, TU Dresden, Dresden, Deutschland.
Josephine FischerQualitätssicherungs-Initiative Pathologie QuIP GmbH, Berlin, Deutschland.
Markus MöbsInstitut für Pathologie, Campus Charité Mitte, Charité - Universitätsmedizin Berlin, Virchowweg 15, 10117, Berlin, Deutschland.
Klaus JunkerZentrum für Pathologie, Klinikum Bremen-Mitte, Bremen, Deutschland.
Jutta KirfelUniversitätsklinikum Schleswig-Holstein, Campus Lübeck, Lübeck, Deutschland.
Sven PernerUniversitätsklinikum Schleswig-Holstein, Campus Lübeck, Lübeck, Deutschland.
Silke LaßmannInstitut für Klinische Pathologie, Universitätsklinikum Freiburg, Freiburg, Deutschland.
Martin WernerInstitut für Klinische Pathologie, Universitätsklinikum Freiburg, Freiburg, Deutschland.
Vanessa BorgmannInstitut für Pathologie und Neuropathologie, Universitätsklinikum Tübingen, Tübingen, Deutschland.
Hendrik BläkerUniversitätsklinikum Leipzig, Leipzig, Deutschland.
Michael HummelInstitut für Pathologie, Campus Charité Mitte, Charité - Universitätsmedizin Berlin, Virchowweg 15, 10117, Berlin, Deutschland. michael.hummel@charite.de.
University Medical Center Freiburg · DEKlinikum Bremen-Mitte · DETU Dresden · DEUniversitäres Kinderwunschzentrum Lübeck · DEUniversitätsklinikum Tübingen · DEUniversity Hospital Leipzig · DEUniversity Hospital Schleswig-Holstein · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Round robin testing is an important instrument for quality assurance. Increasingly, this also applies to the results of molecular diagnostics in pathology, which directly influence therapy decisions in precision oncology. In metastatic colorectal carcinoma (mCRC), the focus has been on detecting KRAS and NRAS mutations, whose absence allows therapy with EGFR blocking antibodies. Recently, BRAF has been added as another predictive marker, since mCRC patients with BRAF V600E mutation benefit significantly from treatment with encorafenib (a BRAF inhibitor) in combination with cetuximab (anti-EGFR antibody) after systemic therapy. Due to the approval of this treatment in 2020, it is a pre-requisite that BRAF V600E mutation detection in diagnostic pathologies is reliably performed. Therefore, this round robin test with BRAF V600E testing either by immunohistochemistry or molecular methods was performed. The round robin test results demonstrate that molecular BRAF V600E detection is currently clearly superior to immunohistochemical detection.

Indexed as

Colorectal NeoplasmsProto-Oncogene Proteins B-rafAntibodies, MonoclonalHumansMutationPrecision MedicineAntibodies, MonoclonalBRAF protein, humanProto-Oncogene Proteins B-rafBRAF mutationCororectal cancerMolecular pathologyPrecision oncologyRound robin test

Identifiers

PMID34807276
PMCPMC8888471
OpenAlexW3215808039

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.