Evidence map›Paper›PMID 31217629›Full record

ArticleGeburtshilfe und Frauenheilkunde2019

Diagnosis and Therapy of Triple-Negative Breast Cancer (TNBC) - Recommendations for Daily Routine Practice.

Andreas Schneeweiss, Carsten Denkert, Peter A Fasching, Carlo Fremd, Oleg Gluz, Cornelia Kolberg-Liedtke, Sibylle Loibl, Hans-Joachim Lück

Open access · hybridAbstract read
In one paragraph

Article in Geburtshilfe und Frauenheilkunde, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 37 citations in OpenAlex.

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  14. [Pembrolizumab as neoadjuvant treatment of early triple-negative breast cancer].Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2020
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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

8 authors at 7 institutions in 1 country.

Andreas SchneeweissNationales Centrum für Tumorerkrankungen (NCT), Universitätsklinikum, Heidelberg, Germany.
Carsten DenkertInstitut für Pathologie, Universitätsklinikum Gießen und Marburg GmbH, Standort Marburg, Philipps-Universität Marburg, Marburg, Germany.
Peter A FaschingFrauenklinik des Universitätsklinikums Erlangen, Comprehensive Cancer Center Erlangen-EMN, Friedrich-Alexander Universität Erlangen-Nürnberg, Erlangen, Germany.
Carlo FremdNationales Centrum für Tumorerkrankungen (NCT), Universitätsklinikum, Heidelberg, Germany.
Oleg GluzBrustzentrum Niederrhein, Evangelisches Krankenhaus Bethesda, Mönchengladbach, Germany.
Cornelia Kolberg-LiedtkeCharité - Universitätsmedizin Berlin, Campus Mitte, Berlin, Germany.
Sibylle LoiblGerman Breast Group c/o GBG Forschungs GmbH, Neu-Isenburg, Germany.
Hans-Joachim LückGynäkologie Onkologie, Gynäkologisch-onkologische Praxis, Hannover, Germany.
University Hospital Heidelberg · DECardiovascular Center Bethanien · DECharité - Universitätsmedizin Berlin · DEEvangelisches Krankenhaus Bethesda Mönchengladbach · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEPraxis für Hämatologie und Onkologie · DEUniversitätsklinikum Gießen und Marburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rapid increase in knowledge in tumour biology and tumour pathogenesis of triple-negative breast cancer (TNBC) has resulted in new therapeutic approaches and new therapeutic concepts for treatment. For years, TNBC has been considered to be a difficult-to-treat tumour due to its generally aggressive tumour biology and in view of limited therapeutic options. The risk of recurrence and metastasis is higher than in the case of other breast cancer subtypes of the same stage. In addition to surgery and radiation in the curative situation, systemic chemotherapy with anthracyclines and/or taxanes is still the therapy of choice. New therapeutic approaches are based on the knowledge that TNBC is a molecularly very heterogeneous disease. Research groups are working to classify TNBC better and better on a molecular level and use this molecular subtyping as the basis for new therapeutic strategies. The most promising new approaches and considerations regarding the therapy of TNBCs are shown below. In addition, the current therapeutic strategies are discussed using a fictitious case history, taking the current data and the resultant therapeutic consequence into account.

Indexed as

BRCA mutationdiagnosis and therapy of TNBCsubtyping of TNBCtriple-negative breast cancer

Identifiers

PMID31217629
PMCPMC6570613
OpenAlexW2953131890

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.