Evidence map›Paper›PMID 28881657›Full record

ArticleOncotarget2017

Tumor biomarker conversion between primary and metastatic breast cancer: mRNA assessment and its concordance with immunohistochemistry.

Stefan Stefanovic, Ralph Wirtz, Thomas M Deutsch, Andreas Hartkopf, Peter Sinn, Zsuzsanna Varga, Bettina Sobottka, Lakis Sotiris, Florin-Andrei Taran, Christoph Domschke and 6 more

Abstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

16 authors.

Stefan Stefanovic *Department of Gynecology and Obstetrics, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Ralph Wirtz *Stratifyer Molecular Pathology GmbH, 50935 Cologne, Germany.
Thomas M DeutschNational Center for Tumor Diseases (NCT) Heidelberg, 69120 Heidelberg, Germany.
Andreas HartkopfDepartment of Women's Health, University Hospital Tübingen, 72076 Tübingen, Germany.
Peter SinnDepartment of Pathology, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Zsuzsanna VargaInstitute of Surgical Pathology, Zurich University Hospital, 8091 Zurich, Switzerland.
Bettina SobottkaInstitute of Surgical Pathology, Zurich University Hospital, 8091 Zurich, Switzerland.
Lakis SotirisStratifyer Molecular Pathology GmbH, 50935 Cologne, Germany.
Florin-Andrei TaranDepartment of Women's Health, University Hospital Tübingen, 72076 Tübingen, Germany.
Christoph DomschkeDepartment of Gynecology and Obstetrics, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Andre HennigsDepartment of Gynecology and Obstetrics, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Sara Y BruckerResearch Institute for Women's Health, Tübingen University Hospital, 72076 Tübingen, Germany.
Christof SohnDepartment of Gynecology and Obstetrics, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Florian SchuetzDepartment of Gynecology and Obstetrics, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Andreas SchneeweissDepartment of Gynecology and Obstetrics, Heidelberg University Hospital, 69120 Heidelberg, Germany.
Markus WallwienerDepartment of Gynecology and Obstetrics, Heidelberg University Hospital, 69120 Heidelberg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biomarker changes between primary (PT) and metastatic tumor (MT) site may be significant in individualizing treatment strategies and can result from actual clonal evolution, biomarker conversion, or technical limitations of diagnostic tests. This study explored biomarker conversion during breast cancer (BC) progression in 67 patients with different tumor subtypes and metastatic sites via mRNA quantification and subsequently analyzed the concordance between real-time qPCR and immunohistochemistry (IHC). Immunostaining for estrogen receptor (ER), progesterone receptor (PR), HER2, and Ki-67 was performed on formalin-fixed, paraffin-embedded PT and MT tissue sections. RT-qPCR was performed using a multiplex RT-qPCR kit for

Indexed as

breast cancerimmunohistochemistryreal-time quantitative polymerase chain reactionreceptor conversiontumor biomarkers

Identifiers

PMID28881657
PMCPMC5584258

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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.