Evidence map›Paper›PMID 30116888›Full record

ArticleVirchows Archiv : an international journal of pathology2018

Immunohistochemical and selected genetic reflex testing of all uterine leiomyosarcomas and STUMPs for ALK gene rearrangement may provide an effective screening tool in identifying uterine ALK-rearranged mesenchymal tumors.

Nikola Ptáková, Markéta Miesbauerová, Ján Kosťun, Petr Grossmann, Henrieta Šidlová, Jaroslav Pavelka, Jiří Presl, Reza Alaghehbandan, Jiří Bouda, Ondrej Ondič

Abstract read
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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 14 citations in OpenAlex.

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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

10 authors at 4 institutions in 3 countries.

Nikola PtákováDepartment of Pathology, Medical Faculty Pilsen, Charles University Prague and Charles University Hospital Pilsen, 304 60, Pilsen, Czech Republic.
Markéta MiesbauerováDepartment of Pathology, Medical Faculty Pilsen, Charles University Prague and Charles University Hospital Pilsen, 304 60, Pilsen, Czech Republic.
Ján KosťunDepartment of Gynecology and Obstetrics, Medical Faculty Pilsen, Charles University Prague and Charles University Hospital Pilsen, Pilsen, Czech Republic.
Petr GrossmannDepartment of Pathology, Medical Faculty Pilsen, Charles University Prague and Charles University Hospital Pilsen, 304 60, Pilsen, Czech Republic.
Henrieta ŠidlováCytopathos, s.r.o, Bratislava, Slovak Republic.
Jaroslav PavelkaBioptická laboratoř, s.r.o, Pilsen, Czech Republic.
Jiří PreslDepartment of Gynecology and Obstetrics, Medical Faculty Pilsen, Charles University Prague and Charles University Hospital Pilsen, Pilsen, Czech Republic.
Reza AlaghehbandanDepartment of Pathology, Royal Columbian Hospital, University of British Columbia, Vancouver, BC, Canada.
Jiří BoudaDepartment of Gynecology and Obstetrics, Medical Faculty Pilsen, Charles University Prague and Charles University Hospital Pilsen, Pilsen, Czech Republic.
Ondrej OndičDepartment of Pathology, Medical Faculty Pilsen, Charles University Prague and Charles University Hospital Pilsen, 304 60, Pilsen, Czech Republic. ondic@medima.cz.ORCID http://orcid.org/0000-0002-4038-5641
Charles University · CZBiopticka Laborator (Czechia) · CZRoyal Columbian Hospital · CASlovak Medical University · SK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We examined the value of targeted molecular screening for the identification of uterine anaplastic lymphoma kinase (ALK)-rearranged mesenchymal tumors, including ALK immunohistochemistry followed by molecular genetic testing, in all uterine leiomyosarcomas and STUMPs (smooth muscle tumors of uncertain malignant potential). All leiomyosarcoma and STUMP cases diagnosed in a 10-year period (2006-2016) at Charles University Faculty of Medicine in Pilsen were retrieved and reviewed. Of 23 cases, one case (LMS [leiomyosarcoma]) was positive for ALK rearrangement, namely, PPP1CB-ALK fusion gene. No specific histologic features (i.e., lymphocytic infiltrate and stromal edema) were observed in this case. This suggests that inflammatory myofibroblastic tumor (IMT)-like histologic features may not be an initial reliable screening tool in identifying uterine IMT cases. Thus, we proposed a two-step IHC and molecular genetic testing (as a reflex test) for IMT in all uterine LMS and STUMP cases. This will enhance the proper detection of such tumors at the population level and ultimately offer patients available targeted therapies.

Indexed as

Gene RearrangementAnaplastic Lymphoma KinaseBiomarkers, TumorFemaleGenetic TestingHumansImmunohistochemistryLeiomyosarcomaReceptor Protein-Tyrosine KinasesRetrospective StudiesSmooth Muscle TumorUterine NeoplasmsALK protein, humanAnaplastic Lymphoma KinaseBiomarkers, TumorReceptor Protein-Tyrosine KinasesALKIMTLeiomyosarcomaMolecular geneticsSTUMP

Identifiers

PMID30116888
OpenAlexW2887232130

What OpenQuestion holds

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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.