Evidence map›Paper›PMID 29135520›Full record

ArticleThe American journal of surgical pathology2018

Epithelial-Myoepithelial Carcinoma: Frequent Morphologic and Molecular Evidence of Preexisting Pleomorphic Adenoma, Common HRAS Mutations in PLAG1-intact and HMGA2-intact Cases, and Occasional TP53, FBXW7, and SMARCB1 Alterations in High-grade Cases.

Soufiane El Hallani, Aaron M Udager, Diana Bell, Isabel Fonseca, Lester D R Thompson, Adel Assaad, Abbas Agaimy, Alyssa M Luvison, Caitlyn Miller, Raja R Seethala and 1 more

Abstract read
In one paragraph

Article in The American journal of surgical pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
7.7field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 100 citations in OpenAlex.

  1. Pooled it
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  5. Oncocytic salivary gland carcinomas.Histology and histopathology · 2026
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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

11 authors at 7 institutions in 3 countries.

Soufiane El HallaniDepartment of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA.
Aaron M UdagerDepartment of Pathology, Michigan Medicine, Ann Arbor, MI.
Diana BellDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Isabel FonsecaPathological Anatomy Institute, Faculdade de Medicina, Universidade de Lisboa & Serviço de Anatomia Patológica, Instituto Português de Oncologia Francisco Gentil, Lisboa, Portugal.
Lester D R ThompsonDepartment of Pathology, Southern California Permanente Medical Group, Woodland Hills, CA.
Adel AssaadDepartment of Pathology, Virginia Mason Hospital, Seattle, WA.
Abbas AgaimyInstitute of Pathology, University Hospital, Erlangen, Germany.
Alyssa M LuvisonDepartment of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA.
Caitlyn MillerDepartment of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA.
Raja R SeethalaDepartment of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA.
Simion ChioseaDepartment of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA.
University of Pittsburgh Medical Center · USMichigan Medicine · USThe University of Texas MD Anderson Cancer Center · USUniversitätsklinikum Erlangen · DEUniversity of Lisbon · PTVirginia Mason Medical Center · USWoodland Hills Medical Center · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOHN C. BYRD · 1988 to 2026
$158.0M
WILD TYPE P53-BASED ADJUVANT IMMUNOTHERAPY FOR SCCHNP50CA097190 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Greg M. Delgoffe · 2004 to 2026
$49.6M
NCI NIH HHS P30 CA047904NCI NIH HHS P50 CA097190
6 · The paper itself

Abstract

We hypothesized that there is a relationship between the preexisting pleomorphic adenoma [PA]), histologic grade of epithelial-myoepithelial carcinomas (EMCAs), and genetic alterations. EMCAs (n=39) were analyzed for morphologic and molecular evidence of preexisting PA (PLAG1, HMGA2 status by fluorescence in situ hybridization, FISH, and FGFR1-PLAG1 fusion by next-generation sequencing, NGS). Twenty-three EMCAs were further analyzed by NGS for mutations and copy number variation in 50 cancer-related genes. On the basis of combined morphologic and molecular evidence of PA, the following subsets of EMCA emerged: (a) EMCAs with morphologic evidence of preexisting PA, but intact PLAG1 and HMGA2 (12/39, 31%), (b) Carcinomas with PLAG1 alterations (9/39, 23%), or (c) HMGA2 alterations (10/39, 26%), and (d) de novo carcinomas, without morphologic or molecular evidence of PA (8/39, 21%). Twelve high-grade EMCAs (12/39, 31%) occurred across all subsets. The median disease-free survival was 80 months (95% confidence interval, 77-84 mo). Disease-free survival and other clinicopathologic parameters did not differ by the above defined subsets. HRAS mutations were more common in EMCAs with intact PLAG1 and HMGA2 (7/9 vs. 1/14, P<0.001). Other genetic abnormalities (TP53 [n=2], FBXW7 [n=1], SMARCB1 deletion [n=1]) were seen only in high-grade EMCAs with intact PLAG1 and HMGA2. We conclude that most EMCAs arose ex PA (31/39, 80%) and the genetic profile of EMCA varies with the absence or presence of preexisting PA and its cytogenetic signature. Progression to higher grade EMCA with intact PLAG1 and HMGA2 correlates with the presence of TP53, FBXW7 mutations, or SMARCB1 deletion.

Indexed as

MutationAdenoma, PleomorphicAdultAgedAged, 80 and overBiomarkers, TumorDisease-Free SurvivalDNA-Binding ProteinsF-Box-WD Repeat-Containing Protein 7FemaleFollow-Up StudiesHMGA2 ProteinHumansIn Situ Hybridization, FluorescenceMaleMiddle AgedBiomarkers, TumorDNA-Binding ProteinsF-Box-WD Repeat-Containing Protein 7FBXW7 protein, humanHMGA2 ProteinHRAS protein, humanPLAG1 protein, humanProto-Oncogene Proteins p21(ras)SMARCB1 ProteinSMARCB1 protein, humanTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID29135520
PMCPMC6530789
OpenAlexW2770994361

What OpenQuestion holds

Textmetadata
LicenceTDM
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.