Evidence map›Paper›PMID 33141488›Full record

ArticleBrain pathology (Zurich, Switzerland)2021

Intracranial mesenchymal tumor with FET-CREB fusion-A unifying diagnosis for the spectrum of intracranial myxoid mesenchymal tumors and angiomatoid fibrous histiocytoma-like neoplasms.

Emily A Sloan, Jason Chiang, Javier E Villanueva-Meyer, Sanda Alexandrescu, Jennifer M Eschbacher, Wesley Wang, Manuela Mafra, Nasir Ud Din, Emily Carr-Boyd, Michael Watson and 23 more

Open access · hybridAbstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

53 citing papers in PubMed, 81 citations in OpenAlex.

  1. Non-Meningothelial Mesenchymal Tumor of the Central Nervous System: Case Report and Literature Review.Neuropathology : official journal of the Japanese Society of Neuropathology · 2026
    Review
  2. Article
  3. Article
  4. Angiomatoid fibrous histiocytoma: a review.Journal of pathology and translational medicine · 2026
    Article
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  6. Article
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  15. Immunohistochemical evaluation of CREM in CREB-rearranged mesenchymal tumors and their mimics.Virchows Archiv : an international journal of pathology · 2025
    Article
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  17. Article
  18. Review
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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

33 authors at 13 institutions in 5 countries.

Emily A SloanDepartment of Pathology, University of California, San Francisco, San Francisco, CA, USA.
Jason ChiangDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0003-3623-8996
Javier E Villanueva-MeyerDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, CA, USA.
Sanda AlexandrescuDepartment of Pathology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Jennifer M EschbacherDepartment of Neuropathology, Barrow Neurological Institute, St Joseph's Hospital and Medical Center, Phoenix, AZ, USA.
Wesley WangDepartment of Pathology, The Ohio State University, Columbus, OH, USA.ORCID 0000-0001-7904-9015
Manuela MafraDepartment of Pathology, The Portuguese Institute of Oncology, Lisbon, Portugal.
Nasir Ud DinSection of Histopathology, Department of Pathology and Laboratory Medicine, Aga Khan University Hospital, Karachi, Pakistan.
Emily Carr-BoydDepartment of Histopathology, ADHB LabPlus, Auckland, New Zealand.
Michael WatsonDepartment of Histopathology, ADHB LabPlus, Auckland, New Zealand.
Michael PunsoniDepartment of Pathology, University of Nebraska Medical Center, Omaha, NE, USA.
Angelica OviedoDepartment of Anatomic Pathology, Dalhousie University, Halifax, Nova Scotia, Canada.
Ahmed GilaniDepartment of Pathology, University of Colorado, Aurora, CO, USA.
Bette K Kleinschmidt-DeMastersDepartment of Pathology, University of Colorado, Aurora, CO, USA.
Dylan J CossDivision of Neuropathology, University of Virginia Health System, Charlottesville, VA, USA.
M Beatriz LopesDivision of Neuropathology, University of Virginia Health System, Charlottesville, VA, USA.
Corey RaffelDepartment of Neurological Surgery, University of California, San Francisco, CA, USA.
Mitchel S BergerDepartment of Neurological Surgery, University of California, San Francisco, CA, USA.
Susan M ChangDivision of Neuro-Oncology, Department of Neurological Surgery, University of California, San Francisco, CA, USA.
Alyssa ReddyDivision of Neuro-Oncology, Department of Neurological Surgery, University of California, San Francisco, CA, USA.
Biswarathan RamaniDepartment of Pathology, University of California, San Francisco, San Francisco, CA, USA.
Sean P FerrisDepartment of Pathology, University of California, San Francisco, San Francisco, CA, USA.
Julieann C LeeDepartment of Pathology, University of California, San Francisco, San Francisco, CA, USA.ORCID 0000-0003-0138-4862
Jeffrey W HofmannDepartment of Pathology, University of California, San Francisco, San Francisco, CA, USA.
Soo-Jin ChoDepartment of Pathology, University of California, San Francisco, San Francisco, CA, USA.
Andrew E HorvaiDepartment of Pathology, University of California, San Francisco, San Francisco, CA, USA.
Melike PekmezciDepartment of Pathology, University of California, San Francisco, San Francisco, CA, USA.ORCID 0000-0003-2548-8359
Tarik TihanDepartment of Pathology, University of California, San Francisco, San Francisco, CA, USA.
Andrew W BollenDepartment of Pathology, University of California, San Francisco, San Francisco, CA, USA.
Fausto J RodriguezDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID 0000-0001-8662-1219
David W EllisonDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN, USA.ORCID 0000-0003-1239-7757
Arie PerryDepartment of Pathology, University of California, San Francisco, San Francisco, CA, USA.
David A SolomonDepartment of Pathology, University of California, San Francisco, San Francisco, CA, USA.ORCID 0000-0003-4571-7999
University of California, San Francisco · USAuckland District Health Board · NZSt. Jude Children's Research Hospital · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Virginia Health System · USAga Khan University Hospital · PKBarrow Neurological Institute · USBoston Children's Hospital · USDalhousie University · CAInstituto Português de Oncologia Francisco Gentil · PTJohns Hopkins University · USNebraska Medical Center · USThe Ohio State University · US

Funding

Cohesin gene mutations in tumorigenesisDP5OD021403 · OD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SOLOMON, DAVID A. · 2015 to 2019
$2.0M
NIH HHS DP5 OD021403
6 · The paper itself

Abstract

Intracranial mesenchymal tumors with FET-CREB fusions are a recently described group of neoplasms in children and young adults characterized by fusion of a FET family gene (usually EWSR1, but rarely FUS) to a CREB family transcription factor (ATF1, CREB1, or CREM), and have been variously termed intracranial angiomatoid fibrous histiocytoma or intracranial myxoid mesenchymal tumor. The clinical outcomes, histologic features, and genomic landscape are not well defined. Here, we studied 20 patients with intracranial mesenchymal tumors proven to harbor FET-CREB fusion by next-generation sequencing (NGS). The 16 female and four male patients had a median age of 14 years (range 4-70). Tumors were uniformly extra-axial or intraventricular and located at the cerebral convexities (n = 7), falx (2), lateral ventricles (4), tentorium (2), cerebellopontine angle (4), and spinal cord (1). NGS demonstrated that eight tumors harbored EWSR1-ATF1 fusion, seven had EWSR1-CREB1, four had EWSR1-CREM, and one had FUS-CREM. Tumors were uniformly well circumscribed and typically contrast enhancing with solid and cystic growth. Tumors with EWSR1-CREB1 fusions more often featured stellate/spindle cell morphology, mucin-rich stroma, and hemangioma-like vasculature compared to tumors with EWSR1-ATF1 fusions that most often featured sheets of epithelioid cells with mucin-poor collagenous stroma. These tumors demonstrated polyphenotypic immunoprofiles with frequent positivity for desmin, EMA, CD99, MUC4, and synaptophysin, but absence of SSTR2A, myogenin, and HMB45 expression. There was a propensity for local recurrence with a median progression-free survival of 12 months and a median overall survival of greater than 60 months, with three patients succumbing to disease (all with EWSR1-ATF1 fusions). In combination with prior case series, this study provides further insight into intracranial mesenchymal tumors with FET-CREB fusion, which represent a distinct group of CNS tumors encompassing both intracranial myxoid mesenchymal tumor and angiomatoid fibrous histiocytoma-like neoplasms.

Indexed as

AdolescentAdultAgedBiomarkers, TumorBrain NeoplasmsChildChild, PreschoolFemaleGene FusionHistiocytoma, Benign FibrousHistiocytoma, Malignant FibrousHumansMaleMiddle AgedOncogene Proteins, FusionYoung AdultBiomarkers, TumorOncogene Proteins, Fusionangiomatoid fibrous histiocytoma (AFH)brain tumorCREBEWSR1intracranial myxoid mesenchymal tumormolecular neuropathologysarcoma

Identifiers

PMID33141488
PMCPMC8089120
OpenAlexW3096208378

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.