Evidence map›Paper›PMID 30633925›Full record

ReviewHuman pathology2019

New fusion sarcomas: histopathology and clinical significance of selected entities.

Markku Miettinen, Anna Felisiak-Golabek, Alejandro Luiña Contreras, John Glod, Rosandra N Kaplan, Jonathan Keith Killian, Jerzy Lasota

Open access · greenAbstract readReview
In one paragraph

Review in Human pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
9.4field-weighted citation impact, top 1% 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

43 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Small round cell sarcomas.Nature reviews. Disease primers · 2022
    Review
  14. Article
  15. Rapid and highly sensitive approach for multiplexed somatic fusion detection.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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

7 authors at 2 institutions in 1 country.

Markku MiettinenLaboratory of Pathology, National Cancer Institute, Bethesda 20892, MD. Electronic address: miettinenmm@mail.nih.gov.
Anna Felisiak-GolabekLaboratory of Pathology, National Cancer Institute, Bethesda 20892, MD.
Alejandro Luiña ContrerasJoint Pathology Center of the Armed Forces, Silver Spring 20910-1290, MD.
John GlodPediatric Oncology Branch, National Cancer Institute, Bethesda 20892, MD.
Rosandra N KaplanPediatric Oncology Branch, National Cancer Institute, Bethesda 20892, MD.
Jonathan Keith KillianGenetics Branch, NIH, Bethesda 20892, Maryland, and Foundation Medicine, Cambridge 02141, MA.
Jerzy LasotaLaboratory of Pathology, National Cancer Institute, Bethesda 20892, MD.
National Cancer Institute · USFoundation Medicine (United States)

Funding

Pediatric Oncology Branch Clinical Care and EducationZIEBC011516 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GLOD, JOHN · 2013 to 2025
$69.1M
Intramural NIH HHS Z99 CA999999Intramural NIH HHS ZIE BC011516
6 · The paper itself

Abstract

Many sarcomas contain gene fusions that can be pathogenetic mechanisms and diagnostic markers. In this article we review selected fusion sarcomas and techniques for their detection. CIC-DUX4 fusion sarcoma is a round cell tumor now considered an entity separate from Ewing sarcoma with a more aggressive clinical course, occurrence in older age, and predilection to soft tissues. It is composed of larger cells than Ewing sarcoma and often has prominent necrosis. Nuclear DUX4 expression is a promising immuno histochemical marker. BCOR-CCNB3 fusion sarcoma is cyclin B3-positive, usually occurs in bone or soft tissue of children, and may mimic a poorly differentiated synovial sarcoma. EWSR1-NFATC2 sarcoma may present in bone or soft tissue. It is typically composed of small round cells in a trabecular pattern in a myxoid matrix resembling myoepithelioma. ACTB-GLI1 fusion sarcoma may mimic a skin adnexal carcinoma, showing focal expression of epithelial markers and S100 protein. NTRK-fusion sarcomas include, in addition to infantile fibrosarcoma with ETV6-NTRK3 fusion, LMNA-NTRK1 fusion sarcoma, a low-grade spindle cell sarcoma seen in peripheral soft tissues in children and young adults. Methods to detect gene fusions include next-generation sequencing panels, anchored multiplex polymerase chain reaction systems to detect partner for a known fusion gene, and comprehensive RNA sequencing to detect virtually all gene fusions. In situ hybridization testing using probes for both fusion partners can be used as an alternative confirmation technique, especially in the absence of satisfactory RNA yield. In addition, fusion protein-related and other immunohistochemical markers can have a high specificity for fusion sarcomas.

Indexed as

HumansOncogene FusionOncogene Proteins, FusionSarcomaSoft Tissue NeoplasmsOncogene Proteins, FusionACTB-GLI1Anchored multiplex PCRBCOR-CCNB3CIC-DUX4EWSR1-NFATC2Fusion sarcomaLMNA-NTRK1

Identifiers

PMID30633925
PMCPMC7443750
OpenAlexW2909146604

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.