Evidence map›Paper›PMID 35443099›Full record

ArticleGenes, chromosomes & cancer2022

Ewing sarcoma and related FET family translocation-associated round cell tumors: A century of clinical and scientific progress.

Robert G Maki, Patrick J Grohar, Cristina R Antonescu

Abstract read
In one paragraph

Article in Genes, chromosomes & cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Molecular basis of EWS interdomain self-association and its role in condensate formation.Protein science : a publication of the Protein Society · 2025
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. A cruel invasion of Ewing's sarcoma of the skull: A rare case report.International journal of surgery case reports · 2023
    Article
  8. Article
  9. Small round cell sarcomas.Nature reviews. Disease primers · 2022
    Review
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

3 authors.

Robert G MakiAbramson Cancer Center, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.ORCID 0000-0002-9853-2528
Patrick J GroharDivision of Oncology, Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Cristina R AntonescuDepartment of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.ORCID 0000-0002-9717-8205

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Targeting Oncogenic Pathways in Genetically Complex SarcomasP50CA217694 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Marc Ladanyi · 2018 to 2026
$21.5M
SPORE in Soft Tissue SarcomaP50CA140146 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SINGER, SAMUEL · 2010 to 2014
$11.1M
Development of Trabectedin Analogs that Target the EWS-FLI1 Transcription FactorR01CA188314 · NCI · VAN ANDEL RESEARCH INSTITUTE · PI GROHAR, PATRICK J · 2015 to 2019
$2.0M
A collaborative approach to analyze and target the EWS-FLI1 transcription factor in patients with Ewing sarcomaU01CA236220 · NCI · SARC · PI GROHAR, PATRICK J · 2019 to 2023
$2.0M
NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA140146NCI NIH HHS P50 CA217694NCI NIH HHS R01 CA188314NCI NIH HHS U01 CA236220
6 · The paper itself

Abstract

The year 2021 marked the centenary of the first publication of a cancer termed diffuse endothelioma of bone by James Ewing. Its unique features were apparent even in the first case series he described. This new diagnosis was clearly distinct from osteogenic sarcoma and myeloma, which were already well recognized at the time. We undertake this summary to better understanding Ewing sarcoma, contrasting the logarithmic evolution of the standard of care of systemic therapy for this and related diagnoses to the exponential understanding of the molecular biology of this family of tumors. We also outline in this manuscript how the finding of genomic relatives within Ewing sarcoma itself and related tumors, first noted nearly 40 years ago, helps us appreciate the need to find therapeutic plans that are specific for each small round blue cell tumor subtype. The advent of next generation sequencing regarding previously unknown small round blue cell tumor subtypes in many ways puts us back in the shoes of James Ewing in 1921, searching anew for clues leading to better treatments for increasingly rare cancer subsets.

Indexed as

SarcomaSarcoma, EwingBiomarkers, TumorHumansMaleOncogene Proteins, FusionTranslocation, GeneticBiomarkers, TumorOncogene Proteins, FusionBCOR::CCNB3CIC::DUX4Ewing sarcomaFET sarcomasmall round cell tumorsystemic therapytranslocation

Identifiers

PMID35443099
PMCPMC9197982

What Socratic 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 Socratic graph.