Evidence map›Paper›PMID 32599807›Full record

ReviewCancers2020

Primary and Metastatic Intracranial Ewing Sarcoma at Diagnosis: Retrospective International Study and Systematic Review.

Lianne M Haveman, Andreas Ranft, Henk van den Berg, Stephanie Klco-Brosius, Ruth Ladenstein, Michael Paulussen, Heribert Juergens, Uta Dirksen, Johannes H M Merks

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Primary Intracranial Ewing Sarcoma WithBrain tumor research and treatment · 2023
    Article
  13. Review
  14. Article
  15. Article
  16. 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

9 authors at 6 institutions in 3 countries.

Lianne M HavemanPrincess Maxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.ORCID 0000-0001-8519-8906
Andreas RanftDepartment of Pediatric Hematology and Oncology, University Children's Hospital of Essen, Center of Pediatric Oncology. 45122 Essen, Germany.
Henk van den BergDepartment of Pediatric Oncology, Academic Medical Center, Emma Children's Hospital, 1105 AZ Amsterdam, The Netherlands.
Stephanie Klco-BrosiusDepartment of Pediatric Hematology and Oncology, University Children's Hospital of Essen, Center of Pediatric Oncology. 45122 Essen, Germany.
Ruth LadensteinChildren's Cancer Research Institute, 1090 Vienna, Austria.
Michael PaulussenVestische Kinder- und Jugendklinik, Witten/Herdecke University, 45711 Datteln, Germany.
Heribert JuergensDepartment of Pediatric Hematology and Oncology, University Children's Hospital, 48149 Muenster, Germany.
Uta DirksenDepartment of Pediatric Hematology and Oncology, University Children's Hospital of Essen, Center of Pediatric Oncology. 45122 Essen, Germany.
Johannes H M MerksPrincess Maxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Essen University Hospital · DEPrincess Máxima Center · NLAmsterdam UMC Location University of Amsterdam · NLSt Anna Children's Hospital · ATUniversity Hospital Münster · DEWitten/Herdecke University · DE

Funding

Deutsche Krebshilfe (DKH) 108128
6 · The paper itself

Abstract

Intracranial Ewing sarcoma (EwS) is rare and publications on primary or metastatic intracranial EwS are minimal. The aim of this study was to describe incidence, clinical behavior, treatment, and factors associated with outcome in patients with primary intracranial EwS or patients with a primary extracranial EwS and cerebral metastases at diagnosis. We reviewed all patients with primary or with metastatic intracranial EwS at diagnosis registered in the International Clinical Trial Euro-E.W.I.N.G.99 (EE99). In total, 17 of 1435 patients (1.2%) presented with primary intracranial EwS; 3 of them had metastatic disease. Four patients (0.3%) with primary extracranial EwS presented with intracranial metastatic lesions. The 3-year event-free survival (EFS) was 64% and overall survival (OS) was 70% in patients with a primary intracranial EwS. Local control in patients with primary intracranial EwS consisted of surgery (6%), radiotherapy (RT) (18%), or both modalities (76%). Univariate analysis showed that patients < 15 years of age had significantly better outcome (EFS: 72%; OS: 76%) compared to those aged above 15 years (EFS: 13%; OS: 25%). In conclusion, primary intracranial EwS and extracranial EwS with cerebral metastases at diagnosis is rare, yet survival is comparable with local and metastatic EwS elsewhere in the body. Age and stage of disease are important prognostic factors. Besides chemotherapeutic treatment, local control with surgical resection combined with RT is recommended whenever feasible.

Indexed as

Ewing sarcomaintracranialmetastaticoutcome

Identifiers

PMID32599807
PMCPMC7352789
OpenAlexW3037009138

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.