Evidence map›Paper›PMID 34324030›Full record

ArticleEuropean journal of orthopaedic surgery & traumatology : orthopedie traumatologie2021

Ewing family tumors of the appendicular skeleton: a retrospective analysis of prognostic factors.

Francesco Muratori, Lorenzo Foschi, Giuliana Roselli, Filippo Frenos, Angela Tamburini, Annarita Palomba, Daniela Greto, Mauro Loi, Giovanni Beltrami, Rodolfo Capanna and 2 more

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Article in European journal of orthopaedic surgery & traumatology : orthopedie traumatologie, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 86% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

12 authors at 4 institutions in 1 country.

Francesco MuratoriDepartment of Orthopaedic Oncology, Azienda Ospedaliera Universitaria Careggi, Largo Palagi 1, Firenze, Italy. fmuratori@inwind.it.ORCID http://orcid.org/0000-0002-8151-9247
Lorenzo FoschiDepartment of Orthopaedic Oncology, Azienda Ospedaliera Universitaria Careggi, Largo Palagi 1, Firenze, Italy.
Giuliana RoselliDepartment of Radiology, Azienda Ospedaliera Universitaria Careggi, Firenze, Italy.
Filippo FrenosDepartment of Orthopaedic Oncology, Azienda Ospedaliera Universitaria Careggi, Largo Palagi 1, Firenze, Italy.
Angela TamburiniDepartment of Paediatric Oncoematology, Azienda Ospedaliera Universitaria Meyer, Firenze, Italy.
Annarita PalombaDepartment of Pathology, Azienda Ospedaliera Universitaria Careggi, Firenze, Italy.
Daniela GretoDepartment of Radiotherapy, Azienda Ospedaliera Universitaria Careggi, Firenze, Italy.
Mauro LoiDepartment of Radiotherapy, Azienda Ospedaliera Universitaria Careggi, Firenze, Italy.
Giovanni BeltramiDepartment of Paediatric Orthopaedics, Azienda Ospedaliera Universitaria Meyer, Firenze, Italy.
Rodolfo CapannaOrthopaedic Clinic, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy.
Nicola MondanelliOrthopaedic Clinic, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
Domenico Andrea CampanacciDepartment of Orthopaedic Oncology, Azienda Ospedaliera Universitaria Careggi, Largo Palagi 1, Firenze, Italy.
Azienda Ospedaliero-Universitaria Careggi · ITMeyer Children's Hospital · ITAzienda Ospedaliera Universitaria Pisana · ITAzienda Ospedaliera Universitaria Senese · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAuthors retrospectively analyzed possible prognostic factors in a series of patients affected by Ewing sarcoma of extremities (eEWS) and treated over a 20-year period at a single institution.

methodsBetween 1997 and 2017, 88 bone eEWS were treated at our institution. Staging, age, gender, tumoral volume, local treatment, surgical margins, post-ChT necrosis were investigated for prognostic correlation with overall survival (OS) and event-free survival (EFS). Median follow-up was 74 months (1-236).

resultsStaging of disease correlated with OS (81% vs 59%, p = 0.01) and not with EFS (68% vs 57%, p = 0.28) in localized vs metastatic eEWS at presentation. Age ≥ 14 years (p = 0.002) and volume ≥ 100 cm3 (p = 0.04) were significant negative prognostic factors. No difference was found in local treatment: OS was 76% vs 63% (p = 0.33), while EFS was 68% vs 49% (p = 0.06) after surgery alone or surgery + radiotherapy, respectively. Regarding surgical margins, OS was 76% vs 38% (p = 0.14), and EFS was 65% vs 33% (p = 0.14) in adequate vs not adequate, respectively. OS was 86% and 68% in good and poor responders, respectively (p = 0.13).

conclusionIn eEWS, metastatic disease at presentation, age > 14 years and tumoral volume > 100 cm

Indexed as

Bone NeoplasmsSarcoma, EwingAdolescentCombined Modality TherapyHumansPrognosisRetrospective StudiesSkeletonAgeBone tumorEwing sarcomaMetastasisTumor volume

Identifiers

PMID34324030
OpenAlexW3184357462

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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.