Literature DB >> 30217290

Extraskeletal versus Skeletal Ewing Sarcoma in the adult population: Controversies in care.

Andrew D Lynch1, Faiz Gani1, Christian F Meyer1, Carol D Morris1, Nita Ahuja1, Fabian M Johnston2.   

Abstract

BACKGROUND AND OBJECTIVES: A lack of consensus exists on the prognosis of extraskeletal Ewing sarcoma (EES) relative to its skeletal (ES) counterpart in adults. This study sought to characterize outcome differences between the two diagnoses.
METHODS: From 2004 to 2014, the NCDB identified 2,660 Ewing Sarcoma patients. Cox proportional hazards regression analysis was used to identify risk factors for overall survival (OS).
RESULTS: EES patients were older, more likely to be female, and have smaller tumors. Among patients with ES, 4.0% received no treatment, 2.5% received local therapy only (surgery and/or radiation), 16.8% received chemotherapy only, while 52.2% received combination therapy (local and chemotherapy), and 17.0% recieived triple therapy (surgery, radiation and chemotherapy). Among patients with EES, 4.3% recived no treatment, 5.6% received local therapy only, 15.6% received chemotherapy only, while 47.0% received combination therapy, and 21.6% received triple therapy. No difference in OS was observed between the two groups (P = 0.816). Factors independently associated with OS for ES included age (HR = 1.26, P = 0.01), Charlson-Deyo Score (CDS) ≥2 (HR = 3.66, P < 0.001), combination therapy (HR = 0.39, P < 0.001) and triple therapy (HR = 0.34, P < 0.001). For EES, factors for OS were age (HR = 1.52, P < 0.001), CDS ≥2 (HR = 1.90, P = 0.02), combination therapy (HR = 0.44, P < 0.001), triple therapy (HR = 0.34, P < 0.001) and PNET histology (HR = 1.33, P = 0.02).
CONCLUSIONS: Demographic, histological, and treatment characteristics differ between adult patients diagnosed with ES and ESS. However, survival and independent predictors of survival are consistent between the two diagnoses.
Copyright © 2018 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  National cancer database; Soft tissue sarcoma; Surgical oncology

Mesh:

Year:  2018        PMID: 30217290     DOI: 10.1016/j.suronc.2018.05.016

Source DB:  PubMed          Journal:  Surg Oncol        ISSN: 0960-7404            Impact factor:   3.279


  6 in total

1.  Intramedullary, periosteal, and extraskeletal Ewing sarcomas: retrospective study of a series of 126 cases in a reference center.

Authors:  F Violon; R Burns; F Mihoubi; V Audard; D Biau; A Feydy; F Larousserie
Journal:  Skeletal Radiol       Date:  2022-02-18       Impact factor: 2.199

2.  A Visualized Dynamic Prediction Model for Lymphatic Metastasis in Ewing's Sarcoma for Smart Medical Services.

Authors:  Wenle Li; Chan Xu; Zhaohui Hu; Shengtao Dong; Haosheng Wang; Qiang Liu; Zhi-Ri Tang; Wanying Li; Bing Wang; Zhi Lei; Chengliang Yin
Journal:  Front Public Health       Date:  2022-05-04

3.  Comorbidities rather than older age define outcome in adult patients with tumors of the Ewing sarcoma family.

Authors:  Jana Käthe Striefler; Maren Schmiester; Franziska Brandes; Anne Dörr; Stefan Pahl; David Kaul; Daniel Rau; Eva-Maria Dobrindt; Georgios Koulaxouzidis; Lars Bullinger; Sven Märdian; Anne Flörcken
Journal:  Cancer Med       Date:  2022-03-16       Impact factor: 4.711

4.  Extraskeletal Ewing sarcoma: A case report.

Authors:  Siham Nasri; Ranya Aqamour; Leila Haddar; Imane Guerrouj; Karim Haddar; Narjisse Aichouni; Imane Kamaoui; Imane Skiker
Journal:  Radiol Case Rep       Date:  2022-10-06

5.  Extraskeletal Ewing's sarcoma: outcomes and CT features of endoceliac lesions.

Authors:  Zeyang Chen; Yang Jiao; Zining Liu; Jiejin Yang; Jiali Sun; Pengyuan Wang
Journal:  Transl Cancer Res       Date:  2021-09       Impact factor: 1.241

Review 6.  Primary Extra-Osseous Ewing Sarcoma of the Thyroid: A Case Report and Review of the Literature.

Authors:  Amanda H Seipel; Hiba Mechahougui; Nicolas Mach; Frédéric Triponez; William C Faquin; Claudio De Vito
Journal:  Head Neck Pathol       Date:  2021-07-26
  6 in total

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