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Published in: Clinical and Translational Oncology 10/2019

01-10-2019 | Ewing's Sarcoma | Research Article

Prognostic factors and survival in Ewing’s sarcoma treated by limb salvage surgery

Authors: J. Alvarez-SanNicolas, I. Gracia-Alegria, L. Trullols-Tarrago, A. Peiro-Ibañez, C. Lamas-Gomez

Published in: Clinical and Translational Oncology | Issue 10/2019

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Abstract

Purpose

Survival in Ewing’s sarcoma (ES) has increased with the use of chemotherapy. Surgical techniques such as limb salvage (LS) have been developed. Survival and adverse events have been widely studied in general series of ES, but there are few specific series of ES cases treated by LS, despite this being the most commonly used (surgical) approach. The aim of this study was to determine survival and prognostic factors in ES patients undergoing LS.

Patients and methods

We analysed all ES patients treated between January 1984 and May 2008 and selected all those treated by systemic multimodal therapy and LS. We assessed the influence of patient characteristics, tumour parameters and therapeutic results in event-free survival (EFS).

Results

Ninety patients were included. Fifty of them were treated by systemic multimodal therapy and locally by LS. ean age was 20 years. Overall survival (OS) was 68.8% and EFS was 60.6% at years. In the univariate analysis, pelvic location, age and response to chemotherapy were associated with poor prognosis. After multivariate analysis, poor response to treatment, pelvis location and age between 12 and 17 years were found to be independent prognostic factors. Dissemination at diagnosis was not a prognostic factor.

Conclusions

OS and EFS in ES treated by LS were similar to findings in previous ES studies. factors are no different, except for the presence of metastasis at diagnosis.
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Metadata
Title
Prognostic factors and survival in Ewing’s sarcoma treated by limb salvage surgery
Authors
J. Alvarez-SanNicolas
I. Gracia-Alegria
L. Trullols-Tarrago
A. Peiro-Ibañez
C. Lamas-Gomez
Publication date
01-10-2019
Publisher
Springer International Publishing
Published in
Clinical and Translational Oncology / Issue 10/2019
Print ISSN: 1699-048X
Electronic ISSN: 1699-3055
DOI
https://doi.org/10.1007/s12094-019-02067-1

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