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dc.creatorDramis A., Grimer R.J., Malizos K., Tillman R.M., Jeys L., Carter S.R.en
dc.date.accessioned2023-01-31T07:36:59Z
dc.date.available2023-01-31T07:36:59Z
dc.date.issued2016
dc.identifier.issn00016462
dc.identifier.urihttp://hdl.handle.net/11615/71213
dc.description.abstractWe are reporting our experience on patients with pelvic Ewing's Sarcoma treated in our unit. We retrospectively reviewed a series of patients with non-metastatic pelvic Ewing's sarcoma treated between 1977 and 2009. Patients were classifed into three groups according to the local treatment received: Group 1. radiotherapy-chemo; Group 2. surgery-chemo and Group 3. radiotherapy-surgery-chemo. Recurrence free and overall survival rates were calculated using the Kaplan-Meier method. In?uence of various factors (age at diagnosis, gender, tumour site and size, chemotherapy response, surgical margins and type of treatment) on survival was assessed with a logistic regression model. A total of 85 patients were treated with a mean follow-up of 65.8 months and mean tumour volume of 435ml. The 5-year survival for all patients was 40.7% decreased to 36.2% at 10 years. A signifcant prognostic factor identifed was chemotherapy response only. There was a trend for improved survival and local control rates for patients who had chemotherapy and surgery and the results were apparent for all tumours irrespective of size but not statistically signifcant. Currently, the optimal management of pelvic Ewing's sarcoma is controversial but our study shows a trend for improved survival for patients treated with chemotherapy and surgery. © 2016, Acta Orthopedica Belgica.en
dc.language.isoenen
dc.sourceActa Orthopaedica Belgicaen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84990032729&partnerID=40&md5=3b29d8d10a4604ba22dcd49a036ba91c
dc.subjectadolescenten
dc.subjectadulten
dc.subjectBone Neoplasmsen
dc.subjectchilden
dc.subjectdisease free survivalen
dc.subjectfemaleen
dc.subjecthumanen
dc.subjectKaplan Meier methoden
dc.subjectmaleen
dc.subjectmiddle ageden
dc.subjectmortalityen
dc.subjectmultimodality cancer therapyen
dc.subjectpathologyen
dc.subjectpelvic girdleen
dc.subjectpreschool childen
dc.subjectretrospective studyen
dc.subjectSarcoma, Ewingen
dc.subjecttumor recurrenceen
dc.subjectyoung adulten
dc.subjectAdolescenten
dc.subjectAdulten
dc.subjectBone Neoplasmsen
dc.subjectChilden
dc.subjectChild, Preschoolen
dc.subjectCombined Modality Therapyen
dc.subjectDisease-Free Survivalen
dc.subjectFemaleen
dc.subjectHumansen
dc.subjectKaplan-Meier Estimateen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectNeoplasm Recurrence, Localen
dc.subjectPelvic Bonesen
dc.subjectRetrospective Studiesen
dc.subjectSarcoma, Ewingen
dc.subjectYoung Adulten
dc.subjectARSMB-KVBMGen
dc.titleNon-Metastatic Pelvic Ewing's Sarcoma: Oncologic outcomes and evaluation of prognostic factorsen
dc.typejournalArticleen


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