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dc.contributor.authorJones, Robin Lewisen
dc.contributor.authorConstantinidou, Anastasiaen
dc.contributor.authorOlmos, Daviden
dc.contributor.authorThway, K.en
dc.contributor.authorFisher, Cyrilen
dc.contributor.authorAl-Muderis, Omaren
dc.contributor.authorScurr, Michelle R.en
dc.contributor.authorJudson, Ian Roberten
dc.creatorJones, Robin Lewisen
dc.creatorConstantinidou, Anastasiaen
dc.creatorOlmos, Daviden
dc.creatorThway, K.en
dc.creatorFisher, Cyrilen
dc.creatorAl-Muderis, Omaren
dc.creatorScurr, Michelle R.en
dc.creatorJudson, Ian Roberten
dc.date.accessioned2018-06-22T09:53:42Z
dc.date.available2018-06-22T09:53:42Z
dc.date.issued2012
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41979
dc.description.abstractBackground: Epithelioid sarcoma is a rare soft tissue sarcoma subtype. The response of this disease to chemotherapy is not well described. The aim of this study was to investigate the response rate and progression-free survival in a series of epithelioid sarcoma patients treated with chemotherapy at a single referral center. Methods: A retrospective search of a prospectively maintained database was made to identify epithelioid sarcoma patients treated with chemotherapy between 1990 and 2009. Radiological response and histological diagnosis were re-reviewed for this study. Results: Twenty-one epithelioid sarcoma patients treated with chemotherapy were identified; follow-up data on palliative chemotherapy was available on 20 of these patients. The median age was 36.5 years (range, 17.4 to 64.8 y) and the male/female ratio was 19:2. Ten patients (50%) were treated with single-agent anthracycline, 9 patients (45%) were treated with a combination therapy (anthracycline and ifosfamide), and 1 patient received trabectedin (5%). Three patients achieved a partial response, 12 had stable disease, and 5 progressed. The median progression-free survival was 29 weeks (95% confidence interval [CI]: 23-35). Seven and 3 patients received second-line and third-line palliative chemotherapy, respectively. The median overall survival from commencing palliative chemotherapy in our series was 51 weeks (95% confidence interval; 29-73). Conclusions: Systemic chemotherapy provides satisfactory palliation in patients with epithelioid sarcoma. However, this is an aggressive disease, responses to chemotherapy are of short duration and there is a need for more effective novel therapies in the treatment of this condition. Copyright © 2012 by Lippincott Williams & Wilkins.en
dc.language.isoengen
dc.sourceAmerican Journal of Clinical Oncology: Cancer Clinical Trialsen
dc.subjectChemotherapyen
dc.subjectEpithelioid sarcomaen
dc.subjectResponse rateen
dc.subjectTime to progressionen
dc.titleRole of palliative chemotherapy in advanced epithelioid sarcomaen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1097/COC.0b013e3182118cf7
dc.description.volume35
dc.description.issue4
dc.description.startingpage351
dc.description.endingpage357
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidConstantinidou, Anastasia [0000-0001-5316-7574]
dc.contributor.orcidJudson, Ian Robert [0000-0002-4766-5304]
dc.gnosis.orcid0000-0001-5316-7574
dc.gnosis.orcid0000-0002-4766-5304


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