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Evaluation of the use and efficacy of (neo)adjuvant chemotherapy in angiosarcoma: a multicentre study.

dc.contributor.authorConstantinidou, Anastasia
dc.contributor.authorSauve, Nicolas
dc.contributor.authorStacchiotti, Silvia
dc.contributor.authorBlay, Jean-Yves
dc.contributor.authorVincenzi, Bruno
dc.contributor.authorGrignani, Giovanni
dc.contributor.authorRutkowski, Piotr
dc.contributor.authorGuida, Michele
dc.contributor.authorHindi, Nadia
dc.contributor.authorKlein, Alexander
dc.contributor.authorThibaud, Valentin
dc.contributor.authorSufliarsky, Jozef
dc.contributor.authorDesar, Ingrid
dc.contributor.authorSteeghs, Neeltje
dc.contributor.authorLitiere, Saskia
dc.contributor.authorGelderblom, Hans
dc.contributor.authorJones, Robin L
dc.date.accessioned2023-02-09T09:39:14Z
dc.date.available2023-02-09T09:39:14Z
dc.date.issued2020
dc.description.abstractAngiosarcomas constitute approximately 2% to 3% of all soft tissue sarcomas, are characterised by an aggressive clinical behaviour and poor outcome. Optimal management of localised angiosarcomas consists of complete surgical resection with or without radiation. However, due to the infiltrating nature of this disease, complete resection is often not possible. Despite optimal management, the outcome of patients with localised disease remains poor. The role of (neo)adjuvant chemotherapy in angiosarcomas remains undefined. The aim of this study is to document the outcome of patients treated with (neo)adjuvant chemotherapy and assess the feasibility of performing a prospective trial by evaluating the number of patients treated at sarcoma referral centres. A retrospective search within participating EORTC (European Organisation for Research and Treatment of Cancer) sites for patients treated with (neo)adjuvant chemotherapy was made. Patients treated between January 2007 and January 2016 were included. A total of 15 institutions participated and 86 patients were evaluable, 43 were treated with neoadjuvant, 27 with adjuvant chemotherapy and 16 with both. At the time of analysis, the median follow-up from diagnosis was 4.6 years. Median overall survival (OS) was 4.9 years (2.9 N) and the percentage alive at 4 years was 57.9 (45.5 to 68.4). The median disease-free survival was 1.4 years (0.9 to 1.7) and the percentage disease-free at 4 years was 26.8% (17.9 to 36.5). The outcome of angiosarcoma patients treated with (neo)adjuvant chemotherapy in this case series compares favourably with previously published data. Due to the aggressive nature of angiosarcoma, a prospective trial of neoadjuvant chemotherapy should be considered.
dc.identifier.doi10.1136/esmoopen-2020-000787
dc.identifier.essn2059-7029
dc.identifier.pmcPMC7451279
dc.identifier.pmid32847839
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7451279/pdf
dc.identifier.unpaywallURLhttps://doi.org/10.1136/esmoopen-2020-000787
dc.identifier.urihttp://hdl.handle.net/10668/16155
dc.issue.number4
dc.journal.titleESMO open
dc.journal.titleabbreviationESMO Open
dc.language.isoen
dc.organizationIBIS
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectadjuvant
dc.subjectangiosarcoma
dc.subjectangiosarcoma surgery
dc.subjectneoadjuvant
dc.subjectsarcoma chemotherapy
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshChemotherapy, Adjuvant
dc.subject.meshFemale
dc.subject.meshHemangiosarcoma
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshProspective Studies
dc.subject.meshRetrospective Studies
dc.subject.meshSarcoma
dc.titleEvaluation of the use and efficacy of (neo)adjuvant chemotherapy in angiosarcoma: a multicentre study.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number5
dspace.entity.typePublication

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