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dc.creatorKyriazoglou A., Bagos P.en
dc.date.accessioned2023-01-31T08:47:54Z
dc.date.available2023-01-31T08:47:54Z
dc.date.issued2021
dc.identifier10.1080/0284186X.2021.1890818
dc.identifier.issn0284186X
dc.identifier.urihttp://hdl.handle.net/11615/75598
dc.description.abstractIntroduction: BCOR rearranged sarcomas comprise a group of malignant mesenchymal tumors that until recently were classified as Ewing sarcomas or as undifferentiated round cell sarcomas. The identification of alterations involving BCOR gene such as BCOR-CCNB3, BCOR-MAML3, ZC3H7B-BCOR fusion genes and BCOR internal tandem duplication (ITD) is characteristic for the differential diagnosis of BCOR rearranged sarcomas. Due to the rarity of these tumors there is no consensus or guidelines regarding the optimal therapeutic algorithm, that clinicians should follow. Patients and methods: Herein we have conducted a meta-analysis of the current reports dealing with the therapeutic approach of BCOR rearranged sarcomas. Results: Meta-analysis of the 57 eligible cases from 10 studies resulted to similar Incidence Rate Ratio (IRR) and overall survival (OS) for patients who received Ewing protocols and non-Ewing oriented treatment. Further similar death rate was reported for both strategies (non-Ewing 20% Vs Ewing 21.8%). Conclusion: Our data support that non-Ewing treatment strategy can be considered a safe option, being at least equal to Ewing protocols. The current study provides a hint toward the optimal therapeutic approach of BCOR rearranged sarcomas. Further, the present study challenges the use of the term Ewing-like sarcomas, since the current literature supports that BCOR rearranged sarcomas deserve their own distinct classification in terms of genetics, pathology and therapy. © 2021 Acta Oncologica Foundation.en
dc.language.isoenen
dc.sourceActa Oncologicaen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85101618671&doi=10.1080%2f0284186X.2021.1890818&partnerID=40&md5=528314669d782da7bb86d49c1522718b
dc.subjectantineoplastic agenten
dc.subjectcisplatinen
dc.subjectcyclophosphamideen
dc.subjectdactinomycinen
dc.subjectdoxorubicinen
dc.subjectepirubicinen
dc.subjectifosfamideen
dc.subjectmethotrexateen
dc.subjectnedaplastinen
dc.subjectunclassified drugen
dc.subjectvincristineen
dc.subjectBCOR protein, humanen
dc.subjectoncoproteinen
dc.subjectrepressor proteinen
dc.subjecttumor markeren
dc.subjectadolescenten
dc.subjectageden
dc.subjectantineoplastic protocolen
dc.subjectArticleen
dc.subjectBCOR rearranged sarcomaen
dc.subjectBCOR rearranged sarcomaen
dc.subjectbone canceren
dc.subjectcancer chemotherapyen
dc.subjectcancer geneticsen
dc.subjectcancer localizationen
dc.subjectcancer mortalityen
dc.subjectcancer radiotherapyen
dc.subjectcancer stagingen
dc.subjectcancer surgeryen
dc.subjectcancer survivalen
dc.subjectcancer therapyen
dc.subjectchilden
dc.subjectEwing sarcomaen
dc.subjectfemaleen
dc.subjectfusion geneen
dc.subjectgene identificationen
dc.subjectgene rearrangementen
dc.subjecthumanen
dc.subjectincidenceen
dc.subjectinfanten
dc.subjectintermethod comparisonen
dc.subjectmaleen
dc.subjectmeta analysisen
dc.subjectmetastasisen
dc.subjectmortality rateen
dc.subjectneoadjuvant chemotherapyen
dc.subjectoncogeneen
dc.subjectosteosarcomaen
dc.subjectoverall survivalen
dc.subjectpatient safetyen
dc.subjectqualitative analysisen
dc.subjectsarcomaen
dc.subjectsex differenceen
dc.subjectsoft tissue canceren
dc.subjecttumor biopsyen
dc.subjectgeneticsen
dc.subjectsoft tissue tumoren
dc.subjectBiomarkers, Tumoren
dc.subjectHumansen
dc.subjectProto-Oncogene Proteinsen
dc.subjectRepressor Proteinsen
dc.subjectSarcomaen
dc.subjectSoft Tissue Neoplasmsen
dc.subjectTaylor and Francis Ltd.en
dc.titleMeta-analysis of BCOR rearranged sarcomas: challenging the therapeutic approachen
dc.typejournalArticleen


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