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dc.contributor.authorGronchi, Alesandroes_ES
dc.contributor.authorStacchiotti, Silviaes_ES
dc.contributor.authorVerderio, P.es_ES
dc.contributor.authorFerrari, Stefanoes_ES
dc.contributor.authorMartín-Broto, Javieres_ES
dc.contributor.authorLópez-Pousa, Antonioes_ES
dc.contributor.authorLlombart-Bosch, Antonioes_ES
dc.contributor.authorDei Tos, Angelo Paoloes_ES
dc.contributor.authorCollini, Paolaes_ES
dc.contributor.authorCruz Jurado, Josefinaes_ES
dc.contributor.authorDe Paoli, A.es_ES
dc.contributor.authorDonati, Davide Maríaes_ES
dc.contributor.authorPoveda, A.es_ES
dc.contributor.authorQuagliuolo, V.es_ES
dc.contributor.authorComandone, A.es_ES
dc.contributor.authorGrignani, Giovannies_ES
dc.contributor.authorMorosi, Carloes_ES
dc.contributor.authorMessina, A.es_ES
dc.contributor.authorDe Sanctis, R.es_ES
dc.contributor.authorBottelli, S.es_ES
dc.contributor.authorPalassini, Elenaes_ES
dc.contributor.authorCasali, Paolo G.es_ES
dc.contributor.authorPicci, Pieroes_ES
dc.date.accessioned2019-05-29T09:31:31Z-
dc.date.available2019-05-29T09:31:31Z-
dc.date.issued2016-12-
dc.identifier.citationAnnals of Oncology 27(12): 2283-2288 (2016)es_ES
dc.identifier.issn0923-7534-
dc.identifier.urihttp://hdl.handle.net/10261/182741-
dc.description.abstract[Background] To report on long-term results of a phase 3 trial comparing three versus five cycles of adjuvant chemotherapy (CT) with full-dose epirubicin+ifosfamide in high-risk soft tissue sarcomas (STS).es_ES
dc.description.abstract[Methods] Patients (pts) were randomized to receive three preoperative cycles of epirubicin 120 mg/m2 and ifosfamide 9 g/m2 (Arm A) or to receive the same three preoperative cycles plus two postoperative cycles (Arm B). Radiotherapy could be either delivered in the preoperative or in the postoperative setting. Non-inferiority of the primary end point, OS, was assessed by the confidence interval of the hazard ratio (HR; Arm A/Arm B) derived from Cox model.es_ES
dc.description.abstract[Results] Between January 2002 and April 2007, 164 pts were assigned to arm A and 164 to arm B. At a median follow-up (FU) of 117 months (IQ range 103–135 months), 123 deaths were recorded: 58 in Arm A and 65 in Arm B. Ten-year OS was 61% for the entire group of patients: 64% in Arm A and 59% in Arm B. The intention-to-treat analysis confirmed that three cycles were not inferior to five cycles (one-sided 95% upper confidence limit was 1.24). A per protocol analysis was consistent with these results. Pts with leiomyosarcoma and undifferentiated pleomorphic sarcoma (UPS) had the lowest, and the highest response rates, respectively. Consistently, Leiomyosarcoma and UPS had the worse and the best prognosis, respectively.es_ES
dc.description.abstract[Conclusions] At a longer FU, the non-inferiority of three cycles of a full-dose conventional CT in comparison to five is confirmed. Response to therapy is also confirmed to be associated with better survival. This regimen is currently tested within an ongoing international trial against three cycles of a neoadjuvant histology-tailored CT (ClinicalTrials.gov Identifier: NCT01710176).es_ES
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.rightsclosedAccesses_ES
dc.subjectSarcomaes_ES
dc.subjectSoft tissue sarcomaes_ES
dc.subjectAdjuvant chemotherapyes_ES
dc.subjectResponsees_ES
dc.subjectQuality of surgeryes_ES
dc.subjectSurvivales_ES
dc.titleShort, full-dose adjuvant chemotherapy (CT) in high-risk adult soft tissue sarcomas (STS): long-term follow-up of a randomized clinical trial from the Italian Sarcoma Group and the Spanish Sarcoma Groupes_ES
dc.typeartículoes_ES
dc.identifier.doi10.1093/annonc/mdw430-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1093/annonc/mdw430es_ES
dc.identifier.e-issn1569-8041-
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
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