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Short, 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 Group.

dc.contributor.authorGronchi, A
dc.contributor.authorStacchiotti, S
dc.contributor.authorVerderio, P
dc.contributor.authorFerrari, S
dc.contributor.authorMartin Broto, J
dc.contributor.authorLopez-Pousa, A
dc.contributor.authorLlombart-Bosch, A
dc.contributor.authorDei Tos, A P
dc.contributor.authorCollini, P
dc.contributor.authorJurado, J Cruz
dc.contributor.authorDe Paoli, A
dc.contributor.authorDonati, D M
dc.contributor.authorPoveda, A
dc.contributor.authorQuagliuolo, V
dc.contributor.authorComandone, A
dc.contributor.authorGrignani, G
dc.contributor.authorMorosi, C
dc.contributor.authorMessina, A
dc.contributor.authorDe Sanctis, R
dc.contributor.authorBottelli, S
dc.contributor.authorPalassini, E
dc.contributor.authorCasali, P G
dc.contributor.authorPicci, Piero
dc.date.accessioned2023-01-25T08:37:55Z
dc.date.available2023-01-25T08:37:55Z
dc.date.issued2016-10-11
dc.description.abstractTo 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). 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. 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. 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).
dc.identifier.doi10.1093/annonc/mdw430
dc.identifier.essn1569-8041
dc.identifier.pmid27733375
dc.identifier.unpaywallURLhttps://doi.org/10.1093/annonc/mdw430
dc.identifier.urihttp://hdl.handle.net/10668/10530
dc.issue.number12
dc.journal.titleAnnals of oncology : official journal of the European Society for Medical Oncology
dc.journal.titleabbreviationAnn Oncol
dc.language.isoen
dc.organizationIBIS
dc.page.number2283-2288
dc.pubmedtypeJournal Article
dc.pubmedtypeRandomized Controlled Trial
dc.rights.accessRightsopen access
dc.subjectadjuvant chemotherapy
dc.subjectquality of surgery
dc.subjectresponse
dc.subjectsarcoma
dc.subjectsoft tissue sarcoma
dc.subjectsurvival
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshChemotherapy, Adjuvant
dc.subject.meshDisease-Free Survival
dc.subject.meshFemale
dc.subject.meshFollow-Up Studies
dc.subject.meshHumans
dc.subject.meshLeiomyosarcoma
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshPrognosis
dc.subject.meshRisk Factors
dc.subject.meshSarcoma
dc.subject.meshTreatment Outcome
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 Group.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number27
dspace.entity.typePublication

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