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dc.contributor.authorBenson, C
dc.contributor.authorRay-Coquard, I
dc.contributor.authorSleijfer, S
dc.contributor.authorLitière, S
dc.contributor.authorBlay, J-Y
dc.contributor.authorLe Cesne, A
dc.contributor.authorPapai, Z
dc.contributor.authorJudson, I
dc.contributor.authorSchöffski, P
dc.contributor.authorChawla, S
dc.contributor.authorGil, T
dc.contributor.authorPiperno-Neumann, S
dc.contributor.authorMarréaud, S
dc.contributor.authorDewji, MR
dc.contributor.authorvan der Graaf, WTA
dc.date.accessioned2016-12-12T13:42:19Z
dc.date.issued2016-07
dc.identifier.citationGynecologic oncology, 2016, 142 (1), pp. 89 - 94
dc.identifier.issn0090-8258
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/324
dc.identifier.eissn1095-6859
dc.identifier.doi10.1016/j.ygyno.2016.03.024
dc.description.abstractBackground Uterine sarcomas are a group of mesenchymal tumours comprising several histologies. They have a high recurrence rate following surgery, modest outcome to systemic therapy, and poor overall survival. Pazopanib is a multi-targeted tyrosine kinase inhibitor approved for non-adipocytic advanced soft tissue sarcomas (STS). Here we investigated whether response to pazopanib in patients with uterine sarcomas differs from that of patients with non-uterine sarcomas.Patients and methods Uterine sarcoma patients were retrieved from all soft tissue sarcoma patients treated with pazopanib in EORTC Phase II (n=10) and Phase III (PALETTE) (n=34) studies. Patient and tumour characteristics, response, progression free and overall survival data were compared.Results Forty-four patients with uterine sarcoma were treated with pazopanib. The majority of patients had uterine leiomyosarcoma (LMS) (n=39, 88.6%) with high grade tumours (n=37, 84.1%) compared to 54.8% (n=164) in the non-uterine population. The median age was 55years (range 33-79) and median follow up was 2.3years. Uterine patients were heavily pre-treated, 61.3% having ≥2 lines of chemotherapy prior to pazopanib compared to 40.8% in the non-uterine population. Five patients (11%), all LMS, had a partial response (95% CI 3.8-24.6). Median progression free survival (PFS) 3.0months (95% CI 2.5-4.7) in uterine versus 4.5 (95% CI 3.7-5.1) in non-uterine STS. Median overall survival (OS) was 17.5months (95% CI 11.1-19.6), longer than the non-uterine population, 11.1months (95% CI 10.2-12.0) (p=0.352).Conclusions Despite heavy pre-treatment, pazopanib shows signs of activity in patients with uterine sarcoma with the similar outcomes to patients with non-uterine STS.
dc.formatPrint-Electronic
dc.format.extent89 - 94
dc.languageeng
dc.language.isoeng
dc.subjectHumans
dc.subjectLeiomyosarcoma
dc.subjectSarcoma
dc.subjectUterine Neoplasms
dc.subjectSulfonamides
dc.subjectPyrimidines
dc.subjectProtein Kinase Inhibitors
dc.subjectPrognosis
dc.subjectSurvival Rate
dc.subjectRetrospective Studies
dc.subjectAdolescent
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectMiddle Aged
dc.subjectFemale
dc.subjectYoung Adult
dc.titleOutcome of uterine sarcoma patients treated with pazopanib: A retrospective analysis based on two European Organisation for Research and Treatment of Cancer (EORTC) Soft Tissue and Bone Sarcoma Group (STBSG) clinical trials 62043 and 62072.
dc.typeJournal Article
dcterms.dateAccepted2016-03-18
rioxxterms.versionofrecord10.1016/j.ygyno.2016.03.024
rioxxterms.licenseref.startdate2016-07
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfGynecologic oncology
pubs.issue1
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical and Translational Sarcoma
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Sarcoma Clinical Trials
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical and Translational Sarcoma
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Sarcoma Clinical Trials
pubs.publication-statusPublished
pubs.volume142
pubs.embargo.termsNot known
icr.researchteamClinical and Translational Sarcomaen_US
icr.researchteamSarcoma Clinical Trialsen_US
dc.contributor.icrauthorvan der Graaf, Wilhelmina
dc.contributor.icrauthorJudson, Ian


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