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Patient-reported outcomes in patients with a germline BRCA mutation and HER2-negative metastatic breast cancer receiving olaparib versus chemotherapy in the OlympiAD trial

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dc.contributor.authorRobson, Mark-
dc.contributor.authorRuddy, Kathryn J.-
dc.contributor.authorIm, Seock-Ah-
dc.contributor.authorSenkus, Elzbieta-
dc.contributor.authorXu, Binghe-
dc.contributor.authorDomchek, Susan M.-
dc.contributor.authorMasuda, Norikazu-
dc.contributor.authorLi, Wei-
dc.contributor.authorTung, Nadine-
dc.contributor.authorArmstrong, Anne-
dc.contributor.authorDelaloge, Suzette-
dc.contributor.authorBannister, Wendy-
dc.contributor.authorGoessl, Carsten-
dc.contributor.authorDegboe, Arnold-
dc.contributor.authorHettle, Robert-
dc.contributor.authorConte, Pierfranco-
dc.date.accessioned2022-03-22T09:10:30Z-
dc.date.available2022-03-22T09:10:30Z-
dc.date.created2019-11-25-
dc.date.created2019-11-25-
dc.date.issued2019-10-
dc.identifier.citationEuropean Journal of Cancer, Vol.120, pp.20-30-
dc.identifier.issn0959-8049-
dc.identifier.other86814-
dc.identifier.urihttps://hdl.handle.net/10371/177197-
dc.description.abstractBackground: The phase III OlympiAD study (NCT02000622) showed a statistically significant progression-free survival benefit with olaparib versus chemotherapy treatment of physician's choice (TPC) in patients with a germline BRCA mutation and human epidermal growth factor receptor 2-negative metastatic breast cancer. From this study, we report the effect of olaparib on health-related quality of life (HRQoL). Methods: Patients were randomised 2:1 to olaparib monotherapy (300 mg twice daily) or single-agent TPC. The primary HRQoL end-point was mean change from baseline in the two-item global health status/QoL score determined from patient-completed European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30-item module (EORTC QLQ-C30) questionnaires and assessed using a mixed model for repeated measures. Symptoms and functioning domains, best overall response and time to deterioration of QoL were also evaluated. Results: Overall questionnaire compliance rates were 93.2% for olaparib and 76.3% for TPC. Between-treatment global health status/QoL comparison showed a significant improvement in the olaparib arm versus the TPC arm, with mean change of 3.9 (standard deviation 1.2) versus -3.6 (2.2), a difference of 7.5 points (95% confidence interval [CI]: 2.48, 12.44; P = 0.0035). A higher proportion of patients in the olaparib arm showed a best overall response of 'improvement' in global health status/QoL (33.7% vs 13.4%). Median time to global health status/QoL deterioration was not reached in olaparib patients and was 15.3 months for TPC patients (hazard ratio: 0.44 [95% CI: 0.25, 0.77]; P = 0.004). For EORTC QLQ-C30 symptoms and functioning subscales, only nausea/vomiting symptom score was worse in the olaparib arm than in the TPC arm (across all visits compared with baseline). Conclusion: HRQoL was consistently improved for patients treated with olaparib, compared with chemotherapy TPC. (C) 2019 The Authors. Published by Elsevier Ltd.-
dc.language영어-
dc.publisherPergamon Press Ltd.-
dc.titlePatient-reported outcomes in patients with a germline BRCA mutation and HER2-negative metastatic breast cancer receiving olaparib versus chemotherapy in the OlympiAD trial-
dc.typeArticle-
dc.contributor.AlternativeAuthor임석아-
dc.identifier.doi10.1016/j.ejca.2019.06.023-
dc.citation.journaltitleEuropean Journal of Cancer-
dc.identifier.wosid000487253300003-
dc.identifier.scopusid2-s2.0-85070926015-
dc.citation.endpage30-
dc.citation.startpage20-
dc.citation.volume120-
dc.identifier.sci000487253300003-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorIm, Seock-Ah-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusEUROPEAN-ORGANIZATION-
dc.subject.keywordPlusGUIDELINES-
dc.subject.keywordAuthorOlaparib-
dc.subject.keywordAuthorOlympiAD-
dc.subject.keywordAuthorHealth-related quality of life-
dc.subject.keywordAuthorEORTC QLQ-C30-
dc.subject.keywordAuthorBreast cancer-
dc.subject.keywordAuthorBRCA-
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  • Department of Medicine
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