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dc.contributor.authorPignata, S.
dc.contributor.authorOza, A.
dc.contributor.authorHall, G.
dc.contributor.authorPardo, B.
dc.contributor.authorMadry, R.
dc.contributor.authorCibula, D.
dc.contributor.authorKlat, J.
dc.contributor.authorMontes, A.
dc.contributor.authorGlasspool, R.
dc.contributor.authorColombo, N.
dc.contributor.authorPete, I.
dc.contributor.authorHerrero, A.
dc.contributor.authorMarin, M. R.
dc.contributor.authorIlieva, R.
dc.contributor.authorTimcheva, C.
dc.contributor.authorBlakeley, C.
dc.contributor.authorTaylor, R.
dc.contributor.authorBarnicle, A.
dc.contributor.authorClamp, Andrew R
dc.date.accessioned2021-09-30T11:56:08Z
dc.date.available2021-09-30T11:56:08Z
dc.date.issued2021en
dc.identifier.citationPignata S, Oza A, Hall G, Pardo B, Madry R, Cibula D, et al. ORZORA: Maintenance olaparib in patients with platinum-sensitive relapsed ovarian cancer: outcomes by somatic and germline BRCA and other homologous recombination repair gene mutation status. Gynecologic Oncology. 2021 Aug;162:S29.en
dc.identifier.doi10.1016/S0090-8258(21)00700-9en
dc.identifier.urihttp://hdl.handle.net/10541/624625
dc.description.abstractObjectives: The Phase III SOLO2 trial (NCT01874353) showed the significant benefit of maintenance olaparib for patients (pts) with platinum-sensitive relapsed ovarian cancer (PSROC) and a BRCA mutation (BRCAm), compared with placebo (median progression-free survival [PFS] 19.1 vs 5.5 months [m], respectively); however, no pts had a confirmed somatic (s) BRCAm and data prospectively evaluating efficacy of olaparib in this pt group were limited. ORZORA (NCT02476968), an open-label, single-arm, multicenter trial, was conducted to assess efficacy and safety of maintenance olaparib in PSROC pts with a BRCAm (s or germline [g]) who were in response to their most recent platinum-based chemotherapy after ≥2 lines of treatment. Methods: Pts underwent prospective central screening for tumor BRCAm status (myChoice CDx, Myriad Genetic Laboratories, Inc.), then s or g BRCAm status was determined by central g testing (BRACAnalysis CDx, Myriad Genetic Laboratories, Inc.). Pts received maintenance olaparib (400 mg bid; capsules) until disease progression. Co-primary endpoints were investigator-assessed PFS (RECIST v1.1) in BRCAm and s cohorts, conducted at 60% maturity. Secondary endpoints included time to second progression or death (PFS2), health-related quality of life (HRQoL; FACT-O trial outcome index) and tolerability. An additional exploratory cohort comprised pts with predefined homologous recombination repair gene mutations (HRRm) excluding BRCAm (Foundatio CDx, Foundation Medicine, Inc.). Conclusions: PFS in pts with PSROC who received maintenance olaparib was similar irrespective of s or g BRCAm status. Activity of maintenance olaparib was also shown in pts with a non-BRCA HRRm. PFS, HRQoL and tolerability were consistent with previous olaparib studies in this population. Results highlight that PSROC pts beyond those with a gBRCAm can benefit from maintenance olaparib.en
dc.language.isoenen
dc.relation.urlhttps://dx.doi.org/10.1016/S0090-8258(21)00700-9en
dc.titleORZORA: Maintenance olaparib in patients with platinum-sensitive relapsed ovarian cancer: outcomes by somatic and germline BRCA and other homologous recombination repair gene mutation statusen
dc.typeOtheren
dc.contributor.departmentIstituto Nazionale Tumori ‘Fondazione G Pascale’, IRCCS, Napoli, Italy, Napoli, Italyen
dc.identifier.journalGynecologic Oncologyen
dc.description.noteen]


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