Efficacy of niraparib by time of surgery and postoperative residual disease status: A post hoc analysis of patients in the PRIMA/ENGOT-OV26/GOG-3012 study

dc.contributor.authorO'Cearbhaill Roisin E.
dc.contributor.authorPérez-Fidalgo Jose-Alejandro
dc.contributor.authorMonk Bradley J.
dc.contributor.authorTusquets Ignacio
dc.contributor.authorMcCormick Colleen
dc.contributor.authorFuentes Jose
dc.contributor.authorMoore Richard G.
dc.contributor.authorVulsteke Christof
dc.contributor.authorShahin Mark S.
dc.contributor.authorForget Frédéric
dc.contributor.authorBradley William H.
dc.contributor.authorHietanen Sakari
dc.contributor.authorO'Malley David M.
dc.contributor.authorDørum Anne
dc.contributor.authorSlomovitz Brian M.
dc.contributor.authorBaumann Klaus
dc.contributor.authorSelle Frédéric
dc.contributor.authorCalvert Paula M.
dc.contributor.authorArtioli Gracia
dc.contributor.authorLevy Tally.
dc.contributor.authorKumar Aalok
dc.contributor.authorMalinowska Izabela A.
dc.contributor.authorLi Yong
dc.contributor.authorGupta Divya
dc.contributor.authorGonzález-Martín Antonio
dc.contributor.organizationfi=synnytys- ja naistentautioppi|en=Obstetrics and Gynaecology|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.74725736230
dc.converis.publication-id175559706
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/175559706
dc.date.accessioned2022-10-28T13:42:09Z
dc.date.available2022-10-28T13:42:09Z
dc.description.abstract<p><strong>Objective</strong><br>To evaluate the association between surgical timing and postoperative residual disease status on the efficacy of niraparib first-line maintenance therapy in patients with newly diagnosed advanced ovarian cancer at high risk of recurrence.</p><p><strong>Methods</strong><br>Post hoc analysis of the phase 3 PRIMA/ENGOT-OV26/GOG-3012 (NCT02655016) study of niraparib in patients with newly diagnosed primary advanced ovarian, primary peritoneal, or fallopian tube cancer with a complete/partial response to first-line platinum-based chemotherapy. Progression-free survival (PFS) was assessed by surgical status (primary debulking surgery [PDS] vs neoadjuvant chemotherapy/interval debulking surgery [NACT/IDS]) and postoperative residual disease status (no visible residual disease [NVRD] vs visible residual disease [VRD]) in the intent-to-treat population.</p><p><strong>Results</strong><br>In PRIMA (<em>N</em> = 733), 236 (32.2%) patients underwent PDS, and 481 (65.6%) received NACT/IDS before enrollment. Median PFS (niraparib vs placebo) and hazard ratios (95% CI) for progression were similar in PDS (13.7 vs 8.2 months; HR, 0.67 [0.47–0.96]) and NACT/IDS (14.2 vs 8.2 months; HR, 0.57 [0.44–0.73]) subgroups. In patients who received NACT/IDS and had NVRD (<em>n</em> = 304), the hazard ratio (95% CI) for progression was 0.65 (0.46–0.91). In patients with VRD following PDS (<em>n</em> = 183) or NACT/IDS (<em>n</em> = 149), the hazard ratios (95% CI) for progression were 0.58 (0.39–0.86) and 0.41 (0.27–0.62), respectively. PFS was not evaluable for patients with PDS and NVRD because of sample size (<em>n</em> = 37).</p><p><strong>Conclusions</strong><br>In this post hoc analysis, niraparib efficacy was similar across PDS and NACT/IDS subgroups. Patients who had NACT/IDS and VRD had the highest reduction in the risk of progression with niraparib maintenance.</p>
dc.format.pagerange36
dc.format.pagerange43
dc.identifier.jour-issn0090-8258
dc.identifier.olddbid183734
dc.identifier.oldhandle10024/166828
dc.identifier.urihttps://www.utupub.fi/handle/11111/41067
dc.identifier.urlhttps://doi.org/10.1016/j.ygyno.2022.04.012
dc.identifier.urnURN:NBN:fi-fe2022081154620
dc.language.isoen
dc.okm.affiliatedauthorHietanen, Sakari
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3123 Gynaecology and paediatricsen_GB
dc.okm.discipline3126 Surgery, anesthesiology, intensive care, radiologyen_GB
dc.okm.discipline3123 Naisten- ja lastentauditfi_FI
dc.okm.discipline3126 Kirurgia, anestesiologia, tehohoito, radiologiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherAcademic Press Inc.
dc.publisher.countryNetherlandsen_GB
dc.publisher.countryAlankomaatfi_FI
dc.publisher.country-codeNL
dc.relation.doi10.1016/j.ygyno.2022.04.012
dc.relation.ispartofjournalGynecologic Oncology
dc.relation.issue1
dc.relation.volume166
dc.source.identifierhttps://www.utupub.fi/handle/10024/166828
dc.titleEfficacy of niraparib by time of surgery and postoperative residual disease status: A post hoc analysis of patients in the PRIMA/ENGOT-OV26/GOG-3012 study
dc.year.issued2022

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