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.author | O'Cearbhaill Roisin E. | |
| dc.contributor.author | Pérez-Fidalgo Jose-Alejandro | |
| dc.contributor.author | Monk Bradley J. | |
| dc.contributor.author | Tusquets Ignacio | |
| dc.contributor.author | McCormick Colleen | |
| dc.contributor.author | Fuentes Jose | |
| dc.contributor.author | Moore Richard G. | |
| dc.contributor.author | Vulsteke Christof | |
| dc.contributor.author | Shahin Mark S. | |
| dc.contributor.author | Forget Frédéric | |
| dc.contributor.author | Bradley William H. | |
| dc.contributor.author | Hietanen Sakari | |
| dc.contributor.author | O'Malley David M. | |
| dc.contributor.author | Dørum Anne | |
| dc.contributor.author | Slomovitz Brian M. | |
| dc.contributor.author | Baumann Klaus | |
| dc.contributor.author | Selle Frédéric | |
| dc.contributor.author | Calvert Paula M. | |
| dc.contributor.author | Artioli Gracia | |
| dc.contributor.author | Levy Tally. | |
| dc.contributor.author | Kumar Aalok | |
| dc.contributor.author | Malinowska Izabela A. | |
| dc.contributor.author | Li Yong | |
| dc.contributor.author | Gupta Divya | |
| dc.contributor.author | González-Martín Antonio | |
| dc.contributor.organization | fi=synnytys- ja naistentautioppi|en=Obstetrics and Gynaecology| | |
| dc.contributor.organization | fi=tyks, vsshp|en=tyks, varha| | |
| dc.contributor.organization-code | 1.2.246.10.2458963.20.74725736230 | |
| dc.converis.publication-id | 175559706 | |
| dc.converis.url | https://research.utu.fi/converis/portal/Publication/175559706 | |
| dc.date.accessioned | 2022-10-28T13:42:09Z | |
| dc.date.available | 2022-10-28T13:42:09Z | |
| 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.pagerange | 36 | |
| dc.format.pagerange | 43 | |
| dc.identifier.jour-issn | 0090-8258 | |
| dc.identifier.olddbid | 183734 | |
| dc.identifier.oldhandle | 10024/166828 | |
| dc.identifier.uri | https://www.utupub.fi/handle/11111/41067 | |
| dc.identifier.url | https://doi.org/10.1016/j.ygyno.2022.04.012 | |
| dc.identifier.urn | URN:NBN:fi-fe2022081154620 | |
| dc.language.iso | en | |
| dc.okm.affiliatedauthor | Hietanen, Sakari | |
| dc.okm.affiliatedauthor | Dataimport, tyks, vsshp | |
| dc.okm.discipline | 3123 Gynaecology and paediatrics | en_GB |
| dc.okm.discipline | 3126 Surgery, anesthesiology, intensive care, radiology | en_GB |
| dc.okm.discipline | 3123 Naisten- ja lastentaudit | fi_FI |
| dc.okm.discipline | 3126 Kirurgia, anestesiologia, tehohoito, radiologia | fi_FI |
| dc.okm.internationalcopublication | international co-publication | |
| dc.okm.internationality | International publication | |
| dc.okm.type | A1 ScientificArticle | |
| dc.publisher | Academic Press Inc. | |
| dc.publisher.country | Netherlands | en_GB |
| dc.publisher.country | Alankomaat | fi_FI |
| dc.publisher.country-code | NL | |
| dc.relation.doi | 10.1016/j.ygyno.2022.04.012 | |
| dc.relation.ispartofjournal | Gynecologic Oncology | |
| dc.relation.issue | 1 | |
| dc.relation.volume | 166 | |
| dc.source.identifier | https://www.utupub.fi/handle/10024/166828 | |
| dc.title | 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.year.issued | 2022 |
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