Full metadata record
DC Field | Value | Language |
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dc.creator | González-Martín, A. (Antonio) | - |
dc.creator | Oza, A.M. (Amit M.) | - |
dc.creator | Embleton, A.C. (Andrew C.) | - |
dc.creator | Pfisterer, J. (Jacobus) | - |
dc.creator | Ledermann, J.A. (Jonathan A.) | - |
dc.creator | Pujade-Lauraine, E. (Eric) | - |
dc.creator | Kristensen, G. (Gunnar) | - |
dc.creator | Bertrand, M.A. (Monique A.) | - |
dc.creator | Beale, P. (Philip) | - |
dc.creator | Cervantes, A. (Andrés) | - |
dc.creator | Kent, E. (Emma) | - |
dc.creator | Kaplan, R.S. (Richard S.) | - |
dc.creator | Parmar, M.K.B. (Mahesh K.B.) | - |
dc.creator | Scotto, N. (Nana) | - |
dc.creator | Perren, T.J. (Timothy J.) | - |
dc.creator | ICON7 investigators | - |
dc.date.accessioned | 2021-09-09T12:24:36Z | - |
dc.date.available | 2021-09-09T12:24:36Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | González-Martín, A. (Antonio); Oza, A.M. (Amit M.); Embleton, A.C. (Andrew C.); et al. "Exploratory outcome analyses according to stage and/or residual disease in the ICON7 trial of carboplatin and paclitaxel with or without bevacizumab for newly diagnosed ovarian cancer". Gynecologic Oncology. 152 (1), 2019, 53 - 60 | es_ES |
dc.identifier.issn | 0090-8258 | - |
dc.identifier.other | PMID: 30449719 | - |
dc.identifier.uri | https://hdl.handle.net/10171/61979 | - |
dc.description.abstract | Objective: In the randomized phase 3 ICON7 trial (ISRCTN91273375), adding bevacizumab to chemotherapy for newly diagnosed ovarian cancer significantly improved progression-free survival (PFS; primary endpoint) but not overall survival (OS; secondary endpoint) in the intent-to-treat (ITT) population. We explored treatment effect according to stage and extent of residual disease. Methods: Patients with stage IIB-IV or high-risk (grade 3/clear-cell) stage I-IIA ovarian cancer were randomized to receive six cycles of carboplatin and paclitaxel either alone or with bevacizumab 7.5 mg/kg every 3 weeks followed by single-agent bevacizumab for 12 further cycles (total duration 12 months). Post hoc exploratory analyses of subgroups defined by stage and extent of residual disease at diagnosis within the stage IIIB-IV population (European indication) was performed. Results: The PFS benefit from bevacizumab was seen consistently in all subgroups explored. The PFS hazard ratio was 0.77 (95% confidence interval [CI], 0.59-0.99) in 411 patients with stage IIIB-IV ovarian cancer with no visible residuum and 0.81 (95% CI, 0.69-0.95) in 749 patients with stage IIIB-IV disease and visible residuum. As in the ITT population, no OS difference was detected in any subgroup except the previously described 'high-risk' subgroup. Safety results in analyzed subgroups were consistent with the overall population. Conclusions: Adding bevacizumab to front-line chemotherapy improves PFS irrespective of stage/residual disease. In patients with stage III with >1 cm residuum, stage IV or inoperable disease, this translates into an OS benefit. No OS benefit or detriment was seen in other subgroups explored. | es_ES |
dc.description.sponsorship | The ICON7 trial was sponsored by the Medical Research Council (MRC) and supported by the National Institute for Health Research through the UK National Cancer Research Network, the MRC, and F. Hoffmann-La Roche. Funding for third-party writing assistance for this manuscript was provided by F. Hoffmann-La Roche Ltd, Basel, Switzerland. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | Elsevier BV | es_ES |
dc.rights | info:eu-repo/semantics/openAccess | es_ES |
dc.subject | Materias Investigacion::Ciencias de la Salud::Oncología | es_ES |
dc.subject | Bevacizumab | es_ES |
dc.subject | Ovarian cancer | es_ES |
dc.subject | Residual disease | es_ES |
dc.subject | Cytoreductive surgery | es_ES |
dc.title | Exploratory outcome analyses according to stage and/or residual disease in the ICON7 trial of carboplatin and paclitaxel with or without bevacizumab for newly diagnosed ovarian cancer | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.description.note | This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). Dataset disponible en: info:eu-repo/semantics/dataset/doi/10.1016/j.ygyno.2018.08.036 | es_ES |
dc.identifier.doi | 10.1016/j.ygyno.2018.08.036 | - |
dadun.citation.endingPage | 60 | es_ES |
dadun.citation.number | 1 | es_ES |
dadun.citation.publicationName | Gynecologic Oncology | es_ES |
dadun.citation.startingPage | 53 | es_ES |
dadun.citation.volume | 152 | es_ES |
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