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dc.creatorSánchez-Lorenzo, M. L. (María Luisa)-
dc.creatorYubero, A. (Alfonso)-
dc.creatorBarquín, A. (Aranzazu)-
dc.creatorEstévez, P. (Purificación)-
dc.creatorPajares, B. (Bella)-
dc.creatorReche, P. (Piedad)-
dc.creatorAlarcón, J. (Jesús)-
dc.creatorCalzas, J. (Julia)-
dc.creatorGaba, L. (Lydia)-
dc.creatorFuentes, J.A. (José Antonio)-
dc.creatorSantaballa, A. (Ana)-
dc.creatorSalvador, C. (Carmen)-
dc.creatorManso, L. (Luis)-
dc.creatorHerrero, A.B. (Ana B.)-
dc.creatorTaus, A. (Álvaro)-
dc.creatorMárquez, R. (Raúl)-
dc.creatorMadani, J. (Julia)-
dc.creatorMerino, M. (María)-
dc.creatorMarquina, G. (Gloria)-
dc.creatorCasado, V. (Victoria)-
dc.creatorConstenla, M. (Manuel)-
dc.creatorGutiérrez, M. (María)-
dc.creatorDosil, A. (Alba)-
dc.creatorGonzález-Martín, A. (Antonio)-
dc.date.accessioned2024-02-08T12:23:45Z-
dc.date.available2024-02-08T12:23:45Z-
dc.date.issued2022-
dc.identifier.citationSánchez-Lorenzo, M. L. (María Luisa); Yubero, A. (Alfonso); Barquín, A. (Aranzazu); et al. "Rucaparib in recurrent ovarian cancer: real-world experience from the rucaparib early access programme in Spain – A GEICO study". BMC Cancer. 22 (1150), 2022, 1 - 10es_ES
dc.identifier.urihttps://hdl.handle.net/10171/68919-
dc.description.abstractBackground: Rucaparib is a poly(ADP-ribose) polymerase inhibitor approved in Europe as maintenance therapy for recurrent platinum-sensitive (Pt-S) ovarian cancer (OC). The Rucaparib Access Programme (RAP) was designed to provide early access to rucaparib for the above-mentioned indication, as well as for patients with BRCA-mutated Pt-S or platinum-resistant (Pt-R) OC and no therapeutic alternatives. Methods: In this observational, retrospective study we analysed the efficacy and safety of rucaparib within the RAP in Spain. Hospitals associated with the Spanish Ovarian Cancer Research Group (GEICO) recruited patients with high-grade epithelial ovarian, fallopian tube, or primary peritoneal cancer treated with rucaparib 600 mg twice daily as maintenance or treatment (Pt-S/Pt-R) in the RAP. Baseline characteristics, efficacy, and safety data were collected. Results: Between July 2020 and February 2021, 51 patients treated in 22 hospitals in the RAP were included in the study. Eighteen patients with a median of 3 (range, 1–6) prior treatment lines received rucaparib as maintenance; median progression-free survival (PFS) for this group was 9.1 months (95% confidence interval [CI], 4.2–11.6 months). Among 33 patients (median 5 [range, 1–9] prior treatment lines) who received rucaparib as treatment, 7 and 26 patients had Pt-S and Pt-R disease, respectively. Median PFS was 10.6 months (95% CI, 2.5 months-not reached) in the Pt-S group and 2.2 months (95% CI, 1.1–3.2 months) in the Pt-R group. Grade ≥ 3 treatment-emergent adverse events were reported in 39% of all patients, the most common being anaemia (12% and 15% in the maintenance and treatment groups, respectively). At data cut-off, 5 patients remained on treatment. Conclusion Efficacy results in these heavily pre-treated patients were similar to those from previous trials. The safety profile of rucaparib in real life was predictable and manageable.es_ES
dc.description.sponsorshipThis study was funded by Clovis Oncology. Medical writing and editorial support were funded by Clovis Oncology.es_ES
dc.language.isoenges_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectRucaparibes_ES
dc.subjectRecurrent ovarian canceres_ES
dc.subjectMaintenancees_ES
dc.subjectTreatmentes_ES
dc.subjectPARP inhibitores_ES
dc.titleRucaparib in recurrent ovarian cancer: real-world experience from the rucaparib early access programme in Spain – A GEICO studyes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://bmccancer.biomedcentral.com/articles/10.1186/s12885-022-10191-5es_ES
dc.editorial.note© The Author(s) 2022. Open Accesses_ES
dadun.citation.endingPage10es_ES
dadun.citation.number1150es_ES
dadun.citation.publicationNameBMC Canceres_ES
dadun.citation.startingPage1es_ES
dadun.citation.volume22es_ES

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