Publication:
A phase II randomised trial of abiraterone acetate plus prednisone in combination with docetaxel or docetaxel plus prednisone after disease progression to abiraterone acetate plus prednisone in patients with metastatic castration-resistant prostate cancer: The ABIDO-SOGUG trial.

dc.contributor.authorCliment, Miguel A
dc.contributor.authorFont, Albert
dc.contributor.authorDuran, Ignacio
dc.contributor.authorPuente, Javier
dc.contributor.authorMendez-Vidal, Maria Jose
dc.contributor.authorSaez, Maria Isabel
dc.contributor.authorSantander-Lobera, Carmen
dc.contributor.authorAngel-Arranz-Arija, Jose
dc.contributor.authorGonzalez-Del-Alba, Aranzazu
dc.contributor.authorSanchez-Hernandez, Alfredo
dc.contributor.authorJuan-Fita, Maria Jose
dc.contributor.authorEsteban, Emilio
dc.contributor.authorAlonso-Gordoa, Teresa
dc.contributor.authorMellado-Gonzalez, Begoña
dc.contributor.authorMaroto, Pablo
dc.contributor.authorLazaro-Quintela, Martin
dc.contributor.authorCassinello-Espinosa, Javier
dc.contributor.authorPerez-Valderrama, Begoña
dc.contributor.authorGarcias, Carmen
dc.contributor.authorCastellano, Daniel
dc.date.accessioned2023-05-03T14:56:07Z
dc.date.available2023-05-03T14:56:07Z
dc.date.issued2022-08-04
dc.description.abstractWe aimed to compare the efficacy and safety of maintaining or withdrawing abiraterone acetate plus prednisone (AAP) in patients with metastatic castration-resistant prostate cancer who had experienced cancer progression to this treatment and were beginning a docetaxel-based therapy. Phase II, randomised, open-label study conducted in patients with metastatic castration-resistant prostate cancer who were asymptomatic or mildly symptomatic. After open-label treatment with AAP, patients who had experienced cancer progression to AAP were randomised to 75 mg/m2 of docetaxel plus AAP or to receive 75 mg/m2 of docetaxel plus 10 mg of prednisone orally daily. The primary outcome was the radiographic progression-free survival rate at 12 months as evaluated by the investigators in all randomised patients. A total of 148 patients were included in open-label treatment with AAP, and of them, 94 patients were randomised to receive either docetaxel plus AAP (intervention group; n = 47) or docetaxel plus prednisone (control group; n = 47). The 12-month radiographic progression-free survival rates did not differ between the intervention group (34.9%; 95% CI 20.7-49.2) and the control group (33.9%; 95% CI 19.5-48.3). There were no significant differences in the time to radiographic progression and the overall survival between the intervention and control groups. Grade 3-5 neutropenia with the combination of docetaxel plus prednisone and AA was more frequent than with docetaxel plus prednisone (59.6% versus 27.7%). Our results indicate that the therapeutic strategy of maintaining AAP added to docetaxel in chemotherapy-naïve patients who have experienced cancer progression to AAP treatment should not be further evaluated and should be avoided in clinical practice.
dc.description.versionSi
dc.identifier.citationCliment MA, Font A, Durán I, Puente J, José Méndez-Vidal M, Sáez MI, et al. A phase II randomised trial of abiraterone acetate plus prednisone in combination with docetaxel or docetaxel plus prednisone after disease progression to abiraterone acetate plus prednisone in patients with metastatic castration-resistant prostate cancer: The ABIDO-SOGUG trial. Eur J Cancer. 2022 Nov;175:110-119
dc.identifier.doi10.1016/j.ejca.2022.08.002
dc.identifier.essn1879-0852
dc.identifier.pmid36099670
dc.identifier.urihttp://hdl.handle.net/10668/22179
dc.journal.titleEuropean journal of cancer (Oxford, England : 1990)
dc.journal.titleabbreviationEur J Cancer
dc.language.isoen
dc.organizationHospital Universitario Reina Sofía
dc.organizationInstituto Maimónides de Investigación Biomédica de Córdoba-IMIBIC
dc.organizationHospital Universitario Virgen de la Victoria
dc.organizationHospital Universitario Regional de Málaga
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number110-119
dc.provenanceRealizada la curación de contenido 05/03/2025
dc.publisherElsevier
dc.pubmedtypeClinical Trial, Phase II
dc.pubmedtypeJournal Article
dc.pubmedtypeRandomized Controlled Trial
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.relation.publisherversionhttps://www.ejcancer.com/article/S0959-8049(22)00467-1/abstract
dc.rights.accessRightsRestricted access
dc.subjectAbiraterone acetate
dc.subjectCombination
dc.subjectDocetaxel
dc.subjectMetastatic castration-resistant prostate cancer
dc.subjectPhase II
dc.subject.decsAcetato de abiraterona
dc.subject.decsNeoplasias de la próstata resistentes a la castración
dc.subject.decsPrednisona
dc.subject.decsProgresión de la enfermedad
dc.subject.decsProtocolos de quimioterapia combinada antineoplásica
dc.subject.decsResultado del tratamiento
dc.subject.meshAbiraterone acetate
dc.subject.meshAntineoplastic combined chemotherapy protocols
dc.subject.meshDisease progression
dc.subject.meshDocetaxel
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshPrednisone
dc.subject.meshProstatic neoplasms, castration-resistant
dc.subject.meshTreatment outcome
dc.titleA phase II randomised trial of abiraterone acetate plus prednisone in combination with docetaxel or docetaxel plus prednisone after disease progression to abiraterone acetate plus prednisone in patients with metastatic castration-resistant prostate cancer: The ABIDO-SOGUG trial.
dc.typeresearch article
dc.volume.number175
dspace.entity.typePublication

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
RISalud_Accesorestringido.pdf
Size:
93.39 KB
Format:
Adobe Portable Document Format