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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorJoshua, Anthony
dc.contributor.authorArmstrong, Andrew
dc.contributor.authorCrumbaker, Megan
dc.contributor.authorScher, Howard I.
dc.contributor.authorde Bono, Johann S
dc.contributor.authorTOMBAL, Bertrand
dc.contributor.authorCarles, Joan
dc.date.accessioned2023-05-18T07:13:06Z
dc.date.available2023-05-18T07:13:06Z
dc.date.issued2022-07
dc.identifier.citationJoshua AM, Armstrong A, Crumbaker M, Scher HI, de Bono J, Tombal B, et al. Statin and metformin use and outcomes in patients with castration-resistant prostate cancer treated with enzalutamide: A meta-analysis of AFFIRM, PREVAIL and PROSPER. Eur J Cancer. 2022 Jul;170:285–95.
dc.identifier.issn0959-8049
dc.identifier.urihttps://hdl.handle.net/11351/9554
dc.descriptionCastration-resistant prostate cancer; Metformin; Overall survival
dc.description.abstractBackground: Statins and metformin are commonly prescribed for patients, including those with prostate cancer. Preclinical and epidemiologic studies of each agent have suggested anti-cancer properties. Methods: Patient data from three randomised, double-blind, placebo-controlled, phase III studies evaluating enzalutamide (AFFIRM, PREVAIL and PROSPER) in patients with castration-resistant prostate cancer were included in this analysis. This post hoc, retrospective study examined the association of statin and metformin on radiographic progression-free survival (rPFS), metastasis-free survival (MFS), toxicity and overall survival (OS). After adjusting for available clinical prognostic variables, multivariate analyses were performed on pooled data from AFFIRM and PREVAIL, all three trials pooled, and each trial individually, to assess differential efficacy in these end-points associated with the baseline use of these medications. Results: In the multivariate analysis of the individual trials, OS and rPFS/MFS were not significantly influenced by statin or metformin use in AFFIRM or PROSPER. However, in PREVAIL, OS was significantly influenced by statin (hazard ratio [HR] 0.72; 95% confidence interval [CI] 0.59-0.89) and rPFS was significantly influenced by metformin (HR, 0.48; 95% CI 0.34-0.70). In pooled analyses, improved OS was significantly associated with statin use but not metformin use for AFFIRM+PREVAIL trials (HR 0.83; 95% CI 0.72-0.96) and AFFIRM+PREVAIL+PROSPER (HR 0.75; 95% CI 0.66-0.85). Conclusions: The association between statin or metformin use and rPFS, MFS and OS was inconsistent across three trials. Analyses of all three trials pooled and AFFIRM+PREVAIL pooled revealed that statin but not metformin use was significantly associated with a reduced risk of death in enzalutamide-treated patients. Additional prospective, controlled studies are warranted.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesEuropean Journal of Cancer;170
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.sourceScientia
dc.subjectPròstata - Càncer - Tractament
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subjectMetformina - Ús terapèutic
dc.subject.meshProstatic Neoplasms, Castration-Resistant
dc.subject.mesh/drug therapy
dc.subject.meshTreatment Outcome
dc.subject.meshMetformin
dc.subject.mesh/therapeutic use
dc.titleStatin and metformin use and outcomes in patients with castration-resistant prostate cancer treated with enzalutamide: A meta-analysis of AFFIRM, PREVAIL and PROSPER
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.ejca.2022.04.005
dc.subject.decsneoplasias prostáticas resistentes a la castración
dc.subject.decs/farmacoterapia
dc.subject.decsresultado del tratamiento
dc.subject.decsmetformina
dc.subject.decs/uso terapéutico
dc.relation.publishversionhttps://doi.org/10.1016/j.ejca.2022.04.005
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Joshua AM, Crumbaker M] Kinghorn Cancer Centre, St. Vincent's Hospital, Sydney, NSW, Australia. [Armstrong A] Duke Cancer Institute Center for Prostate and Urologic Cancers, Duke University, Durham, NC, USA. [Scher HI] Memorial Sloan Kettering Cancer Center, New York, NY, USA. [de Bono J] The Institute of Cancer Research and the Royal Marsden NHS Foundation Trust, London, UK. [Tombal B] Cliniques Universitaires Saint-Luc, Brussels, Belgium. [Carles J] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain
dc.identifier.pmid35643841
dc.identifier.wos000833527200005
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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