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dc.contributor.authorWilson, BE
dc.contributor.authorArmstrong, AJ
dc.contributor.authorde Bono, J
dc.contributor.authorSternberg, CN
dc.contributor.authorRyan, CJ
dc.contributor.authorScher, HI
dc.contributor.authorSmith, MR
dc.contributor.authorRathkopf, D
dc.contributor.authorLogothetis, CJ
dc.contributor.authorChi, KN
dc.contributor.authorJones, RJ
dc.contributor.authorSaad, F
dc.contributor.authorDe Porre, P
dc.contributor.authorTran, N
dc.contributor.authorHu, P
dc.contributor.authorGillessen, S
dc.contributor.authorCarles, J
dc.contributor.authorFizazi, K
dc.contributor.authorJoshua, AM
dc.coverage.spatialEngland
dc.date.accessioned2022-09-05T09:34:45Z
dc.date.available2022-09-05T09:34:45Z
dc.date.issued2022-07-01
dc.identifierS0959-8049(22)00205-2
dc.identifier.citationEuropean Journal of Cancer, 2022, 170 pp. 296 - 304en_US
dc.identifier.issn0959-8049
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5402
dc.identifier.eissn1879-0852
dc.identifier.eissn1879-0852
dc.identifier.doi10.1016/j.ejca.2022.03.042
dc.description.abstractBACKGROUND: The associations of metformin and statins with overall survival (OS) and prostate specific antigen response rate (PSA-RR) in trials in metastatic castration-resistant prostate cancer remain unclear. OBJECTIVE: To determine whether metformin or statins ± abiraterone acetate plus prednisone/prednisolone (AAP) influence OS and PSA-RR. DESIGN, SETTING AND PARTICIPANT: COU-AA-301 and COU-AA-302 patients were stratified by metformin and statin use. Cox proportional hazards models were used to estimate hazards ratio (HR) stratified by concomitant medications, and a random effects model was used to pool HR. We compared PSA-RR using Chi χ2 test. RESULTS: In COU-AA-301-AAP, metformin was associated with improved PSA-RR (41.1% versus 28.6%) but not prolonged OS. In COU-AA-301-placebo-P, there was no association between metformin and prolonged OS or PSA-RR. In COU-AA-302-AAP, metformin was associated with prolonged OS (adjHR 0.69, 95% CI 0.48-0.98) and improved PSA-RR (72.7% versus 60.0%). In COU-AA-302-P, metformin was associated with prolonged OS (adjHR 0.66, 95% CI 0.47-0.93). In pooled analysis, OS was prolonged among those treated with metformin (pooled HR 0.77, 95% CI 0.62-0.95).In COU-AA-301-AAP, statins were associated with an improved OS (adjHR 0.76, 95% CI 0.62-0.93), while there was no difference in COU-AA-301-P. There was no association with statins and OS in either COU-AA-302 groups. When pooling HR, OS was prolonged among those treated with statins (pooled HR 0.78, 95% CI 0.68-0.88). CONCLUSION: Within the limitations of post-hoc sub-analyses, metformin and statins are associated with a prolonged OS and increased PSA-RR, particularly in combination with AAP.
dc.formatPrint-Electronic
dc.format.extent296 - 304
dc.languageeng
dc.language.isoengen_US
dc.publisherELSEVIER SCI LTDen_US
dc.relation.ispartofEuropean Journal of Cancer
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectAbiraterone acetate
dc.subjectMetastatic castration-resistant prostate cancer
dc.subjectMetformin
dc.subjectStatins
dc.subjectAbiraterone Acetate
dc.subjectAntineoplastic Combined Chemotherapy Protocols
dc.subjectCastration
dc.subjectDisease-Free Survival
dc.subjectHumans
dc.subjectHydroxymethylglutaryl-CoA Reductase Inhibitors
dc.subjectMale
dc.subjectMetformin
dc.subjectPrednisone
dc.subjectProstate-Specific Antigen
dc.subjectProstatic Neoplasms, Castration-Resistant
dc.subjectTreatment Outcome
dc.titleEffects of metformin and statins on outcomes in men with castration-resistant metastatic prostate cancer: Secondary analysis of COU-AA-301 and COU-AA-302.en_US
dc.typeJournal Article
dcterms.dateAccepted2022-03-16
dc.date.updated2022-09-05T09:33:38Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1016/j.ejca.2022.03.042en_US
rioxxterms.licenseref.startdate2022-07-01
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/35568679
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Prostate Cancer Targeted Therapy Group
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.1016/j.ejca.2022.03.042
pubs.volume170
icr.researchteamPrCa Targeted Therapyen_US
dc.contributor.icrauthorDe Bono, Johann
icr.provenanceDeposited by Mr Arek Surman on 2022-09-05. Deposit type is initial. No. of files: 1. Files: 1-s2.0-S0959804922002052-main.pdf


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