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dc.contributor.authorGeorge, DJ
dc.contributor.authorDearnaley, DP
dc.date.accessioned2022-04-06T10:02:37Z
dc.date.available2022-04-06T10:02:37Z
dc.date.issued2021-11-01
dc.identifier.citationFuture oncology (London, England), 2021, 17 (33), pp. 4431 - 4446
dc.identifier.issn1479-6694
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5071
dc.identifier.eissn1744-8301
dc.identifier.eissn1744-8301
dc.identifier.doi10.2217/fon-2021-0575
dc.identifier.doi10.2217/fon-2021-0575
dc.description.abstractAndrogen deprivation therapy using gonadotropin-releasing hormone (GnRH) analogues is standard treatment for intermediate and advanced prostate cancer. GnRH agonist therapy results in an initial testosterone flare, and increased metabolic and cardiovascular risks. The GnRH antagonist relugolix is able to reduce serum testosterone levels in men with prostate cancer without inducing testosterone flare. In the HERO Phase III trial, relugolix was superior to leuprolide acetate at rapidly reducing testosterone and continuously suppressing testosterone, with faster post-treatment recovery of testosterone levels. Relugolix was associated with a 54% lower incidence of major adverse cardiovascular events than leuprolide acetate. As the first oral GnRH antagonist approved for the treatment of advanced prostate cancer, relugolix offers a new treatment option.
dc.formatPrint-Electronic
dc.format.extent4431 - 4446
dc.languageeng
dc.language.isoeng
dc.publisherFUTURE MEDICINE LTD
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserved
dc.subjectHumans
dc.subjectProstatic Neoplasms
dc.subjectCardiovascular Diseases
dc.subjectPhenylurea Compounds
dc.subjectPyrimidinones
dc.subjectTestosterone
dc.subjectLeuprolide
dc.subjectTreatment Outcome
dc.subjectIncidence
dc.subjectMale
dc.subjectGonadotropin-Releasing Hormone
dc.subjectRandomized Controlled Trials as Topic
dc.subjectClinical Trials, Phase II as Topic
dc.subjectClinical Trials, Phase III as Topic
dc.titleRelugolix, an oral gonadotropin-releasing hormone antagonist for the treatment of prostate cancer.
dc.typeJournal Article
dcterms.dateAccepted2021-08-03
rioxxterms.versionAM
rioxxterms.versionofrecord10.2217/fon-2021-0575
dc.relation.isPartOfFuture oncology (London, England)
pubs.issue33
pubs.notesNot known
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/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Clinical Academic Radiotherapy (Dearnaley)
pubs.publication-statusPublished
pubs.volume17
pubs.embargo.termsNot known
icr.researchteamClinical Academic Radiotherapy (Dearnaley)
dc.contributor.icrauthorDearnaley, David


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