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dc.contributor.authorAlumkal, JJ
dc.contributor.authorChowdhury, S
dc.contributor.authorLoriot, Y
dc.contributor.authorSternberg, CN
dc.contributor.authorde Bono, JS
dc.contributor.authorTombal, B
dc.contributor.authorCarles, J
dc.contributor.authorFlaig, TW
dc.contributor.authorDorff, TB
dc.contributor.authorPhung, D
dc.contributor.authorForer, D
dc.contributor.authorNoonberg, SB
dc.contributor.authorMansbach, H
dc.contributor.authorBeer, TM
dc.contributor.authorHigano, CS
dc.date.accessioned2017-08-18T15:44:15Z
dc.date.issued2017-10-01
dc.identifier.citationClinical genitourinary cancer, 2017, 15 (5), pp. 610 - 617.e3
dc.identifier.issn1558-7673
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/788
dc.identifier.eissn1938-0682
dc.identifier.doi10.1016/j.clgc.2017.02.007
dc.description.abstractBACKGROUND: The Multinational Phase 3, Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Study of Oral MDV3100 in Chemotherapy-Naive Patients With Progressive Metastatic Prostate Cancer Who Have Failed Androgen Deprivation Therapy (PREVAIL) trial was unique as it included patients with visceral disease. This analysis was designed to describe outcomes for the subgroup of men from PREVAIL with specific sites of visceral disease to help clinicians understand how these patients responded to enzalutamide prior to chemotherapy. PATIENTS AND METHODS: Prespecified analyses examined the coprimary endpoints of radiographic progression-free survival (rPFS) and overall survival (OS) only. All other efficacy analyses were post hoc. The visceral subgroup was divided into liver or lung subsets. Patients with both liver and lung metastases were included in the liver subset. RESULTS: Of the 1717 patients in PREVAIL, 204 (12%) had visceral metastases at screening (liver only or liver/lung metastases, n = 74; lung only metastases, n = 130). In patients with liver metastases, enzalutamide was associated with an improvement in rPFS (hazard ratio [HR], 0.44; 95% confidence interval [CI], 0.22-0.90) but not OS (HR, 1.04; 95% CI, 0.57-1.87). In patients with lung metastases only, the HR for rPFS (0.14; 95% CI, 0.06-0.36) and the HR for OS (0.59; 95% CI, 0.33-1.06) favored enzalutamide over placebo. Patients with liver metastases had worse outcomes than those with lung metastases, regardless of treatment. Enzalutamide was well tolerated in patients with visceral disease. CONCLUSIONS: Enzalutamide is an active first-line treatment option for men with asymptomatic or mildly symptomatic chemotherapy-naive metastatic castration-resistant prostate cancer and visceral disease. Patients with lung-only disease fared better than patients with liver disease, regardless of treatment.
dc.formatPrint-Electronic
dc.format.extent610 - 617.e3
dc.languageeng
dc.language.isoeng
dc.publisherCIG MEDIA GROUP, LP
dc.rights.urihttps://www.rioxx.net/licenses/all-rights-reserved
dc.subjectHumans
dc.subjectLiver Neoplasms
dc.subjectLung Neoplasms
dc.subjectPhenylthiohydantoin
dc.subjectPrognosis
dc.subjectTreatment Outcome
dc.subjectAdministration, Oral
dc.subjectDouble-Blind Method
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectMale
dc.subjectProstatic Neoplasms, Castration-Resistant
dc.titleEffect of Visceral Disease Site on Outcomes in Patients With Metastatic Castration-resistant Prostate Cancer Treated With Enzalutamide in the PREVAIL Trial.
dc.typeJournal Article
dcterms.dateAccepted2017-02-19
rioxxterms.versionofrecord10.1016/j.clgc.2017.02.007
rioxxterms.licenseref.urihttps://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2017-10
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfClinical genitourinary cancer
pubs.issue5
pubs.notes12 months
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.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
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.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.publication-statusPublished
pubs.volume15
pubs.embargo.terms12 months
icr.researchteamProstate Cancer Targeted Therapy Group
dc.contributor.icrauthorDe Bono, Johann


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