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dc.contributor.authorMatsubara, N
dc.contributor.authorde Bono, J
dc.contributor.authorSweeney, C
dc.contributor.authorChi, KN
dc.contributor.authorOlmos, D
dc.contributor.authorSandhu, S
dc.contributor.authorMassard, C
dc.contributor.authorGarcia, J
dc.contributor.authorChen, G
dc.contributor.authorHarris, A
dc.contributor.authorSchenkel, F
dc.contributor.authorSane, R
dc.contributor.authorHinton, H
dc.contributor.authorBracarda, S
dc.contributor.authorSternberg, CN
dc.coverage.spatialUnited States
dc.date.accessioned2023-04-03T11:02:08Z
dc.date.available2023-04-03T11:02:08Z
dc.date.issued2023-04-01
dc.identifierS1558-7673(23)00001-0
dc.identifier.citationClinical Genitourinary Cancer, 2023, 21 (2), pp. 230 - 237.e1
dc.identifier.issn1558-7673
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5732
dc.identifier.eissn1938-0682
dc.identifier.eissn1938-0682
dc.identifier.doi10.1016/j.clgc.2023.01.001
dc.description.abstractPURPOSE: Adding ipatasertib to abiraterone and prednisone/prednisolone significantly improved radiographic progression-free survival for patients with metastatic castration-resistant prostate cancer (mCRPC) with PTEN-loss tumours by immunohistochemistry in the IPATential150 trial (NCT03072238). Here we characterise the safety of these agents in subpopulations and assess manageability of key adverse events (AEs). MATERIALS AND METHODS: In this randomised, double-blind, phase 3 trial, patients with previously untreated asymptomatic or mildly symptomatic mCRPC were randomised 1:1 to receive ipatasertib-abiraterone or placebo-abiraterone (all with prednisone/prednisolone). AEs were analysed, focusing on key AEs of diarrhoea, hyperglycaemia, rash and transaminase increased. RESULTS: 1097 patients received study medication and were assessed for safety (47% with PTEN-loss tumours by immunohistochemistry and 20% were Asian). Ipatasertib was associated with increased Grade 3/4 AEs and AEs leading to treatment discontinuation vs placebo. The rate of discontinuation of ipatasertib was 18% in patients with PTEN-loss and 21% overall. The frequencies of all-grade, Grade 3/4 and serious AEs were similar between the PTEN-loss and overall populations. Diarrhoea, hyperglycaemia, rash and transaminase elevation were more frequent in ipatasertib-treated patients, appearing rapidly after treatment initiation (median onset: 8-43 days for ipatasertib arm and 56-104 days for placebo). The ipatasertib discontinuation rate was 32% and 18% in Asian and non-Asian patients, respectively, despite similar baseline characteristics and Grade 3/4 AE frequencies between groups. CONCLUSIONS: Ipatasertib plus abiraterone had an overall tolerable safety profile consistent with known toxicities. More AEs leading to drug discontinuation were observed with ipatasertib than placebo, but incidence would likely be lessened with prophylactic measures.
dc.formatPrint-Electronic
dc.format.extent230 - 237.e1
dc.languageeng
dc.language.isoeng
dc.publisherCIG MEDIA GROUP, LP
dc.relation.ispartofClinical Genitourinary Cancer
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAKT inhibition
dc.subjectAdverse events
dc.subjectIPATential150
dc.subjectPhase 3
dc.subjectmCRPC
dc.subjectMale
dc.subjectHumans
dc.subjectProstatic Neoplasms, Castration-Resistant
dc.subjectPrednisone
dc.subjectPrednisolone
dc.subjectExanthema
dc.subjectHyperglycemia
dc.subjectAntineoplastic Combined Chemotherapy Protocols
dc.subjectAbiraterone Acetate
dc.titleSafety Profile of Ipatasertib Plus Abiraterone vs Placebo Plus Abiraterone in Metastatic Castration-resistant Prostate Cancer.
dc.typeJournal Article
dcterms.dateAccepted2023-01-02
dc.date.updated2023-04-03T11:01:26Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1016/j.clgc.2023.01.001
rioxxterms.licenseref.startdate2023-04-01
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/36697317
pubs.issue2
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.clgc.2023.01.001
pubs.volume21
icr.researchteamPrCa Targeted Therapy
dc.contributor.icrauthorDe Bono, Johann
icr.provenanceDeposited by Mr Arek Surman on 2023-04-03. Deposit type is initial. No. of files: 1. Files: 1-s2.0-S1558767323000010-main.pdf


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Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by-nc-nd/4.0/