Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/57714
Conference/Presentation Title: 8-year outcomes of enzalutamide (ENZA) versus a non-steroidal anti-androgen (NSAA) for metastatic, hormone-sensitive prostate cancer (ENZAMET; ANZUP 1304).
Authors: Zhang A.Y.;Davis I.D.;Thomas H.;McLaughlin R.A.;Tan T.H.;Pook D.W.;Marx G.M.;Zielinski R.R.;Sandhu S.;Thomson A.;Reaume M.N.;North S.A.;McCaffrey J.;McDermott R.S.;Lawrence N.J.;Horvath L.;Chowdhury S.;Chi K.N.;Stockler M.R.;Sweeney C.
Institution: (Zhang) NHMRC Clinical Trials Centre, University of Sydney, Sydney, NSW, Australia
(Davis) Monash University and Eastern Health, Box Hill, Australia
(Thomas) NHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia
(McLaughlin) Cancer Trials Ireland, Dublin, Ireland
(Tan) Royal Adelaide Hospital, Adelaide, Australia
(Pook) Monash Health, Clayton, Australia
(Marx) Sydney Adventist Hospital and Australian National University, Sydney, Australia
(Zielinski) Orange Hospital & Dubbo Base Hospital & Bathurst Base Hospital, Orange, Dubbo, Bathurst, NSW, Australia
(Sandhu) Peter MacCallum Cancer Centre, Melbourne, Australia
(Thomson) Royal Cornwall Hospitals NHS Trust, Truro, United Kingdom
(Reaume) Ottawa Hospital Cancer Centre, Ottawa, ON, Canada
(North) Division of Medical Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada
(McCaffrey) Cancer Trials Ireland, Dublin, Ireland
(McDermott) Cancer Trials Ireland, Dublin, Ireland
(Lawrence) Te Puriri o Te Ora Cancer and Blood, Te Toka Tumai Auckland, Te Whatu Ora, Auckland, New Zealand
(Horvath) Chris O'Brien Lifehouse, University of Sydney, Sydney, NSW, Australia
(Chowdhury) Guy's, King's, and St. Thomas' Hospitals, and Sarah Cannon Research Institute, London, United Kingdom
(Chi) BC Cancer Agency, University of British Columbia, Vancouver, BC, Canada
(Stockler) NHMRC Clinical Trials Centre, The University of Sydney, Camperdown, NSW, Australia
(Sweeney) South Australian Immunogenomics Cancer Institute, University of Adelaide, Adelaide, SA, Australia
Presentation/Conference Date: 3-Apr-2026
Copyright year: 2025
Publisher: Lippincott Williams and Wilkins
Publication information: Journal of Clinical Oncology. Conference: ASCO MEETING ABSTRACTS. Chicago United States. 43(16) (no pagination), 2025. Article Number: 5090. Date of Publication: 01 Jun 2025.
Abstract: Background: We previously reported that ENZA improved overall survival (OS) after median follow-up times of 34 and 68 months, in comparison with a NSAA, when added to testosterone suppression, with or without concurrent early docetaxel, for mHSPC. We now report outcomes after median follow-up of 98 months. Method(s): Participants (pts) with mHSPC were randomly assigned (1:1) from 31MAR2014-24MAR2017 to treatment with ENZA 160 mg or NSAA, in addition to testosterone suppression. Concurrent early docetaxel was used in 45%. OS was the primary endpoint and analysed with the Kaplan-Meier method, log-rank test for p-values, and Cox regression for hazard ratios (HR). Secondary outcomes included deaths due to prostate cancer (PC) versus (vs) other causes. The numbers of pts experiencing specified adverse events (AE) of grade 3-5 are expressed per 100 person-years of study treatment exposure to account for differing treatment durations. Result(s): After a median follow-up of 98 months, data cut-off 30JUN2024, death was reported in 285/563 (51%) pts assigned ENZA vs 337/562 (60%) assigned NSAA. OS was longer among those assigned ENZA than NSAA (medians 95 vs 70 months; OS at 96 months 50% vs 40%; HR 0.73, 95% CI 0.63 to 0.86; p=0.0001). Clinical PFS also continued to favour ENZA over NSAA (HR 0.49; 95% CI 0.42 to 0.57; p<0.0001). PC accounted for 468 of all 622 deaths, and were less frequent among those assigned ENZA than NSAA (207 vs 261). Deaths due to other causes accounted for a total of 154 deaths, and were similarly frequent among those assigned ENZA vs NSAA (78 vs 76). Mean duration of study treatment was longer for ENZA than NSAA (58 vs 36 months). 185/562 (33%) remain on ENZA with 88% on full dose. G3-5 AE of interest were reported in the following numbers of pts per 100 years of study treatment with ENZA vs NSAA: cardiac disorder 2.2 vs 2.2, nervous system disorder 2.3 vs 2.0, fall 0.70 vs 0.24. Causes of death according to PSA at 7 months are tabulated below. Among those with PSA at 7 months <=0.2, deaths were due to PC in 29%, and other causes in 13%. Among those with PSA at 7 months >0.2, deaths were due to PC in 60%, and other causes in 13%. Conclusion(s): Treatment with enzalutamide continues to confer substantial OS benefits at 8 years. These findings highlight long-term safety, toxicities, non-PC causes of death, and survival outcomes of those with and without PSA <=0.2 at 7 months. ClinicalTrials.gov Identifier NCT02446405. Clinical trial information: NCT02446405. [Table presented]Copyright © 2025 by American Society of Clinical Oncology
Conference Name: ASCO MEETING ABSTRACTS
Conference Start Date: 2025-05-30
Conference End Date: 2025-06-03
Conference Location: Chicago, United States
DOI: http://monash.idm.oclc.org/login?url=https://dx.doi.org/10.1200/JCO.2025.43.16_suppl.5090
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/57714
Type: Conference Abstract
Subjects: heart disease
metastatic castration sensitive prostate cancer
neurologic disease
prostate cancer
antiandrogen
docetaxel
enzalutamide
prostate specific antigen
testosterone
Appears in Collections:Conference Abstracts

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