Effect of docetaxel added to bicalutamide in Hormone-Naive non-metastatic prostate cancer with rising PSA, a randomized clinical trial (SPCG-14)

dc.contributor.authorJosefsson Andreas
dc.contributor.authorJellvert Åsa
dc.contributor.authorHolmberg Erik
dc.contributor.authorBrasso Klaus
dc.contributor.authorPetersen Peter Meidahl
dc.contributor.authorAaltomaa Sirpa
dc.contributor.authorLuukkaa Marjaana
dc.contributor.authorVerhagen Paul
dc.contributor.authorde Wit Ronald
dc.contributor.authorAhlgren Göran
dc.contributor.authorAndren Ove
dc.contributor.authorCastellanos Enrique
dc.contributor.authorSeke Mihalj
dc.contributor.authorWidmark Anders
dc.contributor.authorDamber Jan-Erik
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.converis.publication-id179690712
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/179690712
dc.date.accessioned2025-08-28T02:32:43Z
dc.date.available2025-08-28T02:32:43Z
dc.description.abstractBackgroundHistorically, endocrine therapy was used in a range of scenarios in patients with rising PSA, both as a treatment for locally advanced non-metastatic prostate cancer and PSA recurrence following curative intended therapy. In the present study the objective was to investigate if chemotherapy added to endocrine therapy could improve progression-free survival (PFS).Materials and MethodsPatients with hormone-naive, non-metastatic prostate cancer and rising prostate-specific antigen (PSA), enrolled from Sweden, Denmark, the Netherlands, and Finland, were randomized to long-term bicalutamide (150 mg daily) or plus docetaxel (75 mg/m(2), q3w, 8-10 cycles) without prednisone, after stratification for the site, prior local therapy or not, and PSA doubling time. The primary endpoint was 5-year PFS analyzed with a stratified Cox proportional hazards regression model on intention to treat basis.ResultsBetween 2009 and 2018, a total of 348 patients were randomized; 315 patients had PSA relapse after radical treatment, 33 patients had no prior local therapy. Median follow-up was 4.9 years (IQR 4.0-5.1). Adding docetaxel improved PFS (HR 0.68, 95% CI 0.50-0.93; p = 0.015). Docetaxel showed an advantage for patients with PSA relapse after prior local therapy (HR 0.67, 95% CI 0.49-0.94; p = 0.019). One event of neutropenic infection/fever occurred in 27% of the patients receiving docetaxel. Limitations were slow recruitment, lack of enrolling patients without radical local treatment, and too short follow-up for evaluation of overall survival in patients with PSA relapse.ConclusionDocetaxel improved PFS in patients starting bicalutamide due to PSA relapse after local therapy or localized disease without local therapy. Confirmatory studies of the efficacy of docetaxel in the setting of PSA-only relapse in addition to endocrine therapies may be justified if longer follow-up will show increased metastatic-free survival.
dc.format.pagerange372
dc.format.pagerange380
dc.identifier.eissn1651-226X
dc.identifier.jour-issn0284-186X
dc.identifier.olddbid209273
dc.identifier.oldhandle10024/192300
dc.identifier.urihttps://www.utupub.fi/handle/11111/41434
dc.identifier.urlhttps://doi.org/10.1080/0284186X.2023.2199940
dc.identifier.urnURN:NBN:fi-fe2025082792311
dc.language.isoen
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherTaylor & Francis Ltd
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1080/0284186X.2023.2199940
dc.relation.ispartofjournalActa Oncologica
dc.relation.issue4
dc.relation.volume62
dc.source.identifierhttps://www.utupub.fi/handle/10024/192300
dc.titleEffect of docetaxel added to bicalutamide in Hormone-Naive non-metastatic prostate cancer with rising PSA, a randomized clinical trial (SPCG-14)
dc.year.issued2023

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