Where Should Enzalutamide Be in The Metastatic Castration Resistant Prostate Cancer (mCRPC): A Multi-center Study

dc.authorid0000-0003-4533-0620
dc.authorid0000-0002-1171-8320
dc.contributor.authorKoca, Sinan
dc.contributor.authorOkten, Ilker Nihat
dc.contributor.authorBesiroglu, Mehmet
dc.contributor.authorTelli, Tugba Akin
dc.contributor.authorDemirci, Ayse
dc.contributor.authorKaraagac, Mustafa
dc.contributor.authorKucukarda, Ahmet
dc.date.accessioned2025-05-10T19:57:55Z
dc.date.issued2023
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractObjectives: Enzalutamide(ENZ) is an effective hormonal treatment modality in mCRPC. It can be used before or after docetaxel(DTX) in this setting. Herein, we aimed to show the efficacy of ENZ before or after DTX use and the factors predicting the efficacy.Methods: We retrospectively collected the data of 320 patients from 12 centers who were treated with ENZ in mCRPC. The initial stage, age, line of treatment, serum prostate-specific antigen (PSA) levels before ENZ treatment and at nadir, site of metastasis, gleason score were evaluated.Results: Median age of 320 patients were 69. At a median follow-up of 56 months, 271/320 (84.7%) disease progression and 230/320(71.9%) death had been observed. Median PFS was 11(8.9-13)) and median OS was 25(22.1-27.8) months in all patients group. Median PFS was 10(7.4-12.5) months, 11(8-13.9) months in pre-DT X and post-DT X groups respectively. Median OS was higher in the post-DT X group than the pre-DT X group (28(25.7-30.2) vs 19(15.0-22.9-46.6) (p:0.000). Gleason score >= 8 (HR 0.59, 95%CI 0.46-0.77, p=0.00), presence of non-visceral metastasis (HR 0.72, 95%CI 0.53-0.97, p=0.031), initial PSA value<43(median) (HR 0.70, 95%CI 0.54-0.91, p=0.009), PSA at nadir <2 (HR 0.61, 95%CI 0.44-0.85, p=0.004), >50% decline in PSA (HR 0.27, 95%CI 0.19-0.36, p=0.000) significantly predicted ENZ response regarding rPFS.Conclusion: ENZ has shown equal efficacy before and after DTX treatment in mCRPC regarding rPFS. But OS rate was significantly better in the pre-DT X group. Therefore, we recommend starting with DTX in patients who can tolerate chemotherapy in mCRPC setting.
dc.identifier.doi10.14744/ejmo.2023.69719
dc.identifier.endpage41
dc.identifier.issn2587-196X
dc.identifier.issue1
dc.identifier.scopus2-s2.0-85150276763
dc.identifier.scopusqualityQ2
dc.identifier.startpage34
dc.identifier.trdizinid1166457
dc.identifier.urihttps://doi.org/10.14744/ejmo.2023.69719
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/1166457
dc.identifier.urihttps://hdl.handle.net/20.500.14730/13389
dc.identifier.volume7
dc.identifier.wosWOS:001135809500007
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR-Dizin
dc.language.isoen
dc.publisherKare Publ
dc.relation.ispartofEurasian Journal of Medicine and Oncology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250302
dc.subjectprostate cancer
dc.subjectenzalutamide
dc.subjectdocetaxel
dc.subjectline of treatment
dc.titleWhere Should Enzalutamide Be in The Metastatic Castration Resistant Prostate Cancer (mCRPC): A Multi-center Study
dc.typeArticle

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