Effectiveness and safety of cabazitaxel chemotherapy for metastatic castration-resistant prostatic carcinoma on Turkish patients (The Anatolian Society of Medical Oncology)

dc.authorid0000-0003-4533-0620
dc.authorid0000-0002-7433-3591
dc.authorid0000-0002-4632-9501
dc.authorid0000-0001-8490-3239
dc.authorid0000-0002-0499-8918
dc.authorid0000-0001-6126-5377
dc.contributor.authorSuner, A.
dc.contributor.authorAydin, D.
dc.contributor.authorHacioglu, M. B.
dc.contributor.authorDogu, G. G.
dc.contributor.authorImamoglu, G. I.
dc.contributor.authorMenekse, S.
dc.contributor.authorPilanci, K. N.
dc.date.accessioned2025-05-10T19:28:39Z
dc.date.issued2016
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractOBJECTIVE: Prostate cancer is among the most common cancers in males. Prostate cancer is androgen dependent in the beginning, but as time progresses, it becomes refractory to androgen deprivation treatment. At this stage, docetaxel has been used as standard treatment for years. Cabazitaxel has become the first chemotherapeutic agent which has been shown to increase survival for patients with metastatic Castrate Resistant Prostate Cancer (mCRPC) that progresses after docetaxel. Phase 3 TROPIC study demonstrated that cabazitaxel prolongs survival. PATIENTS AND METHODS: In this study, we evaluated a total of 103 patients who took cabazitaxel chemotherapy for mCRPC diagnosis in 21 centers of Turkey, retrospectively. This study included patients who progressed despite docetaxel treatments, had ECOG performance score between 0-2, and used cabazitaxel treatment. Patients received cabazitaxel 25 mg/m(2) at every 3 weeks, and prednisolone 5 mg twice a day. RESULTS: Median number of cabazitaxel cures was 5.03 (range: 1-17). Cabazitaxel response evaluation detected that 34% of the patients had a partial response, 22.3% had stable disease and 32% had a progressive disease. Grade 3-4 hematological toxicities were neutropenia (28.2%), neutropenic fever (14.5%), anemia (6.7%), and thrombocytopenia (3.8%). In our study, median progression-free survival (PFS) was 7.7 months and overall survival (OS) was 10.6 months. CONCLUSIONS: This study reflects toxicity profile of Turkish patients as a Caucasian race. We suggest that cabazitaxel is a safe and effective treatment option for mCRPC patients who progress after docetaxel. Moreover, ethnicity may play important roles both in treatment response and in toxicity profile.
dc.identifier.endpage1243
dc.identifier.issn1128-3602
dc.identifier.issue7
dc.identifier.pmid27097941
dc.identifier.scopusqualityQ2
dc.identifier.startpage1238
dc.identifier.urihttps://hdl.handle.net/20.500.14730/7420
dc.identifier.volume20
dc.identifier.wosWOS:000376904300006
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherVerduci Publisher
dc.relation.ispartofEuropean Review For Medical and Pharmacological Sciences
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectProstate cancer
dc.subjectCabazitaxel
dc.subjectChemotherapy
dc.subjectToxicities
dc.titleEffectiveness and safety of cabazitaxel chemotherapy for metastatic castration-resistant prostatic carcinoma on Turkish patients (The Anatolian Society of Medical Oncology)
dc.typeArticle

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