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dc.contributor.authorSüner, Ali
dc.contributor.authorAydın, Dinçer
dc.contributor.authorHacıoğlu, Muhammet Bekir
dc.contributor.authorDoǧu, Gamze Gököz
dc.contributor.authorİmamoğlu, Gökşen İnanç
dc.contributor.authorMenekşe, Serkan
dc.contributor.authorPilancı, Kezban Nur
dc.contributor.authorAvcı, Nilüfer
dc.date.accessioned2019-10-17T07:00:47Z
dc.date.available2019-10-17T07:00:47Z
dc.date.issued2016en_US
dc.identifier.issn11283602
dc.identifier.urihttps://hdl.handle.net/20.500.12462/7419
dc.descriptionAvcı, Nilüfer ( Balikesir Author)en_US
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 cabaz-itaxel chemotherapy for mCRPC diagnosis in 21 centers of Turkey, retrospectively. This study included patients who progressed despite doc-etaxel treatments, had ECOG performance score between 0-2, and used cabazitaxel treatment. Patients received cabazitaxel 25 mg/m2 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 hema-tological 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.en_US
dc.language.isoengen_US
dc.publisherVerduci Editoreen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCabazitaxelen_US
dc.subjectChemotherapyen_US
dc.subjectProstate Canceren_US
dc.subjectToxicitiesen_US
dc.titleEffectiveness and safety of cabazitaxel chemotherapy for metastatic castration-resistant prostatic carcinoma on Turkish patients (The Anatolian Society of Medical Oncology)en_US
dc.typearticleen_US
dc.relation.journalEuropean Review for Medical and Pharmacological Sciencesen_US
dc.contributor.departmentTıp Fakültesien_US
dc.identifier.volume20en_US
dc.identifier.issue7en_US
dc.identifier.startpage1238en_US
dc.identifier.endpage1243en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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