Clinical Study on the Efficacy and Continuous Docetaxel Based Chemotherapy Treatment for Castration-Resistant Prostate Cancer

We report a retrospective study on the efficacy, adverse events and the factors for continuous docetaxel (DOC) therapy for patients with castration-resistant prostate cancer (CRPC). Between April 2007 and April 2015, 37 CRPC patients were treated with DOC therapy at Kanazawa Medical University Hospi...

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Veröffentlicht in:Hinyokika kiyo. Acta urologica Japonica. - 1962. - 63(2017), 9 vom: 09. Sept., Seite 351-357
1. Verfasser: Chikazawa, Ippei (VerfasserIn)
Weitere Verfasser: Inoue, Shinya, Nakazawa, Yusuke, Nakai, Dan, Morita, Nobuyo, Tanaka, Tatsuro, Motoo, Yoshiharu, Miyazawa, Katsuhito
Format: Online-Aufsatz
Sprache:Japanese
Veröffentlicht: 2017
Zugriff auf das übergeordnete Werk:Hinyokika kiyo. Acta urologica Japonica
Schlagworte:Journal Article Castration resistant prostate cancer Docetaxel Antineoplastic Agents Taxoids 15H5577CQD
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520 |a We report a retrospective study on the efficacy, adverse events and the factors for continuous docetaxel (DOC) therapy for patients with castration-resistant prostate cancer (CRPC). Between April 2007 and April 2015, 37 CRPC patients were treated with DOC therapy at Kanazawa Medical University Hospital. DOC was administered every 3 weeks at 70 mg/m2. Prostatic specific antigen (PSA) level, adverse events, cycles of DOC therapy, survival time and clinical passage were examined. Fifteen patients showed a decrease in PSA level of 50% or more, 9 patients showed less than 50% decrease in PSA level and 13 patients showed no decrease in PSA level. Adverse effect of grade 3 consisted of neutropenia in 29.7% and leukocytopenia in 10.8%. The median number of treatment cycles was 11.7 courses. The patients were divided into two groups ; the first group comprised of 26 patients who received short-term DOC therapy (≤10 cycles) and the second group comprised of 11 patients who received long-term DOC therapy (≥11 cycles). The 1-year survival rate was 59 and 100% for the short-term and long-term groups, respectively. Long-term treatment was related to pretreatment PSA nadir, time to progression of CRPC and serum lactate dehydrogenase level 
650 4 |a Journal Article 
650 4 |a Castration resistant prostate cancer 
650 4 |a Docetaxel 
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650 7 |a 15H5577CQD  |2 NLM 
700 1 |a Inoue, Shinya  |e verfasserin  |4 aut 
700 1 |a Nakazawa, Yusuke  |e verfasserin  |4 aut 
700 1 |a Nakai, Dan  |e verfasserin  |4 aut 
700 1 |a Morita, Nobuyo  |e verfasserin  |4 aut 
700 1 |a Tanaka, Tatsuro  |e verfasserin  |4 aut 
700 1 |a Motoo, Yoshiharu  |e verfasserin  |4 aut 
700 1 |a Miyazawa, Katsuhito  |e verfasserin  |4 aut 
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