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多西他赛持续化疗治疗去势抵抗性前列腺癌的疗效临床研究

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

作者信息

Chikazawa Ippei, Inoue Shinya, Nakazawa Yusuke, Nakai Dan, Morita Nobuyo, Tanaka Tatsuro, Motoo Yoshiharu, Miyazawa Katsuhito

机构信息

The Department of Urology, Kanazawa Medical University.

The Department of Medical Oncology, Kanazawa Medical University.

出版信息

Hinyokika Kiyo. 2017 Sep;63(9):351-357. doi: 10.14989/ActaUrolJap_63_9_351.

Abstract

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.

摘要

我们报告了一项关于多西他赛(DOC)持续治疗去势抵抗性前列腺癌(CRPC)患者的疗效、不良事件及相关因素的回顾性研究。2007年4月至2015年4月期间,金泽医科大学医院对37例CRPC患者进行了DOC治疗。DOC每3周给药一次,剂量为70mg/m²。检测前列腺特异性抗原(PSA)水平、不良事件、DOC治疗周期、生存时间和临床病程。15例患者PSA水平下降50%或更多,9例患者PSA水平下降不到50%,13例患者PSA水平未下降。3级不良反应包括29.7%的中性粒细胞减少和10.8%的白细胞减少。治疗周期的中位数为11.7个疗程。患者分为两组;第一组包括26例接受短期DOC治疗(≤10个周期)的患者,第二组包括11例接受长期DOC治疗(≥11个周期)的患者。短期和长期组的1年生存率分别为59%和100%。长期治疗与治疗前PSA最低点、CRPC进展时间和血清乳酸脱氢酶水平有关。

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