Determine of the optimal number of cycles of docetaxel in the treatment of metastatic castration-resistant prostate cancer

To determine the optimal number of cycles of docetaxel for metastatic castration-resistant prostate cancer, we retrospectively collected 73 patients receiving varying numbers of docetaxel plus prednisolone and analyzed the clinical outcomes including overall survival, prostate-specific antigen (PSA)...

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Bibliographic Details
Main Authors: Yuan-Chi Shen, Po-Hui Chiang, Hao-Lun Luo, Yao-Chi Chuang, Yen-Ta Chen, Chih-Hsiung Kang, Chun-Chien Hsu, Wei-Ching Lee, Yuan-Tso Cheng
Format: Article
Language:English
Published: Wiley 2016-09-01
Series:Kaohsiung Journal of Medical Sciences
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Online Access:http://www.sciencedirect.com/science/article/pii/S1607551X16301322
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Summary:To determine the optimal number of cycles of docetaxel for metastatic castration-resistant prostate cancer, we retrospectively collected 73 patients receiving varying numbers of docetaxel plus prednisolone and analyzed the clinical outcomes including overall survival, prostate-specific antigen (PSA) response, and adverse events. The study included 33 patients receiving ≤ 10 cycles of docetaxel and 40 patients receiving > 10 cycles. Patients receiving > 10 cycles were younger than those who received ≤ 10 cycles. There was no statistical significant difference in overall survival between the two groups (log-rank test, p = 0.75). Adverse effects were more common among patients receiving ≥ 10 cycles of treatment. A PSA flare-up was observed among six patients (8.2%); the median duration of the PSA surge was 3 weeks (range, 3–12 weeks). The overall survival rates in patients with PSA flare-up were comparable with the patients having PSA response. We concluded that at least four cycles of docetaxel should be administered in metastatic castration-resistant prostate cancer patients in order not to cease treatment prematurely from potentially beneficial chemotherapy. However, administering > 10 cycles does not result in any further improvement in survival and is associated with more adverse effects.
ISSN:1607-551X