Docetaxel with or without estramustine for estramustine refractory castration-resistant prostate cancer: a single institution experience

<p>Abstract</p> <p>Background</p> <p>The significance of combination of docetaxel (DTX) with estramustine phosphate (EMP) in castration-resistant prostate cancer (CRPC) patients remains unclear. In this study, we aimed to retrospectively evaluate the efficacy and toxici...

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Main Authors: Nakano Kazuhiko, Ohta Shigeyuki, Komatsu Kenji, Kubo Taro, Nukui Akinori, Suzuki Kazumi, Kurokawa Shinsuke, Kobayashi Minoru, Morita Tatsuo
Format: Article
Language:English
Published: BMC 2012-02-01
Series:BMC Urology
Online Access:http://www.biomedcentral.com/1471-2490/12/3
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spelling doaj-a4dd9e35ae2e4e00a3746dd8e46555062020-11-24T21:20:19ZengBMCBMC Urology1471-24902012-02-01121310.1186/1471-2490-12-3Docetaxel with or without estramustine for estramustine refractory castration-resistant prostate cancer: a single institution experienceNakano KazuhikoOhta ShigeyukiKomatsu KenjiKubo TaroNukui AkinoriSuzuki KazumiKurokawa ShinsukeKobayashi MinoruMorita Tatsuo<p>Abstract</p> <p>Background</p> <p>The significance of combination of docetaxel (DTX) with estramustine phosphate (EMP) in castration-resistant prostate cancer (CRPC) patients remains unclear. In this study, we aimed to retrospectively evaluate the efficacy and toxicity of DTX with or without EMP and to elucidate the significance of DTX and EMP combination therapy in Japanese EMP-refractory CRPC patients.</p> <p>Methods</p> <p>To compare the efficacy and toxicity of DTX and EMP, we divided CRPC patients, who were confirmed to be resistant to EMP, into the following two groups: group D (n = 28), which included patients treated with DTX (60 mg/m<sup>2</sup>, once in every four weeks) alone, and group DE (n = 33), which included patients treated with a combination of DTX (60 mg/m<sup>2</sup>, once in every four weeks) and EMP (twice daily oral administration at 280 mg).</p> <p>Results</p> <p>Prostate specific antigen (PSA) response (> 50% decline in PSA) was observed in six patients (21%) in group D and eight patients (24%) in group DE. The median time to progression (TTP) was 12.0 months and 6.2 months and the median overall survival (OS) was 26.4 months and 24.3 months in group D and DE, respectively. There was no statistical difference between the two groups in terms of PSA response, TTP, and OS. The incidence of adverse events of grade 3/4 was low in both the groups, and there was no statistical difference between the two groups.</p> <p>Conclusions</p> <p>Although treatment with DTX at 60 mg/m<sup>2 </sup>was effective and highly tolerated in EMP-refractory Japanese CRPC patients, the DTX and EMP combination therapy might not exhibit any survival benefit for CRPC patients.</p> http://www.biomedcentral.com/1471-2490/12/3
collection DOAJ
language English
format Article
sources DOAJ
author Nakano Kazuhiko
Ohta Shigeyuki
Komatsu Kenji
Kubo Taro
Nukui Akinori
Suzuki Kazumi
Kurokawa Shinsuke
Kobayashi Minoru
Morita Tatsuo
spellingShingle Nakano Kazuhiko
Ohta Shigeyuki
Komatsu Kenji
Kubo Taro
Nukui Akinori
Suzuki Kazumi
Kurokawa Shinsuke
Kobayashi Minoru
Morita Tatsuo
Docetaxel with or without estramustine for estramustine refractory castration-resistant prostate cancer: a single institution experience
BMC Urology
author_facet Nakano Kazuhiko
Ohta Shigeyuki
Komatsu Kenji
Kubo Taro
Nukui Akinori
Suzuki Kazumi
Kurokawa Shinsuke
Kobayashi Minoru
Morita Tatsuo
author_sort Nakano Kazuhiko
title Docetaxel with or without estramustine for estramustine refractory castration-resistant prostate cancer: a single institution experience
title_short Docetaxel with or without estramustine for estramustine refractory castration-resistant prostate cancer: a single institution experience
title_full Docetaxel with or without estramustine for estramustine refractory castration-resistant prostate cancer: a single institution experience
title_fullStr Docetaxel with or without estramustine for estramustine refractory castration-resistant prostate cancer: a single institution experience
title_full_unstemmed Docetaxel with or without estramustine for estramustine refractory castration-resistant prostate cancer: a single institution experience
title_sort docetaxel with or without estramustine for estramustine refractory castration-resistant prostate cancer: a single institution experience
publisher BMC
series BMC Urology
issn 1471-2490
publishDate 2012-02-01
description <p>Abstract</p> <p>Background</p> <p>The significance of combination of docetaxel (DTX) with estramustine phosphate (EMP) in castration-resistant prostate cancer (CRPC) patients remains unclear. In this study, we aimed to retrospectively evaluate the efficacy and toxicity of DTX with or without EMP and to elucidate the significance of DTX and EMP combination therapy in Japanese EMP-refractory CRPC patients.</p> <p>Methods</p> <p>To compare the efficacy and toxicity of DTX and EMP, we divided CRPC patients, who were confirmed to be resistant to EMP, into the following two groups: group D (n = 28), which included patients treated with DTX (60 mg/m<sup>2</sup>, once in every four weeks) alone, and group DE (n = 33), which included patients treated with a combination of DTX (60 mg/m<sup>2</sup>, once in every four weeks) and EMP (twice daily oral administration at 280 mg).</p> <p>Results</p> <p>Prostate specific antigen (PSA) response (> 50% decline in PSA) was observed in six patients (21%) in group D and eight patients (24%) in group DE. The median time to progression (TTP) was 12.0 months and 6.2 months and the median overall survival (OS) was 26.4 months and 24.3 months in group D and DE, respectively. There was no statistical difference between the two groups in terms of PSA response, TTP, and OS. The incidence of adverse events of grade 3/4 was low in both the groups, and there was no statistical difference between the two groups.</p> <p>Conclusions</p> <p>Although treatment with DTX at 60 mg/m<sup>2 </sup>was effective and highly tolerated in EMP-refractory Japanese CRPC patients, the DTX and EMP combination therapy might not exhibit any survival benefit for CRPC patients.</p>
url http://www.biomedcentral.com/1471-2490/12/3
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