Oncological outcome of docetaxel-based chemotherapy for Japanese men with metastatic castration-resistant prostate cancer

Abstract Objectives To retrospectively review the oncologic outcomes of docetaxel-based chemotherapy in Japanese men with metastatic castration-resistant prostate cancer (mCRPC). Materials and methods This study included 257 consecutive Japanese patients with mCRPC who were treated with docetaxel-ba...

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Veröffentlicht in:Urologic oncology 2013-08, Vol.31 (6), p.733-738
Hauptverfasser: Miyake, Hideaki, M.D., Ph.D, Sakai, Iori, M.D., Ph.D, Terakawa, Tomoaki, M.D., Ph.D, Harada, Ken-ichi, M.D, Fujisawa, Masato, M.D., Ph.D
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container_issue 6
container_start_page 733
container_title Urologic oncology
container_volume 31
creator Miyake, Hideaki, M.D., Ph.D
Sakai, Iori, M.D., Ph.D
Terakawa, Tomoaki, M.D., Ph.D
Harada, Ken-ichi, M.D
Fujisawa, Masato, M.D., Ph.D
description Abstract Objectives To retrospectively review the oncologic outcomes of docetaxel-based chemotherapy in Japanese men with metastatic castration-resistant prostate cancer (mCRPC). Materials and methods This study included 257 consecutive Japanese patients with mCRPC who were treated with docetaxel-based chemotherapy between April 2007 and March 2010. The prognostic significance of several clinicopathologic factors in these patients was analyzed. Results In these 257 patients, the median age and serum value of prostate-specific antigen (PSA) prior to docetaxel-based chemotherapy were 72 years and 43.0 ng/ml, respectively. Of these patients, 64 (24.9%) and 193 (75.1%) received docetaxel as a weekly (30 mg/m2 ) and 3-weekly (70–75 mg/m2 ) regimen, respectively, and estramustine (EM) was administered in combination with docetaxel in 137 (53.3%). PSA decline was observed in 205 patients (79.8%), including 143 (55.6%) achieving PSA decline ≥ 50%. The median progression-free survival and overall survival (OS) were 4.3 and 25.4 months, respectively. Of several factors examined, univariate analysis identified performance status (PS), PSA value, significant clinical pain, bone metastasis, prior treatment with EM, treatment cycle, and PSA response as significant predictors of OS, of which only PS, significant clinical pain, prior treatment with EM, treatment cycle, and PSA response appeared to be independently related to OS on multivariate analysis. Furthermore, there were significant differences in OS according to positive numbers of these 5 independent risk factors. Conclusions Oncologic outcomes in Japanese mCRPC patients receiving docetaxel-based chemotherapy is generally favorable, and the risk stratification presented in this study may contribute to precisely predicting the prognosis of such patients.
doi_str_mv 10.1016/j.urolonc.2011.06.006
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Materials and methods This study included 257 consecutive Japanese patients with mCRPC who were treated with docetaxel-based chemotherapy between April 2007 and March 2010. The prognostic significance of several clinicopathologic factors in these patients was analyzed. Results In these 257 patients, the median age and serum value of prostate-specific antigen (PSA) prior to docetaxel-based chemotherapy were 72 years and 43.0 ng/ml, respectively. Of these patients, 64 (24.9%) and 193 (75.1%) received docetaxel as a weekly (30 mg/m2 ) and 3-weekly (70–75 mg/m2 ) regimen, respectively, and estramustine (EM) was administered in combination with docetaxel in 137 (53.3%). PSA decline was observed in 205 patients (79.8%), including 143 (55.6%) achieving PSA decline ≥ 50%. The median progression-free survival and overall survival (OS) were 4.3 and 25.4 months, respectively. Of several factors examined, univariate analysis identified performance status (PS), PSA value, significant clinical pain, bone metastasis, prior treatment with EM, treatment cycle, and PSA response as significant predictors of OS, of which only PS, significant clinical pain, prior treatment with EM, treatment cycle, and PSA response appeared to be independently related to OS on multivariate analysis. Furthermore, there were significant differences in OS according to positive numbers of these 5 independent risk factors. Conclusions Oncologic outcomes in Japanese mCRPC patients receiving docetaxel-based chemotherapy is generally favorable, and the risk stratification presented in this study may contribute to precisely predicting the prognosis of such patients.</description><identifier>ISSN: 1078-1439</identifier><identifier>EISSN: 1873-2496</identifier><identifier>DOI: 10.1016/j.urolonc.2011.06.006</identifier><identifier>PMID: 21782481</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aged ; Aged, 80 and over ; Antineoplastic Agents - therapeutic use ; Castration-resistant prostate cancer ; Disease-Free Survival ; Docetaxel ; Humans ; Japan ; Male ; Middle Aged ; Neoplasm Metastasis ; Overall survival ; Prognosis ; Prostate-Specific Antigen - blood ; Prostatic Neoplasms, Castration-Resistant - drug therapy ; Prostatic Neoplasms, Castration-Resistant - pathology ; Retrospective Studies ; Risk ; Taxoids - therapeutic use ; Treatment Outcome ; Urology</subject><ispartof>Urologic oncology, 2013-08, Vol.31 (6), p.733-738</ispartof><rights>Elsevier Inc.</rights><rights>2013 Elsevier Inc.</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-3bf7816aa66cf367d443d80ef484ce7d26a0dc71a7000144570b8a74482ad27b3</citedby><cites>FETCH-LOGICAL-c420t-3bf7816aa66cf367d443d80ef484ce7d26a0dc71a7000144570b8a74482ad27b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1078143911001931$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21782481$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miyake, Hideaki, M.D., Ph.D</creatorcontrib><creatorcontrib>Sakai, Iori, M.D., Ph.D</creatorcontrib><creatorcontrib>Terakawa, Tomoaki, M.D., Ph.D</creatorcontrib><creatorcontrib>Harada, Ken-ichi, M.D</creatorcontrib><creatorcontrib>Fujisawa, Masato, M.D., Ph.D</creatorcontrib><title>Oncological outcome of docetaxel-based chemotherapy for Japanese men with metastatic castration-resistant prostate cancer</title><title>Urologic oncology</title><addtitle>Urol Oncol</addtitle><description>Abstract Objectives To retrospectively review the oncologic outcomes of docetaxel-based chemotherapy in Japanese men with metastatic castration-resistant prostate cancer (mCRPC). Materials and methods This study included 257 consecutive Japanese patients with mCRPC who were treated with docetaxel-based chemotherapy between April 2007 and March 2010. The prognostic significance of several clinicopathologic factors in these patients was analyzed. Results In these 257 patients, the median age and serum value of prostate-specific antigen (PSA) prior to docetaxel-based chemotherapy were 72 years and 43.0 ng/ml, respectively. Of these patients, 64 (24.9%) and 193 (75.1%) received docetaxel as a weekly (30 mg/m2 ) and 3-weekly (70–75 mg/m2 ) regimen, respectively, and estramustine (EM) was administered in combination with docetaxel in 137 (53.3%). PSA decline was observed in 205 patients (79.8%), including 143 (55.6%) achieving PSA decline ≥ 50%. The median progression-free survival and overall survival (OS) were 4.3 and 25.4 months, respectively. Of several factors examined, univariate analysis identified performance status (PS), PSA value, significant clinical pain, bone metastasis, prior treatment with EM, treatment cycle, and PSA response as significant predictors of OS, of which only PS, significant clinical pain, prior treatment with EM, treatment cycle, and PSA response appeared to be independently related to OS on multivariate analysis. Furthermore, there were significant differences in OS according to positive numbers of these 5 independent risk factors. 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Sakai, Iori, M.D., Ph.D ; Terakawa, Tomoaki, M.D., Ph.D ; Harada, Ken-ichi, M.D ; Fujisawa, Masato, M.D., Ph.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-3bf7816aa66cf367d443d80ef484ce7d26a0dc71a7000144570b8a74482ad27b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Castration-resistant prostate cancer</topic><topic>Disease-Free Survival</topic><topic>Docetaxel</topic><topic>Humans</topic><topic>Japan</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm Metastasis</topic><topic>Overall survival</topic><topic>Prognosis</topic><topic>Prostate-Specific Antigen - blood</topic><topic>Prostatic Neoplasms, Castration-Resistant - drug therapy</topic><topic>Prostatic Neoplasms, Castration-Resistant - pathology</topic><topic>Retrospective Studies</topic><topic>Risk</topic><topic>Taxoids - therapeutic use</topic><topic>Treatment Outcome</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miyake, Hideaki, M.D., Ph.D</creatorcontrib><creatorcontrib>Sakai, Iori, M.D., Ph.D</creatorcontrib><creatorcontrib>Terakawa, Tomoaki, M.D., Ph.D</creatorcontrib><creatorcontrib>Harada, Ken-ichi, M.D</creatorcontrib><creatorcontrib>Fujisawa, Masato, M.D., Ph.D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Urologic oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miyake, Hideaki, M.D., Ph.D</au><au>Sakai, Iori, M.D., Ph.D</au><au>Terakawa, Tomoaki, M.D., Ph.D</au><au>Harada, Ken-ichi, M.D</au><au>Fujisawa, Masato, M.D., Ph.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oncological outcome of docetaxel-based chemotherapy for Japanese men with metastatic castration-resistant prostate cancer</atitle><jtitle>Urologic oncology</jtitle><addtitle>Urol Oncol</addtitle><date>2013-08-01</date><risdate>2013</risdate><volume>31</volume><issue>6</issue><spage>733</spage><epage>738</epage><pages>733-738</pages><issn>1078-1439</issn><eissn>1873-2496</eissn><abstract>Abstract Objectives To retrospectively review the oncologic outcomes of docetaxel-based chemotherapy in Japanese men with metastatic castration-resistant prostate cancer (mCRPC). Materials and methods This study included 257 consecutive Japanese patients with mCRPC who were treated with docetaxel-based chemotherapy between April 2007 and March 2010. The prognostic significance of several clinicopathologic factors in these patients was analyzed. Results In these 257 patients, the median age and serum value of prostate-specific antigen (PSA) prior to docetaxel-based chemotherapy were 72 years and 43.0 ng/ml, respectively. Of these patients, 64 (24.9%) and 193 (75.1%) received docetaxel as a weekly (30 mg/m2 ) and 3-weekly (70–75 mg/m2 ) regimen, respectively, and estramustine (EM) was administered in combination with docetaxel in 137 (53.3%). PSA decline was observed in 205 patients (79.8%), including 143 (55.6%) achieving PSA decline ≥ 50%. The median progression-free survival and overall survival (OS) were 4.3 and 25.4 months, respectively. Of several factors examined, univariate analysis identified performance status (PS), PSA value, significant clinical pain, bone metastasis, prior treatment with EM, treatment cycle, and PSA response as significant predictors of OS, of which only PS, significant clinical pain, prior treatment with EM, treatment cycle, and PSA response appeared to be independently related to OS on multivariate analysis. Furthermore, there were significant differences in OS according to positive numbers of these 5 independent risk factors. Conclusions Oncologic outcomes in Japanese mCRPC patients receiving docetaxel-based chemotherapy is generally favorable, and the risk stratification presented in this study may contribute to precisely predicting the prognosis of such patients.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21782481</pmid><doi>10.1016/j.urolonc.2011.06.006</doi><tpages>6</tpages></addata></record>
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subjects Aged
Aged, 80 and over
Antineoplastic Agents - therapeutic use
Castration-resistant prostate cancer
Disease-Free Survival
Docetaxel
Humans
Japan
Male
Middle Aged
Neoplasm Metastasis
Overall survival
Prognosis
Prostate-Specific Antigen - blood
Prostatic Neoplasms, Castration-Resistant - drug therapy
Prostatic Neoplasms, Castration-Resistant - pathology
Retrospective Studies
Risk
Taxoids - therapeutic use
Treatment Outcome
Urology
title Oncological outcome of docetaxel-based chemotherapy for Japanese men with metastatic castration-resistant prostate cancer
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