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Ethinylestradiol Improves Prostate-specific Antigen Levels in Pretreated Castration-resistant Prostate Cancer Patients
Ethinylestradiol was used as palliative treatment for patients with advanced prostate cancer (PCa). However, its use has declined after the development of combined androgen blockade. In the present study, we analyzed the effects of ethinylestradiol on pretreated castration-resistant PCa patients. Tw...
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Published in: | Anticancer research 2010-12, Vol.30 (12), p.5201-5205 |
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creator | IZUMI, Kouji KADONO, Yoshifumi SHIMA, Takashi KONAKA, Hiroyuki MIZOKAMI, Atsushi KOH, Eitetsu NAMIKI, Mikio |
description | Ethinylestradiol was used as palliative treatment for patients with advanced prostate cancer (PCa). However, its use has declined after the development of combined androgen blockade. In the present study, we analyzed the effects of ethinylestradiol on pretreated castration-resistant PCa patients.
Twenty-four Japanese patients were orally administered ethinylestradiol at a dose of 1.5 mg/day and prostate-specific antigen (PSA) was examined. We retrospectively analyzed the proportion of patients achieving a decline in PSA of >50% and progression-free and overall survival rates.
All patients had already been treated with combined androgen blockade followed by one or more salvage therapies. Median follow-up time was 227 (range: 42-1490) days and median ethinylestradiol treatment time was 195 (range: 3-791) days. The proportion of patients achieving a decline in PSA >50% was 70%. Median progression-free survival was estimated as 300 days. At the end of the follow-up period, one patient had died from PCa. Adverse events occurred in three patients, namely elevation of liver enzymes, anorexia, and heart failure in one patient each.
Oral ethinylestradiol administration may be useful for treatment of advanced castration-resistant PCa after salvage therapy with a high PSA response rate and low adverse event rate. |
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Twenty-four Japanese patients were orally administered ethinylestradiol at a dose of 1.5 mg/day and prostate-specific antigen (PSA) was examined. We retrospectively analyzed the proportion of patients achieving a decline in PSA of >50% and progression-free and overall survival rates.
All patients had already been treated with combined androgen blockade followed by one or more salvage therapies. Median follow-up time was 227 (range: 42-1490) days and median ethinylestradiol treatment time was 195 (range: 3-791) days. The proportion of patients achieving a decline in PSA >50% was 70%. Median progression-free survival was estimated as 300 days. At the end of the follow-up period, one patient had died from PCa. Adverse events occurred in three patients, namely elevation of liver enzymes, anorexia, and heart failure in one patient each.
Oral ethinylestradiol administration may be useful for treatment of advanced castration-resistant PCa after salvage therapy with a high PSA response rate and low adverse event rate.</description><identifier>ISSN: 0250-7005</identifier><identifier>EISSN: 1791-7530</identifier><identifier>PMID: 21187513</identifier><language>eng</language><publisher>Attiki: International Institute of Anticancer Research</publisher><subject>Adenocarcinoma - drug therapy ; Aged ; Aged, 80 and over ; Biological and medical sciences ; Disease-Free Survival ; Ethinyl Estradiol - adverse effects ; Ethinyl Estradiol - therapeutic use ; Humans ; Male ; Medical sciences ; Middle Aged ; Nephrology. Urinary tract diseases ; Orchiectomy ; Prostate-Specific Antigen - blood ; Prostatic Neoplasms - blood ; Prostatic Neoplasms - drug therapy ; Prostatic Neoplasms - surgery ; Retrospective Studies ; Salvage Therapy - methods ; Survival Rate ; Tumors ; Tumors of the urinary system ; Urinary tract. Prostate gland</subject><ispartof>Anticancer research, 2010-12, Vol.30 (12), p.5201-5205</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23653098$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21187513$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>IZUMI, Kouji</creatorcontrib><creatorcontrib>KADONO, Yoshifumi</creatorcontrib><creatorcontrib>SHIMA, Takashi</creatorcontrib><creatorcontrib>KONAKA, Hiroyuki</creatorcontrib><creatorcontrib>MIZOKAMI, Atsushi</creatorcontrib><creatorcontrib>KOH, Eitetsu</creatorcontrib><creatorcontrib>NAMIKI, Mikio</creatorcontrib><title>Ethinylestradiol Improves Prostate-specific Antigen Levels in Pretreated Castration-resistant Prostate Cancer Patients</title><title>Anticancer research</title><addtitle>Anticancer Res</addtitle><description>Ethinylestradiol was used as palliative treatment for patients with advanced prostate cancer (PCa). However, its use has declined after the development of combined androgen blockade. In the present study, we analyzed the effects of ethinylestradiol on pretreated castration-resistant PCa patients.
Twenty-four Japanese patients were orally administered ethinylestradiol at a dose of 1.5 mg/day and prostate-specific antigen (PSA) was examined. We retrospectively analyzed the proportion of patients achieving a decline in PSA of >50% and progression-free and overall survival rates.
All patients had already been treated with combined androgen blockade followed by one or more salvage therapies. Median follow-up time was 227 (range: 42-1490) days and median ethinylestradiol treatment time was 195 (range: 3-791) days. The proportion of patients achieving a decline in PSA >50% was 70%. Median progression-free survival was estimated as 300 days. At the end of the follow-up period, one patient had died from PCa. Adverse events occurred in three patients, namely elevation of liver enzymes, anorexia, and heart failure in one patient each.
Oral ethinylestradiol administration may be useful for treatment of advanced castration-resistant PCa after salvage therapy with a high PSA response rate and low adverse event rate.</description><subject>Adenocarcinoma - drug therapy</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Disease-Free Survival</subject><subject>Ethinyl Estradiol - adverse effects</subject><subject>Ethinyl Estradiol - therapeutic use</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Orchiectomy</subject><subject>Prostate-Specific Antigen - blood</subject><subject>Prostatic Neoplasms - blood</subject><subject>Prostatic Neoplasms - drug therapy</subject><subject>Prostatic Neoplasms - surgery</subject><subject>Retrospective Studies</subject><subject>Salvage Therapy - methods</subject><subject>Survival Rate</subject><subject>Tumors</subject><subject>Tumors of the urinary system</subject><subject>Urinary tract. Prostate gland</subject><issn>0250-7005</issn><issn>1791-7530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNpF0M1LwzAYBvAgipvTf0F6EU-FfDQfO44xdTBwBz2XNH2jkTatSTrYf2_Eqaf3kF8eeJ4zNCdySUrJGT5Hc0w5LiXGfIauYvzAWIilYpdoRglRkhM2R4dNenf-2EFMQbdu6IptP4bhALHYhyEmnaCMIxhnnSlWPrk38MUODtDFwvlsIAXIqC3W-jsiucGXAaLLX336y8iv3kAo9hmAT_EaXVjdRbg53QV6fdi8rJ_K3fPjdr3alSOtcCqlqqzQyhCQTWWpzrcyrQVVGaMZN9i2pmG4aoQVIBjHWlLWEKEEFpxqyhbo_ic3d_qccsm6d9FA12kPwxRrRQlfciFVlrcnOTU9tPUYXK_Dsf6dKoO7E9DR6M6G3MjFf8dEHj3P-wXdO3Xo</recordid><startdate>20101201</startdate><enddate>20101201</enddate><creator>IZUMI, Kouji</creator><creator>KADONO, Yoshifumi</creator><creator>SHIMA, Takashi</creator><creator>KONAKA, Hiroyuki</creator><creator>MIZOKAMI, Atsushi</creator><creator>KOH, Eitetsu</creator><creator>NAMIKI, Mikio</creator><general>International Institute of Anticancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20101201</creationdate><title>Ethinylestradiol Improves Prostate-specific Antigen Levels in Pretreated Castration-resistant Prostate Cancer Patients</title><author>IZUMI, Kouji ; KADONO, Yoshifumi ; SHIMA, Takashi ; KONAKA, Hiroyuki ; MIZOKAMI, Atsushi ; KOH, Eitetsu ; NAMIKI, Mikio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p240t-784f6a8c1e7b4f2a1e74cdfe84cca35c0fdcb304b6f6e6350a723b16860652a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adenocarcinoma - drug therapy</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Disease-Free Survival</topic><topic>Ethinyl Estradiol - adverse effects</topic><topic>Ethinyl Estradiol - therapeutic use</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Orchiectomy</topic><topic>Prostate-Specific Antigen - blood</topic><topic>Prostatic Neoplasms - blood</topic><topic>Prostatic Neoplasms - drug therapy</topic><topic>Prostatic Neoplasms - surgery</topic><topic>Retrospective Studies</topic><topic>Salvage Therapy - methods</topic><topic>Survival Rate</topic><topic>Tumors</topic><topic>Tumors of the urinary system</topic><topic>Urinary tract. Prostate gland</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>IZUMI, Kouji</creatorcontrib><creatorcontrib>KADONO, Yoshifumi</creatorcontrib><creatorcontrib>SHIMA, Takashi</creatorcontrib><creatorcontrib>KONAKA, Hiroyuki</creatorcontrib><creatorcontrib>MIZOKAMI, Atsushi</creatorcontrib><creatorcontrib>KOH, Eitetsu</creatorcontrib><creatorcontrib>NAMIKI, Mikio</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Anticancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>IZUMI, Kouji</au><au>KADONO, Yoshifumi</au><au>SHIMA, Takashi</au><au>KONAKA, Hiroyuki</au><au>MIZOKAMI, Atsushi</au><au>KOH, Eitetsu</au><au>NAMIKI, Mikio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ethinylestradiol Improves Prostate-specific Antigen Levels in Pretreated Castration-resistant Prostate Cancer Patients</atitle><jtitle>Anticancer research</jtitle><addtitle>Anticancer Res</addtitle><date>2010-12-01</date><risdate>2010</risdate><volume>30</volume><issue>12</issue><spage>5201</spage><epage>5205</epage><pages>5201-5205</pages><issn>0250-7005</issn><eissn>1791-7530</eissn><abstract>Ethinylestradiol was used as palliative treatment for patients with advanced prostate cancer (PCa). However, its use has declined after the development of combined androgen blockade. In the present study, we analyzed the effects of ethinylestradiol on pretreated castration-resistant PCa patients.
Twenty-four Japanese patients were orally administered ethinylestradiol at a dose of 1.5 mg/day and prostate-specific antigen (PSA) was examined. We retrospectively analyzed the proportion of patients achieving a decline in PSA of >50% and progression-free and overall survival rates.
All patients had already been treated with combined androgen blockade followed by one or more salvage therapies. Median follow-up time was 227 (range: 42-1490) days and median ethinylestradiol treatment time was 195 (range: 3-791) days. The proportion of patients achieving a decline in PSA >50% was 70%. Median progression-free survival was estimated as 300 days. At the end of the follow-up period, one patient had died from PCa. Adverse events occurred in three patients, namely elevation of liver enzymes, anorexia, and heart failure in one patient each.
Oral ethinylestradiol administration may be useful for treatment of advanced castration-resistant PCa after salvage therapy with a high PSA response rate and low adverse event rate.</abstract><cop>Attiki</cop><pub>International Institute of Anticancer Research</pub><pmid>21187513</pmid><tpages>5</tpages></addata></record> |
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subjects | Adenocarcinoma - drug therapy Aged Aged, 80 and over Biological and medical sciences Disease-Free Survival Ethinyl Estradiol - adverse effects Ethinyl Estradiol - therapeutic use Humans Male Medical sciences Middle Aged Nephrology. Urinary tract diseases Orchiectomy Prostate-Specific Antigen - blood Prostatic Neoplasms - blood Prostatic Neoplasms - drug therapy Prostatic Neoplasms - surgery Retrospective Studies Salvage Therapy - methods Survival Rate Tumors Tumors of the urinary system Urinary tract. Prostate gland |
title | Ethinylestradiol Improves Prostate-specific Antigen Levels in Pretreated Castration-resistant Prostate Cancer Patients |
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