Benefits of intermittent/continuous androgen deprivation in patients with advanced prostate cancer
In 1941 Huggins described the effect of castration on prostate cancer. gonadotropin-releasing hormone (GNRH) analogues were introduced in 1985. Complete androgen blockade (association of GNRH analogue with antiandrogen) was introduced by Fernand Labrie to achieve suppression of suprarenal testostero...
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Veröffentlicht in: | Clujul medical 2016, Vol.89 (3), p.419-422 |
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description | In 1941 Huggins described the effect of castration on prostate cancer. gonadotropin-releasing hormone (GNRH) analogues were introduced in 1985. Complete androgen blockade (association of GNRH analogue with antiandrogen) was introduced by Fernand Labrie to achieve suppression of suprarenal testosterone. Long time androgen deprivation lead to androgen independence of the prostate cancer cell. Our principal aim was to demonstrate longer survival rates on prostate cancer patients with intermittent androgen deprivation.
82 patients in the Urology Department of Vasile Goldis West University Arad were included into two groups, with continuous and intermittent androgen deprivation.Treatment efficiency was assessed by the level of testosterone and PSA.Adverse events (AE) and serious adverse events were reported according to Common Terminology Criteria of Adverse Events (CTCAE) of the National Cancer Institute (NCI).
Evolution towards castrate resistant prostate cancer: 12.5% from the intermittent androgen deprivation group and 23.8% from the continuous androgen deprivation groupMortality rate: 15% of patients from the intermittent androgen deprivation group; 19% of patients from the continuous androgen deprivation group.
Better quality of life (Qol) in periods without treatment due to testosteron recovery;Less AE's and metabolic syndrome (MS) related complications;Better survival and longer time of disease control andCost reduction. |
doi_str_mv | 10.15386/cjmed-594 |
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82 patients in the Urology Department of Vasile Goldis West University Arad were included into two groups, with continuous and intermittent androgen deprivation.Treatment efficiency was assessed by the level of testosterone and PSA.Adverse events (AE) and serious adverse events were reported according to Common Terminology Criteria of Adverse Events (CTCAE) of the National Cancer Institute (NCI).
Evolution towards castrate resistant prostate cancer: 12.5% from the intermittent androgen deprivation group and 23.8% from the continuous androgen deprivation groupMortality rate: 15% of patients from the intermittent androgen deprivation group; 19% of patients from the continuous androgen deprivation group.
Better quality of life (Qol) in periods without treatment due to testosteron recovery;Less AE's and metabolic syndrome (MS) related complications;Better survival and longer time of disease control andCost reduction.</description><identifier>ISSN: 1222-2119</identifier><identifier>ISSN: 2602-0807</identifier><identifier>EISSN: 2668-0572</identifier><identifier>EISSN: 2066-8872</identifier><identifier>DOI: 10.15386/cjmed-594</identifier><identifier>PMID: 27547063</identifier><language>eng</language><publisher>Romania: Iuliu Hatieganu University of Medicine and Pharmacy</publisher><subject>Original Research</subject><ispartof>Clujul medical, 2016, Vol.89 (3), p.419-422</ispartof><rights>2016</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2934-7fb6ed682c076c69c43f06da0a79abd2bfd37f685f83b41eacfbb3fa48d3cd8b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990439/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990439/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,729,782,786,887,4026,27930,27931,27932,53798,53800</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27547063$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Muresanu, Horia</creatorcontrib><title>Benefits of intermittent/continuous androgen deprivation in patients with advanced prostate cancer</title><title>Clujul medical</title><addtitle>Clujul Med</addtitle><description>In 1941 Huggins described the effect of castration on prostate cancer. gonadotropin-releasing hormone (GNRH) analogues were introduced in 1985. Complete androgen blockade (association of GNRH analogue with antiandrogen) was introduced by Fernand Labrie to achieve suppression of suprarenal testosterone. Long time androgen deprivation lead to androgen independence of the prostate cancer cell. Our principal aim was to demonstrate longer survival rates on prostate cancer patients with intermittent androgen deprivation.
82 patients in the Urology Department of Vasile Goldis West University Arad were included into two groups, with continuous and intermittent androgen deprivation.Treatment efficiency was assessed by the level of testosterone and PSA.Adverse events (AE) and serious adverse events were reported according to Common Terminology Criteria of Adverse Events (CTCAE) of the National Cancer Institute (NCI).
Evolution towards castrate resistant prostate cancer: 12.5% from the intermittent androgen deprivation group and 23.8% from the continuous androgen deprivation groupMortality rate: 15% of patients from the intermittent androgen deprivation group; 19% of patients from the continuous androgen deprivation group.
Better quality of life (Qol) in periods without treatment due to testosteron recovery;Less AE's and metabolic syndrome (MS) related complications;Better survival and longer time of disease control andCost reduction.</description><subject>Original Research</subject><issn>1222-2119</issn><issn>2602-0807</issn><issn>2668-0572</issn><issn>2066-8872</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpVkUtLnDEYhUNR6qBu-gNKlkX4am5fLptCK1oLghtdh1w1ZSaZJpkR_71xxkq7evOSh5OTcwD4hNFXPFPJz93vVfDTrNgHsCCcywnNghyABSaETARjdQROW0sWMaGU4Ep9BEdEzEwgThfA_gg5xNQbLBGm3ENdpd5D7ueu5J7ypmwaNNnX8hAy9GFd09b0VPKA4XqcBtrgU-qP0PityS54uK6lddMDdK97PQGH0SxbOH2bx-D-6vLu4nq6uf356-L7zeSIomwS0fLguSQOCe64coxGxL1BRihjPbHRUxG5nKOkluFgXLSWRsOkp85LS4_Bt73uemNHJG44q2aph-OVqc-6mKT_v8npUT-UrWZKIUbVEPjyJlDLn01oXa9Sc2G5NDmMGDSWmHIiqaADPdujbvy11RDfn8FI73rRu1706GXAn_819o7-bYG-AMfkjkk</recordid><startdate>2016</startdate><enddate>2016</enddate><creator>Muresanu, Horia</creator><general>Iuliu Hatieganu University of Medicine and Pharmacy</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>2016</creationdate><title>Benefits of intermittent/continuous androgen deprivation in patients with advanced prostate cancer</title><author>Muresanu, Horia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2934-7fb6ed682c076c69c43f06da0a79abd2bfd37f685f83b41eacfbb3fa48d3cd8b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Original Research</topic><toplevel>online_resources</toplevel><creatorcontrib>Muresanu, Horia</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clujul medical</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Muresanu, Horia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Benefits of intermittent/continuous androgen deprivation in patients with advanced prostate cancer</atitle><jtitle>Clujul medical</jtitle><addtitle>Clujul Med</addtitle><date>2016</date><risdate>2016</risdate><volume>89</volume><issue>3</issue><spage>419</spage><epage>422</epage><pages>419-422</pages><issn>1222-2119</issn><issn>2602-0807</issn><eissn>2668-0572</eissn><eissn>2066-8872</eissn><abstract>In 1941 Huggins described the effect of castration on prostate cancer. gonadotropin-releasing hormone (GNRH) analogues were introduced in 1985. Complete androgen blockade (association of GNRH analogue with antiandrogen) was introduced by Fernand Labrie to achieve suppression of suprarenal testosterone. Long time androgen deprivation lead to androgen independence of the prostate cancer cell. Our principal aim was to demonstrate longer survival rates on prostate cancer patients with intermittent androgen deprivation.
82 patients in the Urology Department of Vasile Goldis West University Arad were included into two groups, with continuous and intermittent androgen deprivation.Treatment efficiency was assessed by the level of testosterone and PSA.Adverse events (AE) and serious adverse events were reported according to Common Terminology Criteria of Adverse Events (CTCAE) of the National Cancer Institute (NCI).
Evolution towards castrate resistant prostate cancer: 12.5% from the intermittent androgen deprivation group and 23.8% from the continuous androgen deprivation groupMortality rate: 15% of patients from the intermittent androgen deprivation group; 19% of patients from the continuous androgen deprivation group.
Better quality of life (Qol) in periods without treatment due to testosteron recovery;Less AE's and metabolic syndrome (MS) related complications;Better survival and longer time of disease control andCost reduction.</abstract><cop>Romania</cop><pub>Iuliu Hatieganu University of Medicine and Pharmacy</pub><pmid>27547063</pmid><doi>10.15386/cjmed-594</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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title | Benefits of intermittent/continuous androgen deprivation in patients with advanced prostate cancer |
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