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Outcome of Patients with Hormone-Refractory Prostate Cancer: Prognostic Significance of Prostate-Specific Antigen-Doubling Time and Nadir Prostate-Specific Antigen
Objective Most patients with advanced prostate cancer after prostate-specific antigen (PSA) relapse following maximum androgen blockade rapidly progress to death. The present study was aimed to predict the survival of these serious patients after PSA relapse. Methods Sixty-eight patients with M1b an...
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Published in: | Japanese journal of clinical oncology 2008-01, Vol.38 (1), p.36-42 |
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creator | Tomioka, Susumu Shimbo, Masashi Amiya, Yoshiyasu Nakatsu, Hiroomi Murakami, Shino Shimazaki, Jun |
description | Objective Most patients with advanced prostate cancer after prostate-specific antigen (PSA) relapse following maximum androgen blockade rapidly progress to death. The present study was aimed to predict the survival of these serious patients after PSA relapse. Methods Sixty-eight patients with M1b and 20 patients with T3b, who relapsed and died of cancer within a short period, were studied. PSA-doubling time (PSA-DT) at PSA relapse influenced the outcome after PSA relapse [hazard ratio (CI): 2.000 (1.283–3.226)]; thus, on the basis of the median values of PSA-DT (>2 months) and additionally nadir PSA in previous treatment (≤2 ng/ml), patients were stratified into four groups. Outcome in the respective groups was examined. Results The patients with PSA-DT of >2 months and nadir PSA of ≤2 ng/ml showed the longest survival. The other patients in various classifications proceeded with the similarly worse outcomes, in which PSA-DT still influenced survival [hazard ratio (CI): 0.422 (0.203–0.878)]. In several treatments, estramustine phosphate and dexamethasone were relatively effective. A similar rate of response to these drugs was obtained in all four groups, irrespective of stratifying with PSA-DT and nadir PSA, and this may be possibly due to the intervals between relapse and treatments, in which tumor volume was increased and tumor property was altered. Patients responding to treatment showed prolonged survival. Conclusion Both PSA-DT and nadir PSA were predictive factors for subsequent survival at PSA relapse, and the patients with long PSA-DT and low nadir PSA may show long outcome. |
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The present study was aimed to predict the survival of these serious patients after PSA relapse. Methods Sixty-eight patients with M1b and 20 patients with T3b, who relapsed and died of cancer within a short period, were studied. PSA-doubling time (PSA-DT) at PSA relapse influenced the outcome after PSA relapse [hazard ratio (CI): 2.000 (1.283–3.226)]; thus, on the basis of the median values of PSA-DT (>2 months) and additionally nadir PSA in previous treatment (≤2 ng/ml), patients were stratified into four groups. Outcome in the respective groups was examined. Results The patients with PSA-DT of >2 months and nadir PSA of ≤2 ng/ml showed the longest survival. The other patients in various classifications proceeded with the similarly worse outcomes, in which PSA-DT still influenced survival [hazard ratio (CI): 0.422 (0.203–0.878)]. In several treatments, estramustine phosphate and dexamethasone were relatively effective. A similar rate of response to these drugs was obtained in all four groups, irrespective of stratifying with PSA-DT and nadir PSA, and this may be possibly due to the intervals between relapse and treatments, in which tumor volume was increased and tumor property was altered. Patients responding to treatment showed prolonged survival. Conclusion Both PSA-DT and nadir PSA were predictive factors for subsequent survival at PSA relapse, and the patients with long PSA-DT and low nadir PSA may show long outcome.</description><identifier>ISSN: 0368-2811</identifier><identifier>EISSN: 1465-3621</identifier><identifier>DOI: 10.1093/jjco/hym153</identifier><identifier>PMID: 18258713</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Aged ; Antineoplastic Agents, Hormonal - therapeutic use ; hormone-refractory cancer ; Humans ; Male ; nadir PSA ; Neoplasm Recurrence, Local - blood ; Neoplasm Recurrence, Local - mortality ; Neoplasm Recurrence, Local - pathology ; Neoplasms, Hormone-Dependent - blood ; Neoplasms, Hormone-Dependent - mortality ; Neoplasms, Hormone-Dependent - pathology ; Prognosis ; prostate cancer ; Prostate-Specific Antigen - blood ; Prostatic Neoplasms - blood ; Prostatic Neoplasms - mortality ; Prostatic Neoplasms - pathology ; PSA relapse ; PSA-doubling time ; Survival Rate ; Time Factors ; Treatment Outcome</subject><ispartof>Japanese journal of clinical oncology, 2008-01, Vol.38 (1), p.36-42</ispartof><rights>The Authors (2008). Published by Oxford University Press. All rights reserved 2008</rights><rights>The Authors (2008). Published by Oxford University Press. All rights reserved</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-894f32d1a23961170caf797b32892ee152ab5b21fbadae0ae94493a79f81d2343</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18258713$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tomioka, Susumu</creatorcontrib><creatorcontrib>Shimbo, Masashi</creatorcontrib><creatorcontrib>Amiya, Yoshiyasu</creatorcontrib><creatorcontrib>Nakatsu, Hiroomi</creatorcontrib><creatorcontrib>Murakami, Shino</creatorcontrib><creatorcontrib>Shimazaki, Jun</creatorcontrib><title>Outcome of Patients with Hormone-Refractory Prostate Cancer: Prognostic Significance of Prostate-Specific Antigen-Doubling Time and Nadir Prostate-Specific Antigen</title><title>Japanese journal of clinical oncology</title><addtitle>Jpn J Clin Oncol</addtitle><description>Objective Most patients with advanced prostate cancer after prostate-specific antigen (PSA) relapse following maximum androgen blockade rapidly progress to death. The present study was aimed to predict the survival of these serious patients after PSA relapse. Methods Sixty-eight patients with M1b and 20 patients with T3b, who relapsed and died of cancer within a short period, were studied. PSA-doubling time (PSA-DT) at PSA relapse influenced the outcome after PSA relapse [hazard ratio (CI): 2.000 (1.283–3.226)]; thus, on the basis of the median values of PSA-DT (>2 months) and additionally nadir PSA in previous treatment (≤2 ng/ml), patients were stratified into four groups. Outcome in the respective groups was examined. Results The patients with PSA-DT of >2 months and nadir PSA of ≤2 ng/ml showed the longest survival. The other patients in various classifications proceeded with the similarly worse outcomes, in which PSA-DT still influenced survival [hazard ratio (CI): 0.422 (0.203–0.878)]. In several treatments, estramustine phosphate and dexamethasone were relatively effective. A similar rate of response to these drugs was obtained in all four groups, irrespective of stratifying with PSA-DT and nadir PSA, and this may be possibly due to the intervals between relapse and treatments, in which tumor volume was increased and tumor property was altered. Patients responding to treatment showed prolonged survival. Conclusion Both PSA-DT and nadir PSA were predictive factors for subsequent survival at PSA relapse, and the patients with long PSA-DT and low nadir PSA may show long outcome.</description><subject>Aged</subject><subject>Antineoplastic Agents, Hormonal - therapeutic use</subject><subject>hormone-refractory cancer</subject><subject>Humans</subject><subject>Male</subject><subject>nadir PSA</subject><subject>Neoplasm Recurrence, Local - blood</subject><subject>Neoplasm Recurrence, Local - mortality</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Neoplasms, Hormone-Dependent - blood</subject><subject>Neoplasms, Hormone-Dependent - mortality</subject><subject>Neoplasms, Hormone-Dependent - pathology</subject><subject>Prognosis</subject><subject>prostate cancer</subject><subject>Prostate-Specific Antigen - blood</subject><subject>Prostatic Neoplasms - blood</subject><subject>Prostatic Neoplasms - mortality</subject><subject>Prostatic Neoplasms - pathology</subject><subject>PSA relapse</subject><subject>PSA-doubling time</subject><subject>Survival Rate</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><issn>0368-2811</issn><issn>1465-3621</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkU1vEzEQhi0EoqFw4o4sDlyQqT_Wa5tbCR9BFFq1RaBeLK_XmzrN2sH2CvJ7-KPskohKSIjTSDPPvPOOXgAeE_yCYMWOVisbj663PeHsDpiRquaI1ZTcBTPMaomoJOQAPMh5hTHmshL3wQGRlEtB2Az8PB2Kjb2DsYNnpngXSobffbmGi5j6GBw6d10ytsS0hWcp5mKKg3MTrEsvp8YyjD1v4YVfBt95O01-i-1ZdLFxdhrA41D80gX0Og7N2oclvPTjXRNa-Mm0Pv174yG415l1do_29RB8fvvmcr5AJ6fv3s-PT5CtalWQVFXHaEsMZaomRGBrOqFEw6hU1DnCqWl4Q0nXmNY4bJyqKsWMUJ0kLWUVOwTPdrqbFL8NLhfd-2zdem2Ci0PWAlNRSyVH8Olf4CoOKYzeNCWCYE6pGqHnO8iOf-XkOr1JvjdpqwnWU3B6Ck7vghvpJ3vJoelde8vuk7o1F4fNf5TQDvS5uB9_UJNudC2Y4Hrx9Up_PP_yQV294pqzXwnks8w</recordid><startdate>200801</startdate><enddate>200801</enddate><creator>Tomioka, Susumu</creator><creator>Shimbo, Masashi</creator><creator>Amiya, Yoshiyasu</creator><creator>Nakatsu, Hiroomi</creator><creator>Murakami, Shino</creator><creator>Shimazaki, Jun</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200801</creationdate><title>Outcome of Patients with Hormone-Refractory Prostate Cancer: Prognostic Significance of Prostate-Specific Antigen-Doubling Time and Nadir Prostate-Specific Antigen</title><author>Tomioka, Susumu ; Shimbo, Masashi ; Amiya, Yoshiyasu ; Nakatsu, Hiroomi ; Murakami, Shino ; Shimazaki, Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c469t-894f32d1a23961170caf797b32892ee152ab5b21fbadae0ae94493a79f81d2343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Aged</topic><topic>Antineoplastic Agents, Hormonal - therapeutic use</topic><topic>hormone-refractory cancer</topic><topic>Humans</topic><topic>Male</topic><topic>nadir PSA</topic><topic>Neoplasm Recurrence, Local - blood</topic><topic>Neoplasm Recurrence, Local - mortality</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Neoplasms, Hormone-Dependent - blood</topic><topic>Neoplasms, Hormone-Dependent - mortality</topic><topic>Neoplasms, Hormone-Dependent - pathology</topic><topic>Prognosis</topic><topic>prostate cancer</topic><topic>Prostate-Specific Antigen - blood</topic><topic>Prostatic Neoplasms - blood</topic><topic>Prostatic Neoplasms - mortality</topic><topic>Prostatic Neoplasms - pathology</topic><topic>PSA relapse</topic><topic>PSA-doubling time</topic><topic>Survival Rate</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tomioka, Susumu</creatorcontrib><creatorcontrib>Shimbo, Masashi</creatorcontrib><creatorcontrib>Amiya, Yoshiyasu</creatorcontrib><creatorcontrib>Nakatsu, Hiroomi</creatorcontrib><creatorcontrib>Murakami, Shino</creatorcontrib><creatorcontrib>Shimazaki, Jun</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Japanese journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tomioka, Susumu</au><au>Shimbo, Masashi</au><au>Amiya, Yoshiyasu</au><au>Nakatsu, Hiroomi</au><au>Murakami, Shino</au><au>Shimazaki, Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Outcome of Patients with Hormone-Refractory Prostate Cancer: Prognostic Significance of Prostate-Specific Antigen-Doubling Time and Nadir Prostate-Specific Antigen</atitle><jtitle>Japanese journal of clinical oncology</jtitle><addtitle>Jpn J Clin Oncol</addtitle><date>2008-01</date><risdate>2008</risdate><volume>38</volume><issue>1</issue><spage>36</spage><epage>42</epage><pages>36-42</pages><issn>0368-2811</issn><eissn>1465-3621</eissn><abstract>Objective Most patients with advanced prostate cancer after prostate-specific antigen (PSA) relapse following maximum androgen blockade rapidly progress to death. The present study was aimed to predict the survival of these serious patients after PSA relapse. Methods Sixty-eight patients with M1b and 20 patients with T3b, who relapsed and died of cancer within a short period, were studied. PSA-doubling time (PSA-DT) at PSA relapse influenced the outcome after PSA relapse [hazard ratio (CI): 2.000 (1.283–3.226)]; thus, on the basis of the median values of PSA-DT (>2 months) and additionally nadir PSA in previous treatment (≤2 ng/ml), patients were stratified into four groups. Outcome in the respective groups was examined. Results The patients with PSA-DT of >2 months and nadir PSA of ≤2 ng/ml showed the longest survival. The other patients in various classifications proceeded with the similarly worse outcomes, in which PSA-DT still influenced survival [hazard ratio (CI): 0.422 (0.203–0.878)]. In several treatments, estramustine phosphate and dexamethasone were relatively effective. A similar rate of response to these drugs was obtained in all four groups, irrespective of stratifying with PSA-DT and nadir PSA, and this may be possibly due to the intervals between relapse and treatments, in which tumor volume was increased and tumor property was altered. Patients responding to treatment showed prolonged survival. Conclusion Both PSA-DT and nadir PSA were predictive factors for subsequent survival at PSA relapse, and the patients with long PSA-DT and low nadir PSA may show long outcome.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>18258713</pmid><doi>10.1093/jjco/hym153</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Antineoplastic Agents, Hormonal - therapeutic use hormone-refractory cancer Humans Male nadir PSA Neoplasm Recurrence, Local - blood Neoplasm Recurrence, Local - mortality Neoplasm Recurrence, Local - pathology Neoplasms, Hormone-Dependent - blood Neoplasms, Hormone-Dependent - mortality Neoplasms, Hormone-Dependent - pathology Prognosis prostate cancer Prostate-Specific Antigen - blood Prostatic Neoplasms - blood Prostatic Neoplasms - mortality Prostatic Neoplasms - pathology PSA relapse PSA-doubling time Survival Rate Time Factors Treatment Outcome |
title | Outcome of Patients with Hormone-Refractory Prostate Cancer: Prognostic Significance of Prostate-Specific Antigen-Doubling Time and Nadir Prostate-Specific Antigen |
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