The Effect of Radium-223 Therapy in Agent Orange-Related Prostate Carcinoma
Radium-223 (Ra-223) radioisotope has been reported to increase median survival in bone metastatic prostate carcinoma. The addition of Ra-223 to abiraterone was associated with an increased risk of bone fractures. There has been no comprehensive data for using Ra-223 in veterans who were exposed to A...
Gespeichert in:
Veröffentlicht in: | Federal Practitioner 2020-12, Vol.37 (12), p.570-574 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 574 |
---|---|
container_issue | 12 |
container_start_page | 570 |
container_title | Federal Practitioner |
container_volume | 37 |
creator | Liman, Andrew Shah, Rashmikant Passero, Vida Tan, Jocelyn Rai, Hema Harrold, Laurie Tokarsky, Joyce Liman, Agnes Gupta, Vidhi Gerszten, Kristina |
description | Radium-223 (Ra-223) radioisotope has been reported to increase median survival in bone metastatic prostate carcinoma. The addition of Ra-223 to abiraterone was associated with an increased risk of bone fractures. There has been no comprehensive data for using Ra-223 in veterans who were exposed to Agent Orange (AO+).
We present a retrospective study of veterans with bone metastatic castration-resistant prostate cancer (CRPC) who received standard doses of Ra-223 and other sequential therapies at US Department of Veterans Affairs Pittsburgh Healthcare System in Pennsylvania from January 2014 to January 2019. Veterans were divided into 2 groups: those who were exposed to Agent Orange (AO+) and those who had no exposure (AO-). Time to study was calculated from the initiation of Ra-223. Time to skeletal-related events (SRE), progression of prostate specific antigen (PSA), bone metastasis, and alkaline phosphatase (ALP) were calculated in months using unpaired t test with 2-tailed
values. Median survival was calculated by Kaplan Meier R log-rank test.
There were 34 veterans with bone metastatic CRPC: 17 veterans (50%) were AO+ and 17 veterans (50%) were AO-. The mean age of diagnosis of AO+ veterans was 62 years and 69 years (
= .005) for AO- veterans (the mean Gleason score 8.2 and 8.0, respectively [
= .71]). The median number of Ra-223 cycles was 6 (60%). Ten veterans received Ra-223 as first line (29%) and 24 veterans received Ra-223 later (71%). There were 12 SREs with median survival of 15 months. There was no difference in mean time to SRE between AO+ (8 veterans, 10.6 months) and AO- (4 veterans, 10.3 months) (
= .93). The mean time to PSA progression for AO+ was 5.4 months and AO- was 6.8 months (
= .28). Mean time to bone progression for AO+ was 7.6 months and AO- was 10.1 months (
= .16). Mean time to ALP progression for AO+ and AO- was 6.3 months and 8.7 months, respectively (
= .05). Twenty veterans (58%) had died. Median survival for Ra-223 first was 32 months and for Ra-223 later was 15 months (
= .14; hazard ratio [HR] 0.48; 95% CI, 0.17-1.3). Median survival for AO+ and AO- veterans was 12 months and 18 months, respectively (
= .15; HR, 2.0; 95% CI, 0.77-5.0).
There was no statistical difference between AO+ and AO- veterans in terms of time to SRE, PSA, bone and ALP progression, even though there was a trend of shorter duration in AO+ veterans. There was no median survival difference between Ra-223 first vs Ra-223 later as well as between AO+ a |
doi_str_mv | 10.12788/fp.0062 |
format | Article |
fullrecord | <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7789849</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>33424216</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1782-8c9506b64129372e0a1aefd5e47c9d2410c16bf7122cc0474e2c7ecd0af17ed83</originalsourceid><addsrcrecordid>eNpVUNtKAzEUDKJYrYJfIHn0ZWtu3SQvQin1goVKqeBbSJOTdqV7IbsV-vdGq0WfzsDMmTNnELqiZECZVOo2NANCcnaEzqgWw4xz-XacMJEqE0LLHjpv23dCqGZanqIe54IJRvMz9LxYA56EAK7DdcBz64ttmTHGcSKibXa4qPBoBVWHZ9FWK8jmsLEdePwS67ZLCI9tdEVVl_YCnQS7aeHyZ_bR6_1kMX7MprOHp_FomjkqFcuU00OSL3NBmeaSAbHUQvBDENJpzwQljubLICljzhEhBTAnwXliA5XgFe-ju71vs12W4F0KF-3GNLEobdyZ2hbmP1MVa7OqP4yUSiuhk8HN3sClH9oI4bBLifku1ITGfBWapNd_bx2Evw3yTyvvcLU</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>The Effect of Radium-223 Therapy in Agent Orange-Related Prostate Carcinoma</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Liman, Andrew ; Shah, Rashmikant ; Passero, Vida ; Tan, Jocelyn ; Rai, Hema ; Harrold, Laurie ; Tokarsky, Joyce ; Liman, Agnes ; Gupta, Vidhi ; Gerszten, Kristina</creator><creatorcontrib>Liman, Andrew ; Shah, Rashmikant ; Passero, Vida ; Tan, Jocelyn ; Rai, Hema ; Harrold, Laurie ; Tokarsky, Joyce ; Liman, Agnes ; Gupta, Vidhi ; Gerszten, Kristina</creatorcontrib><description>Radium-223 (Ra-223) radioisotope has been reported to increase median survival in bone metastatic prostate carcinoma. The addition of Ra-223 to abiraterone was associated with an increased risk of bone fractures. There has been no comprehensive data for using Ra-223 in veterans who were exposed to Agent Orange (AO+).
We present a retrospective study of veterans with bone metastatic castration-resistant prostate cancer (CRPC) who received standard doses of Ra-223 and other sequential therapies at US Department of Veterans Affairs Pittsburgh Healthcare System in Pennsylvania from January 2014 to January 2019. Veterans were divided into 2 groups: those who were exposed to Agent Orange (AO+) and those who had no exposure (AO-). Time to study was calculated from the initiation of Ra-223. Time to skeletal-related events (SRE), progression of prostate specific antigen (PSA), bone metastasis, and alkaline phosphatase (ALP) were calculated in months using unpaired t test with 2-tailed
values. Median survival was calculated by Kaplan Meier R log-rank test.
There were 34 veterans with bone metastatic CRPC: 17 veterans (50%) were AO+ and 17 veterans (50%) were AO-. The mean age of diagnosis of AO+ veterans was 62 years and 69 years (
= .005) for AO- veterans (the mean Gleason score 8.2 and 8.0, respectively [
= .71]). The median number of Ra-223 cycles was 6 (60%). Ten veterans received Ra-223 as first line (29%) and 24 veterans received Ra-223 later (71%). There were 12 SREs with median survival of 15 months. There was no difference in mean time to SRE between AO+ (8 veterans, 10.6 months) and AO- (4 veterans, 10.3 months) (
= .93). The mean time to PSA progression for AO+ was 5.4 months and AO- was 6.8 months (
= .28). Mean time to bone progression for AO+ was 7.6 months and AO- was 10.1 months (
= .16). Mean time to ALP progression for AO+ and AO- was 6.3 months and 8.7 months, respectively (
= .05). Twenty veterans (58%) had died. Median survival for Ra-223 first was 32 months and for Ra-223 later was 15 months (
= .14; hazard ratio [HR] 0.48; 95% CI, 0.17-1.3). Median survival for AO+ and AO- veterans was 12 months and 18 months, respectively (
= .15; HR, 2.0; 95% CI, 0.77-5.0).
There was no statistical difference between AO+ and AO- veterans in terms of time to SRE, PSA, bone and ALP progression, even though there was a trend of shorter duration in AO+ veterans. There was no median survival difference between Ra-223 first vs Ra-223 later as well as between AO+ and AO- but there is a trend of worse survival in AO+ veterans.</description><identifier>ISSN: 1078-4497</identifier><identifier>EISSN: 1945-337X</identifier><identifier>DOI: 10.12788/fp.0062</identifier><identifier>PMID: 33424216</identifier><language>eng</language><publisher>United States: Frontline Medical Communications Inc</publisher><ispartof>Federal Practitioner, 2020-12, Vol.37 (12), p.570-574</ispartof><rights>Copyright © 2020 Frontline Medical Communications Inc., Parsippany, NJ, USA.</rights><rights>Copyright © 2020 Frontline Medical Communications Inc., Parsippany, NJ, USA. 2020</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789849/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7789849/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33424216$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liman, Andrew</creatorcontrib><creatorcontrib>Shah, Rashmikant</creatorcontrib><creatorcontrib>Passero, Vida</creatorcontrib><creatorcontrib>Tan, Jocelyn</creatorcontrib><creatorcontrib>Rai, Hema</creatorcontrib><creatorcontrib>Harrold, Laurie</creatorcontrib><creatorcontrib>Tokarsky, Joyce</creatorcontrib><creatorcontrib>Liman, Agnes</creatorcontrib><creatorcontrib>Gupta, Vidhi</creatorcontrib><creatorcontrib>Gerszten, Kristina</creatorcontrib><title>The Effect of Radium-223 Therapy in Agent Orange-Related Prostate Carcinoma</title><title>Federal Practitioner</title><addtitle>Fed Pract</addtitle><description>Radium-223 (Ra-223) radioisotope has been reported to increase median survival in bone metastatic prostate carcinoma. The addition of Ra-223 to abiraterone was associated with an increased risk of bone fractures. There has been no comprehensive data for using Ra-223 in veterans who were exposed to Agent Orange (AO+).
We present a retrospective study of veterans with bone metastatic castration-resistant prostate cancer (CRPC) who received standard doses of Ra-223 and other sequential therapies at US Department of Veterans Affairs Pittsburgh Healthcare System in Pennsylvania from January 2014 to January 2019. Veterans were divided into 2 groups: those who were exposed to Agent Orange (AO+) and those who had no exposure (AO-). Time to study was calculated from the initiation of Ra-223. Time to skeletal-related events (SRE), progression of prostate specific antigen (PSA), bone metastasis, and alkaline phosphatase (ALP) were calculated in months using unpaired t test with 2-tailed
values. Median survival was calculated by Kaplan Meier R log-rank test.
There were 34 veterans with bone metastatic CRPC: 17 veterans (50%) were AO+ and 17 veterans (50%) were AO-. The mean age of diagnosis of AO+ veterans was 62 years and 69 years (
= .005) for AO- veterans (the mean Gleason score 8.2 and 8.0, respectively [
= .71]). The median number of Ra-223 cycles was 6 (60%). Ten veterans received Ra-223 as first line (29%) and 24 veterans received Ra-223 later (71%). There were 12 SREs with median survival of 15 months. There was no difference in mean time to SRE between AO+ (8 veterans, 10.6 months) and AO- (4 veterans, 10.3 months) (
= .93). The mean time to PSA progression for AO+ was 5.4 months and AO- was 6.8 months (
= .28). Mean time to bone progression for AO+ was 7.6 months and AO- was 10.1 months (
= .16). Mean time to ALP progression for AO+ and AO- was 6.3 months and 8.7 months, respectively (
= .05). Twenty veterans (58%) had died. Median survival for Ra-223 first was 32 months and for Ra-223 later was 15 months (
= .14; hazard ratio [HR] 0.48; 95% CI, 0.17-1.3). Median survival for AO+ and AO- veterans was 12 months and 18 months, respectively (
= .15; HR, 2.0; 95% CI, 0.77-5.0).
There was no statistical difference between AO+ and AO- veterans in terms of time to SRE, PSA, bone and ALP progression, even though there was a trend of shorter duration in AO+ veterans. There was no median survival difference between Ra-223 first vs Ra-223 later as well as between AO+ and AO- but there is a trend of worse survival in AO+ veterans.</description><issn>1078-4497</issn><issn>1945-337X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpVUNtKAzEUDKJYrYJfIHn0ZWtu3SQvQin1goVKqeBbSJOTdqV7IbsV-vdGq0WfzsDMmTNnELqiZECZVOo2NANCcnaEzqgWw4xz-XacMJEqE0LLHjpv23dCqGZanqIe54IJRvMz9LxYA56EAK7DdcBz64ttmTHGcSKibXa4qPBoBVWHZ9FWK8jmsLEdePwS67ZLCI9tdEVVl_YCnQS7aeHyZ_bR6_1kMX7MprOHp_FomjkqFcuU00OSL3NBmeaSAbHUQvBDENJpzwQljubLICljzhEhBTAnwXliA5XgFe-ju71vs12W4F0KF-3GNLEobdyZ2hbmP1MVa7OqP4yUSiuhk8HN3sClH9oI4bBLifku1ITGfBWapNd_bx2Evw3yTyvvcLU</recordid><startdate>20201201</startdate><enddate>20201201</enddate><creator>Liman, Andrew</creator><creator>Shah, Rashmikant</creator><creator>Passero, Vida</creator><creator>Tan, Jocelyn</creator><creator>Rai, Hema</creator><creator>Harrold, Laurie</creator><creator>Tokarsky, Joyce</creator><creator>Liman, Agnes</creator><creator>Gupta, Vidhi</creator><creator>Gerszten, Kristina</creator><general>Frontline Medical Communications Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20201201</creationdate><title>The Effect of Radium-223 Therapy in Agent Orange-Related Prostate Carcinoma</title><author>Liman, Andrew ; Shah, Rashmikant ; Passero, Vida ; Tan, Jocelyn ; Rai, Hema ; Harrold, Laurie ; Tokarsky, Joyce ; Liman, Agnes ; Gupta, Vidhi ; Gerszten, Kristina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1782-8c9506b64129372e0a1aefd5e47c9d2410c16bf7122cc0474e2c7ecd0af17ed83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Liman, Andrew</creatorcontrib><creatorcontrib>Shah, Rashmikant</creatorcontrib><creatorcontrib>Passero, Vida</creatorcontrib><creatorcontrib>Tan, Jocelyn</creatorcontrib><creatorcontrib>Rai, Hema</creatorcontrib><creatorcontrib>Harrold, Laurie</creatorcontrib><creatorcontrib>Tokarsky, Joyce</creatorcontrib><creatorcontrib>Liman, Agnes</creatorcontrib><creatorcontrib>Gupta, Vidhi</creatorcontrib><creatorcontrib>Gerszten, Kristina</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Federal Practitioner</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liman, Andrew</au><au>Shah, Rashmikant</au><au>Passero, Vida</au><au>Tan, Jocelyn</au><au>Rai, Hema</au><au>Harrold, Laurie</au><au>Tokarsky, Joyce</au><au>Liman, Agnes</au><au>Gupta, Vidhi</au><au>Gerszten, Kristina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Effect of Radium-223 Therapy in Agent Orange-Related Prostate Carcinoma</atitle><jtitle>Federal Practitioner</jtitle><addtitle>Fed Pract</addtitle><date>2020-12-01</date><risdate>2020</risdate><volume>37</volume><issue>12</issue><spage>570</spage><epage>574</epage><pages>570-574</pages><issn>1078-4497</issn><eissn>1945-337X</eissn><abstract>Radium-223 (Ra-223) radioisotope has been reported to increase median survival in bone metastatic prostate carcinoma. The addition of Ra-223 to abiraterone was associated with an increased risk of bone fractures. There has been no comprehensive data for using Ra-223 in veterans who were exposed to Agent Orange (AO+).
We present a retrospective study of veterans with bone metastatic castration-resistant prostate cancer (CRPC) who received standard doses of Ra-223 and other sequential therapies at US Department of Veterans Affairs Pittsburgh Healthcare System in Pennsylvania from January 2014 to January 2019. Veterans were divided into 2 groups: those who were exposed to Agent Orange (AO+) and those who had no exposure (AO-). Time to study was calculated from the initiation of Ra-223. Time to skeletal-related events (SRE), progression of prostate specific antigen (PSA), bone metastasis, and alkaline phosphatase (ALP) were calculated in months using unpaired t test with 2-tailed
values. Median survival was calculated by Kaplan Meier R log-rank test.
There were 34 veterans with bone metastatic CRPC: 17 veterans (50%) were AO+ and 17 veterans (50%) were AO-. The mean age of diagnosis of AO+ veterans was 62 years and 69 years (
= .005) for AO- veterans (the mean Gleason score 8.2 and 8.0, respectively [
= .71]). The median number of Ra-223 cycles was 6 (60%). Ten veterans received Ra-223 as first line (29%) and 24 veterans received Ra-223 later (71%). There were 12 SREs with median survival of 15 months. There was no difference in mean time to SRE between AO+ (8 veterans, 10.6 months) and AO- (4 veterans, 10.3 months) (
= .93). The mean time to PSA progression for AO+ was 5.4 months and AO- was 6.8 months (
= .28). Mean time to bone progression for AO+ was 7.6 months and AO- was 10.1 months (
= .16). Mean time to ALP progression for AO+ and AO- was 6.3 months and 8.7 months, respectively (
= .05). Twenty veterans (58%) had died. Median survival for Ra-223 first was 32 months and for Ra-223 later was 15 months (
= .14; hazard ratio [HR] 0.48; 95% CI, 0.17-1.3). Median survival for AO+ and AO- veterans was 12 months and 18 months, respectively (
= .15; HR, 2.0; 95% CI, 0.77-5.0).
There was no statistical difference between AO+ and AO- veterans in terms of time to SRE, PSA, bone and ALP progression, even though there was a trend of shorter duration in AO+ veterans. There was no median survival difference between Ra-223 first vs Ra-223 later as well as between AO+ and AO- but there is a trend of worse survival in AO+ veterans.</abstract><cop>United States</cop><pub>Frontline Medical Communications Inc</pub><pmid>33424216</pmid><doi>10.12788/fp.0062</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1078-4497 |
ispartof | Federal Practitioner, 2020-12, Vol.37 (12), p.570-574 |
issn | 1078-4497 1945-337X |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7789849 |
source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
title | The Effect of Radium-223 Therapy in Agent Orange-Related Prostate Carcinoma |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T17%3A21%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Effect%20of%20Radium-223%20Therapy%20in%20Agent%20Orange-Related%20Prostate%20Carcinoma&rft.jtitle=Federal%20Practitioner&rft.au=Liman,%20Andrew&rft.date=2020-12-01&rft.volume=37&rft.issue=12&rft.spage=570&rft.epage=574&rft.pages=570-574&rft.issn=1078-4497&rft.eissn=1945-337X&rft_id=info:doi/10.12788/fp.0062&rft_dat=%3Cpubmed_cross%3E33424216%3C/pubmed_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/33424216&rfr_iscdi=true |