Fractionated stereotactic body radiotherapy for up to five prostate cancer oligometastases: Interim outcomes of a prospective clinical trial
Stereotactic body radiotherapy (SBRT) can delay escalation to systemic treatment in men with oligometastatic prostate cancer (PCa). However, large, prospective studies are still required to evaluate the efficacy of this approach in different patient groups. This is the interim analysis of a prospect...
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Veröffentlicht in: | International journal of cancer 2020-01, Vol.146 (1), p.161-168 |
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creator | Bowden, Patrick See, Andrew W. Frydenberg, Mark Haxhimolla, Hodo Costello, Anthony J. Moon, Daniel Ruljancich, Paul Grummet, Jeremy Crosthwaite, Alan Pranavan, Ganes Peters, Justin S. So, Kevin Gwini, Stella M. McKenzie, Dean P. Nolan, Skye Smyth, Lloyd M.L. Everitt, Craig |
description | Stereotactic body radiotherapy (SBRT) can delay escalation to systemic treatment in men with oligometastatic prostate cancer (PCa). However, large, prospective studies are still required to evaluate the efficacy of this approach in different patient groups. This is the interim analysis of a prospective, single institution study of men relapsing with up to five synchronous lesions following definitive local treatment for primary PCa. Our aim was to determine the proportion of patients not requiring treatment escalation following SBRT. In total, 199 patients were enrolled to receive fractionated SBRT (50 Gray in 10 fractions) to each visible lesion. Fourteen patients were castration resistant at enrolment. The proportion of patients not requiring treatment escalation 2 years following SBRT was 51.7% (95% CI: 44.1–59.3%). The median length of treatment escalation‐free survival over the entire follow‐up period was 27.1 months (95% CI; 21.8–29.4 months). Prior androgen deprivation therapy (ADT) predicted a significantly lower rate of freedom from treatment escalation at 2 years compared to no prior ADT (odds ratio = 0.21, 95% CI: 0.08–0.54, p = 0.001). There was no difference in the efficacy of SBRT when treating 4–5 vs. 1–3 initial lesions. A prostate‐specific antigen (PSA) decline was induced in 75% of patients, with PSA readings falling to an undetectable level in six patients. No late grade three toxicities were observed. These interim results suggest that SBRT can be used to treat up to five synchronous PCa oligometastases to delay treatment escalation.
What's new?
Metastasis‐directed therapy (MDT), involving surgery or stereotactic ablative radiotherapy, is a promising alternative treatment strategy for prostate cancer patients with metastatic disease. It remains unclear, however, which subsets of patients most benefit from MDT. Here, interim analysis of a large prospective trial involving fractionated stereotactic body radiotherapy (SBRT) for prostate cancer patients with up to five synchronous oligometastases shows that 2 years following SBRT, about half of patients did not require treatment escalation. In addition, nearly one‐quarter of patients had prostate‐specific antigen levels below baseline. The findings highlight the promise of SBRT for long‐term suppression of oligometastatic prostate cancer. |
doi_str_mv | 10.1002/ijc.32509 |
format | Article |
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What's new?
Metastasis‐directed therapy (MDT), involving surgery or stereotactic ablative radiotherapy, is a promising alternative treatment strategy for prostate cancer patients with metastatic disease. It remains unclear, however, which subsets of patients most benefit from MDT. Here, interim analysis of a large prospective trial involving fractionated stereotactic body radiotherapy (SBRT) for prostate cancer patients with up to five synchronous oligometastases shows that 2 years following SBRT, about half of patients did not require treatment escalation. In addition, nearly one‐quarter of patients had prostate‐specific antigen levels below baseline. The findings highlight the promise of SBRT for long‐term suppression of oligometastatic prostate cancer.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.32509</identifier><identifier>PMID: 31199504</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Aged ; Androgen Antagonists - therapeutic use ; androgen deprivation therapy ; Cancer ; Castration ; Clinical trials ; Dose Fractionation, Radiation ; Humans ; Lesions ; Male ; Medical research ; Metastasis ; Middle Aged ; Neoplasm Metastasis - radiotherapy ; oligometastases ; Patients ; Prospective Studies ; Prostate cancer ; Prostate-Specific Antigen - blood ; Prostatic Neoplasms - drug therapy ; Prostatic Neoplasms - pathology ; Prostatic Neoplasms - radiotherapy ; Radiation therapy ; Radiosurgery - methods ; stereotactic body radiotherapy ; Toxicity</subject><ispartof>International journal of cancer, 2020-01, Vol.146 (1), p.161-168</ispartof><rights>2019 UICC</rights><rights>2019 UICC.</rights><rights>2020 UICC</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3889-ccb46b90427036617704e6f4c924182668ab1953be5c477a73577bd97448a1383</citedby><cites>FETCH-LOGICAL-c3889-ccb46b90427036617704e6f4c924182668ab1953be5c477a73577bd97448a1383</cites><orcidid>0000-0002-5085-3322</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fijc.32509$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.32509$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31199504$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bowden, Patrick</creatorcontrib><creatorcontrib>See, Andrew W.</creatorcontrib><creatorcontrib>Frydenberg, Mark</creatorcontrib><creatorcontrib>Haxhimolla, Hodo</creatorcontrib><creatorcontrib>Costello, Anthony J.</creatorcontrib><creatorcontrib>Moon, Daniel</creatorcontrib><creatorcontrib>Ruljancich, Paul</creatorcontrib><creatorcontrib>Grummet, Jeremy</creatorcontrib><creatorcontrib>Crosthwaite, Alan</creatorcontrib><creatorcontrib>Pranavan, Ganes</creatorcontrib><creatorcontrib>Peters, Justin S.</creatorcontrib><creatorcontrib>So, Kevin</creatorcontrib><creatorcontrib>Gwini, Stella M.</creatorcontrib><creatorcontrib>McKenzie, Dean P.</creatorcontrib><creatorcontrib>Nolan, Skye</creatorcontrib><creatorcontrib>Smyth, Lloyd M.L.</creatorcontrib><creatorcontrib>Everitt, Craig</creatorcontrib><title>Fractionated stereotactic body radiotherapy for up to five prostate cancer oligometastases: Interim outcomes of a prospective clinical trial</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>Stereotactic body radiotherapy (SBRT) can delay escalation to systemic treatment in men with oligometastatic prostate cancer (PCa). However, large, prospective studies are still required to evaluate the efficacy of this approach in different patient groups. This is the interim analysis of a prospective, single institution study of men relapsing with up to five synchronous lesions following definitive local treatment for primary PCa. Our aim was to determine the proportion of patients not requiring treatment escalation following SBRT. In total, 199 patients were enrolled to receive fractionated SBRT (50 Gray in 10 fractions) to each visible lesion. Fourteen patients were castration resistant at enrolment. The proportion of patients not requiring treatment escalation 2 years following SBRT was 51.7% (95% CI: 44.1–59.3%). The median length of treatment escalation‐free survival over the entire follow‐up period was 27.1 months (95% CI; 21.8–29.4 months). Prior androgen deprivation therapy (ADT) predicted a significantly lower rate of freedom from treatment escalation at 2 years compared to no prior ADT (odds ratio = 0.21, 95% CI: 0.08–0.54, p = 0.001). There was no difference in the efficacy of SBRT when treating 4–5 vs. 1–3 initial lesions. A prostate‐specific antigen (PSA) decline was induced in 75% of patients, with PSA readings falling to an undetectable level in six patients. No late grade three toxicities were observed. These interim results suggest that SBRT can be used to treat up to five synchronous PCa oligometastases to delay treatment escalation.
What's new?
Metastasis‐directed therapy (MDT), involving surgery or stereotactic ablative radiotherapy, is a promising alternative treatment strategy for prostate cancer patients with metastatic disease. It remains unclear, however, which subsets of patients most benefit from MDT. Here, interim analysis of a large prospective trial involving fractionated stereotactic body radiotherapy (SBRT) for prostate cancer patients with up to five synchronous oligometastases shows that 2 years following SBRT, about half of patients did not require treatment escalation. In addition, nearly one‐quarter of patients had prostate‐specific antigen levels below baseline. The findings highlight the promise of SBRT for long‐term suppression of oligometastatic prostate cancer.</description><subject>Aged</subject><subject>Androgen Antagonists - therapeutic use</subject><subject>androgen deprivation therapy</subject><subject>Cancer</subject><subject>Castration</subject><subject>Clinical trials</subject><subject>Dose Fractionation, Radiation</subject><subject>Humans</subject><subject>Lesions</subject><subject>Male</subject><subject>Medical research</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Neoplasm Metastasis - radiotherapy</subject><subject>oligometastases</subject><subject>Patients</subject><subject>Prospective Studies</subject><subject>Prostate cancer</subject><subject>Prostate-Specific Antigen - blood</subject><subject>Prostatic Neoplasms - drug therapy</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Prostatic Neoplasms - radiotherapy</subject><subject>Radiation therapy</subject><subject>Radiosurgery - methods</subject><subject>stereotactic body radiotherapy</subject><subject>Toxicity</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kcFu1DAQhq0KRLctB16gssQFDmnt2I7j3tCKlkWVuNCz5TiT4lU2Tm0HtO_AQzPtlh6QOM1o5pvfM_4JecfZBWesvgxbfyFqxcwRWXFmdMVqrl6RFfZYpblojslJzlvGOFdMviHHgnNjMF2R39fJ-RLi5Ar0NBdIEMtjxdMu9nuaXB9i-QHJzXs6xESXmZZIh_AT6JxiLjhHvZs8JBrHcB93UBxWM-QruplQL-xoXIrHRqZxoO5pbAZ8AiX8GKbg3UhLCm48I68HN2Z4-xxPyd315-_rL9Xtt5vN-tNt5UXbmsr7TjadYbLWTDQN15pJaAbpTS15WzdN6zpulOhAeam100Jp3fVGS9k6LlpxSj4cdHGVhwVysbuQPYyjmyAu2db4l42UQglE3_-DbuOSJtzO1oIL0SqmNFIfD5TH23KCwc54t0t7y5l9tMiiRfbJImTPnxWXbgf9C_nXEwQuD8CvMML-_0p283V9kPwDzkebhw</recordid><startdate>20200101</startdate><enddate>20200101</enddate><creator>Bowden, Patrick</creator><creator>See, Andrew W.</creator><creator>Frydenberg, Mark</creator><creator>Haxhimolla, Hodo</creator><creator>Costello, Anthony J.</creator><creator>Moon, Daniel</creator><creator>Ruljancich, Paul</creator><creator>Grummet, Jeremy</creator><creator>Crosthwaite, Alan</creator><creator>Pranavan, Ganes</creator><creator>Peters, Justin S.</creator><creator>So, Kevin</creator><creator>Gwini, Stella M.</creator><creator>McKenzie, Dean P.</creator><creator>Nolan, Skye</creator><creator>Smyth, Lloyd M.L.</creator><creator>Everitt, Craig</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><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>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5085-3322</orcidid></search><sort><creationdate>20200101</creationdate><title>Fractionated stereotactic body radiotherapy for up to five prostate cancer oligometastases: Interim outcomes of a prospective clinical trial</title><author>Bowden, Patrick ; See, Andrew W. ; Frydenberg, Mark ; Haxhimolla, Hodo ; Costello, Anthony J. ; Moon, Daniel ; Ruljancich, Paul ; Grummet, Jeremy ; Crosthwaite, Alan ; Pranavan, Ganes ; Peters, Justin S. ; So, Kevin ; Gwini, Stella M. ; McKenzie, Dean P. ; Nolan, Skye ; Smyth, Lloyd M.L. ; Everitt, Craig</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3889-ccb46b90427036617704e6f4c924182668ab1953be5c477a73577bd97448a1383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aged</topic><topic>Androgen Antagonists - therapeutic use</topic><topic>androgen deprivation therapy</topic><topic>Cancer</topic><topic>Castration</topic><topic>Clinical trials</topic><topic>Dose Fractionation, Radiation</topic><topic>Humans</topic><topic>Lesions</topic><topic>Male</topic><topic>Medical research</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Neoplasm Metastasis - radiotherapy</topic><topic>oligometastases</topic><topic>Patients</topic><topic>Prospective Studies</topic><topic>Prostate cancer</topic><topic>Prostate-Specific Antigen - blood</topic><topic>Prostatic Neoplasms - drug therapy</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Prostatic Neoplasms - radiotherapy</topic><topic>Radiation therapy</topic><topic>Radiosurgery - methods</topic><topic>stereotactic body radiotherapy</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bowden, Patrick</creatorcontrib><creatorcontrib>See, Andrew W.</creatorcontrib><creatorcontrib>Frydenberg, Mark</creatorcontrib><creatorcontrib>Haxhimolla, Hodo</creatorcontrib><creatorcontrib>Costello, Anthony J.</creatorcontrib><creatorcontrib>Moon, Daniel</creatorcontrib><creatorcontrib>Ruljancich, Paul</creatorcontrib><creatorcontrib>Grummet, Jeremy</creatorcontrib><creatorcontrib>Crosthwaite, Alan</creatorcontrib><creatorcontrib>Pranavan, Ganes</creatorcontrib><creatorcontrib>Peters, Justin S.</creatorcontrib><creatorcontrib>So, Kevin</creatorcontrib><creatorcontrib>Gwini, Stella M.</creatorcontrib><creatorcontrib>McKenzie, Dean P.</creatorcontrib><creatorcontrib>Nolan, Skye</creatorcontrib><creatorcontrib>Smyth, Lloyd M.L.</creatorcontrib><creatorcontrib>Everitt, Craig</creatorcontrib><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>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bowden, Patrick</au><au>See, Andrew W.</au><au>Frydenberg, Mark</au><au>Haxhimolla, Hodo</au><au>Costello, Anthony J.</au><au>Moon, Daniel</au><au>Ruljancich, Paul</au><au>Grummet, Jeremy</au><au>Crosthwaite, Alan</au><au>Pranavan, Ganes</au><au>Peters, Justin S.</au><au>So, Kevin</au><au>Gwini, Stella M.</au><au>McKenzie, Dean P.</au><au>Nolan, Skye</au><au>Smyth, Lloyd M.L.</au><au>Everitt, Craig</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fractionated stereotactic body radiotherapy for up to five prostate cancer oligometastases: Interim outcomes of a prospective clinical trial</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2020-01-01</date><risdate>2020</risdate><volume>146</volume><issue>1</issue><spage>161</spage><epage>168</epage><pages>161-168</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><abstract>Stereotactic body radiotherapy (SBRT) can delay escalation to systemic treatment in men with oligometastatic prostate cancer (PCa). However, large, prospective studies are still required to evaluate the efficacy of this approach in different patient groups. This is the interim analysis of a prospective, single institution study of men relapsing with up to five synchronous lesions following definitive local treatment for primary PCa. Our aim was to determine the proportion of patients not requiring treatment escalation following SBRT. In total, 199 patients were enrolled to receive fractionated SBRT (50 Gray in 10 fractions) to each visible lesion. Fourteen patients were castration resistant at enrolment. The proportion of patients not requiring treatment escalation 2 years following SBRT was 51.7% (95% CI: 44.1–59.3%). The median length of treatment escalation‐free survival over the entire follow‐up period was 27.1 months (95% CI; 21.8–29.4 months). Prior androgen deprivation therapy (ADT) predicted a significantly lower rate of freedom from treatment escalation at 2 years compared to no prior ADT (odds ratio = 0.21, 95% CI: 0.08–0.54, p = 0.001). There was no difference in the efficacy of SBRT when treating 4–5 vs. 1–3 initial lesions. A prostate‐specific antigen (PSA) decline was induced in 75% of patients, with PSA readings falling to an undetectable level in six patients. No late grade three toxicities were observed. These interim results suggest that SBRT can be used to treat up to five synchronous PCa oligometastases to delay treatment escalation.
What's new?
Metastasis‐directed therapy (MDT), involving surgery or stereotactic ablative radiotherapy, is a promising alternative treatment strategy for prostate cancer patients with metastatic disease. It remains unclear, however, which subsets of patients most benefit from MDT. Here, interim analysis of a large prospective trial involving fractionated stereotactic body radiotherapy (SBRT) for prostate cancer patients with up to five synchronous oligometastases shows that 2 years following SBRT, about half of patients did not require treatment escalation. In addition, nearly one‐quarter of patients had prostate‐specific antigen levels below baseline. The findings highlight the promise of SBRT for long‐term suppression of oligometastatic prostate cancer.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>31199504</pmid><doi>10.1002/ijc.32509</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-5085-3322</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aged Androgen Antagonists - therapeutic use androgen deprivation therapy Cancer Castration Clinical trials Dose Fractionation, Radiation Humans Lesions Male Medical research Metastasis Middle Aged Neoplasm Metastasis - radiotherapy oligometastases Patients Prospective Studies Prostate cancer Prostate-Specific Antigen - blood Prostatic Neoplasms - drug therapy Prostatic Neoplasms - pathology Prostatic Neoplasms - radiotherapy Radiation therapy Radiosurgery - methods stereotactic body radiotherapy Toxicity |
title | Fractionated stereotactic body radiotherapy for up to five prostate cancer oligometastases: Interim outcomes of a prospective clinical trial |
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