Early PSA Change after [ 177 Lu]PSMA-617 Radioligand Therapy as a Predicator of Biochemical Response and Overall Survival
Radioligand therapy with [ Lu]PSMA-617 (PSMA-RLT) is a promising therapeutic option for metastatic castration-resistant prostate cancer (mCPRP). This study assessed the prognostic value of early PSA measurements during PSMA-RLT. 27 patients with mCRPC scheduled for PSMA-RLT were prospectively enroll...
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Veröffentlicht in: | Cancers 2021-12, Vol.14 (1), p.149 |
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creator | Kind, Felix Fassbender, Thomas F Andrieux, Geoffroy Boerries, Melanie Meyer, Philipp T Ruf, Juri |
description | Radioligand therapy with [
Lu]PSMA-617 (PSMA-RLT) is a promising therapeutic option for metastatic castration-resistant prostate cancer (mCPRP). This study assessed the prognostic value of early PSA measurements during PSMA-RLT.
27 patients with mCRPC scheduled for PSMA-RLT were prospectively enrolled for a serial short-interval PSA-assessment. Change in PSA (∆%PSA) during two treatment cycles was correlated with biochemical response (BR) and change in tumor volume on PET (TV) after 16 weeks (w16), as well as overall survival (OS). PCWG3 criteria and the recently recommended threshold of ∆%PSA ≤ -30% were assessed for their predictive value.
∆%PSA first correlated with BR, TV and OS after 4 weeks (c1w4). At c1w4, ∆%PSA ≤ -30% was associated with the biochemical response at w16 (
= 0.003) and a longer median OS (
= 0.025), whereas the PCWG3-derived threshold of ∆%PSA ≤ -50% showed no such correlation. In contrast, ∆%PSA ≥ 25% at c1w4 was associated with biochemical progression at w16 (
= 0.003) and a shorter median OS (
< 0.001).
PSA changes as early as four weeks after PSMA-RLT allow a significant prediction of later biochemical and PET-based imaging response, as well as OS. At this early time point, a more lenient threshold for a PSA decrease of at least 30% appears better-suited for the prediction of a positive biochemical response and longer OS. In contrast, the PCWG3-derived threshold for PSA increase (+25%) reliably anticipates biochemical progression and shorter OS. |
doi_str_mv | 10.3390/cancers14010149 |
format | Article |
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Lu]PSMA-617 (PSMA-RLT) is a promising therapeutic option for metastatic castration-resistant prostate cancer (mCPRP). This study assessed the prognostic value of early PSA measurements during PSMA-RLT.
27 patients with mCRPC scheduled for PSMA-RLT were prospectively enrolled for a serial short-interval PSA-assessment. Change in PSA (∆%PSA) during two treatment cycles was correlated with biochemical response (BR) and change in tumor volume on PET (TV) after 16 weeks (w16), as well as overall survival (OS). PCWG3 criteria and the recently recommended threshold of ∆%PSA ≤ -30% were assessed for their predictive value.
∆%PSA first correlated with BR, TV and OS after 4 weeks (c1w4). At c1w4, ∆%PSA ≤ -30% was associated with the biochemical response at w16 (
= 0.003) and a longer median OS (
= 0.025), whereas the PCWG3-derived threshold of ∆%PSA ≤ -50% showed no such correlation. In contrast, ∆%PSA ≥ 25% at c1w4 was associated with biochemical progression at w16 (
= 0.003) and a shorter median OS (
< 0.001).
PSA changes as early as four weeks after PSMA-RLT allow a significant prediction of later biochemical and PET-based imaging response, as well as OS. At this early time point, a more lenient threshold for a PSA decrease of at least 30% appears better-suited for the prediction of a positive biochemical response and longer OS. In contrast, the PCWG3-derived threshold for PSA increase (+25%) reliably anticipates biochemical progression and shorter OS.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers14010149</identifier><identifier>PMID: 35008315</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Antigens ; Cancer therapies ; Castration ; Metastases ; Metastasis ; Patients ; Positron emission tomography ; Prostate cancer ; Prostate-specific antigen ; Regression analysis ; Scintigraphy ; Survival ; Tumors ; Variance analysis</subject><ispartof>Cancers, 2021-12, Vol.14 (1), p.149</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-ee88d158547fcbac730dc2727cdedde0efccb4b8a29933dbc1394bfa394fe66a3</citedby><cites>FETCH-LOGICAL-c421t-ee88d158547fcbac730dc2727cdedde0efccb4b8a29933dbc1394bfa394fe66a3</cites><orcidid>0000-0002-5389-9481 ; 0000-0002-9398-5747 ; 0000-0002-3670-0602</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750166/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750166/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,27926,27927,53793,53795</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35008315$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kind, Felix</creatorcontrib><creatorcontrib>Fassbender, Thomas F</creatorcontrib><creatorcontrib>Andrieux, Geoffroy</creatorcontrib><creatorcontrib>Boerries, Melanie</creatorcontrib><creatorcontrib>Meyer, Philipp T</creatorcontrib><creatorcontrib>Ruf, Juri</creatorcontrib><title>Early PSA Change after [ 177 Lu]PSMA-617 Radioligand Therapy as a Predicator of Biochemical Response and Overall Survival</title><title>Cancers</title><addtitle>Cancers (Basel)</addtitle><description>Radioligand therapy with [
Lu]PSMA-617 (PSMA-RLT) is a promising therapeutic option for metastatic castration-resistant prostate cancer (mCPRP). This study assessed the prognostic value of early PSA measurements during PSMA-RLT.
27 patients with mCRPC scheduled for PSMA-RLT were prospectively enrolled for a serial short-interval PSA-assessment. Change in PSA (∆%PSA) during two treatment cycles was correlated with biochemical response (BR) and change in tumor volume on PET (TV) after 16 weeks (w16), as well as overall survival (OS). PCWG3 criteria and the recently recommended threshold of ∆%PSA ≤ -30% were assessed for their predictive value.
∆%PSA first correlated with BR, TV and OS after 4 weeks (c1w4). At c1w4, ∆%PSA ≤ -30% was associated with the biochemical response at w16 (
= 0.003) and a longer median OS (
= 0.025), whereas the PCWG3-derived threshold of ∆%PSA ≤ -50% showed no such correlation. In contrast, ∆%PSA ≥ 25% at c1w4 was associated with biochemical progression at w16 (
= 0.003) and a shorter median OS (
< 0.001).
PSA changes as early as four weeks after PSMA-RLT allow a significant prediction of later biochemical and PET-based imaging response, as well as OS. At this early time point, a more lenient threshold for a PSA decrease of at least 30% appears better-suited for the prediction of a positive biochemical response and longer OS. In contrast, the PCWG3-derived threshold for PSA increase (+25%) reliably anticipates biochemical progression and shorter OS.</description><subject>Antigens</subject><subject>Cancer therapies</subject><subject>Castration</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Patients</subject><subject>Positron emission tomography</subject><subject>Prostate cancer</subject><subject>Prostate-specific antigen</subject><subject>Regression analysis</subject><subject>Scintigraphy</subject><subject>Survival</subject><subject>Tumors</subject><subject>Variance analysis</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkc1r3DAQxUVpaUKac29F0EsvbiTLluxLYbukbWBLlmxyCkWMpfGugtbaSvbC_vdVmw_S6DASmt97zPAIec_ZZyFadmZgMBgTrxhnvGpfkeOSqbKQsq1eP3sfkdOU7lg-QnAl1VtyJGrGGsHrY3I4h-gPdLma0fkGhjVS6EeM9JZypehi-rVc_ZwVkit6BdYF79YwWHq9wQi7A4VEgS4jWmdgDJGGnn51wWxwmz88vcK0C0PKnllzuc8a7-lqinu3B_-OvOnBJzx9uE_Izbfz6_mPYnH5_WI-WxSmKvlYIDaN5XVTV6o3HRglmDWlKpWxaC0y7I3pqq6Bsm2FsJ3hoq26HnLtUUoQJ-TLve9u6rZoDQ5jnkPvottCPOgATv_fGdxGr8NeN6pmXMps8OnBIIbfE6ZRb10y6D0MGKakS8mblrVMVRn9-AK9C1Mc8nr_qJLVrG4ydXZPmRhSitg_DcOZ_pusfpFsVnx4vsMT_5ij-AMN26Bp</recordid><startdate>20211229</startdate><enddate>20211229</enddate><creator>Kind, Felix</creator><creator>Fassbender, Thomas F</creator><creator>Andrieux, Geoffroy</creator><creator>Boerries, Melanie</creator><creator>Meyer, Philipp T</creator><creator>Ruf, Juri</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5389-9481</orcidid><orcidid>https://orcid.org/0000-0002-9398-5747</orcidid><orcidid>https://orcid.org/0000-0002-3670-0602</orcidid></search><sort><creationdate>20211229</creationdate><title>Early PSA Change after [ 177 Lu]PSMA-617 Radioligand Therapy as a Predicator of Biochemical Response and Overall Survival</title><author>Kind, Felix ; Fassbender, Thomas F ; Andrieux, Geoffroy ; Boerries, Melanie ; Meyer, Philipp T ; Ruf, Juri</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-ee88d158547fcbac730dc2727cdedde0efccb4b8a29933dbc1394bfa394fe66a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antigens</topic><topic>Cancer therapies</topic><topic>Castration</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Patients</topic><topic>Positron emission tomography</topic><topic>Prostate cancer</topic><topic>Prostate-specific antigen</topic><topic>Regression analysis</topic><topic>Scintigraphy</topic><topic>Survival</topic><topic>Tumors</topic><topic>Variance analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kind, Felix</creatorcontrib><creatorcontrib>Fassbender, Thomas F</creatorcontrib><creatorcontrib>Andrieux, Geoffroy</creatorcontrib><creatorcontrib>Boerries, Melanie</creatorcontrib><creatorcontrib>Meyer, Philipp T</creatorcontrib><creatorcontrib>Ruf, Juri</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Biological Science Collection</collection><collection>ProQuest research library</collection><collection>ProQuest Biological Science Journals</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kind, Felix</au><au>Fassbender, Thomas F</au><au>Andrieux, Geoffroy</au><au>Boerries, Melanie</au><au>Meyer, Philipp T</au><au>Ruf, Juri</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Early PSA Change after [ 177 Lu]PSMA-617 Radioligand Therapy as a Predicator of Biochemical Response and Overall Survival</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2021-12-29</date><risdate>2021</risdate><volume>14</volume><issue>1</issue><spage>149</spage><pages>149-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>Radioligand therapy with [
Lu]PSMA-617 (PSMA-RLT) is a promising therapeutic option for metastatic castration-resistant prostate cancer (mCPRP). This study assessed the prognostic value of early PSA measurements during PSMA-RLT.
27 patients with mCRPC scheduled for PSMA-RLT were prospectively enrolled for a serial short-interval PSA-assessment. Change in PSA (∆%PSA) during two treatment cycles was correlated with biochemical response (BR) and change in tumor volume on PET (TV) after 16 weeks (w16), as well as overall survival (OS). PCWG3 criteria and the recently recommended threshold of ∆%PSA ≤ -30% were assessed for their predictive value.
∆%PSA first correlated with BR, TV and OS after 4 weeks (c1w4). At c1w4, ∆%PSA ≤ -30% was associated with the biochemical response at w16 (
= 0.003) and a longer median OS (
= 0.025), whereas the PCWG3-derived threshold of ∆%PSA ≤ -50% showed no such correlation. In contrast, ∆%PSA ≥ 25% at c1w4 was associated with biochemical progression at w16 (
= 0.003) and a shorter median OS (
< 0.001).
PSA changes as early as four weeks after PSMA-RLT allow a significant prediction of later biochemical and PET-based imaging response, as well as OS. At this early time point, a more lenient threshold for a PSA decrease of at least 30% appears better-suited for the prediction of a positive biochemical response and longer OS. In contrast, the PCWG3-derived threshold for PSA increase (+25%) reliably anticipates biochemical progression and shorter OS.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35008315</pmid><doi>10.3390/cancers14010149</doi><orcidid>https://orcid.org/0000-0002-5389-9481</orcidid><orcidid>https://orcid.org/0000-0002-9398-5747</orcidid><orcidid>https://orcid.org/0000-0002-3670-0602</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antigens Cancer therapies Castration Metastases Metastasis Patients Positron emission tomography Prostate cancer Prostate-specific antigen Regression analysis Scintigraphy Survival Tumors Variance analysis |
title | Early PSA Change after [ 177 Lu]PSMA-617 Radioligand Therapy as a Predicator of Biochemical Response and Overall Survival |
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