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Event-free survival after 68 Ga-PSMA-11 PET/CT in recurrent hormone-sensitive prostate cancer (HSPC) patients eligible for salvage therapy

Background/aim Prostate-specific-membrane-antigen/positron emission tomography (PSMA-PET) detects with high accuracy disease-recurrence, leading to changes in the management of biochemically-recurrent (BCR) prostate cancer (PCa). However, data regarding the oncological outcomes of patients who perfo...

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Published in:European journal of nuclear medicine and molecular imaging 2022-07, Vol.49 (9), p.3257-3268
Main Authors: Ceci, Francesco, Rovera, Guido, Iorio, Giuseppe Carlo, Guarneri, Alessia, Chiofalo, Valeria, Passera, Roberto, Oderda, Marco, Dall’Armellina, Sara, Liberini, Virginia, Grimaldi, Serena, Bellò, Marilena, Gontero, Paolo, Ricardi, Umberto, Deandreis, Désirée
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container_issue 9
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container_title European journal of nuclear medicine and molecular imaging
container_volume 49
creator Ceci, Francesco
Rovera, Guido
Iorio, Giuseppe Carlo
Guarneri, Alessia
Chiofalo, Valeria
Passera, Roberto
Oderda, Marco
Dall’Armellina, Sara
Liberini, Virginia
Grimaldi, Serena
Bellò, Marilena
Gontero, Paolo
Ricardi, Umberto
Deandreis, Désirée
description Background/aim Prostate-specific-membrane-antigen/positron emission tomography (PSMA-PET) detects with high accuracy disease-recurrence, leading to changes in the management of biochemically-recurrent (BCR) prostate cancer (PCa). However, data regarding the oncological outcomes of patients who performed PSMA-PET are needed. The aim of this study was to evaluate the incidence of clinically relevant events during follow-up in patients who performed PSMA-PET for BCR after radical treatment. Materials and methods This analysis included consecutive, hormone-sensitive, hormone-free, recurrent PCa patients (HSPC) enrolled through a prospective study. All patients were eligible for salvage therapy, having at least 24 months of follow-up after PSMA-PET. The primary endpoint was the Event-Free Survival (EFS), defined as the time between the PSMA-PET and the date of event/last follow-up. The Kaplan–Meier method was used to estimate the EFS curves. EFS was also investigated by Cox proportional hazards regression. Events were defined as death, radiological progression, or PSA recurrence after therapy. Results One-hundred and seventy-six ( n  = 176) patients were analyzed (median PSA 0.62 [IQR: 0.43–1.00] ng/mL; median follow-up of 35.4 [IQR: 26.5–40.3] months). The EFS was 78.8% at 1 year, 65.2% (2 years), and 52.2% (3 years). Patients experiencing events during study follow-up had a significantly higher median PSA (0.81 [IQR: 0.53–1.28] vs 0.51 [IQR: 0.36–0.80] ng/mL) and a lower PSA doubling time (PSAdt) (5.4 [IQR: 3.7–11.6] vs 12.7 [IQR: 6.6–24.3] months) ( p   0.5 ng/mL, PSAdt ≤ 6 months, and a positive PSMA-PET result were associated with a higher event rate ( p   0.5 ng/mL and PSAdt ≤ 6 months were statistically significant event-predictors in multivariate model ( p  
doi_str_mv 10.1007/s00259-022-05741-9
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However, data regarding the oncological outcomes of patients who performed PSMA-PET are needed. The aim of this study was to evaluate the incidence of clinically relevant events during follow-up in patients who performed PSMA-PET for BCR after radical treatment. Materials and methods This analysis included consecutive, hormone-sensitive, hormone-free, recurrent PCa patients (HSPC) enrolled through a prospective study. All patients were eligible for salvage therapy, having at least 24 months of follow-up after PSMA-PET. The primary endpoint was the Event-Free Survival (EFS), defined as the time between the PSMA-PET and the date of event/last follow-up. The Kaplan–Meier method was used to estimate the EFS curves. EFS was also investigated by Cox proportional hazards regression. Events were defined as death, radiological progression, or PSA recurrence after therapy. Results One-hundred and seventy-six ( n  = 176) patients were analyzed (median PSA 0.62 [IQR: 0.43–1.00] ng/mL; median follow-up of 35.4 [IQR: 26.5–40.3] months). The EFS was 78.8% at 1 year, 65.2% (2 years), and 52.2% (3 years). Patients experiencing events during study follow-up had a significantly higher median PSA (0.81 [IQR: 0.53–1.28] vs 0.51 [IQR: 0.36–0.80] ng/mL) and a lower PSA doubling time (PSAdt) (5.4 [IQR: 3.7–11.6] vs 12.7 [IQR: 6.6–24.3] months) ( p  &lt; 0.001) compared to event-free patients. The Kaplan–Meier curves showed that PSA &gt; 0.5 ng/mL, PSAdt ≤ 6 months, and a positive PSMA-PET result were associated with a higher event rate ( p  &lt; 0.01). No significant differences of event rates were observed in patients who received changes in therapy management after PSMA-PET vs. patients who did not receive therapy changes. Finally, PSA &gt; 0.5 ng/mL and PSAdt ≤ 6 months were statistically significant event-predictors in multivariate model ( p  &lt; 0.001). Conclusion Low PSA and long PSAdt were significant predictors of longer EFS. A lower incidence of events was observed in patients having negative PSMA-PET, since longer EFS was significantly more probable in case of a negative scan.</description><identifier>ISSN: 1619-7070</identifier><identifier>EISSN: 1619-7089</identifier><identifier>DOI: 10.1007/s00259-022-05741-9</identifier><identifier>PMID: 35217883</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Antigens ; Cardiology ; Imaging ; Medicine ; Medicine &amp; Public Health ; Nuclear Medicine ; Oncology ; Oncology – Genitourinary ; Original ; Original Article ; Orthopedics ; Patients ; Positron emission ; Positron emission tomography ; Prostate cancer ; Radiology ; Statistical analysis ; Survival ; Therapy ; Tomography</subject><ispartof>European journal of nuclear medicine and molecular imaging, 2022-07, Vol.49 (9), p.3257-3268</ispartof><rights>The Author(s) 2022</rights><rights>2022. The Author(s).</rights><rights>The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3199-32ba379ae8e9d50b92572ee2e16894dd9dba262652c2697c2df02cd8dc17432e3</citedby><cites>FETCH-LOGICAL-c3199-32ba379ae8e9d50b92572ee2e16894dd9dba262652c2697c2df02cd8dc17432e3</cites><orcidid>0000-0001-9785-5248</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35217883$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ceci, Francesco</creatorcontrib><creatorcontrib>Rovera, Guido</creatorcontrib><creatorcontrib>Iorio, Giuseppe Carlo</creatorcontrib><creatorcontrib>Guarneri, Alessia</creatorcontrib><creatorcontrib>Chiofalo, Valeria</creatorcontrib><creatorcontrib>Passera, Roberto</creatorcontrib><creatorcontrib>Oderda, Marco</creatorcontrib><creatorcontrib>Dall’Armellina, Sara</creatorcontrib><creatorcontrib>Liberini, Virginia</creatorcontrib><creatorcontrib>Grimaldi, Serena</creatorcontrib><creatorcontrib>Bellò, Marilena</creatorcontrib><creatorcontrib>Gontero, Paolo</creatorcontrib><creatorcontrib>Ricardi, Umberto</creatorcontrib><creatorcontrib>Deandreis, Désirée</creatorcontrib><title>Event-free survival after 68 Ga-PSMA-11 PET/CT in recurrent hormone-sensitive prostate cancer (HSPC) patients eligible for salvage therapy</title><title>European journal of nuclear medicine and molecular imaging</title><addtitle>Eur J Nucl Med Mol Imaging</addtitle><addtitle>Eur J Nucl Med Mol Imaging</addtitle><description>Background/aim Prostate-specific-membrane-antigen/positron emission tomography (PSMA-PET) detects with high accuracy disease-recurrence, leading to changes in the management of biochemically-recurrent (BCR) prostate cancer (PCa). However, data regarding the oncological outcomes of patients who performed PSMA-PET are needed. The aim of this study was to evaluate the incidence of clinically relevant events during follow-up in patients who performed PSMA-PET for BCR after radical treatment. Materials and methods This analysis included consecutive, hormone-sensitive, hormone-free, recurrent PCa patients (HSPC) enrolled through a prospective study. All patients were eligible for salvage therapy, having at least 24 months of follow-up after PSMA-PET. The primary endpoint was the Event-Free Survival (EFS), defined as the time between the PSMA-PET and the date of event/last follow-up. The Kaplan–Meier method was used to estimate the EFS curves. EFS was also investigated by Cox proportional hazards regression. Events were defined as death, radiological progression, or PSA recurrence after therapy. Results One-hundred and seventy-six ( n  = 176) patients were analyzed (median PSA 0.62 [IQR: 0.43–1.00] ng/mL; median follow-up of 35.4 [IQR: 26.5–40.3] months). The EFS was 78.8% at 1 year, 65.2% (2 years), and 52.2% (3 years). Patients experiencing events during study follow-up had a significantly higher median PSA (0.81 [IQR: 0.53–1.28] vs 0.51 [IQR: 0.36–0.80] ng/mL) and a lower PSA doubling time (PSAdt) (5.4 [IQR: 3.7–11.6] vs 12.7 [IQR: 6.6–24.3] months) ( p  &lt; 0.001) compared to event-free patients. The Kaplan–Meier curves showed that PSA &gt; 0.5 ng/mL, PSAdt ≤ 6 months, and a positive PSMA-PET result were associated with a higher event rate ( p  &lt; 0.01). No significant differences of event rates were observed in patients who received changes in therapy management after PSMA-PET vs. patients who did not receive therapy changes. Finally, PSA &gt; 0.5 ng/mL and PSAdt ≤ 6 months were statistically significant event-predictors in multivariate model ( p  &lt; 0.001). Conclusion Low PSA and long PSAdt were significant predictors of longer EFS. A lower incidence of events was observed in patients having negative PSMA-PET, since longer EFS was significantly more probable in case of a negative scan.</description><subject>Antigens</subject><subject>Cardiology</subject><subject>Imaging</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Nuclear Medicine</subject><subject>Oncology</subject><subject>Oncology – Genitourinary</subject><subject>Original</subject><subject>Original Article</subject><subject>Orthopedics</subject><subject>Patients</subject><subject>Positron emission</subject><subject>Positron emission tomography</subject><subject>Prostate cancer</subject><subject>Radiology</subject><subject>Statistical analysis</subject><subject>Survival</subject><subject>Therapy</subject><subject>Tomography</subject><issn>1619-7070</issn><issn>1619-7089</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kctu1DAUhiMEohd4ARbIEpt2YWofJ7G9QapGQ4tUxEgd1pbjnMy4yiTBTiL1GXgJnoUnw2XKcFmwsqXz_f-5_Fn2irO3nDF5ERmDQlMGQFkhc071k-yYl1xTyZR-evhLdpSdxHjHGFeg9PPsSBTApVLiOPu6nLEbaRMQSZzC7GfbEtuMGEipvn-7snR1-_GSck5Wy_XFYk18RwK6KYQkI9s-7PoOacQu-tHPSIbQx9GOSJztXDI5u75dLc7JYEefBJFg6ze-apE0fSDRtrPdIBm3GOxw_yJ71tg24svH9zT7_H65XlzTm09XHxaXN9QJrjUVUFkhtUWFui5YpaGQgAjIS6XzutZ1ZaGEsgAHpZYO6oaBq1XtuMwFoDjN3u19h6naYe3SYMG2Zgh-Z8O96a03f1c6vzWbfjapE8tLSAZnjwah_zJhHM3OR4dtazvsp2igFEKz1DxP6Jt_0Lt-Cl1aL1FKFEww8WAIe8ql88WAzWEYzsxD1maftUlZm59ZG51Er_9c4yD5FW4CxB6IqdRtMPzu_R_bH3sgtcY</recordid><startdate>20220701</startdate><enddate>20220701</enddate><creator>Ceci, Francesco</creator><creator>Rovera, Guido</creator><creator>Iorio, Giuseppe Carlo</creator><creator>Guarneri, Alessia</creator><creator>Chiofalo, Valeria</creator><creator>Passera, Roberto</creator><creator>Oderda, Marco</creator><creator>Dall’Armellina, Sara</creator><creator>Liberini, Virginia</creator><creator>Grimaldi, Serena</creator><creator>Bellò, Marilena</creator><creator>Gontero, Paolo</creator><creator>Ricardi, Umberto</creator><creator>Deandreis, Désirée</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9785-5248</orcidid></search><sort><creationdate>20220701</creationdate><title>Event-free survival after 68 Ga-PSMA-11 PET/CT in recurrent hormone-sensitive prostate cancer (HSPC) patients eligible for salvage therapy</title><author>Ceci, Francesco ; 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However, data regarding the oncological outcomes of patients who performed PSMA-PET are needed. The aim of this study was to evaluate the incidence of clinically relevant events during follow-up in patients who performed PSMA-PET for BCR after radical treatment. Materials and methods This analysis included consecutive, hormone-sensitive, hormone-free, recurrent PCa patients (HSPC) enrolled through a prospective study. All patients were eligible for salvage therapy, having at least 24 months of follow-up after PSMA-PET. The primary endpoint was the Event-Free Survival (EFS), defined as the time between the PSMA-PET and the date of event/last follow-up. The Kaplan–Meier method was used to estimate the EFS curves. EFS was also investigated by Cox proportional hazards regression. Events were defined as death, radiological progression, or PSA recurrence after therapy. Results One-hundred and seventy-six ( n  = 176) patients were analyzed (median PSA 0.62 [IQR: 0.43–1.00] ng/mL; median follow-up of 35.4 [IQR: 26.5–40.3] months). The EFS was 78.8% at 1 year, 65.2% (2 years), and 52.2% (3 years). Patients experiencing events during study follow-up had a significantly higher median PSA (0.81 [IQR: 0.53–1.28] vs 0.51 [IQR: 0.36–0.80] ng/mL) and a lower PSA doubling time (PSAdt) (5.4 [IQR: 3.7–11.6] vs 12.7 [IQR: 6.6–24.3] months) ( p  &lt; 0.001) compared to event-free patients. The Kaplan–Meier curves showed that PSA &gt; 0.5 ng/mL, PSAdt ≤ 6 months, and a positive PSMA-PET result were associated with a higher event rate ( p  &lt; 0.01). No significant differences of event rates were observed in patients who received changes in therapy management after PSMA-PET vs. patients who did not receive therapy changes. Finally, PSA &gt; 0.5 ng/mL and PSAdt ≤ 6 months were statistically significant event-predictors in multivariate model ( p  &lt; 0.001). Conclusion Low PSA and long PSAdt were significant predictors of longer EFS. A lower incidence of events was observed in patients having negative PSMA-PET, since longer EFS was significantly more probable in case of a negative scan.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>35217883</pmid><doi>10.1007/s00259-022-05741-9</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-9785-5248</orcidid><oa>free_for_read</oa></addata></record>
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1619-7089
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subjects Antigens
Cardiology
Imaging
Medicine
Medicine & Public Health
Nuclear Medicine
Oncology
Oncology – Genitourinary
Original
Original Article
Orthopedics
Patients
Positron emission
Positron emission tomography
Prostate cancer
Radiology
Statistical analysis
Survival
Therapy
Tomography
title Event-free survival after 68 Ga-PSMA-11 PET/CT in recurrent hormone-sensitive prostate cancer (HSPC) patients eligible for salvage therapy
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