Consolidative Radiotherapy for Metastatic Urothelial Bladder Cancer Patients with No Progression and with No More than Five Residual Metastatic Lesions Following First-Line Systemic Therapy: A Retrospective Analysis

Local consolidative radiotherapy in the treatment of metastatic malignancies has shown promising results in several types of tumors. The objective of this study was to assess consolidative radiotherapy to the bladder and to residual metastases in metastatic urothelial bladder cancer with no progress...

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Veröffentlicht in:Cancers 2023-02, Vol.15 (4), p.1161
Hauptverfasser: Aboudaram, Amélie, Chaltiel, Léonor, Pouessel, Damien, Graff-Cailleaud, Pierre, Benziane-Ouaritini, Nicolas, Sargos, Paul, Schick, Ulrike, Créhange, Gilles, Cohen-Jonathan Moyal, Elizabeth, Chevreau, Christine, Khalifa, Jonathan
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container_start_page 1161
container_title Cancers
container_volume 15
creator Aboudaram, Amélie
Chaltiel, Léonor
Pouessel, Damien
Graff-Cailleaud, Pierre
Benziane-Ouaritini, Nicolas
Sargos, Paul
Schick, Ulrike
Créhange, Gilles
Cohen-Jonathan Moyal, Elizabeth
Chevreau, Christine
Khalifa, Jonathan
description Local consolidative radiotherapy in the treatment of metastatic malignancies has shown promising results in several types of tumors. The objective of this study was to assess consolidative radiotherapy to the bladder and to residual metastases in metastatic urothelial bladder cancer with no progression following first-line systemic therapy. Patients who received first-line therapy for the treatment of metastatic urothelial bladder cancer (mUBC) and who were progression-free following treatment with no more than five residual metastases were retrospectively identified through the database of four Comprehensive Cancer Centers, between January 2005 and December 2018. Among them, patients who received subsequent definitive radiotherapy (of EQD2Gy > 45Gy) to the bladder and residual metastases were included in the consolidative group (irradiated (IR) group), and the other patients were included in the observation group (NIR group). Progression-free survival (PFS) and overall survival (OS) were determined from the start of the first-line chemotherapy using the Kaplan-Meier method. To prevent immortal time bias, a Cox model with time-dependent covariates and 6-month landmark analyses were performed to examine OS and PFS. A total of 91 patients with at least stable disease following first-line therapy and with no more than five residual metastases were analyzed: 51 in the IR group and 40 in the NIR group. Metachronous metastatic disease was more frequent in the NIR group (19% vs. 5%, = 0.02); the median number of metastases in the IR group vs. in the NIR group was 2 (1-9) vs. 3 (1-5) ( = 0.04) at metastatic presentation, and 1 (0-5) vs. 2 (0-5) ( = 0.18) after completion of chemotherapy (residual lesions), respectively. Two grade 3 toxicities (3.9%) and no grade 4 toxicity were reported in the IR group related to radiotherapy. With a median follow up of 85.9 months (95% IC (36.7; 101.6)), median OS and PFS were 21.7 months (95% IC (17.1; 29.7)) and 11.1 months (95% IC (9.9; 14.1)) for the whole cohort, respectively. In multivariable analysis, consolidative radiotherapy conferred a benefit in both PFS (HR = 0.49, = 0.007) and OS (HR = 0.47, = 0.015) in the whole population; in the landmark analysis at 6 months, radiotherapy was associated with improved OS (HR = 0.48, = 0.026), with a trend for PFS (HR = 0.57, = 0.082). Consolidative radiotherapy for mUBC patients who have not progressed after first-line therapy and with limited residual disease seems to confer both
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The objective of this study was to assess consolidative radiotherapy to the bladder and to residual metastases in metastatic urothelial bladder cancer with no progression following first-line systemic therapy. Patients who received first-line therapy for the treatment of metastatic urothelial bladder cancer (mUBC) and who were progression-free following treatment with no more than five residual metastases were retrospectively identified through the database of four Comprehensive Cancer Centers, between January 2005 and December 2018. Among them, patients who received subsequent definitive radiotherapy (of EQD2Gy &gt; 45Gy) to the bladder and residual metastases were included in the consolidative group (irradiated (IR) group), and the other patients were included in the observation group (NIR group). Progression-free survival (PFS) and overall survival (OS) were determined from the start of the first-line chemotherapy using the Kaplan-Meier method. To prevent immortal time bias, a Cox model with time-dependent covariates and 6-month landmark analyses were performed to examine OS and PFS. A total of 91 patients with at least stable disease following first-line therapy and with no more than five residual metastases were analyzed: 51 in the IR group and 40 in the NIR group. Metachronous metastatic disease was more frequent in the NIR group (19% vs. 5%, = 0.02); the median number of metastases in the IR group vs. in the NIR group was 2 (1-9) vs. 3 (1-5) ( = 0.04) at metastatic presentation, and 1 (0-5) vs. 2 (0-5) ( = 0.18) after completion of chemotherapy (residual lesions), respectively. Two grade 3 toxicities (3.9%) and no grade 4 toxicity were reported in the IR group related to radiotherapy. With a median follow up of 85.9 months (95% IC (36.7; 101.6)), median OS and PFS were 21.7 months (95% IC (17.1; 29.7)) and 11.1 months (95% IC (9.9; 14.1)) for the whole cohort, respectively. In multivariable analysis, consolidative radiotherapy conferred a benefit in both PFS (HR = 0.49, = 0.007) and OS (HR = 0.47, = 0.015) in the whole population; in the landmark analysis at 6 months, radiotherapy was associated with improved OS (HR = 0.48, = 0.026), with a trend for PFS (HR = 0.57, = 0.082). Consolidative radiotherapy for mUBC patients who have not progressed after first-line therapy and with limited residual disease seems to confer both OS and PFS benefits. The role of consolidative radiotherapy in the context of avelumab maintenance should be addressed prospectively.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers15041161</identifier><identifier>PMID: 36831503</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Bladder cancer ; Cancer therapies ; Care and treatment ; Chemotherapy ; Clinical trials ; Life Sciences ; Lymphatic system ; Malignancy ; Medical imaging ; Metastases ; Metastasis ; Missing data ; Patients ; Radiation therapy ; Radiotherapy ; Survival ; Testing ; Toxicity ; Tumors ; Urothelial cancer ; Variables</subject><ispartof>Cancers, 2023-02, Vol.15 (4), p.1161</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 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/). 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In multivariable analysis, consolidative radiotherapy conferred a benefit in both PFS (HR = 0.49, = 0.007) and OS (HR = 0.47, = 0.015) in the whole population; in the landmark analysis at 6 months, radiotherapy was associated with improved OS (HR = 0.48, = 0.026), with a trend for PFS (HR = 0.57, = 0.082). Consolidative radiotherapy for mUBC patients who have not progressed after first-line therapy and with limited residual disease seems to confer both OS and PFS benefits. The role of consolidative radiotherapy in the context of avelumab maintenance should be addressed prospectively.</description><subject>Bladder cancer</subject><subject>Cancer therapies</subject><subject>Care and treatment</subject><subject>Chemotherapy</subject><subject>Clinical trials</subject><subject>Life Sciences</subject><subject>Lymphatic system</subject><subject>Malignancy</subject><subject>Medical imaging</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Missing data</subject><subject>Patients</subject><subject>Radiation therapy</subject><subject>Radiotherapy</subject><subject>Survival</subject><subject>Testing</subject><subject>Toxicity</subject><subject>Tumors</subject><subject>Urothelial cancer</subject><subject>Variables</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkk1vEzEQhlcIRKvSMzdkiQsc0vpr11kOSCEiFCmFCtqz5Xhns64cO9hOqvxS_g7epIQ0YlcrrzzP-854PEXxmuALxmp8qZXTECIpMSekIs-KU4oFHVRVzZ8f_J8U5zHe4_wwRkQlXhYnrBqyLGOnxe-xd9Fb06hk1oB-qMb41EFQyw1qfUDXkFRMOajRXegj1iiLPlnVNBDQeFsBuslxcCmiB5M69M2jm-DnAWI03iHlmv3-tQ-AUqccmmyzQTTNKvsdZJlCr4po4q31D8bNMxpiGkyNA_RzExMsMnW7K_EDGmWTFHxcgt4eYOSU3UQTXxUvWmUjnD-uZ8Xd5PPt-Gow_f7l63g0HeiS0jSY8VmLFeEtr3UJpNZt_jTWfDYkogTKmlpwVeKGCobL3GSCdTlsKYeSVzx39Kz4uPNdrmYLaHRuQ1BWLoNZqLCRXhn5NOJMJ-d-Leu65IKLbPB-Z9Adya5GU9nvYT4sOaVsTTL77jFZ8L9WEJNcmKjBWuXAr6KkYoixIIJWGX17hN77VcjN6SlR8xITKv5Rc2VBGtf6XKPuTeVIcIYJznCmLv5D5bfp78I7aE3efyK43Al0vpkYoN0fjGDZj648Gt2seHPYxj3_d1DZH-Ak7SU</recordid><startdate>20230211</startdate><enddate>20230211</enddate><creator>Aboudaram, Amélie</creator><creator>Chaltiel, Léonor</creator><creator>Pouessel, Damien</creator><creator>Graff-Cailleaud, Pierre</creator><creator>Benziane-Ouaritini, Nicolas</creator><creator>Sargos, Paul</creator><creator>Schick, Ulrike</creator><creator>Créhange, Gilles</creator><creator>Cohen-Jonathan Moyal, Elizabeth</creator><creator>Chevreau, Christine</creator><creator>Khalifa, Jonathan</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>Q9U</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4303-8135</orcidid></search><sort><creationdate>20230211</creationdate><title>Consolidative Radiotherapy for Metastatic Urothelial Bladder Cancer Patients with No Progression and with No More than Five Residual Metastatic Lesions Following First-Line Systemic Therapy: A Retrospective Analysis</title><author>Aboudaram, Amélie ; Chaltiel, Léonor ; Pouessel, Damien ; Graff-Cailleaud, Pierre ; Benziane-Ouaritini, Nicolas ; Sargos, Paul ; Schick, Ulrike ; Créhange, Gilles ; Cohen-Jonathan Moyal, Elizabeth ; Chevreau, Christine ; Khalifa, Jonathan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c522t-b4bf0a14f49c5e19cf19cc0c4b8175e23d974a50d2730516110c58f24e5464003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Bladder cancer</topic><topic>Cancer therapies</topic><topic>Care and treatment</topic><topic>Chemotherapy</topic><topic>Clinical trials</topic><topic>Life Sciences</topic><topic>Lymphatic system</topic><topic>Malignancy</topic><topic>Medical imaging</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Missing data</topic><topic>Patients</topic><topic>Radiation therapy</topic><topic>Radiotherapy</topic><topic>Survival</topic><topic>Testing</topic><topic>Toxicity</topic><topic>Tumors</topic><topic>Urothelial cancer</topic><topic>Variables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aboudaram, Amélie</creatorcontrib><creatorcontrib>Chaltiel, Léonor</creatorcontrib><creatorcontrib>Pouessel, Damien</creatorcontrib><creatorcontrib>Graff-Cailleaud, Pierre</creatorcontrib><creatorcontrib>Benziane-Ouaritini, Nicolas</creatorcontrib><creatorcontrib>Sargos, Paul</creatorcontrib><creatorcontrib>Schick, Ulrike</creatorcontrib><creatorcontrib>Créhange, Gilles</creatorcontrib><creatorcontrib>Cohen-Jonathan Moyal, Elizabeth</creatorcontrib><creatorcontrib>Chevreau, Christine</creatorcontrib><creatorcontrib>Khalifa, Jonathan</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</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 Basic</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aboudaram, Amélie</au><au>Chaltiel, Léonor</au><au>Pouessel, Damien</au><au>Graff-Cailleaud, Pierre</au><au>Benziane-Ouaritini, Nicolas</au><au>Sargos, Paul</au><au>Schick, Ulrike</au><au>Créhange, Gilles</au><au>Cohen-Jonathan Moyal, Elizabeth</au><au>Chevreau, Christine</au><au>Khalifa, Jonathan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Consolidative Radiotherapy for Metastatic Urothelial Bladder Cancer Patients with No Progression and with No More than Five Residual Metastatic Lesions Following First-Line Systemic Therapy: A Retrospective Analysis</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2023-02-11</date><risdate>2023</risdate><volume>15</volume><issue>4</issue><spage>1161</spage><pages>1161-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>Local consolidative radiotherapy in the treatment of metastatic malignancies has shown promising results in several types of tumors. The objective of this study was to assess consolidative radiotherapy to the bladder and to residual metastases in metastatic urothelial bladder cancer with no progression following first-line systemic therapy. Patients who received first-line therapy for the treatment of metastatic urothelial bladder cancer (mUBC) and who were progression-free following treatment with no more than five residual metastases were retrospectively identified through the database of four Comprehensive Cancer Centers, between January 2005 and December 2018. Among them, patients who received subsequent definitive radiotherapy (of EQD2Gy &gt; 45Gy) to the bladder and residual metastases were included in the consolidative group (irradiated (IR) group), and the other patients were included in the observation group (NIR group). Progression-free survival (PFS) and overall survival (OS) were determined from the start of the first-line chemotherapy using the Kaplan-Meier method. To prevent immortal time bias, a Cox model with time-dependent covariates and 6-month landmark analyses were performed to examine OS and PFS. A total of 91 patients with at least stable disease following first-line therapy and with no more than five residual metastases were analyzed: 51 in the IR group and 40 in the NIR group. Metachronous metastatic disease was more frequent in the NIR group (19% vs. 5%, = 0.02); the median number of metastases in the IR group vs. in the NIR group was 2 (1-9) vs. 3 (1-5) ( = 0.04) at metastatic presentation, and 1 (0-5) vs. 2 (0-5) ( = 0.18) after completion of chemotherapy (residual lesions), respectively. Two grade 3 toxicities (3.9%) and no grade 4 toxicity were reported in the IR group related to radiotherapy. With a median follow up of 85.9 months (95% IC (36.7; 101.6)), median OS and PFS were 21.7 months (95% IC (17.1; 29.7)) and 11.1 months (95% IC (9.9; 14.1)) for the whole cohort, respectively. In multivariable analysis, consolidative radiotherapy conferred a benefit in both PFS (HR = 0.49, = 0.007) and OS (HR = 0.47, = 0.015) in the whole population; in the landmark analysis at 6 months, radiotherapy was associated with improved OS (HR = 0.48, = 0.026), with a trend for PFS (HR = 0.57, = 0.082). Consolidative radiotherapy for mUBC patients who have not progressed after first-line therapy and with limited residual disease seems to confer both OS and PFS benefits. The role of consolidative radiotherapy in the context of avelumab maintenance should be addressed prospectively.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>36831503</pmid><doi>10.3390/cancers15041161</doi><orcidid>https://orcid.org/0000-0002-4303-8135</orcidid><oa>free_for_read</oa></addata></record>
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source MDPI - Multidisciplinary Digital Publishing Institute; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access
subjects Bladder cancer
Cancer therapies
Care and treatment
Chemotherapy
Clinical trials
Life Sciences
Lymphatic system
Malignancy
Medical imaging
Metastases
Metastasis
Missing data
Patients
Radiation therapy
Radiotherapy
Survival
Testing
Toxicity
Tumors
Urothelial cancer
Variables
title Consolidative Radiotherapy for Metastatic Urothelial Bladder Cancer Patients with No Progression and with No More than Five Residual Metastatic Lesions Following First-Line Systemic Therapy: A Retrospective Analysis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-14T04%3A50%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Consolidative%20Radiotherapy%20for%20Metastatic%20Urothelial%20Bladder%20Cancer%20Patients%20with%20No%20Progression%20and%20with%20No%20More%20than%20Five%20Residual%20Metastatic%20Lesions%20Following%20First-Line%20Systemic%20Therapy:%20A%20Retrospective%20Analysis&rft.jtitle=Cancers&rft.au=Aboudaram,%20Am%C3%A9lie&rft.date=2023-02-11&rft.volume=15&rft.issue=4&rft.spage=1161&rft.pages=1161-&rft.issn=2072-6694&rft.eissn=2072-6694&rft_id=info:doi/10.3390/cancers15041161&rft_dat=%3Cgale_pubme%3EA743010277%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2779450127&rft_id=info:pmid/36831503&rft_galeid=A743010277&rfr_iscdi=true