iRECIST-based versus non-standardized free text reporting of CT scans for monitoring metastatic renal cell carcinoma: a retrospective comparison
Purpose Therapy decision for patients with metastatic renal cell carcinoma (mRCC) is highly dependent on disease monitoring based on radiological reports. The purpose of the study was to compare non-standardized, common practice free text reporting (FTR) on disease response with reporting based on r...
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Veröffentlicht in: | Journal of cancer research and clinical oncology 2022-08, Vol.148 (8), p.2003-2012 |
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container_issue | 8 |
container_start_page | 2003 |
container_title | Journal of cancer research and clinical oncology |
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creator | Schomburg, Laura Malouhi, Amer Grimm, Marc-Oliver Ingwersen, Maja Foller, Susan Leucht, Katharina Teichgräber, Ulf |
description | Purpose
Therapy decision for patients with metastatic renal cell carcinoma (mRCC) is highly dependent on disease monitoring based on radiological reports. The purpose of the study was to compare non-standardized, common practice free text reporting (FTR) on disease response with reporting based on response evaluation criteria in solid tumors modified for immune-based therapeutics (iRECIST).
Methods
Fifty patients with advanced mRCC were included in the retrospective, single-center study. CT scans had been evaluated and FTR prepared in accordance with center’s routine practice. For study purposes, reports were re-evaluated using a dedicated computer program that applied iRECIST. Patients were followed up over a period of 22.8 ± 7.9 months in intervals of 2.7 ± 1.8 months.
Weighted kappa statistics was run to assess strength of agreement. Logistic regression was used to identify predictors for different rating.
Results
Agreement between FTR and iRECIST-based reporting was moderate (kappa 0.38 [95% CI 0.2–0.6] to 0.70 [95% CI 0.5–0.9]). Tumor response or progression according to FTR were not confirmed with iRECIST in 19 (38%) or 11 (22%) patients, respectively, in at least one follow-up examination. With FTR, new lesions were frequently not recognized if they were already identified in the recent prior follow-up examination (odds ratio for too favorable rating of disease response compared to iRECIST: 5.4 [95% CI 2.9–10.1].
Conclusions
Moderate agreement between disease response according to FTR or iRECIST in patients with mRCC suggests the need of standardized quantitative radiological assessment in daily clinical practice. |
doi_str_mv | 10.1007/s00432-022-03997-0 |
format | Article |
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Therapy decision for patients with metastatic renal cell carcinoma (mRCC) is highly dependent on disease monitoring based on radiological reports. The purpose of the study was to compare non-standardized, common practice free text reporting (FTR) on disease response with reporting based on response evaluation criteria in solid tumors modified for immune-based therapeutics (iRECIST).
Methods
Fifty patients with advanced mRCC were included in the retrospective, single-center study. CT scans had been evaluated and FTR prepared in accordance with center’s routine practice. For study purposes, reports were re-evaluated using a dedicated computer program that applied iRECIST. Patients were followed up over a period of 22.8 ± 7.9 months in intervals of 2.7 ± 1.8 months.
Weighted kappa statistics was run to assess strength of agreement. Logistic regression was used to identify predictors for different rating.
Results
Agreement between FTR and iRECIST-based reporting was moderate (kappa 0.38 [95% CI 0.2–0.6] to 0.70 [95% CI 0.5–0.9]). Tumor response or progression according to FTR were not confirmed with iRECIST in 19 (38%) or 11 (22%) patients, respectively, in at least one follow-up examination. With FTR, new lesions were frequently not recognized if they were already identified in the recent prior follow-up examination (odds ratio for too favorable rating of disease response compared to iRECIST: 5.4 [95% CI 2.9–10.1].
Conclusions
Moderate agreement between disease response according to FTR or iRECIST in patients with mRCC suggests the need of standardized quantitative radiological assessment in daily clinical practice.</description><identifier>ISSN: 0171-5216</identifier><identifier>EISSN: 1432-1335</identifier><identifier>DOI: 10.1007/s00432-022-03997-0</identifier><identifier>PMID: 35420348</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Cancer Research ; Hematology ; Internal Medicine ; Kidney cancer ; Medical imaging ; Medicine ; Medicine & Public Health ; Metastases ; Metastasis ; Oncology ; Original Article – Cancer Research ; Original – Cancer Research ; Patients ; Renal cell carcinoma ; Solid tumors</subject><ispartof>Journal of cancer research and clinical oncology, 2022-08, Vol.148 (8), p.2003-2012</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-c404t-901acdce87c6d95c0d74fe7b2c2dd4a255e46b4c107feda194a6d9a69d4b54bc3</citedby><cites>FETCH-LOGICAL-c404t-901acdce87c6d95c0d74fe7b2c2dd4a255e46b4c107feda194a6d9a69d4b54bc3</cites><orcidid>0000-0002-4048-3938</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00432-022-03997-0$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00432-022-03997-0$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35420348$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schomburg, Laura</creatorcontrib><creatorcontrib>Malouhi, Amer</creatorcontrib><creatorcontrib>Grimm, Marc-Oliver</creatorcontrib><creatorcontrib>Ingwersen, Maja</creatorcontrib><creatorcontrib>Foller, Susan</creatorcontrib><creatorcontrib>Leucht, Katharina</creatorcontrib><creatorcontrib>Teichgräber, Ulf</creatorcontrib><title>iRECIST-based versus non-standardized free text reporting of CT scans for monitoring metastatic renal cell carcinoma: a retrospective comparison</title><title>Journal of cancer research and clinical oncology</title><addtitle>J Cancer Res Clin Oncol</addtitle><addtitle>J Cancer Res Clin Oncol</addtitle><description>Purpose
Therapy decision for patients with metastatic renal cell carcinoma (mRCC) is highly dependent on disease monitoring based on radiological reports. The purpose of the study was to compare non-standardized, common practice free text reporting (FTR) on disease response with reporting based on response evaluation criteria in solid tumors modified for immune-based therapeutics (iRECIST).
Methods
Fifty patients with advanced mRCC were included in the retrospective, single-center study. CT scans had been evaluated and FTR prepared in accordance with center’s routine practice. For study purposes, reports were re-evaluated using a dedicated computer program that applied iRECIST. Patients were followed up over a period of 22.8 ± 7.9 months in intervals of 2.7 ± 1.8 months.
Weighted kappa statistics was run to assess strength of agreement. Logistic regression was used to identify predictors for different rating.
Results
Agreement between FTR and iRECIST-based reporting was moderate (kappa 0.38 [95% CI 0.2–0.6] to 0.70 [95% CI 0.5–0.9]). Tumor response or progression according to FTR were not confirmed with iRECIST in 19 (38%) or 11 (22%) patients, respectively, in at least one follow-up examination. With FTR, new lesions were frequently not recognized if they were already identified in the recent prior follow-up examination (odds ratio for too favorable rating of disease response compared to iRECIST: 5.4 [95% CI 2.9–10.1].
Conclusions
Moderate agreement between disease response according to FTR or iRECIST in patients with mRCC suggests the need of standardized quantitative radiological assessment in daily clinical practice.</description><subject>Cancer Research</subject><subject>Hematology</subject><subject>Internal Medicine</subject><subject>Kidney cancer</subject><subject>Medical imaging</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Oncology</subject><subject>Original Article – Cancer Research</subject><subject>Original – Cancer Research</subject><subject>Patients</subject><subject>Renal cell carcinoma</subject><subject>Solid tumors</subject><issn>0171-5216</issn><issn>1432-1335</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kc-OFCEQxonRuOPoC3gwJF68tAIN3dMeTDaTVTfZxETHM6mG6pXNNLRAT9Sn2Ede2lnXPwcPQKj61QdVHyFPOXvJGWtfJcZkLSomyqq7rq3YPbLiS4jXtbpPVoy3vFKCNyfkUUpXrNxVKx6Sk1pJwWq5WZFr9_Fse_5pV_WQ0NIDxjQn6oOvUgZvIVr3o8SHiEgzfss04hRidv6ShoFudzQZ8IkOIdIxeJdDXFIjZij12ZnCe9hTg_uyQTTOhxFeUyjxHEOa0GR3QGrCOEF0KfjH5MEA-4RPbs81-fz2bLd9X118eHe-Pb2ojGQyVx3jYKzBTWsa2ynDbCsHbHthhLUShFIom14aztoBLfBOQuGg6azslexNvSZvjrrT3I9YlHyOsNdTdCPE7zqA039nvPuiL8NBd6KTTMgi8OJWIIavM6asR5eWPsFjmJMWjWJC1ZuWFfT5P-hVmGOZy0J1XCgmC7km4kiZMpgUcbj7DGd6MVwfDdfFcP3TcL1IP_uzjbuSXw4XoD4CaVqswfj77f_I3gAiObqL</recordid><startdate>20220801</startdate><enddate>20220801</enddate><creator>Schomburg, Laura</creator><creator>Malouhi, Amer</creator><creator>Grimm, Marc-Oliver</creator><creator>Ingwersen, Maja</creator><creator>Foller, Susan</creator><creator>Leucht, Katharina</creator><creator>Teichgräber, Ulf</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>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</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/0000-0002-4048-3938</orcidid></search><sort><creationdate>20220801</creationdate><title>iRECIST-based versus non-standardized free text reporting of CT scans for monitoring metastatic renal cell carcinoma: a retrospective comparison</title><author>Schomburg, Laura ; Malouhi, Amer ; Grimm, Marc-Oliver ; Ingwersen, Maja ; Foller, Susan ; Leucht, Katharina ; Teichgräber, Ulf</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-901acdce87c6d95c0d74fe7b2c2dd4a255e46b4c107feda194a6d9a69d4b54bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Cancer Research</topic><topic>Hematology</topic><topic>Internal Medicine</topic><topic>Kidney cancer</topic><topic>Medical imaging</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Oncology</topic><topic>Original Article – Cancer Research</topic><topic>Original – Cancer Research</topic><topic>Patients</topic><topic>Renal cell carcinoma</topic><topic>Solid tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schomburg, Laura</creatorcontrib><creatorcontrib>Malouhi, Amer</creatorcontrib><creatorcontrib>Grimm, Marc-Oliver</creatorcontrib><creatorcontrib>Ingwersen, Maja</creatorcontrib><creatorcontrib>Foller, Susan</creatorcontrib><creatorcontrib>Leucht, Katharina</creatorcontrib><creatorcontrib>Teichgräber, Ulf</creatorcontrib><collection>SpringerOpen</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database (Proquest)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</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>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Research Library</collection><collection>Research Library (Corporate)</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>Journal of cancer research and clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schomburg, Laura</au><au>Malouhi, Amer</au><au>Grimm, Marc-Oliver</au><au>Ingwersen, Maja</au><au>Foller, Susan</au><au>Leucht, Katharina</au><au>Teichgräber, Ulf</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>iRECIST-based versus non-standardized free text reporting of CT scans for monitoring metastatic renal cell carcinoma: a retrospective comparison</atitle><jtitle>Journal of cancer research and clinical oncology</jtitle><stitle>J Cancer Res Clin Oncol</stitle><addtitle>J Cancer Res Clin Oncol</addtitle><date>2022-08-01</date><risdate>2022</risdate><volume>148</volume><issue>8</issue><spage>2003</spage><epage>2012</epage><pages>2003-2012</pages><issn>0171-5216</issn><eissn>1432-1335</eissn><abstract>Purpose
Therapy decision for patients with metastatic renal cell carcinoma (mRCC) is highly dependent on disease monitoring based on radiological reports. The purpose of the study was to compare non-standardized, common practice free text reporting (FTR) on disease response with reporting based on response evaluation criteria in solid tumors modified for immune-based therapeutics (iRECIST).
Methods
Fifty patients with advanced mRCC were included in the retrospective, single-center study. CT scans had been evaluated and FTR prepared in accordance with center’s routine practice. For study purposes, reports were re-evaluated using a dedicated computer program that applied iRECIST. Patients were followed up over a period of 22.8 ± 7.9 months in intervals of 2.7 ± 1.8 months.
Weighted kappa statistics was run to assess strength of agreement. Logistic regression was used to identify predictors for different rating.
Results
Agreement between FTR and iRECIST-based reporting was moderate (kappa 0.38 [95% CI 0.2–0.6] to 0.70 [95% CI 0.5–0.9]). Tumor response or progression according to FTR were not confirmed with iRECIST in 19 (38%) or 11 (22%) patients, respectively, in at least one follow-up examination. With FTR, new lesions were frequently not recognized if they were already identified in the recent prior follow-up examination (odds ratio for too favorable rating of disease response compared to iRECIST: 5.4 [95% CI 2.9–10.1].
Conclusions
Moderate agreement between disease response according to FTR or iRECIST in patients with mRCC suggests the need of standardized quantitative radiological assessment in daily clinical practice.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>35420348</pmid><doi>10.1007/s00432-022-03997-0</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-4048-3938</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Cancer Research Hematology Internal Medicine Kidney cancer Medical imaging Medicine Medicine & Public Health Metastases Metastasis Oncology Original Article – Cancer Research Original – Cancer Research Patients Renal cell carcinoma Solid tumors |
title | iRECIST-based versus non-standardized free text reporting of CT scans for monitoring metastatic renal cell carcinoma: a retrospective comparison |
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