Comparison of whole-body DW-MRI with 2-[18F]FDG PET for staging and treatment monitoring of children with Langerhans cell histiocytosis

Purpose To assess and compare the diagnostic accuracy of whole-body (WB) DW-MRI with 2-[ 18 F]FDG PET for staging and treatment monitoring of children with Langerhans cell histiocytosis (LCH). Methods Twenty-three children with LCH underwent 2-[ 18 F]FDG PET and WB DW-MRI at baseline. Two nuclear me...

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Veröffentlicht in:European journal of nuclear medicine and molecular imaging 2023-05, Vol.50 (6), p.1689-1698
Hauptverfasser: Baratto, Lucia, Nyalakonda, Ramyashree, Theruvath, Ashok J., Sarrami, Amir Hossein, Hawk, Kristina Elizabeth, Rashidi, Ali, Shen, Sa, States, Lisa, Aboian, Mariam, Jeng, Michael, Daldrup-Link, Heike E.
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container_end_page 1698
container_issue 6
container_start_page 1689
container_title European journal of nuclear medicine and molecular imaging
container_volume 50
creator Baratto, Lucia
Nyalakonda, Ramyashree
Theruvath, Ashok J.
Sarrami, Amir Hossein
Hawk, Kristina Elizabeth
Rashidi, Ali
Shen, Sa
States, Lisa
Aboian, Mariam
Jeng, Michael
Daldrup-Link, Heike E.
description Purpose To assess and compare the diagnostic accuracy of whole-body (WB) DW-MRI with 2-[ 18 F]FDG PET for staging and treatment monitoring of children with Langerhans cell histiocytosis (LCH). Methods Twenty-three children with LCH underwent 2-[ 18 F]FDG PET and WB DW-MRI at baseline. Two nuclear medicine physicians and two radiologists independently assessed presence/absence of tumors in 8 anatomical areas. Sixteen children also performed 2-[ 18 F]FDG PET and WB DW-MRI at follow-up. One radiologist and one nuclear medicine physician revised follow-up scans and collected changes in tumor apparent diffusion (ADC) and standardized uptake values (SUV) before and after therapy in all detectable lesions. 2-[ 18 F]FDG PET results were considered the standard of reference for tumor detection and evaluation of treatment response according to Lugano criteria. Sensitivity, specificity, positive and negative predictive values, and diagnostic accuracy of WB DW-MRI at baseline were calculated, and the 95% confidence intervals were estimated by using the Clopper-Pearson (exact) method; changes in tumor SUVs and ADC were compared using a Mann–Whitney U test. Agreement between reviewers was assessed with a Cohen’s weighted kappa coefficient. Analyses were conducted using SAS software version 9.4. Results Agreement between reviewers was perfect (kappa coefficient = 1) for all analyzed regions but spine and neck (kappa coefficient = 0.89 and 0.83, respectively) for 2-[ 18 F]FDG PET images, and abdomen and pelvis (kappa coefficient = 0.65 and 0.88, respectively) for WB DW-MRI. Sensitivity and specificity were 95.5% and 100% for WB DW-MRI compared to 2-[ 18 F]FDG PET. Pre to post-treatment changes in SUV ratio and ADC mean were inversely correlated for all lesions ( r : -0.27, p  = 0·06) and significantly different between responders and non-responders to chemotherapy ( p  = 0.0006 and p  = 0·003 for SUV ratio and ADC mean , respectively). Conclusion Our study showed that WB DW-MRI has similar accuracy to 2-[ 18 F]FDG PET for staging and treatment monitoring of LCH in children. While 2-[ 18 F]FDG PET remains an approved radiological examination for assessing metabolically active disease, WB DW-MRI could be considered as an alternative approach without radiation exposure. The combination of both modalities might have advantages over either approach alone.
doi_str_mv 10.1007/s00259-023-06122-6
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fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10121877</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2771334187</sourcerecordid><originalsourceid>FETCH-LOGICAL-c431t-f3d7aa108e0ee39c084daf3ac3398302373169b876662a207fc116f675a5c5ca3</originalsourceid><addsrcrecordid>eNp9kc9uEzEQxlcIREvhBTggS1y4GMb2xvaeEEqbtlIQCBVxQMhyvN6sq107tR2qPAGvXYct4c-B01ia33wzn7-qek7gNQEQbxIAnTUYKMPACaWYP6iOCScNFiCbh4e3gKPqSUrXAERS2TyujhgXRNTQHFc_5mHc6OhS8Ch06LYPg8Wr0O7Q6Rf8_tMlunW5RxR_JXLxbXF6jj6eXaEuRJSyXju_Rtq3KEer82h9RmPwLoe4bxQ107uhjdZPIkvt1zb22idk7DCg3qXsgtnlkFx6Wj3q9JDss_t6Un1enF3NL_Dyw_nl_N0Sm5qRjDvWCq0JSAvWssaArFvdMW0YayQrPyEY4c1KCs451RREZwjhHRczPTMzo9lJ9XbS3WxXo21NOTrqQW2iG3XcqaCd-rvjXa_W4bsiQCiRQhSFV_cKMdxsbcpqdGlvSHsbtklRIQhjdWEL-vIf9Dpsoy_-FJXAuOSsZoWiE2ViSCna7nANAbUPWk1Bq2JP_Qxa8TL04k8fh5FfyRaATUDa7OOw8ffu_8jeAQJ7tA8</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2803686343</pqid></control><display><type>article</type><title>Comparison of whole-body DW-MRI with 2-[18F]FDG PET for staging and treatment monitoring of children with Langerhans cell histiocytosis</title><source>MEDLINE</source><source>Springer Online Journals Complete</source><creator>Baratto, Lucia ; Nyalakonda, Ramyashree ; Theruvath, Ashok J. ; Sarrami, Amir Hossein ; Hawk, Kristina Elizabeth ; Rashidi, Ali ; Shen, Sa ; States, Lisa ; Aboian, Mariam ; Jeng, Michael ; Daldrup-Link, Heike E.</creator><creatorcontrib>Baratto, Lucia ; Nyalakonda, Ramyashree ; Theruvath, Ashok J. ; Sarrami, Amir Hossein ; Hawk, Kristina Elizabeth ; Rashidi, Ali ; Shen, Sa ; States, Lisa ; Aboian, Mariam ; Jeng, Michael ; Daldrup-Link, Heike E.</creatorcontrib><description>Purpose To assess and compare the diagnostic accuracy of whole-body (WB) DW-MRI with 2-[ 18 F]FDG PET for staging and treatment monitoring of children with Langerhans cell histiocytosis (LCH). Methods Twenty-three children with LCH underwent 2-[ 18 F]FDG PET and WB DW-MRI at baseline. Two nuclear medicine physicians and two radiologists independently assessed presence/absence of tumors in 8 anatomical areas. Sixteen children also performed 2-[ 18 F]FDG PET and WB DW-MRI at follow-up. One radiologist and one nuclear medicine physician revised follow-up scans and collected changes in tumor apparent diffusion (ADC) and standardized uptake values (SUV) before and after therapy in all detectable lesions. 2-[ 18 F]FDG PET results were considered the standard of reference for tumor detection and evaluation of treatment response according to Lugano criteria. Sensitivity, specificity, positive and negative predictive values, and diagnostic accuracy of WB DW-MRI at baseline were calculated, and the 95% confidence intervals were estimated by using the Clopper-Pearson (exact) method; changes in tumor SUVs and ADC were compared using a Mann–Whitney U test. Agreement between reviewers was assessed with a Cohen’s weighted kappa coefficient. Analyses were conducted using SAS software version 9.4. Results Agreement between reviewers was perfect (kappa coefficient = 1) for all analyzed regions but spine and neck (kappa coefficient = 0.89 and 0.83, respectively) for 2-[ 18 F]FDG PET images, and abdomen and pelvis (kappa coefficient = 0.65 and 0.88, respectively) for WB DW-MRI. Sensitivity and specificity were 95.5% and 100% for WB DW-MRI compared to 2-[ 18 F]FDG PET. Pre to post-treatment changes in SUV ratio and ADC mean were inversely correlated for all lesions ( r : -0.27, p  = 0·06) and significantly different between responders and non-responders to chemotherapy ( p  = 0.0006 and p  = 0·003 for SUV ratio and ADC mean , respectively). Conclusion Our study showed that WB DW-MRI has similar accuracy to 2-[ 18 F]FDG PET for staging and treatment monitoring of LCH in children. While 2-[ 18 F]FDG PET remains an approved radiological examination for assessing metabolically active disease, WB DW-MRI could be considered as an alternative approach without radiation exposure. The combination of both modalities might have advantages over either approach alone.</description><identifier>ISSN: 1619-7070</identifier><identifier>EISSN: 1619-7089</identifier><identifier>DOI: 10.1007/s00259-023-06122-6</identifier><identifier>PMID: 36717409</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Accuracy ; Autoimmune diseases ; Cardiology ; Chemotherapy ; Child ; Children ; Coefficients ; Diffusion Magnetic Resonance Imaging - methods ; Fluorine isotopes ; Fluorodeoxyglucose F18 ; Health services ; Histiocytosis ; Histiocytosis, Langerhans-Cell - diagnostic imaging ; Histiocytosis, Langerhans-Cell - therapy ; Humans ; Imaging ; Kappa coefficient ; Langerhans cell histiocytosis ; Lesions ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Medicine ; Medicine &amp; Public Health ; Monitoring ; Neoplasm Staging ; Neoplasms ; Nuclear Medicine ; Oncology ; Original Article ; Orthopedics ; Pelvis ; Physicians ; Positron emission ; Positron emission tomography ; Positron-Emission Tomography - methods ; Radiation effects ; Radiology ; Radiopharmaceuticals ; Telemedicine ; Tumors ; Whole Body Imaging - methods</subject><ispartof>European journal of nuclear medicine and molecular imaging, 2023-05, Vol.50 (6), p.1689-1698</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-f3d7aa108e0ee39c084daf3ac3398302373169b876662a207fc116f675a5c5ca3</citedby><cites>FETCH-LOGICAL-c431t-f3d7aa108e0ee39c084daf3ac3398302373169b876662a207fc116f675a5c5ca3</cites><orcidid>0000-0002-1646-4876</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/s00259-023-06122-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00259-023-06122-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36717409$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baratto, Lucia</creatorcontrib><creatorcontrib>Nyalakonda, Ramyashree</creatorcontrib><creatorcontrib>Theruvath, Ashok J.</creatorcontrib><creatorcontrib>Sarrami, Amir Hossein</creatorcontrib><creatorcontrib>Hawk, Kristina Elizabeth</creatorcontrib><creatorcontrib>Rashidi, Ali</creatorcontrib><creatorcontrib>Shen, Sa</creatorcontrib><creatorcontrib>States, Lisa</creatorcontrib><creatorcontrib>Aboian, Mariam</creatorcontrib><creatorcontrib>Jeng, Michael</creatorcontrib><creatorcontrib>Daldrup-Link, Heike E.</creatorcontrib><title>Comparison of whole-body DW-MRI with 2-[18F]FDG PET for staging and treatment monitoring of children with Langerhans cell histiocytosis</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>Purpose To assess and compare the diagnostic accuracy of whole-body (WB) DW-MRI with 2-[ 18 F]FDG PET for staging and treatment monitoring of children with Langerhans cell histiocytosis (LCH). Methods Twenty-three children with LCH underwent 2-[ 18 F]FDG PET and WB DW-MRI at baseline. Two nuclear medicine physicians and two radiologists independently assessed presence/absence of tumors in 8 anatomical areas. Sixteen children also performed 2-[ 18 F]FDG PET and WB DW-MRI at follow-up. One radiologist and one nuclear medicine physician revised follow-up scans and collected changes in tumor apparent diffusion (ADC) and standardized uptake values (SUV) before and after therapy in all detectable lesions. 2-[ 18 F]FDG PET results were considered the standard of reference for tumor detection and evaluation of treatment response according to Lugano criteria. Sensitivity, specificity, positive and negative predictive values, and diagnostic accuracy of WB DW-MRI at baseline were calculated, and the 95% confidence intervals were estimated by using the Clopper-Pearson (exact) method; changes in tumor SUVs and ADC were compared using a Mann–Whitney U test. Agreement between reviewers was assessed with a Cohen’s weighted kappa coefficient. Analyses were conducted using SAS software version 9.4. Results Agreement between reviewers was perfect (kappa coefficient = 1) for all analyzed regions but spine and neck (kappa coefficient = 0.89 and 0.83, respectively) for 2-[ 18 F]FDG PET images, and abdomen and pelvis (kappa coefficient = 0.65 and 0.88, respectively) for WB DW-MRI. Sensitivity and specificity were 95.5% and 100% for WB DW-MRI compared to 2-[ 18 F]FDG PET. Pre to post-treatment changes in SUV ratio and ADC mean were inversely correlated for all lesions ( r : -0.27, p  = 0·06) and significantly different between responders and non-responders to chemotherapy ( p  = 0.0006 and p  = 0·003 for SUV ratio and ADC mean , respectively). Conclusion Our study showed that WB DW-MRI has similar accuracy to 2-[ 18 F]FDG PET for staging and treatment monitoring of LCH in children. While 2-[ 18 F]FDG PET remains an approved radiological examination for assessing metabolically active disease, WB DW-MRI could be considered as an alternative approach without radiation exposure. The combination of both modalities might have advantages over either approach alone.</description><subject>Accuracy</subject><subject>Autoimmune diseases</subject><subject>Cardiology</subject><subject>Chemotherapy</subject><subject>Child</subject><subject>Children</subject><subject>Coefficients</subject><subject>Diffusion Magnetic Resonance Imaging - methods</subject><subject>Fluorine isotopes</subject><subject>Fluorodeoxyglucose F18</subject><subject>Health services</subject><subject>Histiocytosis</subject><subject>Histiocytosis, Langerhans-Cell - diagnostic imaging</subject><subject>Histiocytosis, Langerhans-Cell - therapy</subject><subject>Humans</subject><subject>Imaging</subject><subject>Kappa coefficient</subject><subject>Langerhans cell histiocytosis</subject><subject>Lesions</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Monitoring</subject><subject>Neoplasm Staging</subject><subject>Neoplasms</subject><subject>Nuclear Medicine</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Orthopedics</subject><subject>Pelvis</subject><subject>Physicians</subject><subject>Positron emission</subject><subject>Positron emission tomography</subject><subject>Positron-Emission Tomography - methods</subject><subject>Radiation effects</subject><subject>Radiology</subject><subject>Radiopharmaceuticals</subject><subject>Telemedicine</subject><subject>Tumors</subject><subject>Whole Body Imaging - methods</subject><issn>1619-7070</issn><issn>1619-7089</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kc9uEzEQxlcIREvhBTggS1y4GMb2xvaeEEqbtlIQCBVxQMhyvN6sq107tR2qPAGvXYct4c-B01ia33wzn7-qek7gNQEQbxIAnTUYKMPACaWYP6iOCScNFiCbh4e3gKPqSUrXAERS2TyujhgXRNTQHFc_5mHc6OhS8Ch06LYPg8Wr0O7Q6Rf8_tMlunW5RxR_JXLxbXF6jj6eXaEuRJSyXju_Rtq3KEer82h9RmPwLoe4bxQ107uhjdZPIkvt1zb22idk7DCg3qXsgtnlkFx6Wj3q9JDss_t6Un1enF3NL_Dyw_nl_N0Sm5qRjDvWCq0JSAvWssaArFvdMW0YayQrPyEY4c1KCs451RREZwjhHRczPTMzo9lJ9XbS3WxXo21NOTrqQW2iG3XcqaCd-rvjXa_W4bsiQCiRQhSFV_cKMdxsbcpqdGlvSHsbtklRIQhjdWEL-vIf9Dpsoy_-FJXAuOSsZoWiE2ViSCna7nANAbUPWk1Bq2JP_Qxa8TL04k8fh5FfyRaATUDa7OOw8ffu_8jeAQJ7tA8</recordid><startdate>20230501</startdate><enddate>20230501</enddate><creator>Baratto, Lucia</creator><creator>Nyalakonda, Ramyashree</creator><creator>Theruvath, Ashok J.</creator><creator>Sarrami, Amir Hossein</creator><creator>Hawk, Kristina Elizabeth</creator><creator>Rashidi, Ali</creator><creator>Shen, Sa</creator><creator>States, Lisa</creator><creator>Aboian, Mariam</creator><creator>Jeng, Michael</creator><creator>Daldrup-Link, Heike E.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</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>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>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1646-4876</orcidid></search><sort><creationdate>20230501</creationdate><title>Comparison of whole-body DW-MRI with 2-[18F]FDG PET for staging and treatment monitoring of children with Langerhans cell histiocytosis</title><author>Baratto, Lucia ; Nyalakonda, Ramyashree ; Theruvath, Ashok J. ; Sarrami, Amir Hossein ; Hawk, Kristina Elizabeth ; Rashidi, Ali ; Shen, Sa ; States, Lisa ; Aboian, Mariam ; Jeng, Michael ; Daldrup-Link, Heike E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-f3d7aa108e0ee39c084daf3ac3398302373169b876662a207fc116f675a5c5ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Accuracy</topic><topic>Autoimmune diseases</topic><topic>Cardiology</topic><topic>Chemotherapy</topic><topic>Child</topic><topic>Children</topic><topic>Coefficients</topic><topic>Diffusion Magnetic Resonance Imaging - methods</topic><topic>Fluorine isotopes</topic><topic>Fluorodeoxyglucose F18</topic><topic>Health services</topic><topic>Histiocytosis</topic><topic>Histiocytosis, Langerhans-Cell - diagnostic imaging</topic><topic>Histiocytosis, Langerhans-Cell - therapy</topic><topic>Humans</topic><topic>Imaging</topic><topic>Kappa coefficient</topic><topic>Langerhans cell histiocytosis</topic><topic>Lesions</topic><topic>Magnetic resonance imaging</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Monitoring</topic><topic>Neoplasm Staging</topic><topic>Neoplasms</topic><topic>Nuclear Medicine</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Orthopedics</topic><topic>Pelvis</topic><topic>Physicians</topic><topic>Positron emission</topic><topic>Positron emission tomography</topic><topic>Positron-Emission Tomography - methods</topic><topic>Radiation effects</topic><topic>Radiology</topic><topic>Radiopharmaceuticals</topic><topic>Telemedicine</topic><topic>Tumors</topic><topic>Whole Body Imaging - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baratto, Lucia</creatorcontrib><creatorcontrib>Nyalakonda, Ramyashree</creatorcontrib><creatorcontrib>Theruvath, Ashok J.</creatorcontrib><creatorcontrib>Sarrami, Amir Hossein</creatorcontrib><creatorcontrib>Hawk, Kristina Elizabeth</creatorcontrib><creatorcontrib>Rashidi, Ali</creatorcontrib><creatorcontrib>Shen, Sa</creatorcontrib><creatorcontrib>States, Lisa</creatorcontrib><creatorcontrib>Aboian, Mariam</creatorcontrib><creatorcontrib>Jeng, Michael</creatorcontrib><creatorcontrib>Daldrup-Link, Heike E.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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Methods Twenty-three children with LCH underwent 2-[ 18 F]FDG PET and WB DW-MRI at baseline. Two nuclear medicine physicians and two radiologists independently assessed presence/absence of tumors in 8 anatomical areas. Sixteen children also performed 2-[ 18 F]FDG PET and WB DW-MRI at follow-up. One radiologist and one nuclear medicine physician revised follow-up scans and collected changes in tumor apparent diffusion (ADC) and standardized uptake values (SUV) before and after therapy in all detectable lesions. 2-[ 18 F]FDG PET results were considered the standard of reference for tumor detection and evaluation of treatment response according to Lugano criteria. Sensitivity, specificity, positive and negative predictive values, and diagnostic accuracy of WB DW-MRI at baseline were calculated, and the 95% confidence intervals were estimated by using the Clopper-Pearson (exact) method; changes in tumor SUVs and ADC were compared using a Mann–Whitney U test. Agreement between reviewers was assessed with a Cohen’s weighted kappa coefficient. Analyses were conducted using SAS software version 9.4. Results Agreement between reviewers was perfect (kappa coefficient = 1) for all analyzed regions but spine and neck (kappa coefficient = 0.89 and 0.83, respectively) for 2-[ 18 F]FDG PET images, and abdomen and pelvis (kappa coefficient = 0.65 and 0.88, respectively) for WB DW-MRI. Sensitivity and specificity were 95.5% and 100% for WB DW-MRI compared to 2-[ 18 F]FDG PET. Pre to post-treatment changes in SUV ratio and ADC mean were inversely correlated for all lesions ( r : -0.27, p  = 0·06) and significantly different between responders and non-responders to chemotherapy ( p  = 0.0006 and p  = 0·003 for SUV ratio and ADC mean , respectively). Conclusion Our study showed that WB DW-MRI has similar accuracy to 2-[ 18 F]FDG PET for staging and treatment monitoring of LCH in children. While 2-[ 18 F]FDG PET remains an approved radiological examination for assessing metabolically active disease, WB DW-MRI could be considered as an alternative approach without radiation exposure. The combination of both modalities might have advantages over either approach alone.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>36717409</pmid><doi>10.1007/s00259-023-06122-6</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-1646-4876</orcidid></addata></record>
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subjects Accuracy
Autoimmune diseases
Cardiology
Chemotherapy
Child
Children
Coefficients
Diffusion Magnetic Resonance Imaging - methods
Fluorine isotopes
Fluorodeoxyglucose F18
Health services
Histiocytosis
Histiocytosis, Langerhans-Cell - diagnostic imaging
Histiocytosis, Langerhans-Cell - therapy
Humans
Imaging
Kappa coefficient
Langerhans cell histiocytosis
Lesions
Magnetic resonance imaging
Magnetic Resonance Imaging - methods
Medicine
Medicine & Public Health
Monitoring
Neoplasm Staging
Neoplasms
Nuclear Medicine
Oncology
Original Article
Orthopedics
Pelvis
Physicians
Positron emission
Positron emission tomography
Positron-Emission Tomography - methods
Radiation effects
Radiology
Radiopharmaceuticals
Telemedicine
Tumors
Whole Body Imaging - methods
title Comparison of whole-body DW-MRI with 2-[18F]FDG PET for staging and treatment monitoring of children with Langerhans cell histiocytosis
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