11C-methionine-PET for differentiating recurrent brain tumor from radiation necrosis: radiomics approach with random forest classifier
Differentiating recurrent brain tumor from radiation necrosis is often difficult. This study aims to investigate the efficacy of 11C-methionine (MET)-PET radiomics for distinguishing recurrent brain tumor from radiation necrosis, as compared with conventional tumor-to-normal cortex (T/N) ratio evalu...
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description | Differentiating recurrent brain tumor from radiation necrosis is often difficult. This study aims to investigate the efficacy of 11C-methionine (MET)-PET radiomics for distinguishing recurrent brain tumor from radiation necrosis, as compared with conventional tumor-to-normal cortex (T/N) ratio evaluation. We enrolled 41 patients with metastatic brain tumor or glioma treated using radiation therapy who underwent MET-PET. The area with a standardized uptake value > 1.3 times that of the normal brain cortex was contoured. Forty-two PET features were extracted and used in a random forest classifier and the diagnostic performance was evaluated using a 10-fold cross-validation scheme. Gini index was measured to identify relevant PET parameters for classification. The reference standard was surgical histopathological analysis or more than 6 months of follow-up with MRI. Forty-four lesions were used for the analysis. Thirty-three and 11 lesions were confirmed as recurrent brain tumor and radiation necrosis, respectively. Radiomics and T/N ratio evaluation showed sensitivities of 90.1% and 60.6%, and specificities of 93.9% and 72.7% with areas under the curve of 0.98 and 0.73, respectively. Gray level co-occurrence matrix dissimilarity was the most pertinent feature for diagnosis. MET-PET radiomics yielded excellent outcome for differentiating recurrent brain tumor from radiation necrosis, which outperformed T/N ratio evaluation. |
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This study aims to investigate the efficacy of 11C-methionine (MET)-PET radiomics for distinguishing recurrent brain tumor from radiation necrosis, as compared with conventional tumor-to-normal cortex (T/N) ratio evaluation. We enrolled 41 patients with metastatic brain tumor or glioma treated using radiation therapy who underwent MET-PET. The area with a standardized uptake value > 1.3 times that of the normal brain cortex was contoured. Forty-two PET features were extracted and used in a random forest classifier and the diagnostic performance was evaluated using a 10-fold cross-validation scheme. Gini index was measured to identify relevant PET parameters for classification. The reference standard was surgical histopathological analysis or more than 6 months of follow-up with MRI. Forty-four lesions were used for the analysis. Thirty-three and 11 lesions were confirmed as recurrent brain tumor and radiation necrosis, respectively. Radiomics and T/N ratio evaluation showed sensitivities of 90.1% and 60.6%, and specificities of 93.9% and 72.7% with areas under the curve of 0.98 and 0.73, respectively. Gray level co-occurrence matrix dissimilarity was the most pertinent feature for diagnosis. MET-PET radiomics yielded excellent outcome for differentiating recurrent brain tumor from radiation necrosis, which outperformed T/N ratio evaluation.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-019-52279-2</identifier><identifier>PMID: 31666650</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>692/4028/67/1922 ; 692/617 ; Algorithms ; Brain cancer ; Brain Neoplasms - diagnostic imaging ; Brain tumors ; Breast - pathology ; Breast - radiation effects ; Diagnosis, Differential ; Female ; Glioma ; Humanities and Social Sciences ; Humans ; Image Processing, Computer-Assisted - methods ; Magnetic resonance imaging ; Male ; Metastases ; Methionine ; Middle Aged ; multidisciplinary ; Necrosis ; Necrosis - diagnostic imaging ; Positron emission tomography ; Positron Emission Tomography Computed Tomography ; Radiation Injuries - pathology ; Radiation therapy ; Radiomics ; Recurrence ; Science ; Science (multidisciplinary)</subject><ispartof>Scientific reports, 2019-10, Vol.9 (1), p.15666-7, Article 15666</ispartof><rights>The Author(s) 2019</rights><rights>2019. 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This study aims to investigate the efficacy of 11C-methionine (MET)-PET radiomics for distinguishing recurrent brain tumor from radiation necrosis, as compared with conventional tumor-to-normal cortex (T/N) ratio evaluation. We enrolled 41 patients with metastatic brain tumor or glioma treated using radiation therapy who underwent MET-PET. The area with a standardized uptake value > 1.3 times that of the normal brain cortex was contoured. Forty-two PET features were extracted and used in a random forest classifier and the diagnostic performance was evaluated using a 10-fold cross-validation scheme. Gini index was measured to identify relevant PET parameters for classification. The reference standard was surgical histopathological analysis or more than 6 months of follow-up with MRI. Forty-four lesions were used for the analysis. Thirty-three and 11 lesions were confirmed as recurrent brain tumor and radiation necrosis, respectively. Radiomics and T/N ratio evaluation showed sensitivities of 90.1% and 60.6%, and specificities of 93.9% and 72.7% with areas under the curve of 0.98 and 0.73, respectively. Gray level co-occurrence matrix dissimilarity was the most pertinent feature for diagnosis. MET-PET radiomics yielded excellent outcome for differentiating recurrent brain tumor from radiation necrosis, which outperformed T/N ratio evaluation.</description><subject>692/4028/67/1922</subject><subject>692/617</subject><subject>Algorithms</subject><subject>Brain cancer</subject><subject>Brain Neoplasms - diagnostic imaging</subject><subject>Brain tumors</subject><subject>Breast - pathology</subject><subject>Breast - radiation effects</subject><subject>Diagnosis, Differential</subject><subject>Female</subject><subject>Glioma</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>Magnetic resonance imaging</subject><subject>Male</subject><subject>Metastases</subject><subject>Methionine</subject><subject>Middle Aged</subject><subject>multidisciplinary</subject><subject>Necrosis</subject><subject>Necrosis - diagnostic imaging</subject><subject>Positron emission tomography</subject><subject>Positron Emission Tomography Computed Tomography</subject><subject>Radiation Injuries - pathology</subject><subject>Radiation therapy</subject><subject>Radiomics</subject><subject>Recurrence</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9UU1vGyEQRVGjJnLyB3qIkHqmZQYWlh4qVVb6IUVKDukZsWvWJvKCC7ut-gf6u4vjNEkvmQsw896bGR4hb4C_Ay7a90VCY1rGwbAGURuGR-QUuWwYCsRXz-4n5LyUO16jQSPBvCYnAlSNhp-SPwBLNvppE1IM0bOby1s6pExXYRh89nEKbgpxTbPv57x_0y67EOk0jxU15DTS7FZ7UIo0-j6nEsqH-1waQ1-o2-1ycv2G_grTpubjqlJqB18m2m9dKWEIPp-R48Ftiz9_OBfk--fL2-VXdnX95dvy0xXrpZYTkyid7Ax2XvdGSDO02DpttMK6rW6V6rzw0kuDWsuGA4ATCtAo5TsJyMWCfDzo7uZu9Ku-LpTd1u5yGF3-bZML9v9KDBu7Tj-tahG0gCrw9kEgpx9zXcLepTnHOrNFAVwJJZumovCA2v9HyX547ADc7u2zB_tstc_e21fZC3LxfLZHyj-zKkAcAKWW4trnp94vyP4FhzOnYw</recordid><startdate>20191030</startdate><enddate>20191030</enddate><creator>Hotta, Masatoshi</creator><creator>Minamimoto, Ryogo</creator><creator>Miwa, Kenta</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><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>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</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>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6790-8804</orcidid></search><sort><creationdate>20191030</creationdate><title>11C-methionine-PET for differentiating recurrent brain tumor from radiation necrosis: radiomics approach with random forest classifier</title><author>Hotta, Masatoshi ; Minamimoto, Ryogo ; Miwa, Kenta</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-424a4b92be7c9349f828a797622047866be3e4e49277450111a3612966eb41203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>692/4028/67/1922</topic><topic>692/617</topic><topic>Algorithms</topic><topic>Brain cancer</topic><topic>Brain Neoplasms - diagnostic imaging</topic><topic>Brain tumors</topic><topic>Breast - pathology</topic><topic>Breast - radiation effects</topic><topic>Diagnosis, Differential</topic><topic>Female</topic><topic>Glioma</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted - methods</topic><topic>Magnetic resonance imaging</topic><topic>Male</topic><topic>Metastases</topic><topic>Methionine</topic><topic>Middle Aged</topic><topic>multidisciplinary</topic><topic>Necrosis</topic><topic>Necrosis - diagnostic imaging</topic><topic>Positron emission tomography</topic><topic>Positron Emission Tomography Computed Tomography</topic><topic>Radiation Injuries - pathology</topic><topic>Radiation therapy</topic><topic>Radiomics</topic><topic>Recurrence</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hotta, Masatoshi</creatorcontrib><creatorcontrib>Minamimoto, Ryogo</creatorcontrib><creatorcontrib>Miwa, Kenta</creatorcontrib><collection>Springer Nature OA Free Journals</collection><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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</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>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</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>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hotta, Masatoshi</au><au>Minamimoto, Ryogo</au><au>Miwa, Kenta</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>11C-methionine-PET for differentiating recurrent brain tumor from radiation necrosis: radiomics approach with random forest classifier</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2019-10-30</date><risdate>2019</risdate><volume>9</volume><issue>1</issue><spage>15666</spage><epage>7</epage><pages>15666-7</pages><artnum>15666</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Differentiating recurrent brain tumor from radiation necrosis is often difficult. This study aims to investigate the efficacy of 11C-methionine (MET)-PET radiomics for distinguishing recurrent brain tumor from radiation necrosis, as compared with conventional tumor-to-normal cortex (T/N) ratio evaluation. We enrolled 41 patients with metastatic brain tumor or glioma treated using radiation therapy who underwent MET-PET. The area with a standardized uptake value > 1.3 times that of the normal brain cortex was contoured. Forty-two PET features were extracted and used in a random forest classifier and the diagnostic performance was evaluated using a 10-fold cross-validation scheme. Gini index was measured to identify relevant PET parameters for classification. The reference standard was surgical histopathological analysis or more than 6 months of follow-up with MRI. Forty-four lesions were used for the analysis. Thirty-three and 11 lesions were confirmed as recurrent brain tumor and radiation necrosis, respectively. Radiomics and T/N ratio evaluation showed sensitivities of 90.1% and 60.6%, and specificities of 93.9% and 72.7% with areas under the curve of 0.98 and 0.73, respectively. Gray level co-occurrence matrix dissimilarity was the most pertinent feature for diagnosis. MET-PET radiomics yielded excellent outcome for differentiating recurrent brain tumor from radiation necrosis, which outperformed T/N ratio evaluation.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>31666650</pmid><doi>10.1038/s41598-019-52279-2</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-6790-8804</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 692/4028/67/1922 692/617 Algorithms Brain cancer Brain Neoplasms - diagnostic imaging Brain tumors Breast - pathology Breast - radiation effects Diagnosis, Differential Female Glioma Humanities and Social Sciences Humans Image Processing, Computer-Assisted - methods Magnetic resonance imaging Male Metastases Methionine Middle Aged multidisciplinary Necrosis Necrosis - diagnostic imaging Positron emission tomography Positron Emission Tomography Computed Tomography Radiation Injuries - pathology Radiation therapy Radiomics Recurrence Science Science (multidisciplinary) |
title | 11C-methionine-PET for differentiating recurrent brain tumor from radiation necrosis: radiomics approach with random forest classifier |
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