Image-Based Molecular Phenotyping of Pancreatic Ductal Adenocarcinoma
To bridge the translational gap between recent discoveries of distinct molecular phenotypes of pancreatic cancer and tangible improvements in patient outcome, there is an urgent need to develop strategies and tools informing and improving the clinical decision process. Radiomics and machine learning...
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Veröffentlicht in: | Journal of clinical medicine 2020-03, Vol.9 (3), p.724 |
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creator | Kaissis, Georgios A Ziegelmayer, Sebastian Lohöfer, Fabian K Harder, Felix N Jungmann, Friederike Sasse, Daniel Muckenhuber, Alexander Yen, Hsi-Yu Steiger, Katja Siveke, Jens Friess, Helmut Schmid, Roland Weichert, Wilko Makowski, Marcus R Braren, Rickmer F |
description | To bridge the translational gap between recent discoveries of distinct molecular phenotypes of pancreatic cancer and tangible improvements in patient outcome, there is an urgent need to develop strategies and tools informing and improving the clinical decision process. Radiomics and machine learning approaches can offer non-invasive whole tumor analytics for clinical imaging data-based classification. The retrospective study assessed baseline computed tomography (CT) from 207 patients with proven pancreatic ductal adenocarcinoma (PDAC). Following expert level manual annotation, Pyradiomics was used for the extraction of 1474 radiomic features. The molecular tumor subtype was defined by immunohistochemical staining for KRT81 and HNF1a as quasi-mesenchymal (QM) vs. non-quasi-mesenchymal (non-QM). A Random Forest machine learning algorithm was developed to predict the molecular subtype from the radiomic features. The algorithm was then applied to an independent cohort of histopathologically unclassifiable tumors with distinct clinical outcomes. The classification algorithm achieved a sensitivity, specificity and ROC-AUC (area under the receiver operating characteristic curve) of 0.84 ± 0.05, 0.92 ± 0.01 and 0.93 ± 0.01, respectively. The median overall survival for predicted QM and non-QM tumors was 16.1 and 20.9 months, respectively, log-rank-test
= 0.02, harzard ratio (HR) 1.59. The application of the algorithm to histopathologically unclassifiable tumors revealed two groups with significantly different survival (8.9 and 39.8 months, log-rank-test
< 0.001, HR 4.33). The machine learning-based analysis of preoperative (CT) imaging allows the prediction of molecular PDAC subtypes highly relevant for patient survival, allowing advanced pre-operative patient stratification for precision medicine applications. |
doi_str_mv | 10.3390/jcm9030724 |
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= 0.02, harzard ratio (HR) 1.59. The application of the algorithm to histopathologically unclassifiable tumors revealed two groups with significantly different survival (8.9 and 39.8 months, log-rank-test
< 0.001, HR 4.33). The machine learning-based analysis of preoperative (CT) imaging allows the prediction of molecular PDAC subtypes highly relevant for patient survival, allowing advanced pre-operative patient stratification for precision medicine applications.</description><identifier>ISSN: 2077-0383</identifier><identifier>EISSN: 2077-0383</identifier><identifier>DOI: 10.3390/jcm9030724</identifier><identifier>PMID: 32155990</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Algorithms ; Antigens ; Cancer ; Chemotherapy ; Classification ; Magnetic resonance imaging ; Pancreatic cancer ; Radiomics ; Tomography ; Tumors</subject><ispartof>Journal of clinical medicine, 2020-03, Vol.9 (3), p.724</ispartof><rights>2020 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 (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 by the authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-68de37e9b3c2486a1c161d25526d81835436fc6956436a16c6196698439ea6ad3</citedby><cites>FETCH-LOGICAL-c406t-68de37e9b3c2486a1c161d25526d81835436fc6956436a16c6196698439ea6ad3</cites><orcidid>0000-0002-7269-5433 ; 0000-0003-2644-2782 ; 0000-0002-8772-4778 ; 0000-0001-8382-8062 ; 0000-0002-9600-4094</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141256/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7141256/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32155990$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kaissis, Georgios A</creatorcontrib><creatorcontrib>Ziegelmayer, Sebastian</creatorcontrib><creatorcontrib>Lohöfer, Fabian K</creatorcontrib><creatorcontrib>Harder, Felix N</creatorcontrib><creatorcontrib>Jungmann, Friederike</creatorcontrib><creatorcontrib>Sasse, Daniel</creatorcontrib><creatorcontrib>Muckenhuber, Alexander</creatorcontrib><creatorcontrib>Yen, Hsi-Yu</creatorcontrib><creatorcontrib>Steiger, Katja</creatorcontrib><creatorcontrib>Siveke, Jens</creatorcontrib><creatorcontrib>Friess, Helmut</creatorcontrib><creatorcontrib>Schmid, Roland</creatorcontrib><creatorcontrib>Weichert, Wilko</creatorcontrib><creatorcontrib>Makowski, Marcus R</creatorcontrib><creatorcontrib>Braren, Rickmer F</creatorcontrib><title>Image-Based Molecular Phenotyping of Pancreatic Ductal Adenocarcinoma</title><title>Journal of clinical medicine</title><addtitle>J Clin Med</addtitle><description>To bridge the translational gap between recent discoveries of distinct molecular phenotypes of pancreatic cancer and tangible improvements in patient outcome, there is an urgent need to develop strategies and tools informing and improving the clinical decision process. Radiomics and machine learning approaches can offer non-invasive whole tumor analytics for clinical imaging data-based classification. The retrospective study assessed baseline computed tomography (CT) from 207 patients with proven pancreatic ductal adenocarcinoma (PDAC). Following expert level manual annotation, Pyradiomics was used for the extraction of 1474 radiomic features. The molecular tumor subtype was defined by immunohistochemical staining for KRT81 and HNF1a as quasi-mesenchymal (QM) vs. non-quasi-mesenchymal (non-QM). A Random Forest machine learning algorithm was developed to predict the molecular subtype from the radiomic features. The algorithm was then applied to an independent cohort of histopathologically unclassifiable tumors with distinct clinical outcomes. The classification algorithm achieved a sensitivity, specificity and ROC-AUC (area under the receiver operating characteristic curve) of 0.84 ± 0.05, 0.92 ± 0.01 and 0.93 ± 0.01, respectively. The median overall survival for predicted QM and non-QM tumors was 16.1 and 20.9 months, respectively, log-rank-test
= 0.02, harzard ratio (HR) 1.59. The application of the algorithm to histopathologically unclassifiable tumors revealed two groups with significantly different survival (8.9 and 39.8 months, log-rank-test
< 0.001, HR 4.33). 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Radiomics and machine learning approaches can offer non-invasive whole tumor analytics for clinical imaging data-based classification. The retrospective study assessed baseline computed tomography (CT) from 207 patients with proven pancreatic ductal adenocarcinoma (PDAC). Following expert level manual annotation, Pyradiomics was used for the extraction of 1474 radiomic features. The molecular tumor subtype was defined by immunohistochemical staining for KRT81 and HNF1a as quasi-mesenchymal (QM) vs. non-quasi-mesenchymal (non-QM). A Random Forest machine learning algorithm was developed to predict the molecular subtype from the radiomic features. The algorithm was then applied to an independent cohort of histopathologically unclassifiable tumors with distinct clinical outcomes. The classification algorithm achieved a sensitivity, specificity and ROC-AUC (area under the receiver operating characteristic curve) of 0.84 ± 0.05, 0.92 ± 0.01 and 0.93 ± 0.01, respectively. The median overall survival for predicted QM and non-QM tumors was 16.1 and 20.9 months, respectively, log-rank-test
= 0.02, harzard ratio (HR) 1.59. The application of the algorithm to histopathologically unclassifiable tumors revealed two groups with significantly different survival (8.9 and 39.8 months, log-rank-test
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subjects | Algorithms Antigens Cancer Chemotherapy Classification Magnetic resonance imaging Pancreatic cancer Radiomics Tomography Tumors |
title | Image-Based Molecular Phenotyping of Pancreatic Ductal Adenocarcinoma |
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