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Amide proton transfer-weighted magnetic resonance image-guided stereotactic biopsy in patients with newly diagnosed gliomas
Pathological assessment using World Health Organization (WHO) criteria is the gold standard for diagnosis of gliomas. However, the accuracy of diagnosis is limited by tissue sampling, particularly for infiltrating, heterogeneous tumours. We assessed the accuracy of amide proton transfer-weighted (AP...
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Published in: | European journal of cancer (1990) 2017-09, Vol.83, p.9-18 |
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creator | Jiang, Shanshan Eberhart, Charles G. Zhang, Yi Heo, Hye-Young Wen, Zhibo Blair, Lindsay Qin, Huamin Lim, Michael Quinones-Hinojosa, Alfredo Weingart, Jon D. Barker, Peter B. Pomper, Martin G. Laterra, John van Zijl, Peter C.M. Blakeley, Jaishri O. Zhou, Jinyuan |
description | Pathological assessment using World Health Organization (WHO) criteria is the gold standard for diagnosis of gliomas. However, the accuracy of diagnosis is limited by tissue sampling, particularly for infiltrating, heterogeneous tumours. We assessed the accuracy of amide proton transfer-weighted (APTw) magnetic resonance imaging (MRI)-guided tissue sampling to identify regions of high-grade glioma via radiographic-histopathologic correlation in patients with newly suspected glioma.
Twenty-four patients with previously undiagnosed gliomas underwent a volumetric APTw MRI prior to their first neurosurgical procedure. A total of 70 specimens were collected via APTw image-directed stereotactic biopsy. Cellularity, necrosis, proliferation and glioma WHO grade were analysed for all specimens and correlated with corresponding APTw signal intensities.
Thirty-three specimens displayed grade-II pathology, 14 grade-III, 15 grade-IV, and eight specimens revealed only peritumoural oedema. Multiple glioma grades were found within a single lesion in six patients. APTw signal intensities of the biopsied sites and the maximum APTw values across all biopsied sites in each patient were significantly higher for high-grade versus low-grade specimens. APTw signal intensities were significantly positively correlated with cellularity (R = 0.757) and proliferation (R = 0.538). Multiple linear regression analysis showed that tumour cellularity and proliferation index were the best predictors of APTw signal intensities.
APTw imaging identified tumour areas of higher cellularity and proliferation, allowing identification of high-grade regions within heterogeneous gliomas. APTw imaging can be readily translated for more widespread use and can assist diagnostic neurosurgical procedures by increasing the accuracy of tumour sampling in patients with infiltrating gliomas.
•APTw images were used to guide diagnostic neurosurgical procedures.•APTw MRI guidance found multiple WHO grades within the same lesion in 25% patients.•APTw hyperintensity identified tumour areas of higher cellularity and proliferation.•Maximum APTw intensity correlated with the histological grade of the tumour. |
doi_str_mv | 10.1016/j.ejca.2017.06.009 |
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Twenty-four patients with previously undiagnosed gliomas underwent a volumetric APTw MRI prior to their first neurosurgical procedure. A total of 70 specimens were collected via APTw image-directed stereotactic biopsy. Cellularity, necrosis, proliferation and glioma WHO grade were analysed for all specimens and correlated with corresponding APTw signal intensities.
Thirty-three specimens displayed grade-II pathology, 14 grade-III, 15 grade-IV, and eight specimens revealed only peritumoural oedema. Multiple glioma grades were found within a single lesion in six patients. APTw signal intensities of the biopsied sites and the maximum APTw values across all biopsied sites in each patient were significantly higher for high-grade versus low-grade specimens. APTw signal intensities were significantly positively correlated with cellularity (R = 0.757) and proliferation (R = 0.538). Multiple linear regression analysis showed that tumour cellularity and proliferation index were the best predictors of APTw signal intensities.
APTw imaging identified tumour areas of higher cellularity and proliferation, allowing identification of high-grade regions within heterogeneous gliomas. APTw imaging can be readily translated for more widespread use and can assist diagnostic neurosurgical procedures by increasing the accuracy of tumour sampling in patients with infiltrating gliomas.
•APTw images were used to guide diagnostic neurosurgical procedures.•APTw MRI guidance found multiple WHO grades within the same lesion in 25% patients.•APTw hyperintensity identified tumour areas of higher cellularity and proliferation.•Maximum APTw intensity correlated with the histological grade of the tumour.</description><identifier>ISSN: 0959-8049</identifier><identifier>EISSN: 1879-0852</identifier><identifier>DOI: 10.1016/j.ejca.2017.06.009</identifier><identifier>PMID: 28704644</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adult ; Aged ; Amide proton transfer-weighted imaging ; Amides ; Biomarkers ; Biopsy ; Biopsy - methods ; Brain cancer ; Brain Neoplasms - diagnostic imaging ; Brain Neoplasms - pathology ; Correlation analysis ; Diagnosis ; Diagnostic systems ; Edema ; Female ; Glioma ; Glioma - diagnostic imaging ; Glioma - pathology ; Histopathologic validation ; Humans ; Image-guided biopsy ; Imaging biomarker ; Imaging, Three-Dimensional ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Magnetic Resonance Spectroscopy - methods ; Male ; Medical diagnosis ; Middle Aged ; Neurosurgery ; Patients ; Prospective Studies ; Protons ; Regression Analysis ; Resonance ; Sampling ; Stereotaxic Techniques ; Tumors</subject><ispartof>European journal of cancer (1990), 2017-09, Vol.83, p.9-18</ispartof><rights>2017 Elsevier Ltd</rights><rights>Copyright © 2017 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Sep 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-138e9fb0373afe82866221cef31a10adcee116cff4b33400b416d8db5436e4da3</citedby><cites>FETCH-LOGICAL-c428t-138e9fb0373afe82866221cef31a10adcee116cff4b33400b416d8db5436e4da3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28704644$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jiang, Shanshan</creatorcontrib><creatorcontrib>Eberhart, Charles G.</creatorcontrib><creatorcontrib>Zhang, Yi</creatorcontrib><creatorcontrib>Heo, Hye-Young</creatorcontrib><creatorcontrib>Wen, Zhibo</creatorcontrib><creatorcontrib>Blair, Lindsay</creatorcontrib><creatorcontrib>Qin, Huamin</creatorcontrib><creatorcontrib>Lim, Michael</creatorcontrib><creatorcontrib>Quinones-Hinojosa, Alfredo</creatorcontrib><creatorcontrib>Weingart, Jon D.</creatorcontrib><creatorcontrib>Barker, Peter B.</creatorcontrib><creatorcontrib>Pomper, Martin G.</creatorcontrib><creatorcontrib>Laterra, John</creatorcontrib><creatorcontrib>van Zijl, Peter C.M.</creatorcontrib><creatorcontrib>Blakeley, Jaishri O.</creatorcontrib><creatorcontrib>Zhou, Jinyuan</creatorcontrib><title>Amide proton transfer-weighted magnetic resonance image-guided stereotactic biopsy in patients with newly diagnosed gliomas</title><title>European journal of cancer (1990)</title><addtitle>Eur J Cancer</addtitle><description>Pathological assessment using World Health Organization (WHO) criteria is the gold standard for diagnosis of gliomas. However, the accuracy of diagnosis is limited by tissue sampling, particularly for infiltrating, heterogeneous tumours. We assessed the accuracy of amide proton transfer-weighted (APTw) magnetic resonance imaging (MRI)-guided tissue sampling to identify regions of high-grade glioma via radiographic-histopathologic correlation in patients with newly suspected glioma.
Twenty-four patients with previously undiagnosed gliomas underwent a volumetric APTw MRI prior to their first neurosurgical procedure. A total of 70 specimens were collected via APTw image-directed stereotactic biopsy. Cellularity, necrosis, proliferation and glioma WHO grade were analysed for all specimens and correlated with corresponding APTw signal intensities.
Thirty-three specimens displayed grade-II pathology, 14 grade-III, 15 grade-IV, and eight specimens revealed only peritumoural oedema. Multiple glioma grades were found within a single lesion in six patients. APTw signal intensities of the biopsied sites and the maximum APTw values across all biopsied sites in each patient were significantly higher for high-grade versus low-grade specimens. APTw signal intensities were significantly positively correlated with cellularity (R = 0.757) and proliferation (R = 0.538). Multiple linear regression analysis showed that tumour cellularity and proliferation index were the best predictors of APTw signal intensities.
APTw imaging identified tumour areas of higher cellularity and proliferation, allowing identification of high-grade regions within heterogeneous gliomas. APTw imaging can be readily translated for more widespread use and can assist diagnostic neurosurgical procedures by increasing the accuracy of tumour sampling in patients with infiltrating gliomas.
•APTw images were used to guide diagnostic neurosurgical procedures.•APTw MRI guidance found multiple WHO grades within the same lesion in 25% patients.•APTw hyperintensity identified tumour areas of higher cellularity and proliferation.•Maximum APTw intensity correlated with the histological grade of the tumour.</description><subject>Adult</subject><subject>Aged</subject><subject>Amide proton transfer-weighted imaging</subject><subject>Amides</subject><subject>Biomarkers</subject><subject>Biopsy</subject><subject>Biopsy - methods</subject><subject>Brain cancer</subject><subject>Brain Neoplasms - diagnostic imaging</subject><subject>Brain Neoplasms - pathology</subject><subject>Correlation analysis</subject><subject>Diagnosis</subject><subject>Diagnostic systems</subject><subject>Edema</subject><subject>Female</subject><subject>Glioma</subject><subject>Glioma - diagnostic imaging</subject><subject>Glioma - pathology</subject><subject>Histopathologic validation</subject><subject>Humans</subject><subject>Image-guided biopsy</subject><subject>Imaging biomarker</subject><subject>Imaging, Three-Dimensional</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Magnetic Resonance Spectroscopy - methods</subject><subject>Male</subject><subject>Medical diagnosis</subject><subject>Middle Aged</subject><subject>Neurosurgery</subject><subject>Patients</subject><subject>Prospective Studies</subject><subject>Protons</subject><subject>Regression Analysis</subject><subject>Resonance</subject><subject>Sampling</subject><subject>Stereotaxic Techniques</subject><subject>Tumors</subject><issn>0959-8049</issn><issn>1879-0852</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kU2L1TAYhYsoznX0D7iQgBs3rW8-2qbgZhjGDxhwo-uQJm_vpLTJNUm9XPzz5nJHFy5cBcJzDsl5quo1hYYC7d7PDc5GNwxo30DXAAxPqh2V_VCDbNnTagdDO9QSxHBVvUhpBoBeCnheXTHZg-iE2FW_blZnkRxiyMGTHLVPE8b6iG7_kNGSVe89ZmdIxBS89gaJK3dY77eSsyRljBiyNmdmdOGQTsR5ctDZoc-JHF1-IB6Py4lYV7pCKqH94sKq08vq2aSXhK8ez-vq-8e7b7ef6_uvn77c3tzXRjCZa8olDtMIvOd6Qslk1zFGDU6cagraGkRKOzNNYuRcAIyCdlbasRW8Q2E1v67eXXrLL39smLJaXTK4LNpj2JKiA5Mt5cCGgr79B53DFn15nWLAeWFaCoViF8rEkFLESR1iWSWeFAV1VqNmdVajzmoUdKqoKaE3j9XbuKL9G_njogAfLgCWLX46jCqZMqJB6yKarGxw_-v_DeqqobE</recordid><startdate>201709</startdate><enddate>201709</enddate><creator>Jiang, Shanshan</creator><creator>Eberhart, Charles G.</creator><creator>Zhang, Yi</creator><creator>Heo, Hye-Young</creator><creator>Wen, Zhibo</creator><creator>Blair, Lindsay</creator><creator>Qin, Huamin</creator><creator>Lim, Michael</creator><creator>Quinones-Hinojosa, Alfredo</creator><creator>Weingart, Jon D.</creator><creator>Barker, Peter B.</creator><creator>Pomper, Martin G.</creator><creator>Laterra, John</creator><creator>van Zijl, Peter C.M.</creator><creator>Blakeley, Jaishri O.</creator><creator>Zhou, Jinyuan</creator><general>Elsevier Ltd</general><general>Elsevier Science Ltd</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>7TO</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>201709</creationdate><title>Amide proton transfer-weighted magnetic resonance image-guided stereotactic biopsy in patients with newly diagnosed gliomas</title><author>Jiang, Shanshan ; Eberhart, Charles G. ; Zhang, Yi ; Heo, Hye-Young ; Wen, Zhibo ; Blair, Lindsay ; Qin, Huamin ; Lim, Michael ; Quinones-Hinojosa, Alfredo ; Weingart, Jon D. ; Barker, Peter B. ; Pomper, Martin G. ; Laterra, John ; van Zijl, Peter C.M. ; Blakeley, Jaishri O. ; Zhou, Jinyuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-138e9fb0373afe82866221cef31a10adcee116cff4b33400b416d8db5436e4da3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Amide proton transfer-weighted imaging</topic><topic>Amides</topic><topic>Biomarkers</topic><topic>Biopsy</topic><topic>Biopsy - methods</topic><topic>Brain cancer</topic><topic>Brain Neoplasms - diagnostic imaging</topic><topic>Brain Neoplasms - pathology</topic><topic>Correlation analysis</topic><topic>Diagnosis</topic><topic>Diagnostic systems</topic><topic>Edema</topic><topic>Female</topic><topic>Glioma</topic><topic>Glioma - diagnostic imaging</topic><topic>Glioma - pathology</topic><topic>Histopathologic validation</topic><topic>Humans</topic><topic>Image-guided biopsy</topic><topic>Imaging biomarker</topic><topic>Imaging, Three-Dimensional</topic><topic>Magnetic resonance imaging</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Magnetic Resonance Spectroscopy - methods</topic><topic>Male</topic><topic>Medical diagnosis</topic><topic>Middle Aged</topic><topic>Neurosurgery</topic><topic>Patients</topic><topic>Prospective Studies</topic><topic>Protons</topic><topic>Regression Analysis</topic><topic>Resonance</topic><topic>Sampling</topic><topic>Stereotaxic Techniques</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jiang, Shanshan</creatorcontrib><creatorcontrib>Eberhart, Charles G.</creatorcontrib><creatorcontrib>Zhang, Yi</creatorcontrib><creatorcontrib>Heo, Hye-Young</creatorcontrib><creatorcontrib>Wen, Zhibo</creatorcontrib><creatorcontrib>Blair, Lindsay</creatorcontrib><creatorcontrib>Qin, Huamin</creatorcontrib><creatorcontrib>Lim, Michael</creatorcontrib><creatorcontrib>Quinones-Hinojosa, Alfredo</creatorcontrib><creatorcontrib>Weingart, Jon D.</creatorcontrib><creatorcontrib>Barker, Peter B.</creatorcontrib><creatorcontrib>Pomper, Martin G.</creatorcontrib><creatorcontrib>Laterra, John</creatorcontrib><creatorcontrib>van Zijl, Peter C.M.</creatorcontrib><creatorcontrib>Blakeley, Jaishri O.</creatorcontrib><creatorcontrib>Zhou, Jinyuan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of cancer (1990)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jiang, Shanshan</au><au>Eberhart, Charles G.</au><au>Zhang, Yi</au><au>Heo, Hye-Young</au><au>Wen, Zhibo</au><au>Blair, Lindsay</au><au>Qin, Huamin</au><au>Lim, Michael</au><au>Quinones-Hinojosa, Alfredo</au><au>Weingart, Jon D.</au><au>Barker, Peter B.</au><au>Pomper, Martin G.</au><au>Laterra, John</au><au>van Zijl, Peter C.M.</au><au>Blakeley, Jaishri O.</au><au>Zhou, Jinyuan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amide proton transfer-weighted magnetic resonance image-guided stereotactic biopsy in patients with newly diagnosed gliomas</atitle><jtitle>European journal of cancer (1990)</jtitle><addtitle>Eur J Cancer</addtitle><date>2017-09</date><risdate>2017</risdate><volume>83</volume><spage>9</spage><epage>18</epage><pages>9-18</pages><issn>0959-8049</issn><eissn>1879-0852</eissn><abstract>Pathological assessment using World Health Organization (WHO) criteria is the gold standard for diagnosis of gliomas. However, the accuracy of diagnosis is limited by tissue sampling, particularly for infiltrating, heterogeneous tumours. We assessed the accuracy of amide proton transfer-weighted (APTw) magnetic resonance imaging (MRI)-guided tissue sampling to identify regions of high-grade glioma via radiographic-histopathologic correlation in patients with newly suspected glioma.
Twenty-four patients with previously undiagnosed gliomas underwent a volumetric APTw MRI prior to their first neurosurgical procedure. A total of 70 specimens were collected via APTw image-directed stereotactic biopsy. Cellularity, necrosis, proliferation and glioma WHO grade were analysed for all specimens and correlated with corresponding APTw signal intensities.
Thirty-three specimens displayed grade-II pathology, 14 grade-III, 15 grade-IV, and eight specimens revealed only peritumoural oedema. Multiple glioma grades were found within a single lesion in six patients. APTw signal intensities of the biopsied sites and the maximum APTw values across all biopsied sites in each patient were significantly higher for high-grade versus low-grade specimens. APTw signal intensities were significantly positively correlated with cellularity (R = 0.757) and proliferation (R = 0.538). Multiple linear regression analysis showed that tumour cellularity and proliferation index were the best predictors of APTw signal intensities.
APTw imaging identified tumour areas of higher cellularity and proliferation, allowing identification of high-grade regions within heterogeneous gliomas. APTw imaging can be readily translated for more widespread use and can assist diagnostic neurosurgical procedures by increasing the accuracy of tumour sampling in patients with infiltrating gliomas.
•APTw images were used to guide diagnostic neurosurgical procedures.•APTw MRI guidance found multiple WHO grades within the same lesion in 25% patients.•APTw hyperintensity identified tumour areas of higher cellularity and proliferation.•Maximum APTw intensity correlated with the histological grade of the tumour.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>28704644</pmid><doi>10.1016/j.ejca.2017.06.009</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Amide proton transfer-weighted imaging Amides Biomarkers Biopsy Biopsy - methods Brain cancer Brain Neoplasms - diagnostic imaging Brain Neoplasms - pathology Correlation analysis Diagnosis Diagnostic systems Edema Female Glioma Glioma - diagnostic imaging Glioma - pathology Histopathologic validation Humans Image-guided biopsy Imaging biomarker Imaging, Three-Dimensional Magnetic resonance imaging Magnetic Resonance Imaging - methods Magnetic Resonance Spectroscopy - methods Male Medical diagnosis Middle Aged Neurosurgery Patients Prospective Studies Protons Regression Analysis Resonance Sampling Stereotaxic Techniques Tumors |
title | Amide proton transfer-weighted magnetic resonance image-guided stereotactic biopsy in patients with newly diagnosed gliomas |
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