Longitudinal brain imaging of five malignant glioma patients treated with bevacizumab using susceptibility-weighted magnetic resonance imaging at 7 T
Abstract Malignant glioma is a rare tumor type characterized by prominent vascular proliferation. Antiangiogenic therapy with the monoclonal antibody bevacizumab is considered as a promising therapeutic strategy, although the effect on tumor vascularization is unclear. High-field susceptibility-weig...
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creator | Grabner, Günther Nöbauer, Iris Elandt, Katarzyna Kronnerwetter, Claudia Woehrer, Adelheid Marosi, Christine Prayer, Daniela Trattnig, Siegfried Preusser, Matthias |
description | Abstract Malignant glioma is a rare tumor type characterized by prominent vascular proliferation. Antiangiogenic therapy with the monoclonal antibody bevacizumab is considered as a promising therapeutic strategy, although the effect on tumor vascularization is unclear. High-field susceptibility-weighted imaging (SWI) visualizes the microvasculature and may contribute to the investigation of antiangiogenic therapy responses in gliomas. We prospectively studied five adult malignant glioma patients treated with bevacizumab-containing regimens. In each patient, we performed three 7-T SWI and T1-weighted imaging investigations (baseline and 2 and 4 weeks after the start of bevacizumab treatment). In addition, we imaged a postmortem brain of a patient with glioblastoma using 7-T SWI and performed detailed histopathological analysis. We observed almost total resolution of brain edema in three of five patients after initiation of bevacizumab therapy. In one case with rapid increase of the lesion size despite bevacizumab therapy, SWI showed progressive increase of irregular hypointense structures, most likely corresponding to increasing amounts of pathological microvasculature. In one case with progressive neurological decline, 7-T images showed multiple intratumoral microhemorrhages after the first bevacizumab application. Correlation of postmortem neuroimaging with histopathology confirmed that SWI-positive structures correspond to tumor vasculature. The experience from our case series indicates that longitudinal 7-T SWI seems to be an appropriate method for investigation of changes in brain tumor vascularization over time under antiangiogenic therapy. |
doi_str_mv | 10.1016/j.mri.2011.08.004 |
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Antiangiogenic therapy with the monoclonal antibody bevacizumab is considered as a promising therapeutic strategy, although the effect on tumor vascularization is unclear. High-field susceptibility-weighted imaging (SWI) visualizes the microvasculature and may contribute to the investigation of antiangiogenic therapy responses in gliomas. We prospectively studied five adult malignant glioma patients treated with bevacizumab-containing regimens. In each patient, we performed three 7-T SWI and T1-weighted imaging investigations (baseline and 2 and 4 weeks after the start of bevacizumab treatment). In addition, we imaged a postmortem brain of a patient with glioblastoma using 7-T SWI and performed detailed histopathological analysis. We observed almost total resolution of brain edema in three of five patients after initiation of bevacizumab therapy. In one case with rapid increase of the lesion size despite bevacizumab therapy, SWI showed progressive increase of irregular hypointense structures, most likely corresponding to increasing amounts of pathological microvasculature. In one case with progressive neurological decline, 7-T images showed multiple intratumoral microhemorrhages after the first bevacizumab application. Correlation of postmortem neuroimaging with histopathology confirmed that SWI-positive structures correspond to tumor vasculature. The experience from our case series indicates that longitudinal 7-T SWI seems to be an appropriate method for investigation of changes in brain tumor vascularization over time under antiangiogenic therapy.</description><identifier>ISSN: 0730-725X</identifier><identifier>EISSN: 1873-5894</identifier><identifier>DOI: 10.1016/j.mri.2011.08.004</identifier><identifier>PMID: 21982163</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>7 T ; Adult ; Aged ; Angiogenesis Inhibitors - therapeutic use ; Antiangiogenic therapy ; Antibodies, Monoclonal, Humanized - therapeutic use ; Bevacizumab ; Brain - pathology ; Brain Neoplasms - drug therapy ; Brain Neoplasms - pathology ; Brain tumors ; Edema ; Female ; Glioblastoma ; Glioma ; Glioma - drug therapy ; Glioma - pathology ; Humans ; Longitudinal Studies ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Male ; Microvasculature ; Middle Aged ; Monoclonal antibodies ; Neuroimaging ; Radiology ; Susceptibility-weighted imaging ; Treatment Outcome ; Tumor ; vascularization</subject><ispartof>Magnetic resonance imaging, 2012, Vol.30 (1), p.139-147</ispartof><rights>Elsevier Inc.</rights><rights>2012 Elsevier Inc.</rights><rights>Copyright © 2012 Elsevier Inc. 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Antiangiogenic therapy with the monoclonal antibody bevacizumab is considered as a promising therapeutic strategy, although the effect on tumor vascularization is unclear. High-field susceptibility-weighted imaging (SWI) visualizes the microvasculature and may contribute to the investigation of antiangiogenic therapy responses in gliomas. We prospectively studied five adult malignant glioma patients treated with bevacizumab-containing regimens. In each patient, we performed three 7-T SWI and T1-weighted imaging investigations (baseline and 2 and 4 weeks after the start of bevacizumab treatment). In addition, we imaged a postmortem brain of a patient with glioblastoma using 7-T SWI and performed detailed histopathological analysis. We observed almost total resolution of brain edema in three of five patients after initiation of bevacizumab therapy. In one case with rapid increase of the lesion size despite bevacizumab therapy, SWI showed progressive increase of irregular hypointense structures, most likely corresponding to increasing amounts of pathological microvasculature. In one case with progressive neurological decline, 7-T images showed multiple intratumoral microhemorrhages after the first bevacizumab application. Correlation of postmortem neuroimaging with histopathology confirmed that SWI-positive structures correspond to tumor vasculature. The experience from our case series indicates that longitudinal 7-T SWI seems to be an appropriate method for investigation of changes in brain tumor vascularization over time under antiangiogenic therapy.</description><subject>7 T</subject><subject>Adult</subject><subject>Aged</subject><subject>Angiogenesis Inhibitors - therapeutic use</subject><subject>Antiangiogenic therapy</subject><subject>Antibodies, Monoclonal, Humanized - therapeutic use</subject><subject>Bevacizumab</subject><subject>Brain - pathology</subject><subject>Brain Neoplasms - drug therapy</subject><subject>Brain Neoplasms - pathology</subject><subject>Brain tumors</subject><subject>Edema</subject><subject>Female</subject><subject>Glioblastoma</subject><subject>Glioma</subject><subject>Glioma - drug therapy</subject><subject>Glioma - pathology</subject><subject>Humans</subject><subject>Longitudinal Studies</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Microvasculature</subject><subject>Middle Aged</subject><subject>Monoclonal antibodies</subject><subject>Neuroimaging</subject><subject>Radiology</subject><subject>Susceptibility-weighted imaging</subject><subject>Treatment Outcome</subject><subject>Tumor</subject><subject>vascularization</subject><issn>0730-725X</issn><issn>1873-5894</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkruO1DAUhiMEYoeFB6BB7qgSbMcZ20JCQitu0kgULBKdZTsn2TPkMtjOrIb34H1xNMsWFFC5-f7f9vlOUTxntGKUbV_tqzFgxSljFVUVpeJBsWFK1mWjtHhYbKisaSl58-2ieBLjnlLa8Lp5XFxwphVn23pT_NrNU49paXGyA3HB4kRwtD1OPZk70uERyGgH7Cc7JdIPOI-WHGxCmFIkKYBN0JJbTDfEwdF6_LmM1pElrgVxiR4OCR0OmE7lLWB_s-K5f4KEngSIcy72cH-nTUSS66fFo84OEZ7dnZfF1_fvrq8-lrvPHz5dvd2VXtQ6la6TgnuppPWq7kTXNIwKoZ3YUtU6xZ3TtRRa-9ZZxbwQIEFkWMiurVXr68vi5bn3EOYfC8RkRsxPHgY7wbxEozlVtBGN-j9JNddNI7eZZGfShznGAJ05hPy7cDKMmlWb2ZuszazaDFUma8uZF3ftixuhvU_88ZSB12cA8jSOCMFEnxV4aDGAT6ad8Z_1b_5K-wEn9Hb4DieI-3kJ2X40zERuqPmy7s26NoxRyjXd1r8B-EbAoQ</recordid><startdate>2012</startdate><enddate>2012</enddate><creator>Grabner, Günther</creator><creator>Nöbauer, Iris</creator><creator>Elandt, Katarzyna</creator><creator>Kronnerwetter, Claudia</creator><creator>Woehrer, Adelheid</creator><creator>Marosi, Christine</creator><creator>Prayer, Daniela</creator><creator>Trattnig, Siegfried</creator><creator>Preusser, Matthias</creator><general>Elsevier Inc</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>7X8</scope><scope>7QO</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>2012</creationdate><title>Longitudinal brain imaging of five malignant glioma patients treated with bevacizumab using susceptibility-weighted magnetic resonance imaging at 7 T</title><author>Grabner, Günther ; Nöbauer, Iris ; Elandt, Katarzyna ; Kronnerwetter, Claudia ; Woehrer, Adelheid ; Marosi, Christine ; Prayer, Daniela ; Trattnig, Siegfried ; Preusser, Matthias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-bf742c787ac83f4f5510449b4608db82bb937499cdba81c44e7e47ac47fd38dc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>7 T</topic><topic>Adult</topic><topic>Aged</topic><topic>Angiogenesis Inhibitors - therapeutic use</topic><topic>Antiangiogenic therapy</topic><topic>Antibodies, Monoclonal, Humanized - therapeutic use</topic><topic>Bevacizumab</topic><topic>Brain - pathology</topic><topic>Brain Neoplasms - drug therapy</topic><topic>Brain Neoplasms - pathology</topic><topic>Brain tumors</topic><topic>Edema</topic><topic>Female</topic><topic>Glioblastoma</topic><topic>Glioma</topic><topic>Glioma - drug therapy</topic><topic>Glioma - pathology</topic><topic>Humans</topic><topic>Longitudinal Studies</topic><topic>Magnetic resonance imaging</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Microvasculature</topic><topic>Middle Aged</topic><topic>Monoclonal antibodies</topic><topic>Neuroimaging</topic><topic>Radiology</topic><topic>Susceptibility-weighted imaging</topic><topic>Treatment Outcome</topic><topic>Tumor</topic><topic>vascularization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grabner, Günther</creatorcontrib><creatorcontrib>Nöbauer, Iris</creatorcontrib><creatorcontrib>Elandt, Katarzyna</creatorcontrib><creatorcontrib>Kronnerwetter, Claudia</creatorcontrib><creatorcontrib>Woehrer, Adelheid</creatorcontrib><creatorcontrib>Marosi, Christine</creatorcontrib><creatorcontrib>Prayer, Daniela</creatorcontrib><creatorcontrib>Trattnig, Siegfried</creatorcontrib><creatorcontrib>Preusser, Matthias</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Magnetic resonance imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grabner, Günther</au><au>Nöbauer, Iris</au><au>Elandt, Katarzyna</au><au>Kronnerwetter, Claudia</au><au>Woehrer, Adelheid</au><au>Marosi, Christine</au><au>Prayer, Daniela</au><au>Trattnig, Siegfried</au><au>Preusser, Matthias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Longitudinal brain imaging of five malignant glioma patients treated with bevacizumab using susceptibility-weighted magnetic resonance imaging at 7 T</atitle><jtitle>Magnetic resonance imaging</jtitle><addtitle>Magn Reson Imaging</addtitle><date>2012</date><risdate>2012</risdate><volume>30</volume><issue>1</issue><spage>139</spage><epage>147</epage><pages>139-147</pages><issn>0730-725X</issn><eissn>1873-5894</eissn><abstract>Abstract Malignant glioma is a rare tumor type characterized by prominent vascular proliferation. Antiangiogenic therapy with the monoclonal antibody bevacizumab is considered as a promising therapeutic strategy, although the effect on tumor vascularization is unclear. High-field susceptibility-weighted imaging (SWI) visualizes the microvasculature and may contribute to the investigation of antiangiogenic therapy responses in gliomas. We prospectively studied five adult malignant glioma patients treated with bevacizumab-containing regimens. In each patient, we performed three 7-T SWI and T1-weighted imaging investigations (baseline and 2 and 4 weeks after the start of bevacizumab treatment). In addition, we imaged a postmortem brain of a patient with glioblastoma using 7-T SWI and performed detailed histopathological analysis. We observed almost total resolution of brain edema in three of five patients after initiation of bevacizumab therapy. In one case with rapid increase of the lesion size despite bevacizumab therapy, SWI showed progressive increase of irregular hypointense structures, most likely corresponding to increasing amounts of pathological microvasculature. In one case with progressive neurological decline, 7-T images showed multiple intratumoral microhemorrhages after the first bevacizumab application. Correlation of postmortem neuroimaging with histopathology confirmed that SWI-positive structures correspond to tumor vasculature. The experience from our case series indicates that longitudinal 7-T SWI seems to be an appropriate method for investigation of changes in brain tumor vascularization over time under antiangiogenic therapy.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>21982163</pmid><doi>10.1016/j.mri.2011.08.004</doi><tpages>9</tpages></addata></record> |
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subjects | 7 T Adult Aged Angiogenesis Inhibitors - therapeutic use Antiangiogenic therapy Antibodies, Monoclonal, Humanized - therapeutic use Bevacizumab Brain - pathology Brain Neoplasms - drug therapy Brain Neoplasms - pathology Brain tumors Edema Female Glioblastoma Glioma Glioma - drug therapy Glioma - pathology Humans Longitudinal Studies Magnetic resonance imaging Magnetic Resonance Imaging - methods Male Microvasculature Middle Aged Monoclonal antibodies Neuroimaging Radiology Susceptibility-weighted imaging Treatment Outcome Tumor vascularization |
title | Longitudinal brain imaging of five malignant glioma patients treated with bevacizumab using susceptibility-weighted magnetic resonance imaging at 7 T |
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