Decreased tumor apparent diffusion coefficient correlates with objective response of pediatric low-grade glioma to bevacizumab
Recent small, retrospective series suggest bevacizumab may be a therapeutic option for recurrent pediatric low-grade glioma (LGG). Assessment of therapeutic responses is complicated by the unpredictable natural history of these tumors. Because diffusion-weighted imaging quantifies microscopic water...
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Veröffentlicht in: | Journal of neuro-oncology 2015-05, Vol.122 (3), p.491-496 |
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description | Recent small, retrospective series suggest bevacizumab may be a therapeutic option for recurrent pediatric low-grade glioma (LGG). Assessment of therapeutic responses is complicated by the unpredictable natural history of these tumors. Because diffusion-weighted imaging quantifies microscopic water motion affected by cellular density and histologic features, we hypothesized that it may be helpful in monitoring therapeutic response of LGG to bevacizumab. We retrospectively reviewed eight consecutive patients, median age 4.8 (range 2.3–12.3) years at initiation of bevacizumab therapy for recurrent or refractory LGG. Patients received 10 mg/kg/dose every 2 weeks (median 16 doses/therapy course). Mean apparent diffusion coefficient (ADC) was measured and analyzed in respect to tumor volume. Following the first treatment course, seven of eight patients had reduced tumor volume (≥25 %) and ADC. The median decrease in tumor volume was 47% (range −6 to 78 %) and the median decrease in ADC was 14 % (range −5 to 30 %). The ADC was significantly decreased during therapy, whereas the decrease in volume was seen only after therapy completion. There was a positive correlation between percent change in tumor volume and ADC (p |
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Assessment of therapeutic responses is complicated by the unpredictable natural history of these tumors. Because diffusion-weighted imaging quantifies microscopic water motion affected by cellular density and histologic features, we hypothesized that it may be helpful in monitoring therapeutic response of LGG to bevacizumab. We retrospectively reviewed eight consecutive patients, median age 4.8 (range 2.3–12.3) years at initiation of bevacizumab therapy for recurrent or refractory LGG. Patients received 10 mg/kg/dose every 2 weeks (median 16 doses/therapy course). Mean apparent diffusion coefficient (ADC) was measured and analyzed in respect to tumor volume. Following the first treatment course, seven of eight patients had reduced tumor volume (≥25 %) and ADC. The median decrease in tumor volume was 47% (range −6 to 78 %) and the median decrease in ADC was 14 % (range −5 to 30 %). The ADC was significantly decreased during therapy, whereas the decrease in volume was seen only after therapy completion. There was a positive correlation between percent change in tumor volume and ADC (p < 0.05). We report a decrease in tumor ADC during initial bevacizumab therapy that is accompanied by a decrease in volume following therapy. Imaging changes in microscopic water motion associated with histology may be useful in monitoring the therapeutic response of LGG to bevacizumab.</description><identifier>ISSN: 0167-594X</identifier><identifier>EISSN: 1573-7373</identifier><identifier>DOI: 10.1007/s11060-015-1754-9</identifier><identifier>PMID: 25758812</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adolescent ; Angiogenesis Inhibitors - therapeutic use ; Bevacizumab - therapeutic use ; Brain - drug effects ; Brain - pathology ; Brain Neoplasms - drug therapy ; Brain Neoplasms - pathology ; Child ; Child, Preschool ; Clinical Study ; Diffusion Magnetic Resonance Imaging ; Female ; Glioma - drug therapy ; Glioma - pathology ; Humans ; Image Processing, Computer-Assisted ; Male ; Medicine ; Medicine & Public Health ; Neurology ; Oncology ; Retrospective Studies</subject><ispartof>Journal of neuro-oncology, 2015-05, Vol.122 (3), p.491-496</ispartof><rights>Springer Science+Business Media New York 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-78ba292fc5daf652e1fa7dcbc3d9a714a79608d4d3ab9378b61b36363f0aa5913</citedby><cites>FETCH-LOGICAL-c475t-78ba292fc5daf652e1fa7dcbc3d9a714a79608d4d3ab9378b61b36363f0aa5913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11060-015-1754-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11060-015-1754-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25758812$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hsu, Christopher H.</creatorcontrib><creatorcontrib>Lober, Robert M.</creatorcontrib><creatorcontrib>Li, Matthew D.</creatorcontrib><creatorcontrib>Partap, Sonia</creatorcontrib><creatorcontrib>Murphy, Patricia A.</creatorcontrib><creatorcontrib>Barnes, Patrick D.</creatorcontrib><creatorcontrib>Fisher, Paul G.</creatorcontrib><creatorcontrib>Yeom, Kristen W.</creatorcontrib><title>Decreased tumor apparent diffusion coefficient correlates with objective response of pediatric low-grade glioma to bevacizumab</title><title>Journal of neuro-oncology</title><addtitle>J Neurooncol</addtitle><addtitle>J Neurooncol</addtitle><description>Recent small, retrospective series suggest bevacizumab may be a therapeutic option for recurrent pediatric low-grade glioma (LGG). Assessment of therapeutic responses is complicated by the unpredictable natural history of these tumors. Because diffusion-weighted imaging quantifies microscopic water motion affected by cellular density and histologic features, we hypothesized that it may be helpful in monitoring therapeutic response of LGG to bevacizumab. We retrospectively reviewed eight consecutive patients, median age 4.8 (range 2.3–12.3) years at initiation of bevacizumab therapy for recurrent or refractory LGG. Patients received 10 mg/kg/dose every 2 weeks (median 16 doses/therapy course). Mean apparent diffusion coefficient (ADC) was measured and analyzed in respect to tumor volume. Following the first treatment course, seven of eight patients had reduced tumor volume (≥25 %) and ADC. The median decrease in tumor volume was 47% (range −6 to 78 %) and the median decrease in ADC was 14 % (range −5 to 30 %). The ADC was significantly decreased during therapy, whereas the decrease in volume was seen only after therapy completion. There was a positive correlation between percent change in tumor volume and ADC (p < 0.05). We report a decrease in tumor ADC during initial bevacizumab therapy that is accompanied by a decrease in volume following therapy. Imaging changes in microscopic water motion associated with histology may be useful in monitoring the therapeutic response of LGG to bevacizumab.</description><subject>Adolescent</subject><subject>Angiogenesis Inhibitors - therapeutic use</subject><subject>Bevacizumab - therapeutic use</subject><subject>Brain - drug effects</subject><subject>Brain - pathology</subject><subject>Brain Neoplasms - drug therapy</subject><subject>Brain Neoplasms - pathology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Clinical Study</subject><subject>Diffusion Magnetic Resonance Imaging</subject><subject>Female</subject><subject>Glioma - drug therapy</subject><subject>Glioma - pathology</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neurology</subject><subject>Oncology</subject><subject>Retrospective Studies</subject><issn>0167-594X</issn><issn>1573-7373</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqFkU2LFDEQhoMo7uzqD_AiAS9eWpN0PrqPsuoqLHhR8Baqk8qYobvTJt276MHfboZZRQSRHAqSp94i9RDyhLMXnDHzsnDONGsYVw03Sjb9PbLjyrSNaU17n-wY16ZRvfx8Rs5LOTDGpGn5Q3ImlFFdx8WO_HiNLiMU9HTdppQpLAtknFfqYwhbiWmmLmEI0cXjrUs54wgrFnob1y80DQd0a7xBmrEsaS5IU6AL-ghrjo6O6bbZZ_BI92NME9A10QFvwMXv2wTDI_IgwFjw8V29IJ_evvl4-a65_nD1_vLVdeOkUWtjugFEL4JTHoJWAnkA493gWt-D4RJMr1nnpW9h6NtKaz60up7AAFTP2wvy_JS75PR1w7LaKRaH4wgzpq1YbozWdXOy-z-qOyGYFkJX9Nlf6CFtea4fOVJcSq2ZrBQ_US6nUjIGu-Q4Qf5mObNHj_bk0VaP9ujR9rXn6V3yNkzof3f8ElcBcQJKfZr3mP8Y_c_Un2p6qjI</recordid><startdate>20150501</startdate><enddate>20150501</enddate><creator>Hsu, Christopher H.</creator><creator>Lober, Robert M.</creator><creator>Li, Matthew D.</creator><creator>Partap, Sonia</creator><creator>Murphy, Patricia A.</creator><creator>Barnes, Patrick D.</creator><creator>Fisher, Paul G.</creator><creator>Yeom, Kristen W.</creator><general>Springer US</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>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20150501</creationdate><title>Decreased tumor apparent diffusion coefficient correlates with objective response of pediatric low-grade glioma to bevacizumab</title><author>Hsu, Christopher H. ; Lober, Robert M. ; Li, Matthew D. ; Partap, Sonia ; Murphy, Patricia A. ; Barnes, Patrick D. ; Fisher, Paul G. ; Yeom, Kristen W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-78ba292fc5daf652e1fa7dcbc3d9a714a79608d4d3ab9378b61b36363f0aa5913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Angiogenesis Inhibitors - therapeutic use</topic><topic>Bevacizumab - therapeutic use</topic><topic>Brain - drug effects</topic><topic>Brain - pathology</topic><topic>Brain Neoplasms - drug therapy</topic><topic>Brain Neoplasms - pathology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Clinical Study</topic><topic>Diffusion Magnetic Resonance Imaging</topic><topic>Female</topic><topic>Glioma - drug therapy</topic><topic>Glioma - pathology</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Neurology</topic><topic>Oncology</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hsu, Christopher H.</creatorcontrib><creatorcontrib>Lober, Robert M.</creatorcontrib><creatorcontrib>Li, Matthew D.</creatorcontrib><creatorcontrib>Partap, Sonia</creatorcontrib><creatorcontrib>Murphy, Patricia A.</creatorcontrib><creatorcontrib>Barnes, Patrick D.</creatorcontrib><creatorcontrib>Fisher, Paul G.</creatorcontrib><creatorcontrib>Yeom, Kristen W.</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>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</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 Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical 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>MEDLINE - Academic</collection><jtitle>Journal of neuro-oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hsu, Christopher H.</au><au>Lober, Robert M.</au><au>Li, Matthew D.</au><au>Partap, Sonia</au><au>Murphy, Patricia A.</au><au>Barnes, Patrick D.</au><au>Fisher, Paul G.</au><au>Yeom, Kristen W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decreased tumor apparent diffusion coefficient correlates with objective response of pediatric low-grade glioma to bevacizumab</atitle><jtitle>Journal of neuro-oncology</jtitle><stitle>J Neurooncol</stitle><addtitle>J Neurooncol</addtitle><date>2015-05-01</date><risdate>2015</risdate><volume>122</volume><issue>3</issue><spage>491</spage><epage>496</epage><pages>491-496</pages><issn>0167-594X</issn><eissn>1573-7373</eissn><abstract>Recent small, retrospective series suggest bevacizumab may be a therapeutic option for recurrent pediatric low-grade glioma (LGG). Assessment of therapeutic responses is complicated by the unpredictable natural history of these tumors. Because diffusion-weighted imaging quantifies microscopic water motion affected by cellular density and histologic features, we hypothesized that it may be helpful in monitoring therapeutic response of LGG to bevacizumab. We retrospectively reviewed eight consecutive patients, median age 4.8 (range 2.3–12.3) years at initiation of bevacizumab therapy for recurrent or refractory LGG. Patients received 10 mg/kg/dose every 2 weeks (median 16 doses/therapy course). Mean apparent diffusion coefficient (ADC) was measured and analyzed in respect to tumor volume. Following the first treatment course, seven of eight patients had reduced tumor volume (≥25 %) and ADC. The median decrease in tumor volume was 47% (range −6 to 78 %) and the median decrease in ADC was 14 % (range −5 to 30 %). The ADC was significantly decreased during therapy, whereas the decrease in volume was seen only after therapy completion. There was a positive correlation between percent change in tumor volume and ADC (p < 0.05). We report a decrease in tumor ADC during initial bevacizumab therapy that is accompanied by a decrease in volume following therapy. Imaging changes in microscopic water motion associated with histology may be useful in monitoring the therapeutic response of LGG to bevacizumab.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>25758812</pmid><doi>10.1007/s11060-015-1754-9</doi><tpages>6</tpages></addata></record> |
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subjects | Adolescent Angiogenesis Inhibitors - therapeutic use Bevacizumab - therapeutic use Brain - drug effects Brain - pathology Brain Neoplasms - drug therapy Brain Neoplasms - pathology Child Child, Preschool Clinical Study Diffusion Magnetic Resonance Imaging Female Glioma - drug therapy Glioma - pathology Humans Image Processing, Computer-Assisted Male Medicine Medicine & Public Health Neurology Oncology Retrospective Studies |
title | Decreased tumor apparent diffusion coefficient correlates with objective response of pediatric low-grade glioma to bevacizumab |
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