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114 Paediatric spinal cord intramedullary gliomas safe maximal extent of resection to optimize neurological and oncological outcomes
ObjectiveLow grade intramedullary spinal cord tumours (IMSCTs) are rare tumours of childhood with potential for significant late morbidity following surgery.We present our institutional experience with surgical treatment of these complex lesions emphasizing consistent definition of extent of resecti...
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Published in: | Archives of disease in childhood 2020-11, Vol.105 (Suppl 2), p.A39-A39 |
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description | ObjectiveLow grade intramedullary spinal cord tumours (IMSCTs) are rare tumours of childhood with potential for significant late morbidity following surgery.We present our institutional experience with surgical treatment of these complex lesions emphasizing consistent definition of extent of resection (EOR), techniques to maximise surgical safety and a novel stratification of residual disease to guide post-operative strategy.MethodsA retrospective review of low-grade IMSCTs treated at GOSH between 2000 and 2019 was conducted. All surgery carried out by a single surgeon with intent of safe maximal resection guided by intra-operative neurophysiological monitoring (IONM). Pre and post-operative MRI were reviewed by neuro-radiologists.EOR was recorded as:Gross Total Resection (GTR) –100% resectionNear Total Resection (NTR) – at least 95% resectionSub Total Resection (STR) – 90% tumour resectionPartial Resection (PR) – less than 90% tumour resectionFurther outcome measures were time to recurrence, need for adjuvant therapy and mobility at last follow-up.ResultsA total of 30 patients underwent surgery. IONM parameters (Motor evoked potentials,D-wave) were used to guide EOR. EORs achieved: GTR = 8, NTR = 4, STR = 9, PR = 9.All patients were alive at last follow up with eighteen patients (60%) remaining radiologically and clinically stable. Twelve patients developed recurrence/progressive disease during surveillance (40%) requiring adjuvant treatment. Progression free survival was significantly better in cases with GTR+NTR in comparison to either STR or PR.Following surgery, 26/30 patients were independently mobile, 1/30 required crutches and 3/30 required a wheelchair.9/30 patients were treated with adjuvant therapy following surgery.ConclusionSurvival rates for low grade IMSCT are excellent. Radical micro-surgical resection, guided by IONM provides an effective means of balancing the objectives of maximal safe resection, functional outcome and tumour control. Small volume residual disease does not compromise long-term oncological outcome. |
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All surgery carried out by a single surgeon with intent of safe maximal resection guided by intra-operative neurophysiological monitoring (IONM). Pre and post-operative MRI were reviewed by neuro-radiologists.EOR was recorded as:Gross Total Resection (GTR) –100% resectionNear Total Resection (NTR) – at least 95% resectionSub Total Resection (STR) – 90% tumour resectionPartial Resection (PR) – less than 90% tumour resectionFurther outcome measures were time to recurrence, need for adjuvant therapy and mobility at last follow-up.ResultsA total of 30 patients underwent surgery. IONM parameters (Motor evoked potentials,D-wave) were used to guide EOR. EORs achieved: GTR = 8, NTR = 4, STR = 9, PR = 9.All patients were alive at last follow up with eighteen patients (60%) remaining radiologically and clinically stable. Twelve patients developed recurrence/progressive disease during surveillance (40%) requiring adjuvant treatment. Progression free survival was significantly better in cases with GTR+NTR in comparison to either STR or PR.Following surgery, 26/30 patients were independently mobile, 1/30 required crutches and 3/30 required a wheelchair.9/30 patients were treated with adjuvant therapy following surgery.ConclusionSurvival rates for low grade IMSCT are excellent. Radical micro-surgical resection, guided by IONM provides an effective means of balancing the objectives of maximal safe resection, functional outcome and tumour control. Small volume residual disease does not compromise long-term oncological outcome.</description><identifier>ISSN: 0003-9888</identifier><identifier>EISSN: 1468-2044</identifier><identifier>DOI: 10.1136/archdischild-2020-gosh.114</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Children ; Glioma ; Magnetic resonance imaging ; Morbidity ; Motor evoked potentials ; Outcome Measures ; Patients ; Pediatrics ; Spinal cord ; Surgery ; Survival ; Tumors</subject><ispartof>Archives of disease in childhood, 2020-11, Vol.105 (Suppl 2), p.A39-A39</ispartof><rights>Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2020 Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2465658616/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2465658616?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,21377,21393,27923,27924,33610,33876,43732,43879,74092,74268</link.rule.ids></links><search><creatorcontrib>Valetopoulou, Alexandra</creatorcontrib><creatorcontrib>Constantinides, Maria</creatorcontrib><creatorcontrib>Silva, Dulanka</creatorcontrib><creatorcontrib>Thompson, Dominic</creatorcontrib><title>114 Paediatric spinal cord intramedullary gliomas safe maximal extent of resection to optimize neurological and oncological outcomes</title><title>Archives of disease in childhood</title><description>ObjectiveLow grade intramedullary spinal cord tumours (IMSCTs) are rare tumours of childhood with potential for significant late morbidity following surgery.We present our institutional experience with surgical treatment of these complex lesions emphasizing consistent definition of extent of resection (EOR), techniques to maximise surgical safety and a novel stratification of residual disease to guide post-operative strategy.MethodsA retrospective review of low-grade IMSCTs treated at GOSH between 2000 and 2019 was conducted. All surgery carried out by a single surgeon with intent of safe maximal resection guided by intra-operative neurophysiological monitoring (IONM). Pre and post-operative MRI were reviewed by neuro-radiologists.EOR was recorded as:Gross Total Resection (GTR) –100% resectionNear Total Resection (NTR) – at least 95% resectionSub Total Resection (STR) – 90% tumour resectionPartial Resection (PR) – less than 90% tumour resectionFurther outcome measures were time to recurrence, need for adjuvant therapy and mobility at last follow-up.ResultsA total of 30 patients underwent surgery. IONM parameters (Motor evoked potentials,D-wave) were used to guide EOR. EORs achieved: GTR = 8, NTR = 4, STR = 9, PR = 9.All patients were alive at last follow up with eighteen patients (60%) remaining radiologically and clinically stable. Twelve patients developed recurrence/progressive disease during surveillance (40%) requiring adjuvant treatment. Progression free survival was significantly better in cases with GTR+NTR in comparison to either STR or PR.Following surgery, 26/30 patients were independently mobile, 1/30 required crutches and 3/30 required a wheelchair.9/30 patients were treated with adjuvant therapy following surgery.ConclusionSurvival rates for low grade IMSCT are excellent. Radical micro-surgical resection, guided by IONM provides an effective means of balancing the objectives of maximal safe resection, functional outcome and tumour control. Small volume residual disease does not compromise long-term oncological outcome.</description><subject>Children</subject><subject>Glioma</subject><subject>Magnetic resonance imaging</subject><subject>Morbidity</subject><subject>Motor evoked potentials</subject><subject>Outcome Measures</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Spinal cord</subject><subject>Surgery</subject><subject>Survival</subject><subject>Tumors</subject><issn>0003-9888</issn><issn>1468-2044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>ALSLI</sourceid><sourceid>CJNVE</sourceid><sourceid>M0P</sourceid><recordid>eNpNkMtKxDAUhoMoOI6-Q9B1Nbem6VIGbzCgC12HNElnMrRNTVIYXbnRB_VJzDAirg7n_B8H_g-Ac4wuMab8SgW9Ni7qtetMQRBBxcrHdc7YAZhhxkU-MnYIZgghWtRCiGNwEuMGIUyEoDPwldHvj88nZY1TKTgN4-gG1UHtg4FuSEH11kxdp8IbXHXO9yrCqFoLe7V1fQbtNtkhQd_CYKPVyfkBJg_9mFzv3i0c7BR851dOZ1gNBvpB_-1-Str3Np6Co1Z10Z79zjl4ub15XtwXy8e7h8X1smgw4azQpWopFaKpjCWi0oIp0ShCMa9oXSPcalJTVJVthUyFypwxqkRbVy2nRNWWzsHF_u8Y_OtkY5IbP4XcN0rCeMlLwTHPVLmnmn4jx5BrhjeJkdwpl_-Vy51yuVOeM0Z_AFsXfXA</recordid><startdate>202011</startdate><enddate>202011</enddate><creator>Valetopoulou, Alexandra</creator><creator>Constantinides, Maria</creator><creator>Silva, Dulanka</creator><creator>Thompson, Dominic</creator><general>BMJ Publishing Group LTD</general><scope>0-V</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88B</scope><scope>88E</scope><scope>88I</scope><scope>8A4</scope><scope>8AF</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>ALSLI</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>CJNVE</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0P</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEDU</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>202011</creationdate><title>114 Paediatric spinal cord intramedullary gliomas safe maximal extent of resection to optimize neurological and oncological outcomes</title><author>Valetopoulou, Alexandra ; Constantinides, Maria ; Silva, Dulanka ; Thompson, Dominic</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1264-c5af3388b7de287c84a8ba2316739901fc293075f70d7058ba43a8f97f632a9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Children</topic><topic>Glioma</topic><topic>Magnetic resonance imaging</topic><topic>Morbidity</topic><topic>Motor evoked potentials</topic><topic>Outcome Measures</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Spinal cord</topic><topic>Surgery</topic><topic>Survival</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Valetopoulou, Alexandra</creatorcontrib><creatorcontrib>Constantinides, Maria</creatorcontrib><creatorcontrib>Silva, Dulanka</creatorcontrib><creatorcontrib>Thompson, Dominic</creatorcontrib><collection>ProQuest Social Sciences Premium Collection</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Education Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Education Periodicals</collection><collection>STEM Database</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>Social Science Premium Collection</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Education Collection</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>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Education Database</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Education</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 Basic</collection><jtitle>Archives of disease in childhood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Valetopoulou, Alexandra</au><au>Constantinides, Maria</au><au>Silva, Dulanka</au><au>Thompson, Dominic</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>114 Paediatric spinal cord intramedullary gliomas safe maximal extent of resection to optimize neurological and oncological outcomes</atitle><jtitle>Archives of disease in childhood</jtitle><date>2020-11</date><risdate>2020</risdate><volume>105</volume><issue>Suppl 2</issue><spage>A39</spage><epage>A39</epage><pages>A39-A39</pages><issn>0003-9888</issn><eissn>1468-2044</eissn><abstract>ObjectiveLow grade intramedullary spinal cord tumours (IMSCTs) are rare tumours of childhood with potential for significant late morbidity following surgery.We present our institutional experience with surgical treatment of these complex lesions emphasizing consistent definition of extent of resection (EOR), techniques to maximise surgical safety and a novel stratification of residual disease to guide post-operative strategy.MethodsA retrospective review of low-grade IMSCTs treated at GOSH between 2000 and 2019 was conducted. All surgery carried out by a single surgeon with intent of safe maximal resection guided by intra-operative neurophysiological monitoring (IONM). Pre and post-operative MRI were reviewed by neuro-radiologists.EOR was recorded as:Gross Total Resection (GTR) –100% resectionNear Total Resection (NTR) – at least 95% resectionSub Total Resection (STR) – 90% tumour resectionPartial Resection (PR) – less than 90% tumour resectionFurther outcome measures were time to recurrence, need for adjuvant therapy and mobility at last follow-up.ResultsA total of 30 patients underwent surgery. IONM parameters (Motor evoked potentials,D-wave) were used to guide EOR. EORs achieved: GTR = 8, NTR = 4, STR = 9, PR = 9.All patients were alive at last follow up with eighteen patients (60%) remaining radiologically and clinically stable. Twelve patients developed recurrence/progressive disease during surveillance (40%) requiring adjuvant treatment. Progression free survival was significantly better in cases with GTR+NTR in comparison to either STR or PR.Following surgery, 26/30 patients were independently mobile, 1/30 required crutches and 3/30 required a wheelchair.9/30 patients were treated with adjuvant therapy following surgery.ConclusionSurvival rates for low grade IMSCT are excellent. Radical micro-surgical resection, guided by IONM provides an effective means of balancing the objectives of maximal safe resection, functional outcome and tumour control. Small volume residual disease does not compromise long-term oncological outcome.</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/archdischild-2020-gosh.114</doi><oa>free_for_read</oa></addata></record> |
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subjects | Children Glioma Magnetic resonance imaging Morbidity Motor evoked potentials Outcome Measures Patients Pediatrics Spinal cord Surgery Survival Tumors |
title | 114 Paediatric spinal cord intramedullary gliomas safe maximal extent of resection to optimize neurological and oncological outcomes |
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