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Paediatric spinal cord low-grade gliomas—evaluation and management of post-surgical residual disease

Purpose To assess the evaluation and management of post-surgical residual disease for low-grade intramedullary spinal cord tumours (IMSCT) in childhood. Methods A single-centre retrospective review of low-grade IMSCTs treated between 2000 and 2019. All surgeries were performed with intent of safe ma...

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Published in:Child's nervous system 2022-03, Vol.38 (3), p.577-586
Main Authors: Silva, A. H. D., Constantinides, M., Valetopoulou, A., Sgardelis, P., Mankad, K., D’Arco, F., Jankovic, I., Thompson, D.
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cited_by cdi_FETCH-LOGICAL-c347t-65bdb395eec7b1406af67a316e6752d29a480bb8fafabcaef854e9d0213caff13
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container_issue 3
container_start_page 577
container_title Child's nervous system
container_volume 38
creator Silva, A. H. D.
Constantinides, M.
Valetopoulou, A.
Sgardelis, P.
Mankad, K.
D’Arco, F.
Jankovic, I.
Thompson, D.
description Purpose To assess the evaluation and management of post-surgical residual disease for low-grade intramedullary spinal cord tumours (IMSCT) in childhood. Methods A single-centre retrospective review of low-grade IMSCTs treated between 2000 and 2019. All surgeries were performed with intent of safe maximal resection guided by intra-operative neurophysiological monitoring (IONM). Pre- and post-operative MRIs were reviewed to assess the extent of resection (EOR), recorded as follows: gross total resection (GTR), near total resection (NTR), sub-total resection (STR) and partial resection (PR). Outcome measures were time to recurrence, need for and modality of additional therapy and ambulatory status at last follow-up. Results Thirty patients underwent surgery for IMSCT (median age 6.9 years). EOR was GTR = 8, NTR = 4, STR = 9, PR = 9. All patients were alive at last follow-up (median follow-up 73 months [IQR 93 months]). Eighteen patients (60%) remained radiologically stable. Twelve patients (40%) developed recurrence during surveillance. Progression free survival was significantly better in cases with GTR + NTR in comparison to either STR or PR ( p  = 0.039). 10/30 (33%) patients were treated with additional therapy. At last follow-up, 26/30 patients were independently mobile. Conclusion Survival rates for low-grade IMSCT are excellent. Radical micro-surgical resection, guided by IONM provides effective means of balancing the objectives of maximal safe resection, functional outcome and tumour control. Whilst evidence of ‘residual disease’ was identified in over 2/3 of immediate post-operative MRI scans, additional treatment was required in only 1/3 of cases. Critical appraisal of post-operative imaging findings is required to better define ‘residual disease’. Small volume residual disease (
doi_str_mv 10.1007/s00381-021-05412-4
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H. D. ; Constantinides, M. ; Valetopoulou, A. ; Sgardelis, P. ; Mankad, K. ; D’Arco, F. ; Jankovic, I. ; Thompson, D.</creator><creatorcontrib>Silva, A. H. D. ; Constantinides, M. ; Valetopoulou, A. ; Sgardelis, P. ; Mankad, K. ; D’Arco, F. ; Jankovic, I. ; Thompson, D.</creatorcontrib><description>Purpose To assess the evaluation and management of post-surgical residual disease for low-grade intramedullary spinal cord tumours (IMSCT) in childhood. Methods A single-centre retrospective review of low-grade IMSCTs treated between 2000 and 2019. All surgeries were performed with intent of safe maximal resection guided by intra-operative neurophysiological monitoring (IONM). Pre- and post-operative MRIs were reviewed to assess the extent of resection (EOR), recorded as follows: gross total resection (GTR), near total resection (NTR), sub-total resection (STR) and partial resection (PR). Outcome measures were time to recurrence, need for and modality of additional therapy and ambulatory status at last follow-up. Results Thirty patients underwent surgery for IMSCT (median age 6.9 years). EOR was GTR = 8, NTR = 4, STR = 9, PR = 9. All patients were alive at last follow-up (median follow-up 73 months [IQR 93 months]). Eighteen patients (60%) remained radiologically stable. Twelve patients (40%) developed recurrence during surveillance. Progression free survival was significantly better in cases with GTR + NTR in comparison to either STR or PR ( p  = 0.039). 10/30 (33%) patients were treated with additional therapy. At last follow-up, 26/30 patients were independently mobile. Conclusion Survival rates for low-grade IMSCT are excellent. Radical micro-surgical resection, guided by IONM provides effective means of balancing the objectives of maximal safe resection, functional outcome and tumour control. Whilst evidence of ‘residual disease’ was identified in over 2/3 of immediate post-operative MRI scans, additional treatment was required in only 1/3 of cases. Critical appraisal of post-operative imaging findings is required to better define ‘residual disease’. Small volume residual disease (&lt; 5%) does not compromise progression-free survival.</description><identifier>ISSN: 0256-7040</identifier><identifier>EISSN: 1433-0350</identifier><identifier>DOI: 10.1007/s00381-021-05412-4</identifier><identifier>PMID: 34855000</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Medicine ; Medicine &amp; Public Health ; Neurosciences ; Neurosurgery ; Original Article</subject><ispartof>Child's nervous system, 2022-03, Vol.38 (3), p.577-586</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021</rights><rights>2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c347t-65bdb395eec7b1406af67a316e6752d29a480bb8fafabcaef854e9d0213caff13</citedby><cites>FETCH-LOGICAL-c347t-65bdb395eec7b1406af67a316e6752d29a480bb8fafabcaef854e9d0213caff13</cites><orcidid>0000-0001-7396-591X ; 0000-0002-1114-9869 ; 0000-0001-5979-9337 ; 0000-0002-2967-2674</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34855000$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Silva, A. H. D.</creatorcontrib><creatorcontrib>Constantinides, M.</creatorcontrib><creatorcontrib>Valetopoulou, A.</creatorcontrib><creatorcontrib>Sgardelis, P.</creatorcontrib><creatorcontrib>Mankad, K.</creatorcontrib><creatorcontrib>D’Arco, F.</creatorcontrib><creatorcontrib>Jankovic, I.</creatorcontrib><creatorcontrib>Thompson, D.</creatorcontrib><title>Paediatric spinal cord low-grade gliomas—evaluation and management of post-surgical residual disease</title><title>Child's nervous system</title><addtitle>Childs Nerv Syst</addtitle><addtitle>Childs Nerv Syst</addtitle><description>Purpose To assess the evaluation and management of post-surgical residual disease for low-grade intramedullary spinal cord tumours (IMSCT) in childhood. Methods A single-centre retrospective review of low-grade IMSCTs treated between 2000 and 2019. All surgeries were performed with intent of safe maximal resection guided by intra-operative neurophysiological monitoring (IONM). Pre- and post-operative MRIs were reviewed to assess the extent of resection (EOR), recorded as follows: gross total resection (GTR), near total resection (NTR), sub-total resection (STR) and partial resection (PR). Outcome measures were time to recurrence, need for and modality of additional therapy and ambulatory status at last follow-up. Results Thirty patients underwent surgery for IMSCT (median age 6.9 years). EOR was GTR = 8, NTR = 4, STR = 9, PR = 9. All patients were alive at last follow-up (median follow-up 73 months [IQR 93 months]). Eighteen patients (60%) remained radiologically stable. Twelve patients (40%) developed recurrence during surveillance. Progression free survival was significantly better in cases with GTR + NTR in comparison to either STR or PR ( p  = 0.039). 10/30 (33%) patients were treated with additional therapy. At last follow-up, 26/30 patients were independently mobile. Conclusion Survival rates for low-grade IMSCT are excellent. Radical micro-surgical resection, guided by IONM provides effective means of balancing the objectives of maximal safe resection, functional outcome and tumour control. Whilst evidence of ‘residual disease’ was identified in over 2/3 of immediate post-operative MRI scans, additional treatment was required in only 1/3 of cases. Critical appraisal of post-operative imaging findings is required to better define ‘residual disease’. 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D.</creatorcontrib><creatorcontrib>Constantinides, M.</creatorcontrib><creatorcontrib>Valetopoulou, A.</creatorcontrib><creatorcontrib>Sgardelis, P.</creatorcontrib><creatorcontrib>Mankad, K.</creatorcontrib><creatorcontrib>D’Arco, F.</creatorcontrib><creatorcontrib>Jankovic, I.</creatorcontrib><creatorcontrib>Thompson, D.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Child's nervous system</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Silva, A. H. 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Medicine & Public Health
Neurosciences
Neurosurgery
Original Article
title Paediatric spinal cord low-grade gliomas—evaluation and management of post-surgical residual disease
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