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Development of prognostic index for primary supratentorial intracerebral tumours
The clinical course of intrinsic supratentorial tumours is variable. Prediction of outcome would be useful in defining patients for specific treatment policies. A retrospective analysis of 560 patients with intrinsic supratentorial tumours was performed. Proportional hazards models for survival were...
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Published in: | Journal of neurology, neurosurgery and psychiatry neurosurgery and psychiatry, 1992-04, Vol.55 (4), p.271-274 |
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description | The clinical course of intrinsic supratentorial tumours is variable. Prediction of outcome would be useful in defining patients for specific treatment policies. A retrospective analysis of 560 patients with intrinsic supratentorial tumours was performed. Proportional hazards models for survival were derived by using a stepwise selection procedure with only clinical and CT features as possible explanatory variables. The variables of prognostic importance were age, a first symptom of epilepsy, focal signs at presentation, a cystic lesion on CT scan, and duration of symptoms before presentation. The model defined a group with a good prognosis (score less than or equal to 9, n = 211) and a group with a poor prognosis (score greater than 9, n = 344). The median survival was 27 months for those with a score less than or equal to 9 or less and three months for those with score greater than 9. An alternative model, not including duration of symptoms, is also capable of defining groups with long (score less than or equal to 16, n = 234) and short (score greater than 16, n = 325) survival. The model may provide a means of classifying patients for inclusion in prospective randomised studies. |
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Prediction of outcome would be useful in defining patients for specific treatment policies. A retrospective analysis of 560 patients with intrinsic supratentorial tumours was performed. Proportional hazards models for survival were derived by using a stepwise selection procedure with only clinical and CT features as possible explanatory variables. The variables of prognostic importance were age, a first symptom of epilepsy, focal signs at presentation, a cystic lesion on CT scan, and duration of symptoms before presentation. The model defined a group with a good prognosis (score less than or equal to 9, n = 211) and a group with a poor prognosis (score greater than 9, n = 344). The median survival was 27 months for those with a score less than or equal to 9 or less and three months for those with score greater than 9. An alternative model, not including duration of symptoms, is also capable of defining groups with long (score less than or equal to 16, n = 234) and short (score greater than 16, n = 325) survival. The model may provide a means of classifying patients for inclusion in prospective randomised studies.</description><identifier>ISSN: 0022-3050</identifier><identifier>EISSN: 1468-330X</identifier><identifier>DOI: 10.1136/jnnp.55.4.271</identifier><identifier>PMID: 1583511</identifier><identifier>CODEN: JNNPAU</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd</publisher><subject>Actuarial Analysis ; Adult ; Aged ; Biological and medical sciences ; Epilepsy - etiology ; Female ; Humans ; Male ; Medical sciences ; Middle Aged ; Neurologic Examination ; Neurology ; Prospective Studies ; Severity of Illness Index ; Supratentorial Neoplasms - complications ; Supratentorial Neoplasms - diagnosis ; Supratentorial Neoplasms - mortality ; Survival Rate ; Tomography, X-Ray Computed ; Tumors of the nervous system. Phacomatoses</subject><ispartof>Journal of neurology, neurosurgery and psychiatry, 1992-04, Vol.55 (4), p.271-274</ispartof><rights>1992 INIST-CNRS</rights><rights>Copyright BMJ Publishing Group LTD Apr 1992</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b509t-f6ed936069c21449391bf3e8ed44e3072a33b4f818e2d105a2018b5e6cbee6c93</citedby><cites>FETCH-LOGICAL-b509t-f6ed936069c21449391bf3e8ed44e3072a33b4f818e2d105a2018b5e6cbee6c93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC489038/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC489038/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5324785$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1583511$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hutton, J L</creatorcontrib><creatorcontrib>Smith, D F</creatorcontrib><creatorcontrib>Sandemann, D</creatorcontrib><creatorcontrib>Foy, P M</creatorcontrib><creatorcontrib>Shaw, M D</creatorcontrib><creatorcontrib>Williams, I R</creatorcontrib><creatorcontrib>Chadwick, D W</creatorcontrib><title>Development of prognostic index for primary supratentorial intracerebral tumours</title><title>Journal of neurology, neurosurgery and psychiatry</title><addtitle>J Neurol Neurosurg Psychiatry</addtitle><description>The clinical course of intrinsic supratentorial tumours is variable. Prediction of outcome would be useful in defining patients for specific treatment policies. A retrospective analysis of 560 patients with intrinsic supratentorial tumours was performed. Proportional hazards models for survival were derived by using a stepwise selection procedure with only clinical and CT features as possible explanatory variables. The variables of prognostic importance were age, a first symptom of epilepsy, focal signs at presentation, a cystic lesion on CT scan, and duration of symptoms before presentation. The model defined a group with a good prognosis (score less than or equal to 9, n = 211) and a group with a poor prognosis (score greater than 9, n = 344). The median survival was 27 months for those with a score less than or equal to 9 or less and three months for those with score greater than 9. An alternative model, not including duration of symptoms, is also capable of defining groups with long (score less than or equal to 16, n = 234) and short (score greater than 16, n = 325) survival. The model may provide a means of classifying patients for inclusion in prospective randomised studies.</description><subject>Actuarial Analysis</subject><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Epilepsy - etiology</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neurologic Examination</subject><subject>Neurology</subject><subject>Prospective Studies</subject><subject>Severity of Illness Index</subject><subject>Supratentorial Neoplasms - complications</subject><subject>Supratentorial Neoplasms - diagnosis</subject><subject>Supratentorial Neoplasms - mortality</subject><subject>Survival Rate</subject><subject>Tomography, X-Ray Computed</subject><subject>Tumors of the nervous system. 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Phacomatoses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hutton, J L</creatorcontrib><creatorcontrib>Smith, D F</creatorcontrib><creatorcontrib>Sandemann, D</creatorcontrib><creatorcontrib>Foy, P M</creatorcontrib><creatorcontrib>Shaw, M D</creatorcontrib><creatorcontrib>Williams, I R</creatorcontrib><creatorcontrib>Chadwick, D W</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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>Nursing & Allied Health Database</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM 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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Science Database</collection><collection>Nursing & Allied Health Premium</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 China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of neurology, neurosurgery and psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hutton, J L</au><au>Smith, D F</au><au>Sandemann, D</au><au>Foy, P M</au><au>Shaw, M D</au><au>Williams, I R</au><au>Chadwick, D W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of prognostic index for primary supratentorial intracerebral tumours</atitle><jtitle>Journal of neurology, neurosurgery and psychiatry</jtitle><addtitle>J Neurol Neurosurg Psychiatry</addtitle><date>1992-04-01</date><risdate>1992</risdate><volume>55</volume><issue>4</issue><spage>271</spage><epage>274</epage><pages>271-274</pages><issn>0022-3050</issn><eissn>1468-330X</eissn><coden>JNNPAU</coden><abstract>The clinical course of intrinsic supratentorial tumours is variable. Prediction of outcome would be useful in defining patients for specific treatment policies. A retrospective analysis of 560 patients with intrinsic supratentorial tumours was performed. Proportional hazards models for survival were derived by using a stepwise selection procedure with only clinical and CT features as possible explanatory variables. The variables of prognostic importance were age, a first symptom of epilepsy, focal signs at presentation, a cystic lesion on CT scan, and duration of symptoms before presentation. The model defined a group with a good prognosis (score less than or equal to 9, n = 211) and a group with a poor prognosis (score greater than 9, n = 344). The median survival was 27 months for those with a score less than or equal to 9 or less and three months for those with score greater than 9. An alternative model, not including duration of symptoms, is also capable of defining groups with long (score less than or equal to 16, n = 234) and short (score greater than 16, n = 325) survival. The model may provide a means of classifying patients for inclusion in prospective randomised studies.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd</pub><pmid>1583511</pmid><doi>10.1136/jnnp.55.4.271</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actuarial Analysis Adult Aged Biological and medical sciences Epilepsy - etiology Female Humans Male Medical sciences Middle Aged Neurologic Examination Neurology Prospective Studies Severity of Illness Index Supratentorial Neoplasms - complications Supratentorial Neoplasms - diagnosis Supratentorial Neoplasms - mortality Survival Rate Tomography, X-Ray Computed Tumors of the nervous system. Phacomatoses |
title | Development of prognostic index for primary supratentorial intracerebral tumours |
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