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The current consensus on the clinical management of intracranial ependymoma and its distinct molecular variants.

Identifieur interne : 000205 ( PubMed/Checkpoint ); précédent : 000204; suivant : 000206

The current consensus on the clinical management of intracranial ependymoma and its distinct molecular variants.

Auteurs : Kristian W. Pajtler [Allemagne] ; Stephen C. Mack [États-Unis] ; Vijay Ramaswamy [Canada] ; Christian A. Smith [Canada] ; Hendrik Witt [Allemagne] ; Amy Smith [États-Unis] ; Jordan R. Hansford [Australie] ; Katja Von Hoff [Allemagne] ; Karen D. Wright [États-Unis] ; Eugene Hwang [États-Unis] ; Didier Frappaz [France] ; Yonehiro Kanemura [Japon] ; Maura Massimino [Italie] ; Cécile Faure-Conter [France] ; Piergiorgio Modena [Italie] ; Uri Tabori [Canada] ; Katherine E. Warren [États-Unis] ; Eric C. Holland [États-Unis] ; Koichi Ichimura [Japon] ; Felice Giangaspero [Italie] ; David Castel [France] ; Andreas Von Deimling [Allemagne] ; Marcel Kool [Allemagne] ; Peter B. Dirks [Canada] ; Richard G. Grundy [Royaume-Uni] ; Nicholas K. Foreman [États-Unis] ; Amar Gajjar [États-Unis] ; Andrey Korshunov [Allemagne] ; Jonathan Finlay [États-Unis] ; Richard J. Gilbertson [Royaume-Uni] ; David W. Ellison [États-Unis] ; Kenneth D. Aldape [Canada] ; Thomas E. Merchant [États-Unis] ; Eric Bouffet [Canada] ; Stefan M. Pfister [Allemagne] ; Michael D. Taylor [Canada]

Source :

RBID : pubmed:27858204

Descripteurs français

English descriptors

Abstract

Multiple independent genomic profiling efforts have recently identified clinically and molecularly distinct subgroups of ependymoma arising from all three anatomic compartments of the central nervous system (supratentorial brain, posterior fossa, and spinal cord). These advances motivated a consensus meeting to discuss: (1) the utility of current histologic grading criteria, (2) the integration of molecular-based stratification schemes in future clinical trials for patients with ependymoma and (3) current therapy in the context of molecular subgroups. Discussion at the meeting generated a series of consensus statements and recommendations from the attendees, which comment on the prognostic evaluation and treatment decisions of patients with intracranial ependymoma (WHO Grade II/III) based on the knowledge of its molecular subgroups. The major consensus among attendees was reached that treatment decisions for ependymoma (outside of clinical trials) should not be based on grading (II vs III). Supratentorial and posterior fossa ependymomas are distinct diseases, although the impact on therapy is still evolving. Molecular subgrouping should be part of all clinical trials henceforth.

DOI: 10.1007/s00401-016-1643-0
PubMed: 27858204


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pubmed:27858204

Le document en format XML

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<nlm:affiliation>Department of Neuropathology, University of Heidelberg, Heidelberg, Germany.</nlm:affiliation>
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<nlm:affiliation>Li Ka Shing Centre, CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.</nlm:affiliation>
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<name sortKey="Ellison, David W" sort="Ellison, David W" uniqKey="Ellison D" first="David W" last="Ellison">David W. Ellison</name>
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<name sortKey="Aldape, Kenneth D" sort="Aldape, Kenneth D" uniqKey="Aldape K" first="Kenneth D" last="Aldape">Kenneth D. Aldape</name>
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<orgName type="university">Université de Toronto</orgName>
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<name sortKey="Merchant, Thomas E" sort="Merchant, Thomas E" uniqKey="Merchant T" first="Thomas E" last="Merchant">Thomas E. Merchant</name>
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<nlm:affiliation>Department of Radiological Sciences, St Jude Children's Research Hospital, Memphis, TN, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Radiological Sciences, St Jude Children's Research Hospital, Memphis, TN</wicri:regionArea>
<placeName>
<region type="state">Tennessee</region>
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<name sortKey="Bouffet, Eric" sort="Bouffet, Eric" uniqKey="Bouffet E" first="Eric" last="Bouffet">Eric Bouffet</name>
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<nlm:affiliation>Division of Hematology/Oncology, Hospital for Sick Children, Toronto, ON, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
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<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), Heidelberg</wicri:regionArea>
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<region type="land" nuts="1">Bade-Wurtemberg</region>
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<term>Ependymoma (therapy)</term>
<term>Humans</term>
<term>Neoplasm Staging</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Animaux</term>
<term>Consensus</term>
<term>Humains</term>
<term>Prise en charge de la maladie</term>
<term>Stade de la tumeur</term>
<term>Tumeurs du cerveau ()</term>
<term>Tumeurs du cerveau (anatomopathologie)</term>
<term>Tumeurs du cerveau (génétique)</term>
<term>Tumeurs du cerveau (métabolisme)</term>
<term>Épendymome ()</term>
<term>Épendymome (anatomopathologie)</term>
<term>Épendymome (génétique)</term>
<term>Épendymome (métabolisme)</term>
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<term>Tumeurs du cerveau</term>
<term>Épendymome</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Brain Neoplasms</term>
<term>Ependymoma</term>
</keywords>
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<term>Tumeurs du cerveau</term>
<term>Épendymome</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Brain Neoplasms</term>
<term>Ependymoma</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Tumeurs du cerveau</term>
<term>Épendymome</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Brain Neoplasms</term>
<term>Ependymoma</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en">
<term>Brain Neoplasms</term>
<term>Ependymoma</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Consensus</term>
<term>Disease Management</term>
<term>Humans</term>
<term>Neoplasm Staging</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Animaux</term>
<term>Consensus</term>
<term>Humains</term>
<term>Prise en charge de la maladie</term>
<term>Stade de la tumeur</term>
<term>Tumeurs du cerveau</term>
<term>Épendymome</term>
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<front>
<div type="abstract" xml:lang="en">Multiple independent genomic profiling efforts have recently identified clinically and molecularly distinct subgroups of ependymoma arising from all three anatomic compartments of the central nervous system (supratentorial brain, posterior fossa, and spinal cord). These advances motivated a consensus meeting to discuss: (1) the utility of current histologic grading criteria, (2) the integration of molecular-based stratification schemes in future clinical trials for patients with ependymoma and (3) current therapy in the context of molecular subgroups. Discussion at the meeting generated a series of consensus statements and recommendations from the attendees, which comment on the prognostic evaluation and treatment decisions of patients with intracranial ependymoma (WHO Grade II/III) based on the knowledge of its molecular subgroups. The major consensus among attendees was reached that treatment decisions for ependymoma (outside of clinical trials) should not be based on grading (II vs III). Supratentorial and posterior fossa ependymomas are distinct diseases, although the impact on therapy is still evolving. Molecular subgrouping should be part of all clinical trials henceforth.</div>
</front>
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<Year>2016</Year>
<Month>11</Month>
<Day>18</Day>
</DateCreated>
<DateCompleted>
<Year>2017</Year>
<Month>09</Month>
<Day>22</Day>
</DateCompleted>
<DateRevised>
<Year>2017</Year>
<Month>09</Month>
<Day>22</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1432-0533</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>133</Volume>
<Issue>1</Issue>
<PubDate>
<Year>2017</Year>
<Month>Jan</Month>
</PubDate>
</JournalIssue>
<Title>Acta neuropathologica</Title>
<ISOAbbreviation>Acta Neuropathol.</ISOAbbreviation>
</Journal>
<ArticleTitle>The current consensus on the clinical management of intracranial ependymoma and its distinct molecular variants.</ArticleTitle>
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<MedlinePgn>5-12</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1007/s00401-016-1643-0</ELocationID>
<Abstract>
<AbstractText>Multiple independent genomic profiling efforts have recently identified clinically and molecularly distinct subgroups of ependymoma arising from all three anatomic compartments of the central nervous system (supratentorial brain, posterior fossa, and spinal cord). These advances motivated a consensus meeting to discuss: (1) the utility of current histologic grading criteria, (2) the integration of molecular-based stratification schemes in future clinical trials for patients with ependymoma and (3) current therapy in the context of molecular subgroups. Discussion at the meeting generated a series of consensus statements and recommendations from the attendees, which comment on the prognostic evaluation and treatment decisions of patients with intracranial ependymoma (WHO Grade II/III) based on the knowledge of its molecular subgroups. The major consensus among attendees was reached that treatment decisions for ependymoma (outside of clinical trials) should not be based on grading (II vs III). Supratentorial and posterior fossa ependymomas are distinct diseases, although the impact on therapy is still evolving. Molecular subgrouping should be part of all clinical trials henceforth.</AbstractText>
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<LastName>Pajtler</LastName>
<ForeName>Kristian W</ForeName>
<Initials>KW</Initials>
<AffiliationInfo>
<Affiliation>Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), Heidelberg, Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Pediatric Oncology, Hematology and Immunology, University Hospital Heidelberg, Heidelberg, Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>German Cancer Consortium (DKTK), Heidelberg, Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Mack</LastName>
<ForeName>Stephen C</ForeName>
<Initials>SC</Initials>
<AffiliationInfo>
<Affiliation>Department of Stem Cell Biology and Regenerative Medicine, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Molecular Medicine, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, OH, USA.</Affiliation>
</AffiliationInfo>
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<LastName>Ramaswamy</LastName>
<ForeName>Vijay</ForeName>
<Initials>V</Initials>
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<Affiliation>Division of Neurosurgery, Arthur & Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, ON, Canada.</Affiliation>
</AffiliationInfo>
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<Affiliation>Division of Hematology/Oncology, Hospital for Sick Children, Toronto, ON, Canada.</Affiliation>
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<Affiliation>Division of Neurosurgery, Arthur & Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, ON, Canada.</Affiliation>
</AffiliationInfo>
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<LastName>Witt</LastName>
<ForeName>Hendrik</ForeName>
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<Affiliation>Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), Heidelberg, Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Pediatric Oncology, Hematology and Immunology, University Hospital Heidelberg, Heidelberg, Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>German Cancer Consortium (DKTK), Heidelberg, Germany.</Affiliation>
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<LastName>Smith</LastName>
<ForeName>Amy</ForeName>
<Initials>A</Initials>
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<Affiliation>Arnold Palmer Hospital, Orlando, FL, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Hansford</LastName>
<ForeName>Jordan R</ForeName>
<Initials>JR</Initials>
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<Affiliation>Royal Children's Hospital, Melbourne, VIC, Australia.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>von Hoff</LastName>
<ForeName>Katja</ForeName>
<Initials>K</Initials>
<AffiliationInfo>
<Affiliation>Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Wright</LastName>
<ForeName>Karen D</ForeName>
<Initials>KD</Initials>
<AffiliationInfo>
<Affiliation>Department of Oncology, St Jude Children's Research Hospital, Memphis, TN, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hwang</LastName>
<ForeName>Eugene</ForeName>
<Initials>E</Initials>
<AffiliationInfo>
<Affiliation>Center for Cancer and Blood Disorders, Children's National Medical Center, Washington, DC, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Frappaz</LastName>
<ForeName>Didier</ForeName>
<Initials>D</Initials>
<AffiliationInfo>
<Affiliation>Pediatric Neuro-Oncology Centre Léon Bérard, Lyon, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Kanemura</LastName>
<ForeName>Yonehiro</ForeName>
<Initials>Y</Initials>
<AffiliationInfo>
<Affiliation>Department of Neurosurgery and Institute for Clinical Research, Osaka National Hospital, Osaka, Japan.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Massimino</LastName>
<ForeName>Maura</ForeName>
<Initials>M</Initials>
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<Affiliation>Fondazione IRCCS-Istituto Nazionale dei Tumori, Milan, Italy.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Faure-Conter</LastName>
<ForeName>Cécile</ForeName>
<Initials>C</Initials>
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<Affiliation>Pediatric Neuro-Oncology Centre Léon Bérard, Lyon, France.</Affiliation>
</AffiliationInfo>
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<LastName>Modena</LastName>
<ForeName>Piergiorgio</ForeName>
<Initials>P</Initials>
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<Affiliation>Laboratory of Genetics, Pathology Unit, S. Anna General Hospital, Como, Italy.</Affiliation>
</AffiliationInfo>
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<LastName>Tabori</LastName>
<ForeName>Uri</ForeName>
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<LastName>Warren</LastName>
<ForeName>Katherine E</ForeName>
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<LastName>Holland</LastName>
<ForeName>Eric C</ForeName>
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<Affiliation>Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.</Affiliation>
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<LastName>Ichimura</LastName>
<ForeName>Koichi</ForeName>
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<Affiliation>Division of Brain Tumor Translational Research, National Cancer Center Research Institute, Tokyo, Japan.</Affiliation>
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<LastName>Giangaspero</LastName>
<ForeName>Felice</ForeName>
<Initials>F</Initials>
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<Affiliation>Department of Radiological Sciences, Oncology and Anatomical Pathology, Sapienza University, Rome, Italy.</Affiliation>
</AffiliationInfo>
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<LastName>Castel</LastName>
<ForeName>David</ForeName>
<Initials>D</Initials>
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</AffiliationInfo>
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<Affiliation>UMR8203 "Vectorologie and Thérapeutiques Anticancéreuses", CNRS, Gustave Roussy, Univ. Paris-Sud, Université Paris-Saclay, Villejuif, France.</Affiliation>
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<LastName>von Deimling</LastName>
<ForeName>Andreas</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Department of Neuropathology, University of Heidelberg, Heidelberg, Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Clinical Cooperation Unit Neuropathology, German Cancer Research Center (DKFZ), Heidelberg, Germany.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Kool</LastName>
<ForeName>Marcel</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), Heidelberg, Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>German Cancer Consortium (DKTK), Heidelberg, Germany.</Affiliation>
</AffiliationInfo>
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<Affiliation>Division of Neurosurgery, Arthur & Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, ON, Canada.</Affiliation>
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<LastName>Grundy</LastName>
<ForeName>Richard G</ForeName>
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<Affiliation>Children's Brain Tumour Research Centre, The Medical School, University of Nottingham, Nottingham, UK.</Affiliation>
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<LastName>Foreman</LastName>
<ForeName>Nicholas K</ForeName>
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<Affiliation>Department of Pediatrics, University of Colorado Denver, Aurora, CO, USA.</Affiliation>
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<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Department of Neuropathology, University of Heidelberg, Heidelberg, Germany.</Affiliation>
</AffiliationInfo>
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<Affiliation>Clinical Cooperation Unit Neuropathology, German Cancer Research Center (DKFZ), Heidelberg, Germany.</Affiliation>
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<LastName>Finlay</LastName>
<ForeName>Jonathan</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Nationwide Children's Hospital and the Ohio State University, Columbus, OH, USA.</Affiliation>
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<Author ValidYN="Y">
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<ForeName>Richard J</ForeName>
<Initials>RJ</Initials>
<AffiliationInfo>
<Affiliation>Li Ka Shing Centre, CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.</Affiliation>
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</Author>
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<LastName>Ellison</LastName>
<ForeName>David W</ForeName>
<Initials>DW</Initials>
<AffiliationInfo>
<Affiliation>Department of Pathology, St Jude Children's Research Hospital, Memphis, TN, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Aldape</LastName>
<ForeName>Kenneth D</ForeName>
<Initials>KD</Initials>
<AffiliationInfo>
<Affiliation>Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Merchant</LastName>
<ForeName>Thomas E</ForeName>
<Initials>TE</Initials>
<AffiliationInfo>
<Affiliation>Department of Radiological Sciences, St Jude Children's Research Hospital, Memphis, TN, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Bouffet</LastName>
<ForeName>Eric</ForeName>
<Initials>E</Initials>
<AffiliationInfo>
<Affiliation>Division of Hematology/Oncology, Hospital for Sick Children, Toronto, ON, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Pfister</LastName>
<ForeName>Stefan M</ForeName>
<Initials>SM</Initials>
<AffiliationInfo>
<Affiliation>Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), Heidelberg, Germany. s.pfister@dkfz.de.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Pediatric Oncology, Hematology and Immunology, University Hospital Heidelberg, Heidelberg, Germany. s.pfister@dkfz.de.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>German Cancer Consortium (DKTK), Heidelberg, Germany. s.pfister@dkfz.de.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Taylor</LastName>
<ForeName>Michael D</ForeName>
<Initials>MD</Initials>
<AffiliationInfo>
<Affiliation>Division of Neurosurgery, Arthur & Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, ON, Canada. mdtaylor@sickkids.ca.</Affiliation>
</AffiliationInfo>
</Author>
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<Language>eng</Language>
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<GrantID>P01 CA096832</GrantID>
<Acronym>CA</Acronym>
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