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The international diffuse intrinsic pontine glioma registry: an infrastructure to accelerate collaborative research for an orphan disease.

Identifieur interne : 004168 ( Ncbi/Merge ); précédent : 004167; suivant : 004169

The international diffuse intrinsic pontine glioma registry: an infrastructure to accelerate collaborative research for an orphan disease.

Auteurs : Joshua Baugh [États-Unis] ; Ute Bartels [Canada] ; James Leach [États-Unis] ; Blaise Jones [États-Unis] ; Brooklyn Chaney [États-Unis] ; Katherine E. Warren [États-Unis] ; Jenavieve Kirkendall [États-Unis] ; Renee Doughman [États-Unis] ; Cynthia Hawkins [Canada] ; Lili Miles [États-Unis] ; Christine Fuller [États-Unis] ; Tim Hassall [Australie] ; Eric Bouffet [Canada] ; Adam Lane [États-Unis] ; Darren Hargrave [Royaume-Uni] ; Jacques Grill [France] ; Lindsey M. Hoffman [États-Unis] ; Chris Jones [Royaume-Uni] ; Alex Towbin [États-Unis] ; Sharon A. Savage [États-Unis] ; Michelle Monje [États-Unis] ; Xiao-Nan Li [États-Unis] ; David S. Ziegler [Australie] ; Sophie Veldhuijzen Van Zanten [Pays-Bas] ; Christof M. Kramm [Allemagne] ; Dannis G. Van Vuurden [Pays-Bas] ; Maryam Fouladi [États-Unis]

Source :

RBID : pubmed:28093680

Abstract

Diffuse intrinsic pontine glioma (DIPG), a rare, often fatal childhood brain tumor, remains a major therapeutic challenge. In 2012, investigators, funded by the DIPG Collaborative (a philanthropic partnership among 29 private foundations), launched the International DIPG Registry (IDIPGR) to advance understanding of DIPG. Comprised of comprehensive deidentified but linked clinical, imaging, histopathological, and genomic repositories, the IDIPGR uses standardized case report forms for uniform data collection; serial imaging and histopathology are centrally reviewed by IDIPGR neuro-radiologists and neuro-pathologists, respectively. Tissue and genomic data, and cell cultures derived from autopsies coordinated by the IDIPGR are available to investigators for studies approved by the Scientific Advisory Committee. From April 2012 to December 2016, 670 patients diagnosed with DIPG have been enrolled from 55 participating institutions in the US, Canada, Australia and New Zealand. The radiology repository contains 3558 studies from 448 patients. The pathology repository contains tissue on 81 patients with another 98 samples available for submission. Fresh DIPG tissue from seven autopsies has been sent to investigators to develop primary cell cultures. The bioinformatics repository contains next-generation sequencing data on 66 tumors. Nine projects using data/tissue from the IDIPGR by 13 principle investigators from around the world are now underway. The IDIPGR, a successful alliance among philanthropic agencies and investigators, has developed and maintained a highly collaborative, hypothesis-driven research infrastructure for interdisciplinary and translational projects in DIPG to improve diagnosis, response assessment, treatment and outcome for patients.

DOI: 10.1007/s11060-017-2372-5
PubMed: 28093680

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<name sortKey="Fouladi, Maryam" sort="Fouladi, Maryam" uniqKey="Fouladi M" first="Maryam" last="Fouladi">Maryam Fouladi</name>
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<series>
<title level="j">Journal of neuro-oncology</title>
<idno type="eISSN">1573-7373</idno>
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<div type="abstract" xml:lang="en">Diffuse intrinsic pontine glioma (DIPG), a rare, often fatal childhood brain tumor, remains a major therapeutic challenge. In 2012, investigators, funded by the DIPG Collaborative (a philanthropic partnership among 29 private foundations), launched the International DIPG Registry (IDIPGR) to advance understanding of DIPG. Comprised of comprehensive deidentified but linked clinical, imaging, histopathological, and genomic repositories, the IDIPGR uses standardized case report forms for uniform data collection; serial imaging and histopathology are centrally reviewed by IDIPGR neuro-radiologists and neuro-pathologists, respectively. Tissue and genomic data, and cell cultures derived from autopsies coordinated by the IDIPGR are available to investigators for studies approved by the Scientific Advisory Committee. From April 2012 to December 2016, 670 patients diagnosed with DIPG have been enrolled from 55 participating institutions in the US, Canada, Australia and New Zealand. The radiology repository contains 3558 studies from 448 patients. The pathology repository contains tissue on 81 patients with another 98 samples available for submission. Fresh DIPG tissue from seven autopsies has been sent to investigators to develop primary cell cultures. The bioinformatics repository contains next-generation sequencing data on 66 tumors. Nine projects using data/tissue from the IDIPGR by 13 principle investigators from around the world are now underway. The IDIPGR, a successful alliance among philanthropic agencies and investigators, has developed and maintained a highly collaborative, hypothesis-driven research infrastructure for interdisciplinary and translational projects in DIPG to improve diagnosis, response assessment, treatment and outcome for patients.</div>
</front>
</TEI>
<pubmed>
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<PMID Version="1">28093680</PMID>
<DateCreated>
<Year>2017</Year>
<Month>01</Month>
<Day>17</Day>
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<DateRevised>
<Year>2017</Year>
<Month>10</Month>
<Day>30</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">1573-7373</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>132</Volume>
<Issue>2</Issue>
<PubDate>
<Year>2017</Year>
<Month>Apr</Month>
</PubDate>
</JournalIssue>
<Title>Journal of neuro-oncology</Title>
<ISOAbbreviation>J. Neurooncol.</ISOAbbreviation>
</Journal>
<ArticleTitle>The international diffuse intrinsic pontine glioma registry: an infrastructure to accelerate collaborative research for an orphan disease.</ArticleTitle>
<Pagination>
<MedlinePgn>323-331</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1007/s11060-017-2372-5</ELocationID>
<Abstract>
<AbstractText>Diffuse intrinsic pontine glioma (DIPG), a rare, often fatal childhood brain tumor, remains a major therapeutic challenge. In 2012, investigators, funded by the DIPG Collaborative (a philanthropic partnership among 29 private foundations), launched the International DIPG Registry (IDIPGR) to advance understanding of DIPG. Comprised of comprehensive deidentified but linked clinical, imaging, histopathological, and genomic repositories, the IDIPGR uses standardized case report forms for uniform data collection; serial imaging and histopathology are centrally reviewed by IDIPGR neuro-radiologists and neuro-pathologists, respectively. Tissue and genomic data, and cell cultures derived from autopsies coordinated by the IDIPGR are available to investigators for studies approved by the Scientific Advisory Committee. From April 2012 to December 2016, 670 patients diagnosed with DIPG have been enrolled from 55 participating institutions in the US, Canada, Australia and New Zealand. The radiology repository contains 3558 studies from 448 patients. The pathology repository contains tissue on 81 patients with another 98 samples available for submission. Fresh DIPG tissue from seven autopsies has been sent to investigators to develop primary cell cultures. The bioinformatics repository contains next-generation sequencing data on 66 tumors. Nine projects using data/tissue from the IDIPGR by 13 principle investigators from around the world are now underway. The IDIPGR, a successful alliance among philanthropic agencies and investigators, has developed and maintained a highly collaborative, hypothesis-driven research infrastructure for interdisciplinary and translational projects in DIPG to improve diagnosis, response assessment, treatment and outcome for patients.</AbstractText>
</Abstract>
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<LastName>Grill</LastName>
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<LastName>Savage</LastName>
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</AffiliationInfo>
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<LastName>Monje</LastName>
<ForeName>Michelle</ForeName>
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<Affiliation>Stanford University and Lucile Packard Children's Hospital, Palo Alto, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Li</LastName>
<ForeName>Xiao-Nan</ForeName>
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<Affiliation>Texas Children's Hospital, Houston, TX, USA.</Affiliation>
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<LastName>Ziegler</LastName>
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<Affiliation>Sydney Children's Hospital, Randwick, NSW, Australia.</Affiliation>
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<AffiliationInfo>
<Affiliation>Children's Cancer Institute, University of New South Wales, Kensington, Australia.</Affiliation>
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<LastName>Veldhuijzen van Zanten</LastName>
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<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">Brain tumor</Keyword>
<Keyword MajorTopicYN="N">Diffuse intrinsic pontine glioma</Keyword>
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