Evidence map›Paper›PMID 35287168›Full record

ReviewNeuro-oncology2022

Opportunities and challenges for the development of "core outcome sets" in neuro-oncology.

Christopher P Millward, Terri S Armstrong, Heather Barrington, Andrew R Brodbelt, Helen Bulbeck, Anthony Byrne, Linda Dirven, Carrol Gamble, Paul L Grundy, Abdurrahman I Islim and 20 more

Open access · hybridAbstract readReview
In one paragraph

Review in Neuro-oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
7.1field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 18 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors at 17 institutions in 7 countries.

Christopher P MillwardInstitute of Systems, Molecular, & Integrative Biology, University of Liverpool, Liverpool, UK.ORCID 0000-0001-7727-1157
Terri S ArmstrongNeuro-Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA.
Heather BarringtonInstitute of Population Health, University of Liverpool, Liverpool, UK.
Andrew R BrodbeltInstitute of Systems, Molecular, & Integrative Biology, University of Liverpool, Liverpool, UK.
Helen BulbeckBrainstrust-The Brain Cancer People, Cowes, UK.
Anthony ByrneDepartment of Palliative Care, Cardiff and Vale UHB, Cardiff, UK.
Linda DirvenDepartment of Neurology, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0001-9157-9895
Carrol GambleInstitute of Population Health, University of Liverpool, Liverpool, UK.
Paul L GrundyDepartment of Neurosurgery, University Hospital Southampton, Southampton, UK.
Abdurrahman I IslimInstitute of Systems, Molecular, & Integrative Biology, University of Liverpool, Liverpool, UK.
Mohsen JavadpourNational Centre for Neurosurgery, Beaumont Hospital, Dublin, Ireland.
Sumirat M KeshwaraInstitute of Systems, Molecular, & Integrative Biology, University of Liverpool, Liverpool, UK.
Sandhya T KrishnaDepartment of Neurosurgery. Alder Hey Children's NHS Foundation Trust, Liverpool, UK.
Conor L MallucciDepartment of Neurosurgery. Alder Hey Children's NHS Foundation Trust, Liverpool, UK.ORCID 0000-0002-5509-0547
Anthony G MarsonDepartment of Neurology, The Walton Centre NHS Foundation Trust, Liverpool, UK.
Michael W McDermottDivision of Neuroscience, Florida International University, Florida, USA.
Torstein R MelingDepartment of Neurosurgery, Geneva University Hospital, Geneva, Switzerland.
Kathy OliverInternational Brain Tumour Alliance, Surrey, UK.
Barry PizerInstitute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.
Puneet PlahaNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.
Matthias PreusserDivision of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.ORCID 0000-0003-3541-2315
Thomas SantariusDepartment of Neurosurgery, Addenbrooke's Hospital & University of Cambridge, Cambridge, UK.
Nisaharan SrikandarajahInstitute of Systems, Molecular, & Integrative Biology, University of Liverpool, Liverpool, UK.
Martin J B TaphoornDepartment of Neurology, Leiden University Medical Center, Leiden, the Netherlands.
Colin WattsInstitute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.
Michael WellerDepartment of Neurology, University Hospital and University of Zurich, Zürich, Switzerland.ORCID 0000-0002-1748-174X
Paula R WilliamsonInstitute of Population Health, University of Liverpool, Liverpool, UK.
Gelareh ZadehDepartment of Surgery, University of Toronto, Toronto, Canada.ORCID 0000-0002-6637-4502
Amir H Zamanipoor NajafabadiUniversity Neurosurgical Center Holland, Leiden University Medical Centre, Haaglanden Medical Center, Haga Teaching Hospitals, Leiden and The Hague, the Netherlands.
Michael D JenkinsonInstitute of Systems, Molecular, & Integrative Biology, University of Liverpool, Liverpool, UK.
University of Liverpool · GBAlder Hey Children's NHS Foundation Trust · GBLeiden University Medical Center · NLBeaumont Hospital · IEBrain Tumour Charity · GBCardiff and Vale University Health Board · GBFlorida International University · USLeiden University · NLMedical University of Vienna · ATNational Cancer Institute · USUniversity Hospital of Geneva · CHUniversity Hospital Southampton NHS Foundation Trust · GBUniversity of Birmingham · GBUniversity of Cambridge · GBUniversity of Oxford · GBUniversity of Toronto · CAUniversity of Zurich · CH

Funding

Natural History and Specimen Banking for Patients with CNS TumorsZIABC011768 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ARMSTRONG, TERRI S. · 2017 to 2024
$6.7M
Marie Curie MCCC-FCO-11-C
6 · The paper itself

Abstract

Core Outcome Sets (COS) define minimum outcomes to be measured and reported in clinical effectiveness trials for a particular health condition/health area. Despite recognition as critical to clinical research design for other health areas, none have been developed for neuro-oncology. COS development projects should carefully consider: scope (how the COS should be used), stakeholders involved in development (including patients as both research partners and participants), and consensus methodologies used (typically a Delphi survey and consensus meeting), as well as dissemination plans. Developing COS for neuro-oncology is potentially challenging due to extensive tumor subclassification (including molecular stratification), different symptoms related to anatomical tumor location, and variation in treatment options. Development of a COS specific to tumor subtype, in a specific location, for a particular intervention may be too narrow and would be unlikely to be used. Equally, a COS that is applicable across a wider area of neuro-oncology may be too broad and therefore lack specificity. This review describes why and how a COS may be developed, and discusses challenges for their development, specific to neuro-oncology. The COS under development are briefly described, including: adult glioma, incidental/untreated meningioma, meningioma requiring intervention, and adverse events from surgical intervention for pediatric brain tumors.

Indexed as

Meningeal NeoplasmsMeningiomaAdultChildConsensusDelphi TechniqueHumansResearch DesignTreatment Outcomeclinical trialcore outcome seteffectivenessgliomameningioma

Identifiers

PMID35287168
PMCPMC9248398
OpenAlexW4220994793

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.