Evidence map›Paper›PMID 29931654›Full record

ReviewCurrent treatment options in oncology2018

Precision Neuro-oncology: the Role of Genomic Testing in the Management of Adult and Pediatric Gliomas.

Lori A Ramkissoon, Nicholas Britt, Alexander Guevara, Emily Whitt, Eric Severson, Pratheesh Sathyan, Laurie Gay, Julia Elvin, Jeffrey S Ross, Charlotte Brown and 6 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current treatment options in oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. The road-map for establishment of a prognostic molecular marker panel in glioma using liquid biopsy: current status and future directions.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  4. Article
  5. Article
  6. Article
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

16 authors.

Lori A RamkissoonUniversity of North Carolina School of Medicine, Chapel Hill, NC, USA.
Nicholas BrittFoundation Medicine, Inc, 7010 Kit Creek Road, Morrisville, NC, 27560, USA.
Alexander GuevaraFoundation Medicine, Inc, 7010 Kit Creek Road, Morrisville, NC, 27560, USA.
Emily WhittFoundation Medicine, Inc, 7010 Kit Creek Road, Morrisville, NC, 27560, USA.
Eric SeversonFoundation Medicine, Inc, 7010 Kit Creek Road, Morrisville, NC, 27560, USA.
Pratheesh SathyanFoundation Medicine, Inc, Cambridge, MA, USA.
Laurie GayFoundation Medicine, Inc, Cambridge, MA, USA.
Julia ElvinFoundation Medicine, Inc, Cambridge, MA, USA.
Jeffrey S RossFoundation Medicine, Inc, Cambridge, MA, USA.
Charlotte BrownFoundation Medicine, Inc, 7010 Kit Creek Road, Morrisville, NC, 27560, USA.
Kimberly Stogner-UnderwoodDepartment of Pathology, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Ryan MottDepartment of Pathology, Wake Forest School of Medicine, Winston-Salem, NC, USA.
David KramSection of Pediatric Hematology-Oncology, Department of Pediatrics, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Roy StrowdSection of Hematology-Oncology, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Glenn J LesserSection of Hematology-Oncology, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Shakti H RamkissoonFoundation Medicine, Inc, 7010 Kit Creek Road, Morrisville, NC, 27560, USA. sramkissoon@foundationmedicine.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

opinion statementIn recent years, large-scale genomic studies have expanded our knowledge regarding genomic drivers in tumors of the central nervous system. While histopathologic analysis of brain tumors remains the primary method for tumor classification, the clinical utility of molecular and genomic testing to support and/or complement tumor classification continues to expand. This approach enhances diagnostic accuracy and provides clinicians with objective data to facilitate discussions regarding prognosis and treatment decisions, including selection of clinical trials. Ensuring accurate diagnoses is fundamental to the management of brain tumor patients. However, given the morphologic overlap among primary brain tumors, genomic data can be used to help distinguish tumor lineage. In its clearest form, we have embraced the concept of an integrated diagnosis, which combines traditional histopathology findings with molecular and genomic data. Patient prognosis varies significantly based on a tumor's genomic profile. For neuro-oncology patients, outcome studies linking diagnoses with genomic profiles show significant differences based on tumor biomarkers such as IDH1/2, H3F3A, BRAF, and CDKN2A and TERT status. Therefore, easy access to reliable genomic data is important in understanding a patient's disease and developing a clinical strategy wherein targeted molecular or immune therapies can be incorporated into the discussion.

Indexed as

Precision MedicineAge FactorsBiomarkers, TumorBrain NeoplasmsClinical Trials as TopicCombined Modality TherapyDisease ManagementGenetic Predisposition to DiseaseGenetic TestingGenomicsGliomaHumansImmunotherapyMolecular Targeted TherapyNeoplasm GradingNeoplasm StagingBiomarkers, TumorComprehensive genomic profilingGliomaImmunotherapyTargeted therapy

Identifiers

What OpenQuestion holds

Textmetadata
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.