Evidence map›Paper›PMID 33192972›Full record

ReviewFrontiers in neurology2020

Genomic Profiling of Circulating Tumor DNA From Cerebrospinal Fluid to Guide Clinical Decision Making for Patients With Primary and Metastatic Brain Tumors.

Lori A Ramkissoon, Worthy Pegram, James Haberberger, Natalie Danziger, Glenn Lesser, Roy Strowd, Sonika Dahiya, Thomas J Cummings, Wenya Linda Bi, Malak Abedalthagafi and 17 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Guideline
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  16. Prognostic value of plasma circulating tumor DNA fraction across four common cancer types: a real-world outcomes study.Annals of oncology : official journal of the European Society for Medical Oncology · 2023
    Article
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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

27 authors at 8 institutions in 2 countries.

Lori A RamkissoonDepartment of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Worthy PegramFoundation Medicine, Inc., Morrisville, NC, United States.
James HaberbergerFoundation Medicine, Inc., Morrisville, NC, United States.
Natalie DanzigerFoundation Medicine, Inc., Cambridge, MA, United States.
Glenn LesserSection of Medical Oncology and Hematology, Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC, United States.
Roy StrowdSection of Medical Oncology and Hematology, Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC, United States.
Sonika DahiyaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MI, United States.
Thomas J CummingsDepartment of Pathology, Duke University Medical Center, Durham, NC, United States.
Wenya Linda BiDepartment of Neurosurgery, Brigham and Women's Hospital, Boston, MA, United States.
Malak AbedalthagafiGenomics Research Department, Saudi Human Genome Project, King Fahad Medical City and King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Pratheesh SathyanFoundation Medicine, Inc., Cambridge, MA, United States.
Kimberly McGregorFoundation Medicine, Inc., Cambridge, MA, United States.
Prasanth ReddyFoundation Medicine, Inc., Cambridge, MA, United States.
Eric SeversonFoundation Medicine, Inc., Morrisville, NC, United States.
Erik WilliamsFoundation Medicine, Inc., Morrisville, NC, United States.
Douglas LinFoundation Medicine, Inc., Cambridge, MA, United States.
Claire EdgerlyFoundation Medicine, Inc., Morrisville, NC, United States.
Richard S P HuangFoundation Medicine, Inc., Morrisville, NC, United States.
Amanda HemmerichFoundation Medicine, Inc., Morrisville, NC, United States.
James CreedenFoundation Medicine, Inc., Cambridge, MA, United States.
Charlotte BrownFoundation Medicine, Inc., Morrisville, NC, United States.
Jeffrey VenstromFoundation Medicine, Inc., Cambridge, MA, United States.
Priti HegdeFoundation Medicine, Inc., Cambridge, MA, United States.
Jeffrey S RossFoundation Medicine, Inc., Cambridge, MA, United States.
Brian M AlexanderFoundation Medicine, Inc., Cambridge, MA, United States.
Julia ElvinFoundation Medicine, Inc., Cambridge, MA, United States.
Shakti H RamkissoonFoundation Medicine, Inc., Morrisville, NC, United States.
Foundation Medicine (United States)Atrium Health Wake Forest Baptist · USBrigham and Women's Hospital · USDuke Medical Center · USKing Abdulaziz City for Science and Technology · SAUniversity of North Carolina at Chapel Hill · USWake Forest Baptist Comprehensive Cancer CenterWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite advances in systemic therapies for solid tumors, the development of brain metastases remains a significant contributor to overall cancer mortality and requires improved methods for diagnosing and treating these lesions. Similarly, the prognosis for malignant primary brain tumors remains poor with little improvement in overall survival over the last several decades. In both primary and metastatic central nervous system (CNS) tumors, the challenge from a clinical perspective centers on detecting CNS dissemination early and understanding how CNS lesions differ from the primary tumor, in order to determine potential treatment strategies. Acquiring tissue from CNS tumors has historically been accomplished through invasive neurosurgical procedures, which restricts the number of patients to those who can safely undergo a surgical procedure, and for which such interventions will add meaningful value to the care of the patient. In this review we discuss the potential of analyzing cell free DNA shed from tumor cells that is contained within the cerebrospinal fluid (CSF) as a sensitive and minimally invasive method to detect and characterize primary and metastatic tumors in the CNS.

Indexed as

brain tumorcirculating tumor DNA (ctDNA)CSF (cerebrospinal fluid)genomic profilingmetastatic disease

Identifiers

PMID33192972
PMCPMC7604477
OpenAlexW3093677865

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.