Evidence map›Paper›PMID 29705034›Full record

ArticleJournal of magnetic resonance (San Diego, Calif. : 1997)2018

Preclinical MRI: Studies of the irradiated brain.

Joel R Garbow, Christina I Tsien, Scott C Beeman

Open access · greenAbstract read
In one paragraph

Article in Journal of magnetic resonance (San Diego, Calif. : 1997), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 49% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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

3 authors at 2 institutions in 1 country.

Joel R GarbowDepartment of Radiology, Washington University, Saint Louis, MO, United States; The Alvin J. Siteman Cancer Center, Washington University, Saint Louis, MO, United States. Electronic address: garbow@wustl.edu.
Christina I TsienDepartment of Radiation Oncology, Washington University, Saint Louis, MO, United States.
Scott C BeemanDepartment of Radiology, Washington University, Saint Louis, MO, United States.
Washington University in St. Louis · USAlvin J. Siteman Cancer Center

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI AIMEE S JAMES · 2001 to 2026
$128.0M
IMAGING BIOMARKERS FOR RADIATION-INDUCED NECROSISR01CA155365 · NCI · WASHINGTON UNIVERSITY · PI GARBOW, JOEL RICHARD · 2011 to 2015
$1.5M
MR ADIPOSE-O2 QUANTIFICATION AND THE HYPOXIA-DRIVEN INSULIN RESISTANCE HYPOTHESISK01DK109119 · NIDDK · WASHINGTON UNIVERSITY · PI BEEMAN, SCOTT CHARLES · 2016 to 2020
$652k
NCI NIH HHS P30 CA091842NCI NIH HHS R01 CA155365NIDDK NIH HHS K01 DK109119
6 · The paper itself

Abstract

Radiation therapy (RT) plays a central role in the treatment of primary brain tumors. However, despite recent advances in RT treatment, local recurrences following therapy remain common. Radiation necrosis (RN) is a severe, late complication of radiation therapy in the brain. RN is a serious clinical problem often associated with devastating neurologic complications. Therapeutic strategies, including neuroprotectants, have been described, but have not been widely translated in routine clinical use. We have developed a mouse model that recapitulates all of the major pathologic features of late-onset RN for the purposes of characterizing the basic pathogenesis of RN, identifying non-invasive (imaging) biomarkers of RN that might allow for the radiologic discernment of tumor and RN, systematic testing of tumor and RN therapeutics, and exploring the complex interplay between RN pathogenesis and tumor recurrence. Herein, we describe the fundamental clinical challenges associated with RN and the progress made towards addressing these challenges by combining our novel mouse model of late-onset RN and magnetic resonance imaging (MRI). MRI techniques discussed include conventional T1- and T2-weighted imaging, diffusion-weighted imaging, magnetization transfer, and measures of tissue oxygenation. Studies of RN mitigation and neuroprotection are described, including the use of anti-VEGF antibodies, and inhibitors of GSK-3β, HIF-1α, and CXCR4. We conclude with some future perspectives on the irradiated brain and the study and treatment of recurrent tumor growing in an irradiated tumor microenvironment.

Indexed as

AnimalsAntibodies, BlockingBiomarkersBrainBrain NeoplasmsHumansImage Processing, Computer-AssistedMagnetic Resonance ImagingMiceNecrosisNeoplasm Recurrence, LocalNerve Tissue ProteinsNeuroprotective AgentsRadiation Injuries, ExperimentalRadiation-Protective AgentsRadiotherapyAntibodies, BlockingBiomarkersNerve Tissue ProteinsNeuroprotective AgentsRadiation-Protective AgentsMagnetic resonance imagingRadiated brainRadiation necrosis

Identifiers

PMID29705034
PMCPMC6029718
OpenAlexW2802775515

What OpenQuestion holds

Textmetadata
LicenceTDM
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.