Evidence map›Paper›PMID 30346623›Full record

ArticleNeuro-oncology2019

Multimodal imaging-defined subregions in newly diagnosed glioblastoma: impact on overall survival.

Flóra John, Edit Bosnyák, Natasha L Robinette, Alit J Amit-Yousif, Geoffrey R Barger, Keval D Shah, Sharon K Michelhaugh, Neil V Klinger, Sandeep Mittal, Csaba Juhász

Registry-linked trialAbstract read
In one paragraph

Article in Neuro-oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02367469 (Tryptophan Metabolism in Human Brain Tumors), which is not on this map. Cited by 33 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 3 pooled it
–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.

NCT02367469 completednot on this map

Tryptophan Metabolism in Human Brain Tumors

TypeobservationalSponsorWayne State UniversityRan2014 to 2021Enrolled105ConditionsBrain Tumors
3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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  14. Exploring the association of glioma tumor residuals from incongruent [European journal of nuclear medicine and molecular imaging · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Flóra JohnDepartment of Pediatrics, Wayne State University, Detroit, Michigan.
Edit BosnyákDepartment of Pediatrics, Wayne State University, Detroit, Michigan.
Natasha L RobinetteDepartment of Oncology, Wayne State University, Detroit, Michigan.
Alit J Amit-YousifDepartment of Oncology, Wayne State University, Detroit, Michigan.
Geoffrey R BargerDepartment of Neurology, Wayne State University, Detroit, Michigan.
Keval D ShahDepartment of Neurology, Wayne State University, Detroit, Michigan.
Sharon K MichelhaughDepartment of Neurosurgery, Wayne State University, Detroit, Michigan.
Neil V Klinger
Sandeep MittalDepartment of Neurosurgery, Wayne State University, Detroit, Michigan.
Csaba JuhászDepartment of Pediatrics, Wayne State University, Detroit, Michigan.

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI PAUL M STEMMER · 1985 to 2026
$68.4M
Tryptophan Metabolism in Human Brain TumorsR01CA123451 · NCI · WAYNE STATE UNIVERSITY · PI JUHASZ, CSABA, MITTAL, SANDEEP · 2008 to 2018
$3.1M
NCI NIH HHS P30 CA022453NCI NIH HHS R01 CA123451
6 · The paper itself

Abstract

backgroundAlthough glioblastomas are heterogeneous brain-infiltrating tumors, their treatment is mostly focused on the contrast-enhancing tumor mass. In this study, we combined conventional MRI, diffusion-weighted imaging (DWI), and amino acid PET to explore imaging-defined glioblastoma subregions and evaluate their potential prognostic value.

methodsContrast-enhanced T1, T2/fluid attenuated inversion recovery (FLAIR) MR images, apparent diffusion coefficient (ADC) maps from DWI, and alpha-[11C]-methyl-L-tryptophan (AMT)-PET images were analyzed in 30 patients with newly diagnosed glioblastoma. Five tumor subregions were identified based on a combination of MRI contrast enhancement, T2/FLAIR signal abnormalities, and AMT uptake on PET. ADC and AMT uptake tumor/contralateral normal cortex (T/N) ratios in these tumor subregions were correlated, and their prognostic value was determined.

resultsA total of 115 MRI/PET-defined subregions were analyzed. Most tumors showed not only a high-AMT uptake (T/N ratio > 1.65, N = 27) but also a low-uptake subregion (N = 21) within the contrast-enhancing tumor mass. High AMT uptake extending beyond contrast enhancement was also common (N = 25) and was associated with low ADC (r = -0.40, P = 0.05). Higher AMT uptake in the contrast-enhancing tumor subregions was strongly prognostic for overall survival (hazard ratio: 7.83; 95% CI: 1.98-31.02, P = 0.003), independent of clinical and molecular genetic prognostic variables. Nonresected high-AMT uptake subregions predicted the sites of tumor progression on posttreatment PET performed in 10 patients.

conclusionsGlioblastomas show heterogeneous amino acid uptake with high-uptake regions often extending into non-enhancing brain with high cellularity; nonresection of these predict the site of posttreatment progression. High tryptophan uptake values in MRI contrast-enhancing tumor subregions are a strong, independent imaging marker for longer overall survival.

Indexed as

Diffusion Magnetic Resonance ImagingDisease ProgressionFemaleFollow-Up StudiesGlioblastomaHumansMaleMiddle AgedMultimodal ImagingNeoplasm Recurrence, LocalPositron-Emission TomographyPrognosisSurvival RateTryptophanTryptophanamino aciddiffusion-weighted imagingglioblastomapositron emission tomographysurvival

Identifiers

PMID30346623
PMCPMC6374760

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Registered trials

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.