Evidence map›Paper›PMID 32410409›Full record

ArticleKorean journal of radiology2020

Prognostic Value of Dynamic Contrast-Enhanced MRI-Derived Pharmacokinetic Variables in Glioblastoma Patients: Analysis of Contrast-Enhancing Lesions and Non-Enhancing T2 High-Signal Intensity Lesions.

Yeonah Kang, Eun Kyoung Hong, Jung Hyo Rhim, Roh Eul Yoo, Koung Mi Kang, Tae Jin Yun, Ji Hoon Kim, Chul Ho Sohn, Sun Won Park, Seung Hong Choi

Open access · hybridAbstract read
In one paragraph

Article in Korean journal of radiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 8 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

10 authors at 1 institution in 1 country.

Yeonah KangDepartment of Radiology, Haeundae Paik Hospital, Inje University College of Medicine, Busan, Korea.ORCID 0000-0002-5078-3213
Eun Kyoung HongDepartment of Radiology, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0002-5440-0451
Jung Hyo RhimDepartment of Radiology, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, Korea.ORCID 0000-0001-5822-9770
Roh Eul YooDepartment of Radiology, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0002-5625-5921
Koung Mi KangDepartment of Radiology, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0001-9643-2008
Tae Jin YunDepartment of Radiology, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0001-8441-4574
Ji Hoon KimDepartment of Radiology, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0002-6349-6950
Chul Ho SohnDepartment of Radiology, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0003-0039-5746
Sun Won Park *Department of Radiology, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, Korea.ORCID 0000-0002-5063-2685
Seung Hong Choi *Department of Radiology, Seoul National University Hospital, Seoul, Korea.ORCID 0000-0002-0412-2270
Seoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate pharmacokinetic variables from contrast-enhancing lesions (CELs) and non-enhancing T2 high signal intensity lesions (NE-T2HSILs) on dynamic contrast-enhanced (DCE) magnetic resonance (MR) imaging for predicting progression-free survival (PFS) in glioblastoma (GBM) patients. MATERIALS AND

methodsSixty-four GBM patients who had undergone preoperative DCE MR imaging and received standard treatment were retrospectively included. We analyzed the pharmacokinetic variables of the volume transfer constant (Ktrans) and volume fraction of extravascular extracellular space within the CEL and NE-T2HSIL of the entire tumor. Univariate and multivariate Cox regression analyses were performed using preoperative clinical characteristics, pharmacokinetic variables of DCE MR imaging, and postoperative molecular biomarkers to predict PFS.

resultsThe increased mean Ktrans of the CEL, increased 95th percentile Ktrans of the CELs, and absence of methylated O⁶-methylguanine-DNA methyltransferase promoter were relevant adverse variables for PFS in the univariate analysis (

conclusionAmong the pharmacokinetic variables extracted from CELs and NE-T2HSILs on preoperative DCE MR imaging, the mean Ktrans of CELs exhibits potential as a useful imaging predictor of PFS in GBM patients.

Indexed as

Magnetic Resonance ImagingAdultAgedBrain NeoplasmsContrast MediaFemaleGlioblastomaHumansImage Processing, Computer-AssistedKaplan-Meier EstimateMaleMiddle AgedPreoperative CarePrognosisProgression-Free SurvivalProportional Hazards ModelsContrast MediaDynamic contrast-enhanced MR imagingGlioblastoma multiformeParameter imagingPreoperative analysisPrognosis prediction

Identifiers

PMID32410409
PMCPMC7231611
OpenAlexW3021992682

What OpenQuestion holds

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LicenceCC BY-NC
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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.