Evidence map›Paper›PMID 36294385›Full record

ArticleJournal of clinical medicine2022

A Head-to-Head Comparison of

Ana María Garcia Vicente, Julián Pérez-Beteta, Mariano Amo-Salas, Jesús J Bosque, Edel Noriega-Álvarez, Ángel María Soriano Castrejon, Víctor M Pérez-García

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Auxiliary Value of [Cancers · 2025
    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

7 authors at 2 institutions in 1 country.

Ana María Garcia VicenteNuclear Medicine Department, University General Hospital, 13005 Ciudad Real, Spain.
Julián Pérez-BetetaMathematical Oncology Laboratory (MOLAB), Department of Mathematics, Faculty of Medicine, Castilla-La Mancha University, 13005 Ciudad Real, Spain.ORCID 0000-0003-0317-6215
Mariano Amo-SalasDepartment of Mathematics, Faculty of Medicine, Castilla-La Mancha University, 13005 Ciudad Real, Spain.ORCID 0000-0002-0956-2531
Jesús J BosqueMathematical Oncology Laboratory (MOLAB), Department of Mathematics, Faculty of Medicine, Castilla-La Mancha University, 13005 Ciudad Real, Spain.
Edel Noriega-ÁlvarezNuclear Medicine Department, University General Hospital, 13005 Ciudad Real, Spain.ORCID 0000-0002-2725-8920
Ángel María Soriano CastrejonNuclear Medicine Department, University General Hospital, 13005 Ciudad Real, Spain.
Víctor M Pérez-GarcíaMathematical Oncology Laboratory (MOLAB), Department of Mathematics, Faculty of Medicine, Castilla-La Mancha University, 13005 Ciudad Real, Spain.ORCID 0000-0002-6575-495X
University of Castilla-La Mancha · ESHospital General Universitario de Ciudad Real · ES

Funding

Ministry of Economy, Industry and Competitiveness MTM2015-71200-RRegional Government of Castile-La Mancha SBPLY/17/180501/000154
6 · The paper itself

Abstract

(1) Aim: To study the associations between imaging parameters derived from contrast-enhanced MRI (CE-MRI) and 18F-fluorocholine PET/CT and their performance as prognostic predictors in isocitrate dehydrogenase wild-type (IDH-wt) high-grade gliomas. (2) Methods: A prospective, multicenter study (FuMeGA: Functional and Metabolic Glioma Analysis) including patients with baseline CE-MRI and 18F-fluorocholine PET/CT and IDH wild-type high-grade gliomas. Clinical variables such as performance status, extent of surgery and adjuvant treatments (Stupp protocol vs others) were obtained and used to discriminate overall survival (OS) and progression-free survival (PFS) as end points. Multilesionality was assessed on the visual analysis of PET/CT and CE-MRI images. After tumor segmentation, standardized uptake value (SUV)-based variables for PET/CT and volume-based and geometrical variables for PET/CT and CE-MRI were calculated. The relationships among imaging techniques variables and their association with prognosis were evaluated using Pearson’s chi-square test and the t-test. Receiver operator characteristic, Kaplan−Meier and Cox regression were used for the survival analysis. (3) Results: 54 patients were assessed. The median PFS and OS were 5 and 11 months, respectively. Significant strong relationships between volume-dependent variables obtained from PET/CT and CE-MRI were found (r > 0.750, p < 0.05). For OS, significant associations were found with SUVmax, SUVpeak, SUVmean and sphericity (HR: 1.17, p = 0.035; HR: 1.24, p = 0.042; HR: 1.62, p = 0.040 and HR: 0.8, p = 0.022, respectively). Among clinical variables, only Stupp protocol and age showed significant associations with OS and PFS. No CE-MRI derived variables showed significant association with prognosis. In multivariate analysis, age (HR: 1.04, p = 0.002), Stupp protocol (HR: 2.81, p = 0.001), multilesionality (HR: 2.20, p = 0.013) and sphericity (HR: 0.79, p = 0.027) derived from PET/CT showed independent associations with OS. For PFS, only age (HR: 1.03, p = 0.021) and treatment protocol (HR: 2.20, p = 0.008) were significant predictors. (4) Conclusions: 18F-fluorocholine PET/CT metabolic and radiomic variables were robust prognostic predictors in patients with IDH-wt high-grade gliomas, outperforming CE-MRI derived variables.

Indexed as

18F-Fluorocholine PET/CTcontrast enhanced-MRIIDH wild-type gliomamultiple gliomaprognosisSUVpeak to centroid distance

Identifiers

PMID36294385
PMCPMC9605635
OpenAlexW4306385328

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.