Evidence map›Paper›PMID 22169956›Full record

ArticleJournal of neuro-oncology2012

Independent prognostic value of pre-treatment 18-FDG-PET in high-grade gliomas.

Cécile Colavolpe, Philippe Metellus, Julien Mancini, Maryline Barrie, Céline Béquet-Boucard, Dominique Figarella-Branger, Olivier Mundler, Olivier Chinot, Eric Guedj

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In one paragraph

Article in Journal of neuro-oncology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 19% 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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it, 51 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Imaging in Neuro-oncology.Seminars in neurology · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Radiomics in Oncological PET/CT: Clinical Applications.Nuclear medicine and molecular imaging · 2018
    Review
  12. IDH mutation is paradoxically associated with higherEuropean journal of nuclear medicine and molecular imaging · 2017
    Article
  13. Hypoxic glucose metabolism in glioblastoma as a potential prognostic factor.European journal of nuclear medicine and molecular imaging · 2017
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Quantifying tumour heterogeneity in 18F-FDG PET/CT imaging by texture analysis.European journal of nuclear medicine and molecular imaging · 2013
    Review
  20. 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

9 authors at 3 institutions in 1 country.

Cécile ColavolpeAPHM, Hôpital de la Timone, Service Central de Biophysique et Médecine Nucléaire, 13005 Marseille, France.
Philippe Metellus
Julien Mancini
Maryline Barrie
Céline Béquet-Boucard
Dominique Figarella-Branger
Olivier Mundler
Olivier Chinot
Eric Guedj
Hôpital de la Timone · FRAix-Marseille Université · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prognostic value of PET with (18F)-fluoro-2-deoxy-D: -glucose (FDG) has been shown in high-grade gliomas (HGG), but not compared with consensual prognostic factors. We sought to evaluate the independent predictive value of pre-treatment FDG-PET on overall (OS) and event-free survival (EFS). We retrospectively analyzed 41 patients with histologically-confirmed HGG (31 glioblastomas and 10 anaplastic gliomas). The pre-treatment uptake of FDG was assessed qualitatively by five-step visual metabolic grading, and quantitatively by the ratio between the tumor and contralateral maximal standardized uptake value (T/CL). EFS and OS following PET were compared with FDG uptake by univariate analysis, and by two multivariate analyses: one including main consensual prognostic factors (age, KPS, extent of surgery and histological grade), and the other including the classification system of the Radiation Therapy Oncology Group (Recursive Partitioning Analysis, RPA). Median OS and EFS were 13.8 and 7.4 months, respectively, for glioblastomas, and over 25.8 and 12 months, respectively, for anaplastic gliomas (P = 0.040 and P = 0.027). The T/CL ratio predicted OS in the entire group [P = 0.003; Hazard Ratio (HR) = 2.3] and in the glioblastoma subgroup (P = 0.018; HR = 2), independently of age, Karnofsky performance status, histological grade, and surgery, and independently of RPA classification. T/CL ratio tended to predict EFS in the whole group (P = 0.052). The prognostic value of visual metabolic grade on OS was less significant than T/CL ratio, both in the entire group and in the glioblastoma subgroup (P = 0.077 and P = 0.059). Quantitative evaluation of the ratio between the maximal tumor and contralateral uptake in pre-treatment FDG-PET provides significant additional prognostic information in newly-diagnosed HGG, independently of consensual prognostic factors.

Indexed as

Fluorodeoxyglucose F18RadiopharmaceuticalsAdultBrain NeoplasmsDisease-Free SurvivalFemaleGliomaHumansKaplan-Meier EstimateMaleMiddle AgedNeoplasm GradingPositron-Emission TomographyPredictive Value of TestsPrognosisRetrospective StudiesFluorodeoxyglucose F18Radiopharmaceuticals

Identifiers

PMID22169956
OpenAlexW2062603316

What OpenQuestion holds

Textmetadata
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.