Evidence map›Paper›PMID 30847823›Full record

ArticleMolecular imaging and biology2019

Pre-Therapeutic Total Lesion Glycolysis on [

Marius E Mayerhoefer, Anton Staudenherz, Barbara Kiesewetter, Michael Weber, Ingrid Simonitsch-Klupp, Peter Gibbs, Werner Dolak, Julius Lukas, Markus Raderer

Open access · hybridAbstract read
In one paragraph

Article in Molecular imaging and biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Is There a Role for [Cancers · 2022
    Article
  4. Article
  5. Article
  6. Review
  7. MRI and PET/MRI in hematologic malignancies.Journal of magnetic resonance imaging : JMRI · 2020
    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

9 authors at 2 institutions in 2 countries.

Marius E MayerhoeferDepartment of Biomedical Imaging and Image-guided Therapy, Division of General and Pediatric Radiology, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria. marius.mayerhoefer@meduniwien.ac.at.ORCID http://orcid.org/0000-0001-8786-8686
Anton StaudenherzDepartment of Biomedical Imaging and Image-guided Therapy, Division of Nuclear Medicine, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Barbara KiesewetterDepartment of Medicine I, Medical University of Vienna, Vienna, Austria.
Michael WeberDepartment of Biomedical Imaging and Image-guided Therapy, Division of General and Pediatric Radiology, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Ingrid Simonitsch-KluppInstitute of Pathology, Medical University Vienna, Vienna, Austria.
Peter GibbsDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Werner DolakDepartment of Medicine III, Medical University of Vienna, Vienna, Austria.
Julius LukasDepartment of Ophthalmology and Optometry, Medical University of Vienna, Vienna, Austria.
Markus RadererDepartment of Medicine I, Medical University of Vienna, Vienna, Austria.
Medical University of Vienna · ATMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeStandardized uptake values (SUV), total metabolic tumor volumes (TMTV), and total lesion glycolysis (TLG) based on positron emission tomography with 2-deoxy-2-[ PROCEDURES: Pre-therapeutic [

resultsAfter 2 years, progression had occurred in 12/61 patients (CD20-anitbody group 6/35). TLG emerged as the only significant prognostic factor for 2-year PFS in the multivariate analyses with forward selection, both in entire cohort (hazard ratio HR, 1.001; 95 % CI, 1.001-1.002; P < 0.0001) and in the CD20-antibody group (HR, 1.001; 95 % CI, 1.001-1.002; P = 0.001). However, in the entire population, where 8/26 patients with a TLG > 90 (30.8 %) vs. 4/35 patients with a TLG ≤ 90 (11.4 %) showed progression within the 2-year observation period, TLG-based separation of risk groups failed (HR, 0.35; 95 % CI, 0.10-1.15; P = 0.069); whereas in the CD20-antibody group, where 6/16 patients with a TLG > 90 (37.5 %) vs. 0/19 patients with a TLG ≤ 90 (0.0 %) showed progression, risk group separation was successful (HR, 0.010; 95 % CI, 0.0001-8.068; P = 0.003).

conclusionsTLG may improve early risk stratification of MALT lymphoma patients treated with CD20-antibody-based immunotherapy.

Indexed as

GlycolysisImmunotherapyPositron-Emission TomographyProgression-Free SurvivalAgedAntibodiesAntigens, CD20FemaleFluorodeoxyglucose F18HumansKaplan-Meier EstimateLymphoma, B-Cell, Marginal ZoneMaleMiddle AgedPrognosisProportional Hazards ModelsAntibodiesAntigens, CD20Fluorodeoxyglucose F18DeoxyglucoseLymphomaPositron emission tomographyPrognosis

Identifiers

PMID30847823
PMCPMC7604829
OpenAlexW2921136265

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.