Evidence map›Paper›PMID 31832803›Full record

ArticleEJNMMI research2019

Dual time point [

Pierre Lovinfosse, Caroline Rousseau, Jean-Yves Pierga, Francis Bouchet, Alexandre Cochet, Jean-Louis Alberini, Sylvie Girault, Pierre Vera, Pierre Olivier, Lionel Uwer and 8 more

Open access · goldAbstract read
In one paragraph

Article in EJNMMI research, 2019. 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
0.2field-weighted citation impact, top 41% 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, 5 citations in OpenAlex.

  1. Radiology. Imaging cancer · 2025
    Trial
  2. 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

18 authors at 7 institutions in 1 country.

Pierre LovinfosseNuclear Medicine Department and Inserm UMR_S 1066 MINT, University of Angers, Angers, France.
Caroline RousseauNuclear Medicine Department, West Cancer Institut (ICO), René Gauducheau Centre, Saint Herblain, France.
Jean-Yves PiergaNuclear Medicine Department, Curie Institut, Paris, France.
Francis BouchetNuclear Medicine Department and Inserm UMR_S 1066 MINT, University of Angers, Angers, France.
Alexandre CochetNuclear Medicine Department, Georges-François Leclerc Centre, Dijon, France.
Jean-Louis AlberiniNuclear Medicine Department, Curie Institut, Saint-Cloud, France.
Sylvie GiraultNuclear Medicine Department, West Cancer Institut (ICO), Paul Papin Centre, Angers, France.
Pierre VeraNuclear Medicine Department, Henri Becquerel Centre, Rouen, France.
Pierre OlivierNuclear Medicine Department, University of Nancy, Nancy, France.
Lionel UwerNuclear Medicine Department, Institut de cancerologie de lorraine, Vandoeuvre-les-, Nancy, France.
Florent CachinNuclear Medicine Department, Jean Perrin Center, Clermont Ferrand, France.
Benoit ScarwellNuclear Medicine Department, Centre Hospitalier de la Cote Basque, Bayonne, France.
Jérome LemonnierUniCancer R&D, Paris, France.
Emmanuelle FourmeNuclear Medicine Department, Curie Institut, Saint-Cloud, France.
Christel MesleardUniCancer R&D, Paris, France.
Anne-Laure MartinUniCancer R&D, Paris, France.
Franck LacœuilleNuclear Medicine Department and Inserm UMR_S 1066 MINT, University of Angers, Angers, France.
Olivier-François CouturierNuclear Medicine Department and Inserm UMR_S 1066 MINT, University of Angers, Angers, France. ocouturier70@me.com.ORCID http://orcid.org/0000-0002-4900-7807
Inserm · FRInstitut Curie · FRUniCancer Group · FRCentre Georges François Leclerc · FRCentre Hospitalier de la Côte Basque · FRCentre Jean Perrin · FRInstitut de Cancérologie de Lorraine · FR

Funding

FLT 0105/05 NA
6 · The paper itself

Abstract

purposeFor differentiating tumor from inflammation and normal tissues, fluorodeoxyglucose ([

methodsBefore any treatment, 85 womens with de novo unifocal breast cancer underwent three PET acquisitions at 33.94 ± 8.01 min (PET30), 61.45 ± 8.30 min (PET60), and 81.06 ± 12.12 min (PET80) after [

resultsThere was a significant increase in SUVmax over time for breast lesions (5.58 ± 3.80; 5.97 ± 4.56; 6.19 ± 4.42; p < 0.0001) (m ± SD for PET30, PET60, and PET80, respectively), and bone marrow (for T4, 8.21 ± 3.17, 9.64 ± 3.66, 10.85 ± 3.63, p < 0.0001; for humeral head, 3.36 ± 1.79, 3.87 ± 1.89, 4.39 ± 2.00, p < 0.0001). A significant decrease in SUVmax over time was observed for liver (6.79 ± 2.03; 6.24 ± 1.99; 5.57 ± 1.74; p < 0.0001), muscle (0.95 ± 0.28; 0.93 ± 0.29; 0.86 ± 0.20; p < 0.027), and aorta (1.18 ± 0.34; 1.01 ± 0.32; 0.97 ± 0.30; p < 0.0001). No significant difference was observed for SUVmax in contralateral breast (0.8364 ± 0.40; 0.78 ± 0.38; 0.80 ± 0.35).

conclusion[

Indexed as

Breast cancerFLTFluorothymidinePositron emission tomography

Identifiers

PMID31832803
PMCPMC6908533
OpenAlexW2996270163

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.