Evidence map›Paper›PMID 40493048›Full record

ArticlePediatric radiology2025

Acquisition matters - how do scan parameters affect apparent diffusion coefficient estimates in pediatric rhabdomyosarcoma.

Cyrano Chatziantoniou, Roelof van Ewijk, Madeleine Adams, Patrizia Bertolini, Gianni Bisogno, Amine Bouhamama, Pablo Caro-Dominguez, Valérie Charon, Ana Coma, Rana Dandis and 30 more

Abstract readMulticenter Study
In one paragraph

Article in Pediatric radiology, 2025. 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
–field-weighted citation impact
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.

  1. Article
  2. 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

40 authors.

Cyrano ChatziantoniouUniversity Medical Center Utrecht, Utrecht, Heidelberglaan 100, 3584 CX, Netherlands. c.chatziantoniou-3@umcutrecht.nl.
Roelof van EwijkPrincess Máxima Center, Utrecht, Netherlands. R.vanEwijk-2@prinsesmaximacentrum.nl.
Madeleine AdamsNoah's Ark Children's Hospital for Wales, Cardiff, United Kingdom.
Patrizia BertoliniUniversity Hospital of Parma, Parma, Italy.
Gianni BisognoUniversity of Padua, Padova, Italy.
Amine BouhamamaCentre Léon Bérard, Lyon, France.
Pablo Caro-DominguezHospital Universitario Virgen del Rocío, Seville, Spain.
Valérie CharonCentre Hospitalier Universitaire de Rennes, Rennes, France.
Ana ComaVall d'Hebron Hospital Universitari, Barcelona, Spain.
Rana DandisPrincess Máxima Center, Utrecht, Netherlands.
Christine DevalckQueen Fabiola Children's University Hospital, Brussels, Belgium.
Giulia De DonnoUniversity Medical Center Utrecht, Utrecht, Heidelberglaan 100, 3584 CX, Netherlands.
Andrea FerrariFondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Marta FioccoPrincess Máxima Center, Utrecht, Netherlands.
Soledad GallegoVall d'Hebron Hospital Universitari, Barcelona, Spain.
Chiara GiraudoUniversity of Padua, Padova, Italy.
Heidi GlosliOslo University Hospital, Oslo, Norway.
Simone A J Ter HorstWilhelmina Children's Hospital, Utrecht, Netherlands.
Meriel JenneyNoah's Ark Children's Hospital for Wales, Cardiff, United Kingdom.
Willemijn M KleinRadboud University Nijmegen Medical Centre, Nijmegen, Netherlands.
Alexander LeemansUniversity Medical Center Utrecht, Utrecht, Heidelberglaan 100, 3584 CX, Netherlands.
Julie LeseurCentre Eugène Marquis, Rennes, France.
Henry C MandevilleRoyal Marsden Hospital, London, United Kingdom.
Kieran McHughGreat Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
Johannes H M MerksPrincess Máxima Center, Utrecht, Netherlands.
Veronique Minard-ColinInstitut Gustave Roussy, Villejuif, France.
Salma MoallaInstitut Gustave Roussy, Villejuif, France.
Carlo MorosiFondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Daniel OrbachInstitute Curie, Paris, France.
Lil-Sofie Ording MüllerOslo University Hospital, Oslo, Norway.
Erika PaceRoyal Marsden NHS Foundation Trust, London, United Kingdom.
Pier Luigi Di PaoloBambino Gesù Children's Hospital, Rome, Italy.
Katia PerruccioAzienda Ospedaliera di Perugia, Perugia, Italy.
Lucia QuagliettaDepartment of Hemato-Oncology and Cell Therapy, Santobono-Pausilipon Children's Hospital, Naples, Italy.
Marleen RenardUniversitair Ziekenhuis Leuven, Leuven, Belgium.
Rick R van RijnDepartment of Radiology and Nuclear Medicine, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands.
Antonio RuggieroCatholic University of the Sacred Heart, Milan, Italy.
Sara I SirventHospital Infantil Universitario Niño Jesús, Madrid, Spain.
Reineke A SchootPrincess Máxima Center, Utrecht, Netherlands.
Alberto De LucaUniversity Medical Center Utrecht, Utrecht, Heidelberglaan 100, 3584 CX, Netherlands.

Funding

Stichting Kinderen Kankervrij 357
6 · The paper itself

Abstract

backgroundThe apparent diffusion coefficient (ADC) derived from diffusion-weighted imaging (DWI) is a potential biomarker for treatment response in pediatric rhabdomyosarcoma. Due to its rarity, investigations into this marker require multicenter approaches, which can result in variability in acquisition parameters.

objectiveTo evaluate the impact of different acquisition parameters on ADC estimates in a multicenter dataset of rhabdomyosarcoma patients. MATERIALS AND

methodsWe included 114 pediatric and adolescent rhabdomyosarcoma patients from 22 treatment centers (195 scans). Median age: 6.0 years (0.3-21.8). We evaluated the impact of voxel size, (number of) b-values, and echo time on tumor ADC values. The effect of the highest b-value was separately investigated on a subset of scans with five or more b-values.

resultsWe observed a large variability in key acquisition parameters in the overall cohort, and for individual imaging centers. No parameter showed a significant effect on ADC estimates of the whole cohort when corrected for multiple-comparisons. Decreasing the highest b-value within the same acquisition caused ADC to decrease on average by 2.8% per 100 s mm

conclusionWhile we observed wide variation of acquisition parameters within a multicenter cohort, this did not lead to significant cross-sectional differences of tumor ADC. However, we found that modifying the highest b-value between baseline and follow-up can impact longitudinal ADC estimates. As such, we recommend the highest b-value to remain constant. This retrospective study was reviewed and approved by the Internal Review Board (UMC Utrecht, reference ID: 18-412).

Indexed as

Diffusion Magnetic Resonance ImagingImage Interpretation, Computer-AssistedRhabdomyosarcomaAdolescentChildChild, PreschoolFemaleHumansInfantMaleRetrospective StudiesYoung AdultAdolescentChildDiffusion magnetic resonance imagingRhabdomyosarcoma

Identifiers

PMID40493048
PMCPMC12321683

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.