Evidence map›Paper›PMID 39983076›Full record

ArticleJCO precision oncology2025

Urinary Catecholamines Predict Relapse During Complete Remission in High-Risk Neuroblastoma.

Yvette A H Matser, Atia Samim, Marta Fiocco, Marieke van de Mheen, Maria van der Ham, Monique G M de Sain-van der Velden, Nanda M Verhoeven-Duif, Martine van Grotel, Kathelijne C J M Kraal, Miranda P Dierselhuis and 5 more

Abstract read
In one paragraph

Article in JCO precision oncology, 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. Effect ofJCO precision oncology · 2026
    Article
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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

15 authors.

Yvette A H MatserPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0002-7182-3202
Atia SamimPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0001-6165-0902
Marta FioccoPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0001-5588-0277
Marieke van de MheenPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Maria van der HamDepartment of Genetics, Section Metabolic Diagnostics, Wilhelmina Children's Hospital, Utrecht, the Netherlands.
Monique G M de Sain-van der VeldenDepartment of Genetics, Section Metabolic Diagnostics, Wilhelmina Children's Hospital, Utrecht, the Netherlands.ORCID 0000-0003-3033-4397
Nanda M Verhoeven-DuifDepartment of Genetics, Section Metabolic Diagnostics, Wilhelmina Children's Hospital, Utrecht, the Netherlands.
Martine van GrotelPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Kathelijne C J M KraalPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Miranda P DierselhuisPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Natasha K A van EijkelenburgPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0002-0526-3737
Karin P S LangenbergPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0002-6780-0585
Max M van NoeselPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0003-0503-5838
André B P van KuilenburgLaboratory Genetic Metabolic Diseases, Amsterdam UMC, Free University Amsterdam, Amsterdam, the Netherlands.ORCID 0000-0002-7989-4910
Godelieve A M TytgatPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID 0000-0003-4452-0748

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeUrinary catecholamine metabolites are well-known biomarkers for the diagnosis (Dx) of neuroblastoma, but their clinical significance in determining therapy response during treatment is not well established. Therefore, catecholamines are not included in criteria for assessing response and complete remission (CR). This study investigated the use of urinary catecholamines in response monitoring and predicting survival outcomes.

methodsFrom 2005 to 2021, a panel of eight urinary catecholamines were measured in patients with high-risk neuroblastoma at Dx and at standard evaluation moments during treatment. At the same time points, response and CR were assessed according to the revised International Neuroblastoma Response Criteria.

resultsThe total cohort consists of 153 high-risk patients, and at least one of the eight metabolites was elevated (ie, catecholamine status positive) in 141 of 146 (97%), 104 of 128 (81%), and 39 of 69 (57%) patients at Dx, postinduction, and at CR, respectively. Primary tumor resection significantly reduced catecholamine levels (

conclusionCatecholamine measurements contribute to the assessment of CR and identifies patients with high-risk neuroblastoma with an increased risk of relapse and death.

Indexed as

CatecholaminesNeoplasm Recurrence, LocalNeuroblastomaAdolescentBiomarkers, TumorChildChild, PreschoolFemaleHumansInfantMalePrognosisRemission InductionBiomarkers, TumorCatecholamines

Identifiers

PMID39983076
PMCPMC11867808

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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.