Evidence map›Paper›PMID 42016573›Full record

ArticleHemaSphere2026

Integration of circulating tumor DNA profiling in the risk stratification of classical Hodgkin lymphoma in children, adolescents, and young adults.

Mathieu Simonin, Mathieu Viennot, Stéphanie Haouy, Stéphane Ducassou, Catherine Curtillet, Nathalie Garnier, Aurélie Phulpin, Catherine Paillard, Charlotte Rigaud, Marie-Laure Couec and 18 more

Abstract read
In one paragraph

Article in HemaSphere, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

28 authors.

Mathieu SimoninDepartment of Pediatric Hematology and Oncology Armand Trousseau University Hospital, AP-HP, Sorbonne Université Paris France.ORCID https://orcid.org/0000-0002-0448-8811
Mathieu ViennotDepartment of Hematology, Center Henri Becquerel University of Rouen, INSERM UMR1245 Rouen France.
Stéphanie HaouyDepartment of Pediatric Oncology and Haematology University Hospital of Montpellier Montpellier France.
Stéphane DucassouDepartment of Pediatric Oncology and Haematology University Hospital of Bordeaux Bordeaux France.
Catherine CurtilletDepartment of Pediatric Hematology and Oncology APHM, La Timone Hospital Marseille France.
Nathalie GarnierInstitute of Pediatric Hematology and Oncology Hospices Civils de Lyon Lyon France.
Aurélie PhulpinPediatric Oncology and Hematology Department University Hospital of Nancy (CHRU Nancy) Nancy France.
Catherine PaillardDepartment of Pediatric Hematology and Oncology Hautepierre University Hospital Strasbourg France.
Charlotte RigaudDepartments of Pediatric and Adolescent Oncology, Gustave Roussy Université Paris-Saclay Villejuif France.
Marie-Laure CouecPediatric Hematology and Oncology Department University Hospital of Nantes Nantes France.
Liana CarausuDepartment of Pediatric Hematology and Oncology Centre Hospitalo-Universitaire de Brest Brest France.
Jacinthe BonneauDepartment of Pediatric Hematology and Oncology Rennes University Hospital Rennes France.
Isabelle PellierPediatric Immuno-Hemato-Oncology Angers University Hospital, CRCI2NA, UMR Inserm CNRS, Université d'Angers, Université de Nantes Angers France.
Melissa BarbatiDepartment of Pediatric Hematology-Oncology CHRU Lille Lille France.
Frédéric MillotDepartment of Pediatric Hematology-Oncology CHU Poitiers Poitiers France.
Marie-Émilie DourtheDepartment of Pediatric Hematology and Immunology Robert Debré University Hospital, AP-HP and Université de Paris Paris France.
Justina KanoldDepartment of Pediatric Hematology-Oncology University Hospital of Clermont-Ferrand Clermont-Ferrand France.
Pascale SchneiderPediatric Hematology, Immunology, Oncology and Stem Cells Transplantation Rouen University Hospital Charles Nicolle CHU Rouen Rouen France.
Jean-Louis StephanDepartment of Pediatrics Centre Hospitalier Universitaire Saint-Etienne Saint-Priest en Jarez France.
Camille LegliseDepartment of Pediatric Oncology, Hematology, Immunology University Hospital of Amiens Amiens France.
Claire PluchartPediatric Oncology and Hematology Department Reims University Hospital Reims France.
Pierre-Julien ViaillyDepartment of Hematology, Center Henri Becquerel University of Rouen, INSERM UMR1245 Rouen France.
Victor MichelDepartment of Hematology, Center Henri Becquerel University of Rouen, INSERM UMR1245 Rouen France.
Sabah BoudjemaaPathology Department Armand Trousseau University Hospital, AP-HP, Sorbonne Université Paris France.
Bénédicte JoncaDepartment of Nuclear Medicine University Hospital Tenon Paris France.
Thierry LeblancDepartment of Pediatric Hematology-Oncology CHU Poitiers Poitiers France.ORCID https://orcid.org/0000-0003-2463-9346
Judith Landman-ParkerDepartment of Pediatric Hematology and Oncology Armand Trousseau University Hospital, AP-HP, Sorbonne Université Paris France.
Fabrice JardinDepartment of Hematology, Center Henri Becquerel University of Rouen, INSERM UMR1245 Rouen France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to define the potential role of circulating tumor DNA (ctDNA) in children, adolescents, and young adults (CAYA) with classical Hodgkin lymphoma (cHL). This prospective trial was conducted in France between 2019 and 2023 and recruited CAYA patients (≤25 years old) with a new diagnosis of cHL. Patients were treated according to the EuroNet-PHL-C2 trial (EudraCT: 2012-004053-88), and plasma ctDNA evaluations were performed at diagnosis, after two cycles of chemotherapy, and in case of relapse. Two hundred and seventy-five patients were included. Median age at diagnosis was 15 years (range 2-22), and 47% of the patients were treated as advanced stages (treatment level 3 [TL-3]). Using an 18-gene amplicon-based next-generation sequencing (NGS) targeted panel encompassing the most frequently mutated genes in cHL, at least one mutation was detected in 236/275 patients (86%). B-symptoms, erythrocyte sedimentation rate, and advanced stages were significantly associated with the level of ctDNA at diagnosis.

Identifiers

PMID42016573
PMCPMC13093264

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Registered trials

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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.