Evidence map›Paper›PMID 41704060›Full record

ArticleBritish journal of haematology2026

Efficacy of immune checkpoint inhibitors in paediatric, adolescent and young adults with primary refractory or relapsed classical Hodgkin lymphoma: A national multicentre real-world study.

Marlène Pouthier, Nathalie Garnier, Amaury Leruste, Charlotte Rigaud, Catherine Curtillet, Stéphane Ducassou, Marilyne Poirée, Marie-Emilie Dourthe, Cécile Pochon, Marie-Laure Couec and 8 more

Abstract readMulticenter Study
In one paragraph

Article in British journal of haematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Marlène PouthierSIREDO Oncology Center, Institut Curie, Paris, France.
Nathalie GarnierInstitut d'Hématologie et d'Oncologie Pédiatrique, Hospices Civils de Lyon, Lyon, France.
Amaury LerusteSIREDO Oncology Center, Institut Curie, Paris, France.ORCID https://orcid.org/0000-0002-6891-9588
Charlotte RigaudDepartment of Pediatric and Adolescent Oncology, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
Catherine CurtilletDepartment of Pediatric Hematology, Immunology and Oncology, AP-HM, La Timone Children's Hospital, Marseille, France.
Stéphane DucassouDepartment of Pediatric Oncology and Haematology, University Hospital of Bordeaux, Bordeaux, France.
Marilyne PoiréeDepartment of Pediatric Hematology-Oncology, University Hospital Nice, Nice, France.
Marie-Emilie DourtheDepartment of Pediatric Hematology and Immunology, Robert Debré University Hospital, AP-HP, Université Paris Cité, Paris, France.
Cécile PochonDepartment of Pediatric Hematology and Oncology, University Hospital of Nancy, Nancy, France.
Marie-Laure CouecDepartment of Pediatric Hematology and Oncology, University Hospital of Nantes, Nantes, France.
Jacinthe Bonneau-LagacherieDepartment of Pediatric Hematology and Oncology, Rennes University Hospital, Rennes, France.
Françoise MontraversDepartment of Nuclear Medicine, Tenon Hospital, AP-HP, Sorbonne Université, Paris, France.
Sabah BoudjemaaDepartment of Pathology, Armand Trousseau Hospital, AP-HP, Sorbonne Université, Paris, France.
Bénédicte JoncaDepartment of Nuclear Medicine, Tenon Hospital, AP-HP, Sorbonne Université, Paris, France.
Stéphanie HaouyDepartment of Pediatric Hematology and Oncology, University Hospital of Montpellier, Montpellier, France.
Thierry LeblancDepartment of Pediatric Hematology and Immunology, Robert Debré University Hospital, AP-HP, Université Paris Cité, Paris, France.ORCID https://orcid.org/0000-0003-2463-9346
Judith Landman ParkerDepartment of Pediatric Hematology and Oncology, Trousseau Hospital, AP-HP, Sorbonne Université, Paris, France.
Mathieu SimoninDepartment of Pediatric Hematology and Oncology, Trousseau Hospital, AP-HP, Sorbonne Université, Paris, France.ORCID https://orcid.org/0000-0002-0448-8811

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Classical Hodgkin lymphoma (cHL) is the most frequent lymphoma in children, adolescents and young adults (CAYA). Despite therapeutic advances, around 15% of patients relapse or have refractory (R/R) disease. Conventional salvage regimens remain effective but are associated with substantial long-term toxicity. Immune checkpoint inhibitors (CPIs), such as nivolumab and pembrolizumab, and the anti-CD30 antibody-drug conjugate brentuximab vedotin (BV) have recently demonstrated encouraging efficacy with improved safety. We conducted a retrospective, multicentre nationwide study to assess the real-world efficacy of CPI in CAYA patients (<18 years) with R/R cHL treated outside clinical trials in France between August 2015 and May 2023. Twenty-seven patients from 11 centres were included. Median age at CPI initiation was 16 years; 70% had advanced disease. Prior treatments included BV (44%), autologous stem cell transplantation (22%) and allogeneic transplantation (4%). Nivolumab was used in 89%, frequently combined with BV (67%). The overall response rate was 93%, with 63% achieving complete metabolic response. After a median follow-up of 28 months, 3-year progression-free survival and overall survival were 48% and 95%, respectively, and toxicities were manageable. These findings strongly support CPI as a highly effective and well-tolerated treatment option for the CAYA population with R/R cHL even in heavily pretreated patients.

Indexed as

Hodgkin DiseaseImmune Checkpoint InhibitorsAdolescentAdultChildFemaleFranceHumansMaleRecurrenceRetrospective StudiesTreatment OutcomeYoung AdultImmune Checkpoint Inhibitorsadolescentbrentuximab vedotinCAYAcheckpoint inhibitorclassical Hodgkin lymphomanivolumabpaediatricrefractoryrelapse

Identifiers

PMID41704060
PMCPMC13071494

What OpenQuestion holds

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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.