Evidence map›Paper›PMID 40820816›Full record

Trial reportHaematologica2026

Impact of minimal residual disease on the outcome of hematopoietic stem cell transplantation for childhood acute lymphoblastic leukemia within the FORUM trial.

Adriana Balduzzi, Evgenia Glogova, Christina Peters, Petr Sedlacek, Jean-Hugues Dalle, Franco Locatelli, Roland Meisel, Birgit Burkhardt, Jochen Buechner, Jacek Wachowiak and 14 more

Abstract readRandomized Controlled TrialClinical Trial, Phase IIIMulticenter Study
In one paragraph

Trial report in Haematologica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Trial
  2. Article
  3. 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

24 authors.

Adriana BalduzziPediatric Department, Fondazione IRCCS San Gerardo, Monza, Italy; School of Medicine and Surgery, Milano-Bicocca University, Monza. adriana.balduzzi@unimib.it.
Evgenia GlogovaSt. Anna Children's Cancer Research Institute, Vienna.
Christina PetersSt. Anna Children's Cancer Research Institute, Vienna, Austria; St. Anna Children's Hospital, Medical University Vienna, Vienna.
Petr SedlacekDepartment of Pediatric Hematology and Oncology, University Hospital Motol, Prague, Czech Republic.
Jean-Hugues DalleHemato-Immunology Department, Robert-Debré Hospital, GHU AP-HP Nord, Paris, France; Université Paris Cité, Paris.
Franco LocatelliDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Ospedale Pediatrico Bambino Gesù, Roma, Italy; Catholic University of the Sacred Heart, Rome.
Roland MeiselDepartment of Pediatric Oncology, Hematology and Clinical Immunology, Division of Pediatric Stem Cell Therapy, Medical Faculty, Heinrich Heine University, Duesseldorf.
Birgit BurkhardtDepartment of Pediatric Hematology and Oncology, University Children's Hospital Muenster, Muenster.
Jochen BuechnerDepartment of Pediatric Hematology and Oncology, Oslo University Hospital, Oslo.
Jacek WachowiakDepartment of Pediatric Oncology, Hematology and Transplantology, University of Medical Sciences, Poznań.
Marc BieringsPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands; Utrecht University Children's Hospital, Utrecht.
Raquel StaciukHospital de Pediatría "Prof. Dr. Juan P. Garrahan," Buenos Aires, and Hospital Sor Maria Ludovica, La Plata, Buenos Aires.
Stelios GraphakosAghia Sophia Children's University Hospital, Athens.
Tayfun GüngörEleonore Foundation and Children's Research Center, Zürich.
Akif YesilipekPediatric Stem Cell Transplantation Unit, Antalya Medical park Hospital Antalya.
Peter SvecDepartment of Pediatric Hematology and Oncology, National Institute of Children's Diseases, Comenius University, Bratislava.
Julia PalmaFaculty of Medicine, Hospital Luis Calvo Mackenna, Department of Pediatrics-Bone Marrow Transplantation Unit, University of Chile, Santiago.
Gergely KrivanPediatric Hematology and Stem Cell Transplantation Department, Central Hospital of Southern Pest, National Institute of Hematology and Infectious Diseases, Budapest.
Cristina Diaz-de-HerediaDivision of Pediatric Hematology and Oncology, University Hospital Vall d'Hebron, Barcelona.
Francesca LimidoSchool of Medicine and Surgery, Milano-Bicocca University, Monza.
Marc AnsariCANSEARCH Research Platform for Pediatric Oncology and Hematology, Faculty of Medicine, Department of Pediatrics, Gynecology and Obstetrics, University of Geneva, Switzerland; Department of Women, Child and Adolescent, Division of Pediatric Oncology and Hematology, University Geneva Hospitals, Geneva.
Krzysztof KalwakDepartment of Pediatric Hematology/Oncology and BMT, Wroclaw Medical University, Wroclaw.
Peter BaderDepartment of Pediatrics, Division for Stem Cell Transplantation, Immunology, Goethe University, University Hospital Frankfurt am Main.
Marianne IfversenDepartment of Pediatric and Adolescent Medicine, Rigshospitalet, Copenhagen University Hospital.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the randomized cohort of the international phase-III FORUM trial, which showed the superiority of total-body irradiation (TBI) over chemotherapy-based conditioning prior to hematopoietic stem cell transplantation (HSCT) for pediatric acute lymphoblastic leukemia (ALL), type of conditioning and remission phase, but not pre-HSCT minimal residual disease (MRD), were associated with outcome. We report the impact of MRD within the extended FORUM cohort. Patients (N=1,014) aged 4-21 years old, transplanted from a matched donor who had ≥1 MRD measurement prior to and/or 100 days and/or one year after HSCT were eligible. A threshold of 0.01% defined MRD positivity versus negativity. Prior to HSCT, 21% of patients were MRDpos. Three-year event-free survival (EFS) was 0.73 and 0.59 (P<0.001), and 3-year cumulative incidence of relapse (CIR) was 0.20 and 0.33 (P<0.001) in MRDneg and MRDpos patients, respectively. The level of MRD positivity pre-HSCT (<0.1% vs. ≥0.1%) did not significantly affect outcome. Pre-HSCT MRDneg and TBI/etoposide conditioning were associated with a 2-fold lower risk of relapse, whereas MRDpos had a 2-fold higher risk of any failure and/or death. No detrimental effect of MRDpos pre-HSCT could be demonstrated in patients with T-cell ALL. MRDpos versus MRDneg patients at day 100 had an EFS of 0.47 versus 0.77 (P<0.001) and a CIR of 0.51 versus 0.17 (P<0.001), respectively, but post-HSCT MRDpos did not necessarily imply relapse. In conclusion, the MRD status pre-HSCT and at day 100 post-HSCT was a strong prognostic factor for children transplanted for ALL in the extended FORUM cohort.

Indexed as

Hematopoietic Stem Cell TransplantationNeoplasm, ResidualPrecursor Cell Lymphoblastic Leukemia-LymphomaAdolescentAdultChildChild, PreschoolFemaleHumansMalePrognosisTransplantation ConditioningTreatment OutcomeYoung Adult

Identifiers

PMID40820816
PMCPMC12775767

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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.