Evidence map›Paper›PMID 40921705›Full record

ReviewBritish journal of haematology2025

An old leukaemia in young patients-Genetic characteristics of paediatric chronic myeloid leukaemia.

Markus Metzler, Susan Branford, Nobuko Hijiya, Kathleen Sakamoto

Abstract readReview
In one paragraph

Review in British journal of haematology, 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. Review
  2. 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

4 authors.

Markus MetzlerPediatric Oncology and Hematology, Department of Pediatrics and Adolescent Medicine, University Hospital Erlangen, Erlangen, Germany.
Susan BranfordDepartment of Genetics and Molecular Pathology, Centre for Cancer Biology, SA Pathology, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0002-5095-7981
Nobuko HijiyaPediatric Hematology Oncology and Stem Cell Transplant, Columbia University Irving Medical Center, New York, New York, USA.ORCID https://orcid.org/0000-0002-0199-054X
Kathleen SakamotoDepartment of Pediatrics, Stanford University, Stanford, California, USA.

Funding

Clinical Trials Specialist in Developmental TherapeuticsR50CA278916 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Nobuko Hijiya · 2023 to 2026
$704k
National Cancer Institute (NCI) 5R50CA278916-02NCI NIH HHS R50 CA278916Pediatric Cancer Research FoundationStanford Maternal & Child Health Research Institute
6 · The paper itself

Abstract

Chronic myeloid leukaemia (CML) accounts for 2% of leukaemias in children and 9% in adolescents. While the BCR::ABL1 fusion gene remains a hallmark across all age groups, emerging evidence suggests that paediatric CML exhibits unique biological and clinical characteristics compared to its adult counterpart. Children often present with more aggressive clinical features and show distinct treatment response patterns. Recent genomic and transcriptomic studies have highlighted a higher prevalence of germline variants in haematopoiesis-related genes and unique cytogenetic alterations, as well as age-specific distributions of BCR and ABL1 breakpoints. Transcriptomic profiling of paediatric CML stem cells reveals differential expression signatures that suggest the presence of distinct signalling networks. Somatic mutations-particularly in ASXL1-are observed at diagnosis in some children, though their prognostic relevance remains uncertain. Additionally, while the BCR::ABL1 transcript subtype is known to affect treatment-free remission in adults, its role in paediatric CML is still unclear. Collectively, these findings support the notion that paediatric CML may constitute a biologically distinct disease rather than simply a younger form of adult CML. To advance risk stratification and develop age-specific treatment approaches, larger international studies and comprehensive genomic analyses are urgently needed.

Indexed as

Fusion Proteins, bcr-ablLeukemia, Myelogenous, Chronic, BCR-ABL PositiveAdolescentChildHumansMutationFusion Proteins, bcr-ablBCR::ABL1 fusion transcriptschildren and adolescentschronic myeloid leukaemiagenetic predispositiongermline variantspaediatric CMLsomatic variants

Identifiers

PMID40921705
PMCPMC13502535

What Socratic holds

Textmetadata
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 Socratic graph.