Evidence map›Paper›PMID 40356267›Full record

ArticleEuropean journal of haematology2025

Genetic Landscape and Risk Stratification of AML With Hyperdiploid Karyotype.

Ehsan Bahrami Hezaveh, Jiong Yan, Davidson Zhao, Collins Wangulu, Winnie Lo, Cuihong Wei, Hong Chang

Abstract read
In one paragraph

Article in European journal of haematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

7 authors.

Ehsan Bahrami HezavehDepartment of Laboratory Hematology, University Health Network, Toronto, Ontario, Canada.ORCID https://orcid.org/0009-0007-9518-9879
Jiong YanDepartment of Laboratory Hematology, University Health Network, Toronto, Ontario, Canada.
Davidson ZhaoDepartment of Laboratory Hematology, University Health Network, Toronto, Ontario, Canada.
Collins WanguluDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Winnie LoDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Cuihong WeiDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Hong ChangDepartment of Laboratory Hematology, University Health Network, Toronto, Ontario, Canada.ORCID https://orcid.org/0000-0003-3106-2776

Funding

The study was partially supported by Academic Enrichment Fund from University Health Network (UHN) Pathology Associates
6 · The paper itself

Abstract

Hyperdiploid karyotype (HK) (49-65 chromosomes) in acute myeloid leukemia (AML) is rare. Recently, HK-AML with only numerical changes has been reclassified into an intermediate risk group in the updated 2022 European LeukemiaNet (ELN) risk classification, which has historically been classified into an adverse risk group. However, there are limited data in the literature concerning whether these new exclusion criteria are appropriate, and the genetic landscape of HK-AML remains unclear. We retrospectively analyzed a cohort of HK-AML diagnosed at our institution. Among 124 cases, 72 (58.1%) had concurrent adverse risk cytogenetic abnormalities (HK-ADV), 33 (26.6%) had other concurrent structural abnormalities (HK-STR) and 19 (15.3%) had numerical changes alone (HK-NUM). The most frequently gained chromosomes were chromosomes 8, 22, 21, and 19. TP53 mutation was associated with HK-ADV, and a higher frequency of mutations in DNA methylation genes was present in HK-NUM and HK-STR. Patients with HK-NUM had significantly longer overall survival (OS) and event-free survival (EFS) compared to those with HK-ADV. In the adjusted model accounting for confounders, the HK-STR outcome was superior to that of HK-ADV but was not significantly different from that of HK-NUM. In addition, patients with a modal chromosome number of 49-53 had more favorable survival than those with ≥ 54 chromosomes. Our data support the reclassification of HK-NUM patients in the intermediate risk group and suggest that HK-STR might also be more appropriately classified into the intermediate risk group.

Indexed as

DiploidyLeukemia, Myeloid, AcuteAbnormal KaryotypeAdultAgedAged, 80 and overBiomarkers, TumorChromosome AberrationsFemaleHumansKaryotypeKaryotypingMaleMiddle AgedMutationPrognosisBiomarkers, Tumoracute myeloid leukemiacomplex karyotypecytogeneticsgene mutationhyperdiploid karyotypeprognosis

Identifiers

PMID40356267
PMCPMC12224555

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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.