Evidence map›Paper›PMID 40247105›Full record

ReviewLeukemia2025

T-cell acute lymphoblastic leukaemia: subtype prevalence, clinical outcome, and emerging targeted treatments.

Maxim Buckley, David T Yeung, Deborah L White, Laura N Eadie

Abstract readReview
In one paragraph

Review in Leukemia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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.

Maxim BuckleyBlood Cancer, Precision Medicine Theme, South Australian Health and Medical Research Institute, Adelaide, SA, Australia.ORCID 0000-0002-0241-7243
David T YeungBlood Cancer, Precision Medicine Theme, South Australian Health and Medical Research Institute, Adelaide, SA, Australia.
Deborah L WhiteBlood Cancer, Precision Medicine Theme, South Australian Health and Medical Research Institute, Adelaide, SA, Australia.ORCID 0000-0003-4844-333X
Laura N EadieBlood Cancer, Precision Medicine Theme, South Australian Health and Medical Research Institute, Adelaide, SA, Australia. laura.eadie@sahmri.com.ORCID 0000-0003-1912-7602

Funding

Cancer Council South Australia 22234
6 · The paper itself

Abstract

T-cell Acute Lymphoblastic Leukaemia (T-ALL) is a high-risk hematological disease constituting ~20% of acute leukemias. To date, the only subtype recognized by the World Health Organization's International Consensus Classification is early T-cell precursor ALL. To improve clinical outcomes, several studies have investigated and defined T-ALL genomic subtypes within cohorts of varied ages and geographical locations. These studies have also utilized differing analysis methods including whole transcriptome, exome, or genome sequencing as well as immunophenotyping and cytogenetic testing. As a result, there are significant differences in reported subtypes as well as the frequency at which each occurs. The reported clinical outcomes for specific genomic alterations also depend on patient demographics and treatment protocols. This review synthesizes the data from four T-ALL genomic landscape studies establishing consensus and highlighting differences, details clinical outcomes for the most common genomic alterations observed in T-ALL patients, and proposes novel avenues for future investigation and treatment.

Indexed as

Molecular Targeted TherapyPrecursor T-Cell Lymphoblastic Leukemia-LymphomaBiomarkers, TumorHumansPrevalencePrognosisTreatment OutcomeBiomarkers, Tumor

Identifiers

PMID40247105
PMCPMC12133571

What OpenQuestion holds

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LicenceCC BY
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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.