Evidence map›Paper›PMID 23974192›Full record

ArticleBlood2013

Independent prognostic value of BCR-ABL1-like signature and IKZF1 deletion, but not high CRLF2 expression, in children with B-cell precursor ALL.

Arian van der Veer, Esmé Waanders, Rob Pieters, Marieke E Willemse, Simon V Van Reijmersdal, Lisa J Russell, Christine J Harrison, William E Evans, Vincent H J van der Velden, Peter M Hoogerbrugge and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 150 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
150citing papers in PubMed, 3 pooled it
31.0field-weighted citation impact, top 1% of its field
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

150 citing papers in PubMed, 3 syntheses or guidelines pooled it, 292 citations in OpenAlex.

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90 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 8 institutions in 4 countries.

Arian van der VeerDepartment of Pediatric Oncology, Erasmus University Medical Center-Sophia Children's Hospital, Rotterdam, The Netherlands;
Esmé Waanders
Rob Pieters
Marieke E Willemse
Simon V Van Reijmersdal
Lisa J Russell
Christine J Harrison
William E Evans
Vincent H J van der Velden
Peter M Hoogerbrugge
Frank Van Leeuwen
Gabriele Escherich
Martin A Horstmann
Leila Mohammadi Khankahdani
Dimitris Rizopoulos
Hester A De Groot-Kruseman
Edwin Sonneveld
Roland P Kuiper
Monique L Den Boer
Erasmus MC · NLRadboud University Medical Center · NLStichting Kinderoncologie Nederland · NLNewcastle University · GBRadboud University Nijmegen · NLSt. Jude Children's Research Hospital · USUniversität Hamburg · DEUniversity Medical Center Hamburg-Eppendorf · DE

Funding

PHARMACOGENOMICS OF CHILDHOOD LEUKEMIA (ALL)R37CA036401 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI EVANS, WILLIAM E · 1987 to 2014
$9.7M
NCI NIH HHS R37 CA036401
6 · The paper itself

Abstract

Most relapses in childhood B-cell precursor acute lymphoblastic leukemia (BCP-ALL) are not predicted using current prognostic features. Here, we determined the co-occurrence and independent prognostic relevance of 3 recently identified prognostic features: BCR-ABL1-like gene signature, deletions in IKZF1, and high CRLF2 messenger RNA expression (CRLF2-high). These features were determined in 4 trials representing 1128 children with ALL: DCOG ALL-8, ALL9, ALL10, and Cooperative ALL (COALL)-97/03. BCR-ABL1-like, IKZF1-deleted, and CRLF2-high cases constitute 33.7% of BCR-ABL1-negative, MLL wild-type BCP-ALL cases, of which BCR-ABL1-like and IKZF1 deletion (co)occurred most frequently. Higher cumulative incidence of relapse was found for BCR-ABL1-like and IKZF1-deleted, but not CRLF2-high, cases relative to remaining BCP-ALL cases, reflecting the observations in each of the cohorts analyzed separately. No relapses occurred among cases with CRLF2-high as single feature, whereas 62.9% of all relapses in BCR-ABL1-negative, MLL wild-type BCP-ALL occurred in cases with BCR-ABL1-like signature and/or IKZF1 deletion. Both the BCR-ABL1-like signature and IKZF1 deletions were prognostic features independent of conventional prognostic markers in a multivariate model, and both remained prognostic among cases with intermediate minimal residual disease. The BCR-ABL1-like signature and an IKZF1 deletion, but not CRLF2-high, are prognostic factors and are clinically of importance to identify high-risk patients who require more intensive and/or alternative therapies.

Indexed as

AdolescentChildChild, PreschoolFemaleFusion Proteins, bcr-ablHumansIkaros Transcription FactorIncidenceInfantMalePrecursor B-Cell Lymphoblastic Leukemia-LymphomaPrecursor Cell Lymphoblastic Leukemia-LymphomaPredictive Value of TestsPrognosisReceptors, CytokineRecurrenceBCR-ABL1 fusion protein, humanCRLF2 protein, humanFusion Proteins, bcr-ablIkaros Transcription FactorIKZF1 protein, humanReceptors, Cytokine

Identifiers

PMID23974192
PMCPMC3795461
OpenAlexW2096709475

What OpenQuestion 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 OpenQuestion graph.