Evidence map›Paper›PMID 26202931›Full record

ArticleLeukemia2016

Prognostic value of rare IKZF1 deletion in childhood B-cell precursor acute lymphoblastic leukemia: an international collaborative study.

J M Boer, A van der Veer, D Rizopoulos, M Fiocco, E Sonneveld, H A de Groot-Kruseman, R P Kuiper, P Hoogerbrugge, M Horstmann, M Zaliova and 22 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
9.6field-weighted citation impact, top 2% 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

58 citing papers in PubMed, 103 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Genomic Determinants of Outcome in Acute Lymphoblastic Leukemia.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Article
  14. Article
  15. Multifaceted roles ofFrontiers in oncology · 2024
    Review
  16. Article
  17. Article
  18. Article
  19. Observational
  20. 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

32 authors at 16 institutions in 9 countries.

J M BoerDepartment of Pediatric Oncology, Erasmus MC-Sophia Children's Hospital, Rotterdam, The Netherlands.
A van der VeerDepartment of Pediatric Oncology, Erasmus MC-Sophia Children's Hospital, Rotterdam, The Netherlands.
D RizopoulosDepartment of Biostatistics, Erasmus MC, Rotterdam, The Netherlands.
M FioccoDCOG, Dutch Childhood Oncology Group, the Hague, The Netherlands.
E SonneveldDCOG, Dutch Childhood Oncology Group, the Hague, The Netherlands.
H A de Groot-KrusemanDCOG, Dutch Childhood Oncology Group, the Hague, The Netherlands.
R P KuiperDepartment of Human Genetics, Radboud University Medical Center and Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands.
P HoogerbruggeDCOG, Dutch Childhood Oncology Group, the Hague, The Netherlands.
M HorstmannCOALL Study Group, Research Centre and Clinic for Pediatric Oncology, University Medical Centre Eppendorf, Hamburg, Germany.
M ZaliovaBFM-G, Berlin-Frankfurt-Münster-Germany Study Group, University of Schleswig-Holstein, Kiel, Germany.
C PalmiAIEOP, Associazione Italiana Ematologia Oncologia Pediatrica, University of Milano-Bicocca, Monza, Italy.
J TrkaCLIP, Childhood Leukaemia Investigation Prague, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
E FronkovaCLIP, Childhood Leukaemia Investigation Prague, Second Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
M EmerencianoPediatric Haematology and Oncology Program, Research Centre, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.
M do Socorro Pombo-de-OliveiraPediatric Haematology and Oncology Program, Research Centre, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.
W MlynarskiPPLLSG, Polish Pediatric Leukaemia Lymphoma Study Group, Department of Pediatrics, Oncology, Haematology and Diabetology, Medical University of Lodz, Lodz, Poland.
T SzczepanskiPPLLSG, Polish Pediatric Leukaemia Lymphoma Study Group, Department of Pediatric Hematology and Oncology, Medical University of Silesia, Zabrze, Poland.
K NebralChildren's Cancer Research Institute, St Anna Kinderkrebsforschung, Vienna, Austria.
A AttarbaschiBFM-A, Berlin-Frankfurt-Münster-Austria Study Group, Department of Pediatric Hematology and Oncology, St Anna Children's Hospital, Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.
N VennANZCHOG, Australian and New Zealand Children's Oncology Group, Children's Cancer Institute Australia, Lowy Cancer Research Centre, UNSW, Sydney, Australia.
R SuttonANZCHOG, Australian and New Zealand Children's Oncology Group, Children's Cancer Institute Australia, Lowy Cancer Research Centre, UNSW, Sydney, Australia.ORCID http://orcid.org/0000-0002-0188-6005
C J SchwabLeukaemia Research Cytogenetics Group, Northern Institute for Cancer Research, Newcastle University, Newcastle-upon-Tyne, UK.
A EnshaeiLeukaemia Research Cytogenetics Group, Northern Institute for Cancer Research, Newcastle University, Newcastle-upon-Tyne, UK.
A VoraDepartment of Haematology, Sheffield Children's Hospital, Sheffield, UK.
M StanullaPediatric Hematology and Oncology, Hannover Medical School, Hannover, Germany.
M SchrappeBFM-G, Berlin-Frankfurt-Münster-Germany Study Group, University of Schleswig-Holstein, Kiel, Germany.
G CazzanigaAIEOP, Associazione Italiana Ematologia Oncologia Pediatrica, University of Milano-Bicocca, Monza, Italy.
V ConterAIEOP, Associazione Italiana Ematologia Oncologia Pediatrica, University of Milano-Bicocca, Monza, Italy.
M ZimmermannPediatric Hematology and Oncology, Hannover Medical School, Hannover, Germany.
A V MoormanLeukaemia Research Cytogenetics Group, Northern Institute for Cancer Research, Newcastle University, Newcastle-upon-Tyne, UK.
R PietersDepartment of Pediatric Oncology, Erasmus MC-Sophia Children's Hospital, Rotterdam, The Netherlands.
M L den BoerDepartment of Pediatric Oncology, Erasmus MC-Sophia Children's Hospital, Rotterdam, The Netherlands.
Stichting Kinderoncologie Nederland · NLAssociazione Italiana Ematologia Oncologia Pediatrica · ITCharles University · CZNewcastle University · GBChildren's Cancer Institute Australia · AUErasmus MC - Sophia Children’s Hospital · NLInstituto Nacional de Câncer - INCA · BRMedizinische Hochschule Hannover · DESt Anna Children's Hospital · ATErasmus MC · NLLeiden University · NLMedical University of Lodz · PLMedical University of Silesia · PLRadboud University Nijmegen · NLSheffield Children's Hospital · GBUniversität Hamburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deletions in IKZF1 are found in ~15% of children with B-cell precursor acute lymphoblastic leukemia (BCP-ALL). There is strong evidence for the poor prognosis of IKZF1 deletions affecting exons 4-7 and exons 1-8, but evidence for the remaining 33% of cases harboring other variants of IKZF1 deletions is lacking. In an international multicenter study we analyzed the prognostic value of these rare variants in a case-control design. Each IKZF1-deleted case was matched to three IKZF1 wild-type controls based on cytogenetic subtype, treatment protocol, risk stratification arm, white blood cell count and age. Hazard ratios for the prognostic impact of rare IKZF1 deletions on event-free survival were calculated by matched pair Cox regression. Matched pair analysis for all 134 cases with rare IKZF1 deletions together revealed a poor prognosis (P<0.001) that was evident in each risk stratification arm. Rare variant types with the most unfavorable event-free survival were DEL 2-7 (P=0.03), DEL 2-8 (P=0.002) and DEL-Other (P<0.001). The prognosis of each type of rare variant was equal or worse compared with the well-known major DEL 4-7 and DEL 1-8 IKZF1 deletion variants. We therefore conclude that all variants of rare IKZF1 deletions are associated with an unfavorable prognosis in pediatric BCP-ALL.

Indexed as

Gene DeletionAdolescentAdultChildChild, PreschoolCore Binding Factor Alpha 2 SubunitETS Translocation Variant 6 ProteinHumansIkaros Transcription FactorInfantInternational CooperationOncogene Proteins, FusionPrecursor B-Cell Lymphoblastic Leukemia-LymphomaPrognosisProportional Hazards ModelsCore Binding Factor Alpha 2 SubunitETS Translocation Variant 6 ProteinIkaros Transcription FactorIKZF1 protein, humanOncogene Proteins, FusionTEL-AML1 fusion protein

Identifiers

PMID26202931
OpenAlexW1919084303

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.