Evidence map›Paper›PMID 23826732›Full record

Trial reportBritish journal of haematology2013

High EVI1 expression is associated with MLL rearrangements and predicts decreased survival in paediatric acute myeloid leukaemia: a report from the children's oncology group.

Phoenix A Ho, Todd A Alonzo, Robert B Gerbing, Jessica A Pollard, Betsy Hirsch, Susana C Raimondi, Todd Cooper, Alan S Gamis, Soheil Meshinchi

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in British journal of haematology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. HighFrontiers in oncology · 2021
    Article
  11. Review
  12. Article
  13. Prognostic Value ofIranian journal of pathology · 2018
    Review
  14. Article
  15. Article
  16. Article
  17. Collaborative Efforts Driving Progress in Pediatric Acute Myeloid Leukemia.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2015
    Review
  18. Article
  19. Article
  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

9 authors at 7 institutions in 1 country.

Phoenix A HoClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98103, USA. pho@fhcrc.org
Todd A Alonzo
Robert B Gerbing
Jessica A Pollard
Betsy Hirsch
Susana C Raimondi
Todd Cooper
Alan S Gamis
Soheil Meshinchi
Arcadia · USChildren's Oncology Group · USMasonic Cancer CenterSeattle Children's Hospital · USSt. Jude Children's Research Hospital · USUniversity of Southern California · USUniversity of Washington · US

Funding

COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
Biology/prognostic implications of Flt3 mutations in AMLR01CA114563 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MESHINCHI, SOHEIL · 2005 to 2016
$4.4M
NCI NIH HHS R01 CA114563NCI NIH HHS R21 CA10262NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA98543
6 · The paper itself

Abstract

Ectopic viral integration site-1 (EVI1) is highly expressed in certain cytogenetic subsets of adult acute myeloid leukaemia (AML), and has been associated with inferior survival. We sought to examine the clinical and biological associations of EVI1(high) , defined as expression in excess of normal controls, in paediatric AML. EVI1 mRNA expression was measured via quantitative real-time polymerase chain reaction in diagnostic specimens obtained from 206 patients. Expression levels were correlated with clinical features and outcome. EVI1(high) was present in 58/206 (28%) patients. MLL rearrangements occurred in 40% of EVI1(high) patients as opposed to 12% of the EVI1(low/absent) patients (P < 0·001). No abnormalities of 3q26 were found in EVI1(high) patients by conventional cytogenetic analysis, nor were cryptic 3q26 abnormalities detected in a subset of patients screened by next-generation sequencing. French-American-British class M7 was enriched in the EVI1(high) group, accounting for 24% of these patients. EVI1(high) patients had significantly lower 5-year overall survival from study entry (51% vs. 68%, P = 0·015). However, in multivariate analysis including other established prognostic markers, EVI1 expression did not retain independent prognostic significance. EVI1 expression is currently being studied in a larger cohort of patients enrolled on subsequent Children's Oncology Group trials, to determine if EVI1(high) has prognostic value in MLL-rearranged or intermediate-risk subsets.

Indexed as

Gene RearrangementAdolescentAdultAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorChildChild, PreschoolDNA-Binding ProteinsFemaleHumansInfantKaplan-Meier EstimateLeukemia, Myeloid, AcuteMaleMDS1 and EVI1 Complex Locus ProteinMyeloid-Lymphoid Leukemia ProteinBiomarkers, TumorDNA-Binding ProteinsMDS1 and EVI1 Complex Locus ProteinMECOM protein, humanMyeloid-Lymphoid Leukemia ProteinRNA, MessengerRNA, NeoplasmTranscription Factorsacute myeloid leukaemiaEVI1MLLpaediatric cancer

Identifiers

PMID23826732
PMCPMC3754879
OpenAlexW1971278976

What OpenQuestion holds

Textmetadata
LicenceTDM
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.