Evidence map›Paper›PMID 22378655›Full record

ArticlePediatric blood & cancer2012

FLT3 mutation status is a predictor of early death in pediatric acute promyelocytic leukemia: a report from the Children's Oncology Group.

Matthew A Kutny, Barry K Moser, Kristina Laumann, James H Feusner, Alan Gamis, John Gregory, Richard A Larson, Bayard L Powell, Wendy Stock, Cheryl L Willman and 2 more

Abstract read
In one paragraph

Article in Pediatric blood & cancer, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 53 citations in OpenAlex.

  1. Trial
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  4. Article
  5. Favorable outcome ofClinical case reports · 2023
    Article
  6. Article
  7. Article
  8. Advances in Pediatric Acute Promyelocytic Leukemia.Children (Basel, Switzerland) · 2020
    Review
  9. Article
  10. The Impact ofCancers · 2019
    Review
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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

12 authors at 11 institutions in 1 country.

Matthew A KutnyClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA. mkutny@peds.uab.edu
Barry K Moser
Kristina Laumann
James H Feusner
Alan Gamis
John Gregory
Richard A Larson
Bayard L Powell
Wendy Stock
Cheryl L Willman
William G Woods
Soheil Meshinchi
University of Chicago · USChildren's Mercy Hospital · USDuke Medical Center · USEmory University · USFred Hutch Cancer Center · USGoryeb Children's Hospital · USMayo Clinic · USOakland University · USUniversity of New Mexico · USUniversity of Washington · USWake Forest University · US

Funding

COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
CANCER AND LEUKEMIA GROUP B MINORITY SATELLITE SUPPLEMENU10CA031946 · NCI · UNIVERSITY OF CHICAGO · PI BERTAGNOLLI, MONICA M · 1985 to 2013
$158.4M
CANCER &LEUKEMIA GROUP B STATISTICAL CENTERU10CA033601 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SARGENT, DANIEL J. · 1985 to 2013
$69.4M
Children's Oncology Group Statistics &Data Center GrantU10CA098413 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ANDERSON, JAMES R · 2003 to 2013
$67.5M
Support for Human Specimen Banking in NCI-Supported Cancer Clinical TrialsU24CA114766 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI RAMIREZ MILAN, NILSA DEL CARMEN · 2005 to 2014
$14.5M
PEDIATRIC ONCOLOGY RESEARCH TRAINING PROGRAMT32CA009351 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Elizabeth R Lawlor, SOHEIL MESHINCHI · 1985 to 2026
$7.0M
Biology/prognostic implications of Flt3 mutations in AMLR01CA114563 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MESHINCHI, SOHEIL · 2005 to 2016
$4.4M
Accurate Prediction of Acute Myeloid Leukemia RelapseR21CA104964 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MESHINCHI, SOHEIL · 2004 to 2005
$311k
NCI NIH HHS CA31946NCI NIH HHS CA33601NCI NIH HHS R01 CA114563NCI NIH HHS R01-CA114563NCI NIH HHS R21 CA104964NCI NIH HHS R21 CA 104964-02NCI NIH HHS T32 CA009351NCI NIH HHS T32CA009351NCI NIH HHS U10 CA031946NCI NIH HHS U10 CA033601NCI NIH HHS U10 CA098413NCI NIH HHS U10 CA098543NCI NIH HHS U10-CA98413NCI NIH HHS U10-CA98543NCI NIH HHS U24 CA114766NCI NIH HHS U24-CA114766
6 · The paper itself

Abstract

backgroundFLT3 mutations (FLT3/Mut) are prevalent in de novo AML and are associated with early relapse. The prevalence and prognostic significance of FLT3/Mut have not been well defined in childhood acute promyelocytic leukemia (APL). PROCEDURE: Diagnostic specimens from 104 pediatric APL patients were screened for FLT3/Mut (FLT3/ITD or FLT3/ALM). FLT3/Mut status was correlated with disease characteristics and clinical outcome for patients treated on CALGB C9710 (n = 50).

resultsForty-two of the 104 patients (40%) had either FLT3/ITD (n = 28, 27%) or FLT3/ALM (n = 15, 14%). Median diagnostic WBC count was 23,400 cells/µl vs. 3,600 cells/µl for those with and without FLT3/Mut (P < 0.001), and similar results for the cohort of 50 patients treated on C9710 (P < 0.001). In patients treated on C9710, presence of a FLT3 mutation was highly correlated with diagnostic WBC count >10,000 (P = 0.004), microgranular variant histology (P = 0.035), and a lower remission rate (P = 0.009). In patients who received ATRA (C9710 or CCG-2911, n = 8), those with FLT3/Mut had an induction death rate of 30% (7/23) compared to 3% (1/35) in FLT3/WT patients (P = 0.005). In patients with high WBC counts (>10,000), those with FLT3/Mut had a significantly higher risk of induction death versus FLT3/WT patients (47% vs. 0%, P = 0.05). FLT3/Mut was not associated with adverse outcome in those who survived induction therapy.

conclusionsFLT3/Mut are prevalent in pediatric APL and are associated with high WBC count and increased induction death. This study provides further evidence for testing APL patients for FLT3/Mut and the potential role for FLT3 inhibitors in this disease.

Indexed as

MutationAdolescentChildChild, PreschoolDisease-Free SurvivalFemalefms-Like Tyrosine Kinase 3HumansInfantLeukemia, Promyelocytic, AcuteLeukocyte CountMalePrognosisSurvival RateYoung AdultFLT3 protein, humanfms-Like Tyrosine Kinase 3

Identifiers

PMID22378655
PMCPMC3368997
OpenAlexW1983261603

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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.