Evidence map›Paper›PMID 18378853›Full record

Trial reportBlood2008

High BAALC expression associates with other molecular prognostic markers, poor outcome, and a distinct gene-expression signature in cytogenetically normal patients younger than 60 years with acute myeloid leukemia: a Cancer and Leukemia Group B (CALGB) study.

Christian Langer, Michael D Radmacher, Amy S Ruppert, Susan P Whitman, Peter Paschka, Krzysztof Mrózek, Claudia D Baldus, Tamara Vukosavljevic, Chang-Gong Liu, Mary E Ross and 7 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00002925 (Phase I Study of MDR Modulation With PSC-833), which is not on this map. Cited by 72 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 2 pooled it
12.5field-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.

NCT00002925 phase1 / phase2completednot on this map

Phase I Study of MDR Modulation With PSC-833 (NSC# 648265) With a Pilot Study of Cytogenetic Risk-Adapted Consolidation Followed by a Phase II Pilot Study of Immunotherapy With RIL-2 (NSC # 373364) in Previously Untreated Patients With AML< 60 Years

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran1997 to 2010Enrolled410ConditionsLeukemiaArmsara-C, Daunorubicin, Etoposide, PSC-833, Aldesleukin
3 · Its place in the literature

Who cites it

72 citing papers in PubMed, 2 syntheses or guidelines pooled it, 189 citations in OpenAlex.

  1. The M2 macrophage markerOncoimmunology · 2020
    Pooled it
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  14. The Prognostic Significance of the BMI-1 and BAALC Genes in Adult Patients with Acute Myeloid Leukemia.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2020
    Article
  15. Review
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12 more citing papers are in PubMed but not listed here.

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

17 authors at 9 institutions in 2 countries.

Christian LangerDivision of Hematology and Oncology, Department of Internal Medicine, Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA.
Michael D Radmacher
Amy S Ruppert
Susan P Whitman
Peter Paschka
Krzysztof Mrózek
Claudia D Baldus
Tamara Vukosavljevic
Chang-Gong Liu
Mary E Ross
Bayard L Powell
Albert de la Chapelle
Jonathan E Kolitz
Richard A Larson
Guido Marcucci
Clara D Bloomfield
Cancer and Leukemia Group B (CALGB)
Cancer Genetics (United States) · USCharité - Universitätsmedizin Berlin · DEDuke Medical Center · USDuke University Hospital · USNationwide Children's Hospital · USNorth Shore University Hospital · USThe Ohio State University · USUniversity of Chicago · USWake Forest University · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Cancer and Leukemia Group B Human Specimen RepositoriesU24CA114725 · NCI · UNIVERSITY OF CHICAGO · PI BERTAGNOLLI, MONICA M · 2005 to 2014
$11.1M
Cancer and Leukemia Group B - Leukemia Correlative SciencesU10CA101140 · NCI · OHIO STATE UNIVERSITY · PI MARCUCCI, GUIDO · 2003 to 2013
$10.3M
Cancer and Leukemia Group B - The Ohio State UniversityU10CA077658 · NCI · OHIO STATE UNIVERSITY · PI BLOOMFIELD, CLARA D · 1998 to 2013
$6.0M
Functional Characterization of MLL Gene FusionsR01CA089341 · NCI · OHIO STATE UNIVERSITY · PI CALIGIURI, MICHAEL A · 2002 to 2013
$2.8M
BAALC in neurogenesis and hematopoiesisR01CA098933 · NCI · OHIO STATE UNIVERSITY · PI DE LA CHAPELLE, ALBERT · 2004 to 2007
$1.2M
FLT3 GENOTYPES IN ACUTE MYELOID LEUKEMIAK01CA096887 · NCI · OHIO STATE UNIVERSITY · PI WHITMAN, SUSAN P · 2002 to 2006
$649k
NCI NIH HHS CA016058NCI NIH HHS CA077658NCI NIH HHS CA089341NCI NIH HHS CA096887NCI NIH HHS CA098933NCI NIH HHS CA101140NCI NIH HHS CA114725NCI NIH HHS K01 CA096887NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA089341NCI NIH HHS R01 CA098933NCI NIH HHS U10 CA077658NCI NIH HHS U10 CA101140NCI NIH HHS U24 CA114725
6 · The paper itself

Abstract

BAALC expression is considered an independent prognostic factor in cytogenetically normal acute myeloid leukemia (CN-AML), but has yet to be investigated together with multiple other established prognostic molecular markers in CN-AML. We analyzed BAALC expression in 172 primary CN-AML patients younger than 60 years of age, treated similarly on CALGB protocols. High BAALC expression was associated with FLT3-ITD (P = .04), wild-type NPM1 (P < .001), mutated CEBPA (P = .003), MLL-PTD (P = .009), absent FLT3-TKD (P = .005), and high ERG expression (P = .05). In multivariable analysis, high BAALC expression independently predicted lower complete remission rates (P = .04) when adjusting for ERG expression and age, and shorter survival (P = .04) when adjusting for FLT3-ITD, NPM1, CEBPA, and white blood cell count. A gene-expression signature of 312 probe sets differentiating high from low BAALC expressers was identified. High BAALC expression was associated with overexpression of genes involved in drug resistance (MDR1) and stem cell markers (CD133, CD34, KIT). Global microRNA-expression analysis did not reveal significant differences between BAALC expression groups. However, an analysis of microRNAs that putatively target BAALC revealed a potentially interesting inverse association between expression of miR-148a and BAALC. We conclude that high BAALC expression is an independent adverse prognostic factor and is associated with a specific gene-expression profile.

Indexed as

Gene ExpressionAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorGene Expression ProfilingHumansKaplan-Meier EstimateLeukemia, Myeloid, AcuteNeoplasm ProteinsNucleophosminOligonucleotide Array Sequence AnalysisPrognosisReverse Transcriptase Polymerase Chain ReactionRNA, MessengerTreatment OutcomeBAALC protein, humanBiomarkers, TumorNeoplasm ProteinsNPM1 protein, humanNucleophosminRNA, Messenger

Identifiers

PMID18378853
PMCPMC2396728
OpenAlexW2082416593

What OpenQuestion holds

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Registered trials

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.