Evidence map›Paper›PMID 25512507›Full record

Trial reportProceedings of the National Academy of Sciences of the United States of America2014

Expression and prognostic impact of lncRNAs in acute myeloid leukemia.

Ramiro Garzon, Stefano Volinia, Dimitrios Papaioannou, Deedra Nicolet, Jessica Kohlschmidt, Pearlly S Yan, Krzysztof Mrózek, Donna Bucci, Andrew J Carroll, Maria R Baer and 14 more

Abstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 147 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
147citing papers in PubMed, 3 pooled it
8.4field-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

147 citing papers in PubMed, 3 syntheses or guidelines pooled it, 231 citations in OpenAlex.

  1. Pooled it
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  3. Pooled it
  4. Trial
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  6. Article
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  11. MALNC: a new mutant NPM1/IDH2Cancer gene therapy · 2025
    Article
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  16. Article
  17. Review
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  19. Article
  20. Non-coding RNA research · 2024
    Review

87 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

24 authors at 11 institutions in 2 countries.

Ramiro GarzonThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210; carlo.croce@osumc.edu ramiro.garzon@osumc.edu clara.bloomfield@osumc.edu.
Stefano VoliniaDepartment of Morphology, Surgery, and Experimental Medicine, University of Ferrara, Ferrara, FE 44121, Italy;
Dimitrios PapaioannouThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210;
Deedra NicoletThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210; Alliance for Clinical Trials in Oncology Statistics and Data Center, Mayo Clinic, Rochester, MN 55905;
Jessica KohlschmidtThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210; Alliance for Clinical Trials in Oncology Statistics and Data Center, Mayo Clinic, Rochester, MN 55905;
Pearlly S YanThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210;
Krzysztof MrózekThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210;
Donna BucciThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210;
Andrew J CarrollDepartment of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294;
Maria R BaerGreenebaum Cancer Center, University of Maryland, Baltimore, MD 21201;
Meir WetzlerRoswell Park Cancer Institute, Buffalo, NY 14263;
Thomas H CarterHolden Comprehensive Cancer Center, University of Iowa, Iowa City, IA 52242;
Bayard L PowellThe Comprehensive Cancer Center of Wake Forest University, Winston-Salem, NC 27157;
Jonathan E KolitzNorth Shore Cancer Institute, Lake Success, NY 11042;
Joseph O MooreDepartment of Medicine, Division of Hematology-Oncology, Duke University and Durham VA Medical Centers, Durham, NC 27701; and.
Ann-Kathrin EisfeldThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210;
James S BlachlyThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210;
William BlumThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210;
Michael A CaligiuriThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210;
Richard M StoneDana-Farber Cancer Institute, Harvard University, Boston, MA 02215.
Guido MarcucciThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210;
Carlo M CroceThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210; carlo.croce@osumc.edu ramiro.garzon@osumc.edu clara.bloomfield@osumc.edu.
John C ByrdThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210;
Clara D BloomfieldThe Ohio State University Comprehensive Cancer Center, Columbus, OH 43210; carlo.croce@osumc.edu ramiro.garzon@osumc.edu clara.bloomfield@osumc.edu.
The Ohio State University · USAlliance for Clinical Trials in Oncology · USDana-Farber Cancer Institute · USDurham VA Medical Center · USNorthwell Health · USRoswell Park Comprehensive Cancer Center · USUniversity of Alabama at Birmingham · USUniversity of Ferrara · ITUniversity of Iowa · USUniversity of Maryland, Baltimore · USWake Forest University · US

Funding

Member Site CoreU10CA180821 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Evanthia Galanis · 2014 to 2026
$177.3M
Statistics CoreU10CA180882 · NCI · MAYO CLINIC ROCHESTER · PI Sumithra Jay Mandrekar · 2014 to 2026
$115.0M
THE ALLIANCE NCTN BIOREPOSITORY AND BIOSPECIMEN RESOURCEU24CA196171 · NCI · WASHINGTON UNIVERSITY · PI Mine Cicek, Wendy Frankel · 2015 to 2026
$35.0M
SPORE Leukemia Tissue BankP50CA140158 · NCI · OHIO STATE UNIVERSITY · PI MARCUCCI, GUIDO · 2009 to 2013
$11.2M
Cancer and Leukemia Group B - Leukemia Correlative SciencesU10CA101140 · NCI · OHIO STATE UNIVERSITY · PI MARCUCCI, GUIDO · 2003 to 2013
$10.3M
OSU as Network Lead Academic Participating Site for the NCI NCTNU10CA180850 · NCI · OHIO STATE UNIVERSITY · PI BLUM, KRISTIE A, CHAKRAVARTI, ARNAB · 2014 to 2018
$6.8M
ITSC for Leukemia: Novel Molecular Strategies for NCTN: "Individualized" TherapieU10CA180861 · NCI · OHIO STATE UNIVERSITY · PI BLOOMFIELD, CLARA D, MARCUCCI, GUIDO · 2014 to 2018
$3.4M
NCI NIH HHS CA101140NCI NIH HHS CA180861NCI NIH HHS P50 CA140158NCI NIH HHS P50-CA140158-05NCI NIH HHS U10 CA101140NCI NIH HHS U10 CA180821NCI NIH HHS U10 CA180850NCI NIH HHS U10 CA180861NCI NIH HHS U10 CA180882NCI NIH HHS U24 CA196171
6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) are transcripts longer than 200 nucleotides, located within the intergenic stretches or overlapping antisense transcripts of protein coding genes. LncRNAs are involved in numerous biological roles including imprinting, epigenetic regulation, apoptosis, and cell cycle. To determine whether lncRNAs are associated with clinical features and recurrent mutations in older patients (aged ≥60 y) with cytogenetically normal (CN) acute myeloid leukemia (AML), we evaluated lncRNA expression in 148 untreated older CN-AML cases using a custom microarray platform. An independent set of 71 untreated older patients with CN-AML was used to validate the outcome scores using RNA sequencing. Distinctive lncRNA profiles were found associated with selected mutations, such as internal tandem duplications in the FLT3 gene (FLT3-ITD) and mutations in the NPM1, CEBPA, IDH2, ASXL1, and RUNX1 genes. Using the lncRNAs most associated with event-free survival in a training cohort of 148 older patients with CN-AML, we derived a lncRNA score composed of 48 lncRNAs. Patients with an unfavorable compared with favorable lncRNA score had a lower complete response (CR) rate [P < 0.001, odds ratio = 0.14, 54% vs. 89%], shorter disease-free survival (DFS) [P < 0.001, hazard ratio (HR) = 2.88] and overall survival (OS) (P < 0.001, HR = 2.95). The validation set analyses confirmed these results (CR, P = 0.03; DFS, P = 0.009; OS, P = 0.009). Multivariable analyses for CR, DFS, and OS identified the lncRNA score as an independent marker for outcome. In conclusion, lncRNA expression in AML is closely associated with recurrent mutations. A small subset of lncRNAs is correlated strongly with treatment response and survival.

Indexed as

Gene Expression Regulation, LeukemicCase-Control StudiesDisease-Free SurvivalFemaleHumansLeukemia, Myeloid, AcuteMaleMiddle AgedMutationNeoplasm ProteinsNucleophosminRNA, Long NoncodingRNA, NeoplasmSequence Analysis, RNASurvival RateNeoplasm ProteinsNPM1 protein, humanNucleophosminRNA, Long NoncodingRNA, Neoplasmacute myeloid leukemialncRNAsoutcome

Identifiers

PMID25512507
PMCPMC4284555
OpenAlexW2040452735

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.