Evidence map›Paper›PMID 27229714›Full record

ArticleHaematologica2016

Characterization of leukemias with ETV6-ABL1 fusion.

Marketa Zaliova, Anthony V Moorman, Giovanni Cazzaniga, Martin Stanulla, Richard C Harvey, Kathryn G Roberts, Sue L Heatley, Mignon L Loh, Marina Konopleva, I-Ming Chen and 19 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

40 citing papers in PubMed, 90 citations in OpenAlex.

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  11. Review
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  14. Review
  15. Review
  16. International journal of molecular sciences · 2023
    Article
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  18. Myeloproliferative Neoplasm Driven byCurrent oncology (Toronto, Ont.) · 2023
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  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

29 authors at 19 institutions in 11 countries.

Marketa ZaliovaCLIP, Department of Pediatric Hematology and Oncology, 2 Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic marketa.zaliova@lfmotol.cuni.cz jan.zuna@lfmotol.cuni.cz.
Anthony V MoormanLeukaemia Research Cytogenetics Group, Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne, UK.
Giovanni CazzanigaCentro Ricerca Tettamanti, Clinica Pediatrica, Università di Milano-Bicocca, Fondazione MBBM/Ospedale San Gerardo, Monza, Italy.
Martin StanullaPediatric Hematology and Oncology, Hannover Medical School, Germany.
Richard C HarveyUniversity of New Mexico Cancer Center, Albuquerque, NM, USA.
Kathryn G RobertsDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Sue L HeatleySouth Australia Health and Medical Research Institute, Adelaide, Australia.
Mignon L LohDepartment of Pediatrics, Hematology-Oncology, Benioff Children's Hospital, and the Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
Marina KonoplevaDepartment of Leukemia, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
I-Ming ChenUniversity of New Mexico Cancer Center, Albuquerque, NM, USA.
Olga ZimmermannovaCLIP, Department of Pediatric Hematology and Oncology, 2 Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
Claire SchwabLeukaemia Research Cytogenetics Group, Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne, UK.
Owen SmithDepartment of Haematology, Our Lady's Children's Hospital, Dublin, Ireland.
Marie-Joelle MozziconacciDepartment of Cancer Biology, Institut Paoli Calmettes, Marseille, France.
Christian ChabannonDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Myungshin KimDepartment of Laboratory Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
J H Frederik FalkenburgDepartment of Hematology, Leiden University Medical Center, The Netherlands.
Alice NortonBirmingham Children's Hospital, NHS Foundation Trust, UK.
Karen MarshallDepartment of Cytogenetics, Leicester Royal Infirmary NHS Trust, UK.
Oskar A HaasSt. Anna Children's Hospital, Childrens Cancer Research Institute, Vienna, Austria.
Julia StarkovaCLIP, Department of Pediatric Hematology and Oncology, 2 Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
Jan StuchlyCLIP, Department of Pediatric Hematology and Oncology, 2 Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
Stephen P HungerDepartment of Pediatrics and the Center for Childhood Cancer Research, Children's Hospital of Philadelphia and the University of Pennsylvania Perelman School of Medicine, PA, USA.
Deborah WhiteSouth Australia Health and Medical Research Institute, Adelaide, Australia.
Charles G MullighanDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Cheryl L WillmanUniversity of New Mexico Cancer Center, Albuquerque, NM, USA.
Jan StaryCLIP, Department of Pediatric Hematology and Oncology, 2 Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
Jan TrkaCLIP, Department of Pediatric Hematology and Oncology, 2 Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic.
Jan ZunaCLIP, Department of Pediatric Hematology and Oncology, 2 Faculty of Medicine, Charles University and University Hospital Motol, Prague, Czech Republic marketa.zaliova@lfmotol.cuni.cz jan.zuna@lfmotol.cuni.cz.
Charles University · CZInstitut Paoli-Calmettes · FRNewcastle University · GBSouth Australian Health and Medical Research Institute · AUSt. Jude Children's Research Hospital · USBirmingham Children's Hospital · GBCatholic University of Korea · KRLeicester Royal Infirmary · GBLeiden University Medical Center · NLMedizinische Hochschule Hannover · DENew Mexico Cancer Center · USOur Lady's Hospital · IESt Anna Children's Hospital · ATThe University of Texas MD Anderson Cancer Center · USUniversity of California, San Francisco · USUniversity of Milano-Bicocca · ITUniversity of New Mexico · USUniversity of Pennsylvania · USUNM Comprehensive Cancer Center

Funding

COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
Children's Oncology Group Statistics &Data Center GrantU10CA098413 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI DEVIDAS, MEENAKSHI · 2003 to 2013
$67.5M
CPML - Project 3: Genome-wide Studies of Adverse EffectsP50GM115279 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI LOH, MIGNON LEE-CHEUN, RELLING, MARY V · 2015 to 2019
$15.1M
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
NCI NIH HHS U10 CA098413NCI NIH HHS U10 CA098543NCI NIH HHS U24 CA114766NIGMS NIH HHS P50 GM115279
6 · The paper itself

Abstract

To characterize the incidence, clinical features and genetics of ETV6-ABL1 leukemias, representing targetable kinase-activating lesions, we analyzed 44 new and published cases of ETV6-ABL1-positive hematologic malignancies [22 cases of acute lymphoblastic leukemia (13 children, 9 adults) and 22 myeloid malignancies (18 myeloproliferative neoplasms, 4 acute myeloid leukemias)]. The presence of the ETV6-ABL1 fusion was ascertained by cytogenetics, fluorescence in-situ hybridization, reverse transcriptase-polymerase chain reaction and RNA sequencing. Genomic and gene expression profiling was performed by single nucleotide polymorphism and expression arrays. Systematic screening of more than 4,500 cases revealed that in acute lymphoblastic leukemia ETV6-ABL1 is rare in childhood (0.17% cases) and slightly more common in adults (0.38%). There is no systematic screening of myeloproliferative neoplasms; however, the number of ETV6-ABL1-positive cases and the relative incidence of acute lymphoblastic leukemia and myeloproliferative neoplasms suggest that in adulthood ETV6-ABL1 is more common in BCR-ABL1-negative chronic myeloid leukemia-like myeloproliferations than in acute lymphoblastic leukemia. The genomic profile of ETV6-ABL1 acute lymphoblastic leukemia resembled that of BCR-ABL1 and BCR-ABL1-like cases with 80% of patients having concurrent CDKN2A/B and IKZF1 deletions. In the gene expression profiling all the ETV6-ABL1-positive samples clustered in close vicinity to BCR-ABL1 cases. All but one of the cases of ETV6-ABL1 acute lymphoblastic leukemia were classified as BCR-ABL1-like by a standardized assay. Over 60% of patients died, irrespectively of the disease or age subgroup examined. In conclusion, ETV6-ABL1 fusion occurs in both lymphoid and myeloid leukemias; the genomic profile and clinical behavior resemble BCR-ABL1-positive malignancies, including the unfavorable prognosis, particularly of acute leukemias. The poor outcome suggests that treatment with tyrosine kinase inhibitors should be considered for patients with this fusion.

Indexed as

AdolescentAdultAgedAlternative SplicingChildChild, PreschoolCluster AnalysisDNA Copy Number VariationsETS Translocation Variant 6 ProteinFemaleGene Expression ProfilingHumansInfantIn Situ Hybridization, FluorescenceLeukemiaMaleETS Translocation Variant 6 ProteinOncogene Proteins, FusionProtein-Tyrosine KinasesTEL-ABL fusion protein, human

Identifiers

PMID27229714
PMCPMC5060025
OpenAlexW2397706354

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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.