Evidence map›Paper›PMID 27121471›Full record

Trial reportBlood2016

Development and validation of a comprehensive genomic diagnostic tool for myeloid malignancies.

Thomas McKerrell, Thaidy Moreno, Hannes Ponstingl, Niccolo Bolli, João M L Dias, German Tischler, Vincenza Colonna, Bridget Manasse, Anthony Bench, David Bloxham and 22 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
6.1field-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

34 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
  2. Article
  3. Observational
  4. Article
  5. Detection ofCancers · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Haematologica · 2021
    Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

32 authors at 11 institutions in 6 countries.

Thomas McKerrellWellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom; Department of Haematology, Haemato-oncology Diagnostic Service, Cambridge University Hospitals National Health Service Trust, Cambridge, United Kingdom; Department of Haematology, University of Cambridge, Cambridge, United Kingdom;
Thaidy MorenoInstituto de Biomedicina y Biotecnología de Cantabria, Cantabria, Spain;
Hannes PonstinglWellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom;
Niccolo BolliWellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom; Division of Haematology, Fondazione IRCCS Istituto Nazionale dei Tumori, University of Milan, Milan, Italy;
João M L DiasCancer Molecular Diagnosis Laboratory, National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, United Kingdom;
German TischlerWellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom;
Vincenza ColonnaWellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom; National Research Council, Institute of Genetics and Biophysics, Naples, Italy;
Bridget ManasseDepartment of Haematology, Haemato-oncology Diagnostic Service, Cambridge University Hospitals National Health Service Trust, Cambridge, United Kingdom;
Anthony BenchDepartment of Haematology, Haemato-oncology Diagnostic Service, Cambridge University Hospitals National Health Service Trust, Cambridge, United Kingdom;
David BloxhamDepartment of Haematology, Haemato-oncology Diagnostic Service, Cambridge University Hospitals National Health Service Trust, Cambridge, United Kingdom;
Bram HermanAgilent Technologies, Cheadle, United Kingdom;
Danielle FletcherAgilent Technologies, Cheadle, United Kingdom;
Naomi ParkWellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom;
Michael A QuailWellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom;
Nicla ManesWellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom; Department of Haematology, University of Cambridge, Cambridge, United Kingdom;
Clare HodkinsonDepartment of Haematology, University of Cambridge, Cambridge, United Kingdom;
Joanna BaxterDepartment of Haematology, University of Cambridge, Cambridge, United Kingdom;
Jorge SierraDepartment of Haematology, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain;
Theodora FoukaneliDepartment of Haematology, Haemato-oncology Diagnostic Service, Cambridge University Hospitals National Health Service Trust, Cambridge, United Kingdom;
Alan J WarrenDepartment of Haematology, Haemato-oncology Diagnostic Service, Cambridge University Hospitals National Health Service Trust, Cambridge, United Kingdom; Department of Haematology, University of Cambridge, Cambridge, United Kingdom; Cambridge Institute for Medical Research, Cambridge, United Kingdom; Wellcome Trust-Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom;
Jianxiang ChiThe Center for the Study of Haematological Malignancies, Nicosia, Cyprus; The Karaiskakio Foundation, Nicosia, Cyprus;
Paul CosteasThe Center for the Study of Haematological Malignancies, Nicosia, Cyprus; The Karaiskakio Foundation, Nicosia, Cyprus;
Roland RadDepartment of Medicine II, Klinikum Rechts der Isar, Technische Universität München, Munich, Germany; German Cancer Consortium, German Cancer Research Center, Heidelberg, Germany;
Brian HuntlyDepartment of Haematology, Haemato-oncology Diagnostic Service, Cambridge University Hospitals National Health Service Trust, Cambridge, United Kingdom; Department of Haematology, University of Cambridge, Cambridge, United Kingdom; Cambridge Institute for Medical Research, Cambridge, United Kingdom; Wellcome Trust-Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom;
Carolyn GroveDepartment of Haematology, PathWest/Sir Charles Gairdner Hospital, Perth, Australia; and Pathology and Laboratory Medicine, University of Western Australia, Perth, Australia.
Zemin NingWellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom;
Chris Tyler-SmithWellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom;
Ignacio VarelaInstituto de Biomedicina y Biotecnología de Cantabria, Cantabria, Spain;
Mike ScottDepartment of Haematology, Haemato-oncology Diagnostic Service, Cambridge University Hospitals National Health Service Trust, Cambridge, United Kingdom; Department of Haematology, University of Cambridge, Cambridge, United Kingdom;
Josep NomdedeuDepartment of Haematology, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain;
Ville MustonenWellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom;
George S VassiliouWellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom; Department of Haematology, Haemato-oncology Diagnostic Service, Cambridge University Hospitals National Health Service Trust, Cambridge, United Kingdom; Department of Haematology, University of Cambridge, Cambridge, United Kingdom;ORCID 0000-0003-4337-8022
National Health Service · GBWellcome Sanger Institute · GBUniversity of Cambridge · GBAgilent Technologies (United Kingdom) · GBCenter for the Study of Childhood and Adolescence · CYHospital de Sant Pau · ESInstituto de Biomedicina y Biotecnología de Cantabria · ESGerman Cancer Research Center · DENational Institute for Health Research · GBThe University of Western Australia · AUUniversity of Milan · IT

Funding

Medical Research Council MC_PC_12009Medical Research Council MC_U105161083Medical Research Council MR/L003368/1Medical Research Council MR/M010392/1Wellcome TrustWorldwide Cancer Research 14-1069
6 · The paper itself

Abstract

The diagnosis of hematologic malignancies relies on multidisciplinary workflows involving morphology, flow cytometry, cytogenetic, and molecular genetic analyses. Advances in cancer genomics have identified numerous recurrent mutations with clear prognostic and/or therapeutic significance to different cancers. In myeloid malignancies, there is a clinical imperative to test for such mutations in mainstream diagnosis; however, progress toward this has been slow and piecemeal. Here we describe Karyogene, an integrated targeted resequencing/analytical platform that detects nucleotide substitutions, insertions/deletions, chromosomal translocations, copy number abnormalities, and zygosity changes in a single assay. We validate the approach against 62 acute myeloid leukemia, 50 myelodysplastic syndrome, and 40 blood DNA samples from individuals without evidence of clonal blood disorders. We demonstrate robust detection of sequence changes in 49 genes, including difficult-to-detect mutations such as FLT3 internal-tandem and mixed-lineage leukemia (MLL) partial-tandem duplications, and clinically significant chromosomal rearrangements including MLL translocations to known and unknown partners, identifying the novel fusion gene MLL-DIAPH2 in the process. Additionally, we identify most significant chromosomal gains and losses, and several copy neutral loss-of-heterozygosity mutations at a genome-wide level, including previously unreported changes such as homozygosity for DNMT3A R882 mutations. Karyogene represents a dependable genomic diagnosis platform for translational research and for the clinical management of myeloid malignancies, which can be readily adapted for use in other cancers.

Indexed as

Hematologic NeoplasmsLeukemia, MyeloidMyelodysplastic SyndromesCarrier ProteinsDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3AFemalefms-Like Tyrosine Kinase 3ForminsGenomicsHistone-Lysine N-MethyltransferaseHumansMaleMutationMyeloid-Lymphoid Leukemia ProteinOncogene Proteins, FusionCarrier ProteinsDIAPH2 protein, humanDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNMT3A protein, humanFLT3 protein, humanfms-Like Tyrosine Kinase 3ForminsHistone-Lysine N-MethyltransferaseKMT2A protein, humanMyeloid-Lymphoid Leukemia ProteinOncogene Proteins, Fusion

Identifiers

PMID27121471
PMCPMC4937362
OpenAlexW2343944287

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.