Evidence map›Paper›PMID 27128508›Full record

ArticleEpigenetics2016

Prognostic impact of epigenetic classification in chronic lymphocytic leukemia: The case of subset #2.

Sujata Bhoi, Viktor Ljungström, Panagiotis Baliakas, Mattias Mattsson, Karin E Smedby, Gunnar Juliusson, Richard Rosenquist, Larry Mansouri

Open access · bronzeAbstract readValidation Study
In one paragraph

Article in Epigenetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Towards precision medicine in lymphoid malignancies.Journal of internal medicine · 2022
    Review
  6. Article
  7. Article
  8. Altered DNA Methylation Profiles inInternational journal of molecular sciences · 2021
    Article
  9. Chromatin network markers of leukemia.Bioinformatics (Oxford, England) · 2020
    Article
  10. Review
  11. Article
  12. Article
  13. Chronic lymphocytic leukaemia.Nature reviews. Disease primers · 2017
    Review
  14. 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

8 authors at 4 institutions in 1 country.

Sujata Bhoia Department of Immunology , Genetics and Pathology, Science for Life Laboratory, Uppsala University , Sweden.
Viktor Ljungströma Department of Immunology , Genetics and Pathology, Science for Life Laboratory, Uppsala University , Sweden.
Panagiotis Baliakasa Department of Immunology , Genetics and Pathology, Science for Life Laboratory, Uppsala University , Sweden.
Mattias Mattssona Department of Immunology , Genetics and Pathology, Science for Life Laboratory, Uppsala University , Sweden.
Karin E Smedbyc Department of Medicine Solna , Clinical Epidemiology Unit, Karolinska Institutet , Stockholm , Sweden.
Gunnar Juliussond Department of Laboratory Medicine , Stem Cell Center, Hematology and Transplantation, Lund University , Lund , Sweden.
Richard Rosenquista Department of Immunology , Genetics and Pathology, Science for Life Laboratory, Uppsala University , Sweden.
Larry Mansouria Department of Immunology , Genetics and Pathology, Science for Life Laboratory, Uppsala University , Sweden.
Science for Life Laboratory · SEUppsala University · SEKarolinska Institutet · SELund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Based on the methylation status of 5 single CpG sites, a novel epigenetic classification of chronic lymphocytic leukemia (CLL) was recently proposed, classifying CLL patients into 3 clinico-biological subgroups with different outcome, termed memory like CLL (m-CLL), naïve like CLL (n-CLL), and a third intermediate CLL subgroup (i-CLL). While m-CLL and n-CLL patients at large corresponded to patients carrying mutated and unmutated IGHV genes, respectively, limited information exists regarding the less defined i-CLL group. Using pyrosequencing, we investigated the prognostic impact of the proposed 5 CpG signature in a well-characterized CLL cohort (135 cases), including IGHV-mutated and unmutated patients as well as clinically aggressive stereotyped subset #2 patients. Overall, we confirmed the signature's association with established prognostic markers. Moreover, in the presence of the IGHV mutational status, the epigenetic signature remained independently associated with both time-to-first-treatment and overall survival in multivariate analyses. As a prime finding, we observed that subset #2 patients were predominantly classified as i-CLL, probably reflecting their borderline IGHV mutational status (97-99% germline identity), though having a similarly poor prognosis as n-CLL patients. In summary, we validated the epigenetic classifier as an independent factor in CLL prognostication and provide further evidence that subset #2 is a member of the i-CLL group, hence supporting the existence of a third, intermediate epigenetic subgroup.

Indexed as

DNA MethylationEpigenesis, GeneticAdultAgedBiomarkers, TumorFemaleHumansLeukemia, Prolymphocytic, B-CellMaleMiddle AgedMutationPrognosisSurvival AnalysisBiomarkers, TumorCLLepigenetic classificationmethylationprognosis

Identifiers

PMID27128508
PMCPMC4939912
OpenAlexW2343709847

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.