Evidence map›Paper›PMID 26848054›Full record

Trial reportBritish journal of haematology2016

The Dohner fluorescence in situ hybridization prognostic classification of chronic lymphocytic leukaemia (CLL): the CLL Research Consortium experience.

Daniel L Van Dyke, Lillian Werner, Laura Z Rassenti, Donna Neuberg, Emanuella Ghia, Nyla A Heerema, Paola Dal Cin, Marie Dell Aquila, Chandrika Sreekantaiah, Andrew W Greaves and 2 more

Open access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in British journal of haematology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

37 citing papers in PubMed, 76 citations in OpenAlex.

  1. Trial
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  7. CAD204520 TargetsInternational journal of molecular sciences · 2024
    Article
  8. Association of Cytogenetics Aberrations andGlobal medical genetics · 2024
    Article
  9. Article
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  11. Article
  12. Review
  13. Rare GermlineJournal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Article
  14. Article
  15. Article
  16. Article
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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

12 authors at 7 institutions in 1 country.

Daniel L Van DykeDepartments of Laboratory Medicine and Pathology and Internal Medicine, Mayo Clinic, Rochester, MN, USA.
Lillian WernerBiostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA.
Laura Z RassentiMoores University of California San Diego Cancer Center, La Jolla, CA, USA.
Donna NeubergBiostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA.
Emanuella GhiaMoores University of California San Diego Cancer Center, La Jolla, CA, USA.
Nyla A HeeremaDepartment of Pathology, The Ohio State University, Columbus, OH, USA.
Paola Dal CinBrigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Marie Dell AquilaMoores University of California San Diego Cancer Center, La Jolla, CA, USA.
Chandrika SreekantaiahNorth Shore-LIJ Health System, Long Island, NY, USA.
Andrew W GreavesMoores University of California San Diego Cancer Center, La Jolla, CA, USA.
Thomas J KippsMoores University of California San Diego Cancer Center, La Jolla, CA, USA.
Neil E KayDepartments of Laboratory Medicine and Pathology and Internal Medicine, Mayo Clinic, Rochester, MN, USA.
University of California, San Diego · USDana-Farber Cancer Institute · USHarvard University · USMayo Clinic in Arizona · USMayo Clinic in Florida · USNorthwell Health · USThe Ohio State University · US

Funding

Tissue CoreP01CA081534 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KIPPS, THOMAS J · 2000 to 2016
$59.5M
NCI NIH HHS P01 CA081534
6 · The paper itself

Abstract

This study revisited the Dohner prognostic hierarchy in a cohort of 1585 well-documented patients with chronic lymphocytic leukaemia. The duration of both time to first treatment (TTFT) and overall survival (OS) were significantly longer than observed previously, and this is at least partly due to improved therapeutic options. Deletion 13q remains the most favourable prognostic group with median TTFT and OS from fluorescence in situ hybridization (FISH) testing of 72 months and >12 years, respectively. Deletion 11q had the poorest median TTFT (22 months) and 17p deletion the poorest median OS (5 years). The percentages of abnormal nuclei were significantly associated with differential TTFT for the trisomy 12, 13q and 17p deletion cohorts but not for the 11q deletion cohort. From the date of the first FISH study, patients with >85% 13q deletion nuclei had a notably shorter TTFT (24 months). Patients with ≤20% 17p deletion nuclei had longer median TTFT and OS from the date of the first FISH study (44 months and 11 years), and were more likely to be IGHV mutated.

Indexed as

Chromosome DeletionIn Situ Hybridization, FluorescenceChromosomes, HumanDisease-Free SurvivalFemaleFollow-Up StudiesHumansLeukemia, Lymphocytic, Chronic, B-CellMaleSurvival Ratechronic lymphocytic leukaemiacytogeneticsfluorescence in situ hybridizationleukaemia

Identifiers

PMID26848054
PMCPMC4963001
OpenAlexW2271365036

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.