Evidence map›Paper›PMID 27151266›Full record

Trial reportBritish journal of haematology2016

The morphology of CLL revisited: the clinical significance of prolymphocytes and correlations with prognostic/molecular markers in the LRF CLL4 trial.

David Oscier, Monica Else, Estella Matutes, Ricardo Morilla, Jonathan C Strefford, Daniel Catovsky

Open access · hybridAbstract readRandomized Controlled Trial
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 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. [Prognostic value of prolymphocyte percentage in chronic lymphocytic leukemia].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Journal of hematology · 2023
    Article
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  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
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  18. B-cell lymphomas with discordance between pathological features and clinical behavior.Virchows Archiv : an international journal of pathology · 2017
    Article
  19. Review
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

6 authors at 3 institutions in 1 country.

David OscierDepartment of Molecular Pathology, Royal Bournemouth Hospital, Bournemouth, UK.
Monica ElseDivision of Molecular Pathology, The Institute of Cancer Research, London, UK.
Estella MatutesDivision of Molecular Pathology, The Institute of Cancer Research, London, UK.
Ricardo MorillaDivision of Molecular Pathology, The Institute of Cancer Research, London, UK.
Jonathan C StreffordCancer Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Daniel CatovskyDivision of Molecular Pathology, The Institute of Cancer Research, London, UK.
Institute of Cancer Research · GBRoyal Bournemouth Hospital · GBUniversity of Southampton · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Historically, an increase in the percentage and number of circulating prolymphocytes in chronic lymphocytic leukaemia (CLL) has been associated with strong expression of surface immunoglobulin, trisomy 12 and a poor outcome. This study re-examines the biological and clinical significance of increased peripheral blood prolymphocytes in 508 patients at entry into the randomized UK Leukaemia Research Fund CLL4 trial. It also investigates the associations between increased prolymphocytes and a comprehensive array of biomarkers. 270 patients (53%) had <5% prolymphocytes, 167 (33%) had 5-9%, 60 (12%) had 10-14% and 11 (2%) had ≥15% prolymphocytes. We show that a higher proportion of prolymphocytes (≥10%) was independently associated with NOTCH1 mutations (P = 0·006), absence of 13q deletion (P = 0·001), high CD38 expression (P = 0·02) and unmutated IGHV genes (P = 0·01). Deaths due to Richter syndrome were significantly more common amongst patients who had ≥10% vs <10% prolymphocytes (13% vs 2%) respectively (P < 0·0001). ≥10% prolymphocytes was also associated with a shorter progression-free survival (Hazard ratio [HR] 1·50 [95% confidence interval [CI]: 1·16-1·93], P = 0·002) and overall survival (HR 1·99 [95% CI: 1·53-2·59], P < 0·0001). Our data support the routine examination of blood films in CLL and suggest that a finding of an increased proportion of prolymphocytes may be a trigger for further evaluation of clinical and laboratory features of progressive disease.

Indexed as

ADP-ribosyl Cyclase 1AdultAgedAged, 80 and overBiomarkers, TumorChromosome DeletionChromosome DisordersChromosomes, Human, Pair 13Disease-Free SurvivalFemaleHumansLeukemia, Lymphocytic, Chronic, B-CellLymphocytesLymphocyte SubsetsMaleMembrane GlycoproteinsADP-ribosyl Cyclase 1Biomarkers, TumorCD38 protein, humanMembrane GlycoproteinsNOTCH1 protein, humanReceptor, Notch1Chronic lymphocytic leukaemiamolecular markersmorphologyprognostic markersprolymphocytes

Identifiers

PMID27151266
PMCPMC4995732
OpenAlexW2345827498

What OpenQuestion holds

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Registered trials

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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.