Evidence map›Paper›PMID 41324573›Full record

ArticleJournal of the National Cancer Institute2026

Lymphocyte count and risk of chronic lymphocytic leukemia.

Simon Pahnke, Karine Alcala, Connie Bulos Salim, Ricardo Cortez Cardoso Penha, Hanla A Park, James Mckay, Mattias Johansson

Abstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Simon PahnkeDepartment of Immunology, Genetics and Pathology, Cancer Precision Medicine, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-3541-2027
Karine AlcalaGenomic Epidemiology Branch, International Agency for Research on Cancer (IARC/World Health Organization), Lyon, France.ORCID 0000-0003-2308-9880
Connie Bulos SalimGenomic Epidemiology Branch, International Agency for Research on Cancer (IARC/World Health Organization), Lyon, France.
Ricardo Cortez Cardoso PenhaGenomic Epidemiology Branch, International Agency for Research on Cancer (IARC/World Health Organization), Lyon, France.ORCID 0000-0002-2847-1993
Hanla A ParkGenomic Epidemiology Branch, International Agency for Research on Cancer (IARC/World Health Organization), Lyon, France.ORCID 0000-0001-8055-3729
James MckayGenomic Epidemiology Branch, International Agency for Research on Cancer (IARC/World Health Organization), Lyon, France.ORCID 0000-0002-1787-3874
Mattias JohanssonGenomic Epidemiology Branch, International Agency for Research on Cancer (IARC/World Health Organization), Lyon, France.ORCID 0000-0002-3116-5081

Funding

NCI NIH HHS UO1CA257679World Health Organization 001
6 · The paper itself

Abstract

backgroundElevated absolute lymphocyte count is often used as a first indication for diagnostic investigation of chronic lymphocytic leukemia (CLL). The absolute risk of CLL as a function of age, sex, and absolute lymphocyte count has not been described.

methodsWe used information about prediagnostic absolute lymphocyte cell count on 475 399 longitudinally followed research participants from UK Biobank, with a median follow-up of 11.6 years, during which 854 participants were diagnosed with CLL. A CLL risk model was developed based on sex, age at recruitment, and prediagnostic absolute lymphocyte count using flexible parametric survival modelling.

resultsCompared with research participants who had absolute lymphocyte counts below 2 × 109/L, the risk of CLL was almost 8 times higher for individuals with absolute lymphocyte counts of 3 to 4 × 109/L (hazard ratio = 7.76, 95% CI = 6.24 to 9.65). The absolute risk of CLL was 2-fold higher in male than in female individuals. For 60-year-old persons with absolute lymphocyte counts of 5 ×109/L, 10-year CLL risk was estimated at 6.5% (95% CI = 5.6% to 7.5%) for men and 3.5% (95% CI = 3.0% to 4.1%) for women. The 10-year risk of CLL for participants with absolute lymphocyte counts of 5 ×109/L varied between 0.91% (95% CI = 0.68% to 1.2%) for a 40-year-old woman and 12% (95% CI = 11% to 15%) for a 70-year-old man.

conclusionThe absolute risk of CLL is strongly influenced by age, sex, and absolute lymphocyte count. A crude absolute lymphocyte count cutoff to indicate further investigation for CLL without taking age and sex into consideration will identify some individuals who are at low risk. These results may be considered when establishing guidelines for clinical management in patients with elevated absolute lymphocyte counts.

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellAdultAgedAged, 80 and overAge FactorsFemaleFollow-Up StudiesHumansLongitudinal StudiesLymphocyte CountMaleMiddle AgedRisk AssessmentRisk FactorsSex FactorsUnited Kingdom

Identifiers

PMID41324573
PMCPMC13064517

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.