Evidence map›Paper›PMID 42057558›Full record

ArticleInternational journal of cancer2026

Adverse Health Events in Chronic Myeloid Leukaemia Patients Treated With Tyrosine Kinase Inhibitors 2009-2019: A Real-World Study From the UK's Haematological Malignancy Research Network.

Eleanor Kane, Alexandra Smith, Debra Howell, Catherine Cargo, Kate Rothwell, Simone Green, Russell Patmore, Eve Roman

Abstract read
In one paragraph

Article in International journal of cancer, 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

8 authors.

Eleanor KaneEpidemiology and Cancer Statistics Group, Department of Health Sciences, University of York, York, UK.ORCID https://orcid.org/0000-0002-7438-9982
Alexandra SmithEpidemiology and Cancer Statistics Group, Department of Health Sciences, University of York, York, UK.ORCID https://orcid.org/0000-0002-1111-966X
Debra HowellEpidemiology and Cancer Statistics Group, Department of Health Sciences, University of York, York, UK.ORCID https://orcid.org/0000-0002-7521-7402
Catherine CargoHaematological Malignancy Diagnostic Service, St James's University Hospital, Leeds, UK.ORCID https://orcid.org/0000-0002-5185-0190
Kate RothwellDepartment of Clinical Haematology, Leeds Teaching Hospital NHS Trust, Leeds, UK.
Simone GreenQueen's Centre for Oncology and Haematology, Castle Hill Hospital, Cottingham, UK.
Russell PatmoreQueen's Centre for Oncology and Haematology, Castle Hill Hospital, Cottingham, UK.ORCID https://orcid.org/0000-0002-0925-9014
Eve RomanEpidemiology and Cancer Statistics Group, Department of Health Sciences, University of York, York, UK.ORCID https://orcid.org/0000-0001-7603-3704

Funding

Cancer Research UK and Blood Cancer UK 29685National Institute for Health and Care Research (NIHR) Leeds Biomedical Research Centre (BRC) NIHR203331
6 · The paper itself

Abstract

Outcomes among patients with chronic myeloid leukaemia (CML) improved markedly when tyrosine kinase inhibitors (TKIs) were introduced into routine clinical practice around the turn of the century. Nonetheless, adverse events still occur, survival remains suboptimal and the long-term health impact of the disease and its treatment is poorly understood. Using data from an established UK population-based cohort of haematological malignancies, we compared the morbidity of 411 CML patients treated with TKIs 2009-2019 to that of individually age- and sex-matched general population-based controls (n = 4099). Over the course of follow-up (to March 2021, median 5.3, interquartile range 3.0-8.2 years), patients were more likely than controls to die from cardiovascular or respiratory diseases; Hazard Ratios of 1.9, 95% Confidence Interval, 95% CI = 1.2-2.8 and 2.4, 95% CI 1.2-4.9 respectively. Hospital admissions for cardiovascular or respiratory conditions were similarly elevated; HR = 1.6, 95% CI 1.3-1.9; HR = 2.3, 95% CI 1.6-3.4 respectively. The risk of a cardiovascular admission varied over time; being increased in the first year (HR = 2.4, 95% CI 1.5-3.8), and then again 5 years or more after starting TKI therapy (HR = 2.3, 95% CI 1.5-3.6); no increase was evident in the intervening years (HR = 1.1, 95% CI 0.8-1.7). While not related to excess mortality, admissions for infections and gastrointestinal conditions occurred more frequently among cases than controls; the increased risk remaining largely constant over the course of follow-up. In the era of TKIs, these real-world analyses revealed that CML patients are at increased risk of severe cardiovascular events several years after starting treatment, and that admission for infections and gastrointestinal conditions are raised throughout.

Indexed as

Cardiovascular DiseasesLeukemia, Myelogenous, Chronic, BCR-ABL PositiveProtein Kinase InhibitorsAdultAgedCase-Control StudiesFemaleHumansMaleMiddle AgedRespiratory Tract DiseasesUnited KingdomProtein Kinase Inhibitorscardiovascular eventschronic myeloid leukaemiamorbiditymortalitytyrosine kinase inhibitor

Identifiers

PMID42057558
PMCPMC13397138

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.