Prognostic significance of troponin in patients with malignancy (NIHR Health Informatics Collaborative TROP-MALIGNANCY study).

Biomarkers Cancer Cardio-oncology Malignancy Mortality Troponin

Journal

Cardio-oncology (London, England)
ISSN: 2057-3804
Titre abrégé: Cardiooncology
Pays: England
ID NLM: 101689938

Informations de publication

Date de publication:
05 Jul 2024
Historique:
received: 10 02 2024
accepted: 28 05 2024
medline: 6 7 2024
pubmed: 6 7 2024
entrez: 5 7 2024
Statut: epublish

Résumé

Cardiac troponin is commonly raised in patients presenting with malignancy. The prognostic significance of raised troponin in these patients is unclear. We sought to investigate the relation between troponin and mortality in a large, well characterised cohort of patients with a routinely measured troponin and a primary diagnosis of malignancy. We used the National Institute for Health Research (NIHR) Health Informatics Collaborative data of 5571 patients, who had troponin levels measured at 5 UK cardiac centres between 2010 and 2017 and had a primary diagnosis of malignancy. Patients were classified into solid tumour or haematological malignancy subgroups. Peak troponin levels were standardised as a multiple of each laboratory's 99th -percentile upper limit of normal (xULN). 4649 patients were diagnosed with solid tumours and 922 patients with haematological malignancies. Raised troponin was an independent predictor of mortality in all patients (Troponin > 10 vs. <1 adjusted HR 2.01, 95% CI 1.73 to 2.34), in solid tumours (HR 1.84, 95% CI 1.55 to 2.19), and in haematological malignancy (HR 2.72, 95% CI 1.99 to 3.72). There was a significant trend in increasing mortality risk across troponin categories in all three subgroups (p < 0.001). Raised troponin level is associated with increased mortality in patients with a primary diagnosis of malignancy regardless of cancer subtype. Mortality risk is stable for patients with a troponin level below the ULN but increases as troponin level increases above the ULN in the absence of acute coronary syndrome.

Sections du résumé

BACKGROUND BACKGROUND
Cardiac troponin is commonly raised in patients presenting with malignancy. The prognostic significance of raised troponin in these patients is unclear.
OBJECTIVES OBJECTIVE
We sought to investigate the relation between troponin and mortality in a large, well characterised cohort of patients with a routinely measured troponin and a primary diagnosis of malignancy.
METHODS METHODS
We used the National Institute for Health Research (NIHR) Health Informatics Collaborative data of 5571 patients, who had troponin levels measured at 5 UK cardiac centres between 2010 and 2017 and had a primary diagnosis of malignancy. Patients were classified into solid tumour or haematological malignancy subgroups. Peak troponin levels were standardised as a multiple of each laboratory's 99th -percentile upper limit of normal (xULN).
RESULTS RESULTS
4649 patients were diagnosed with solid tumours and 922 patients with haematological malignancies. Raised troponin was an independent predictor of mortality in all patients (Troponin > 10 vs. <1 adjusted HR 2.01, 95% CI 1.73 to 2.34), in solid tumours (HR 1.84, 95% CI 1.55 to 2.19), and in haematological malignancy (HR 2.72, 95% CI 1.99 to 3.72). There was a significant trend in increasing mortality risk across troponin categories in all three subgroups (p < 0.001).
CONCLUSION CONCLUSIONS
Raised troponin level is associated with increased mortality in patients with a primary diagnosis of malignancy regardless of cancer subtype. Mortality risk is stable for patients with a troponin level below the ULN but increases as troponin level increases above the ULN in the absence of acute coronary syndrome.

Identifiants

pubmed: 38970129
doi: 10.1186/s40959-024-00238-w
pii: 10.1186/s40959-024-00238-w
doi:

Types de publication

Journal Article

Langues

eng

Pagination

41

Subventions

Organisme : British Heart Foundation
ID : CH/1999001/11735
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/14/76/30933
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RE/18/4/34215
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/19/17/34172
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/20/18/34972
Pays : United Kingdom

Informations de copyright

© 2024. The Author(s).

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Auteurs

Nathan A Samuel (NA)

NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare NHS Trust, London, U.K.
NIHR Oxford Biomedical Research Centre, University of Oxford and Oxford University Hospitals NHS Foundation Trust, Oxford, U.K.

Alistair Roddick (A)

NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare NHS Trust, London, U.K.
NIHR Oxford Biomedical Research Centre, University of Oxford and Oxford University Hospitals NHS Foundation Trust, Oxford, U.K.

Ben Glampson (B)

NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare NHS Trust, London, U.K.

Abdulrahim Mulla (A)

NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare NHS Trust, London, U.K.

Jim Davies (J)

NIHR Oxford Biomedical Research Centre, University of Oxford and Oxford University Hospitals NHS Foundation Trust, Oxford, U.K.

Dimitri Papadimitriou (D)

NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare NHS Trust, London, U.K.

Vasileios Panoulas (V)

NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare NHS Trust, London, U.K.
National Heart and Lung Institute, Imperial College London, London, U.K.

Erik Mayer (E)

NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare NHS Trust, London, U.K.
Department of Surgery & Cancer, Imperial College London, London, UK.

Kerrie Woods (K)

NIHR Oxford Biomedical Research Centre, University of Oxford and Oxford University Hospitals NHS Foundation Trust, Oxford, U.K.

Anoop D Shah (AD)

Hospitals Biomedical Research Centre, NIHR University College London, University College London and University College London Hospitals NHS Foundation Trust, London, U.K.

Sanjay Gautama (S)

NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare NHS Trust, London, U.K.

Paul Elliott (P)

NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare NHS Trust, London, U.K.
Health Data Research UK, London Substantive Site, London, U.K.

Harry Hemmingway (H)

Hospitals Biomedical Research Centre, NIHR University College London, University College London and University College London Hospitals NHS Foundation Trust, London, U.K.
Health Data Research UK, London Substantive Site, London, U.K.

Bryan Williams (B)

Hospitals Biomedical Research Centre, NIHR University College London, University College London and University College London Hospitals NHS Foundation Trust, London, U.K.

Folkert W Asselbergs (FW)

Hospitals Biomedical Research Centre, NIHR University College London, University College London and University College London Hospitals NHS Foundation Trust, London, U.K.

Narbeh Melikian (N)

NIHR King's Biomedical Research Centre, King's College London and King's College Hospital NHS Foundation Trust, London, U.K.

Rajesh Kharbanda (R)

NIHR Oxford Biomedical Research Centre, University of Oxford and Oxford University Hospitals NHS Foundation Trust, Oxford, U.K.

Ajay M Shah (AM)

NIHR King's Biomedical Research Centre, King's College London and King's College Hospital NHS Foundation Trust, London, U.K.

Divaka Perera (D)

NIHR King's Biomedical Research Centre, King's College London and Guy's and St Thomas' NHS Foundation Trust, London, U.K.

Riyaz S Patel (RS)

Hospitals Biomedical Research Centre, NIHR University College London, University College London and University College London Hospitals NHS Foundation Trust, London, U.K.

Keith M Channon (KM)

NIHR Oxford Biomedical Research Centre, University of Oxford and Oxford University Hospitals NHS Foundation Trust, Oxford, U.K.

Jamil Mayet (J)

NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare NHS Trust, London, U.K.. j.mayet@imperial.ac.uk.
National Heart and Lung Institute, Imperial College London, London, U.K.. j.mayet@imperial.ac.uk.
Imperial College Healthcare NHS Trust, Hammersmith Hospital, NHLI offices, B Block 2nd Floor, Du Cane Road, W12 0HS, London, U.K.. j.mayet@imperial.ac.uk.

Anoop S V Shah (ASV)

NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare NHS Trust, London, U.K.
National Heart and Lung Institute, Imperial College London, London, U.K.
London School of Hygiene Tropical Medicine, London, U.K.

Amit Kaura (A)

NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare NHS Trust, London, U.K.
National Heart and Lung Institute, Imperial College London, London, U.K.

Classifications MeSH