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173 Prognostic significance of troponin in patients with malignancy (nihr health informatics collaborative trop-malignancy study)
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  1. Amit Kaura1,
  2. Nathan A Samuel2,
  3. Alistair Roddick3,
  4. Benjamin Glampson4,
  5. Abdulrahim Mulla5,
  6. Jim Davies6,
  7. Vasileios Panoulas7,
  8. Kerrie Woods8,
  9. Anoop D Shah9,
  10. Sanjay Gautama10,
  11. Paul Elliott11,
  12. Harry Hemingway12,
  13. Bryan Williams13,
  14. Folkert W Asselbergs14,
  15. Narbeh Melikian15,
  16. Ajay M Shah16,
  17. Rajesh Kharbanda17,
  18. Divaka Perera18,
  19. Riyaz S Patel19,
  20. Keith M Channon20,
  21. Anoop SV Shah21,
  22. Jamil Mayet22
  1. 1NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare, Hammersmith Hospital, National Heart and Lung Institute, London, GLN W12 0HS, United Kingdom
  2. 2NIHR Oxford Biomedical Research Centre, University of Oxford and Oxford University Hospitals
  3. 3NIHR Oxford Biomedical Research Centre, University of Oxford and Oxford University Hospitals
  4. 4NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare
  5. 5NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare
  6. 6NIHR Oxford Biomedical Research Centre, University of Oxford and Oxford University Hospitals
  7. 7NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare
  8. 8NIHR Oxford Biomedical Research Centre, University of Oxford and Oxford University Hospitals
  9. 9NIHR UCL Biomedical Research Centre, UCL and UCL Hospitals
  10. 10NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare
  11. 11NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare
  12. 12NIHR UCL Biomedical Research Centre, UCL and UCL Hospitals
  13. 13NIHR UCL Biomedical Research Centre, UCL and UCL Hospitals
  14. 14NIHR UCL Biomedical Research Centre, UCL and UCL Hospitals
  15. 15NIHR King’s Biomedical Research Centre, King’s College London and King’s College Hospital
  16. 16NIHR King’s Biomedical Research Centre, King’s College London and King’s College Hospital
  17. 17NIHR Oxford Biomedical Research Centre, University of Oxford and Oxford University Hospitals
  18. 18NIHR King’s Biomedical Research Centre, King’s College London and Guy’s and St Thomas’
  19. 19NIHR UCL Biomedical Research Centre, UCL and UCL Hospitals
  20. 20NIHR Oxford Biomedical Research Centre, University of Oxford and Oxford University Hospitals
  21. 21NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare
  22. 22NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare

Abstract

Background Cardiac troponin is commonly raised in patients with malignancy and may aid clinicians in risk prediction. The prognostic significance of raised troponin in these patients with known malignancies remains unclear. We sought to investigate the relation between troponin and mortality in a large, well characterised cohort of patients undergoing cardiac troponin testing with a concomitant malignancy. MethodsA retrospective cohort study was carried out using the National Institute for Health Research Health Informatics Collaborative Cardiovascular dataset of all consecutive patients who had a troponin measured at five hospitals (Imperial, University College London, Oxford, King’s and Guy’s and St Thomas’) between 2010 and 2017. Patients with a primary inpatient diagnosis of malignancy who had at least one cTn measurement during their hospital stay were identified. Patients were classified into solid tumour or haematological malignancy subgroups. Survival analyses were performed using multivariate Cox-Regression analyses and Kaplan-Meier plots. The peak cTn level (highest level measured), standardised to the upper limit of normal (ULN), was used for all analyses.Results5571 patients undergoing troponin testing had a primary diagnosis of malignancy and comprised of twenty-one different cancer types. 4649 patients were diagnosed with solid tumours and 922 patients were diagnosed with haematological malignancies. Patients with raised troponin had a higher burden of cardiovascular comorbidities compared to patients with a troponin level below the ULN. The median follow-up in the cohort was 14 months (interquartile range 2–39 months). At 1-year follow-up, 2495 (42%) of patients died.Figure 1 shows Kaplan-Meier plots for patients stratified by troponin level. Patients with a troponin level >1xULN had a higher risk of death compared to patients with a troponin level <1xULN (Figure 1A). A similar trend was shown in cancer subtypes (Figure 1B-C). Raised troponin was an independent predictor of mortality in all patients with malignancy (adjusted hazard ratio 1.66, 95% confidence interval [CI] 1.52–1.81), in solid tumours (adjusted hazard ratio 1.63, 95% CI 1.48–1.81) and in haematological malignancy (adjusted hazard ratio 1.75, 95% CI 1.44 to 2.13) when compared to troponin level below the ULN.

Abstract 173 Figure 1

One-year Kaplan-Meier survival curves for different troponin levels in patients with (A) any malignancy, (B) solid tumours or (C) haematological malignancy

Conclusion Raised troponin level was associated with increased mortality in patients with malignancy regardless of cancer subtype. Troponin may be more widely useful in the risk stratification of patients with cancer. Although the appropriate management of patients in response to raised troponin in the absence of acute coronary syndrome is not clear, stratification of clinical risk of mortality can be helpful in general decision making.

Conflict of Interest No conflicts of interest

  • Malignancy
  • Mortality
  • Troponin

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