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ePoster Display

1831P - Prevalence of cardiovascular disease in patients diagnosed with six common curable malignancies: A Virtual Cardio-Oncology Research Institute (VICORI) national registry dataset analysis

Date

16 Sep 2021

Session

ePoster Display

Topics

Cancer Treatment in Patients with Comorbidities;  Cancer in Older Adults;  Cancer Prevention

Tumour Site

Breast Cancer

Presenters

Nicolò Matteo Luca Battisti

Citation

Annals of Oncology (2021) 32 (suppl_5): S1237-S1256. 10.1016/annonc/annonc701

Authors

N.M.L. Battisti1, C. Welch2, M. DeBelder3, J. Deanfield4, C. Weston5, M.D. Peake6, M. Sweeting2, D. Adlam7, A. Ring8

Author affiliations

  • 1 Department Of Medicine - Breast Unit, The Royal Marsden Hospital (Sutton) - NHS Foundation Trust, SM2 5PT - Sutton/GB
  • 2 Biostatistics Research Team - Department Of Health Sciences, University of Leicester, LE1 7RH - Leicester/GB
  • 3 National Institute For Cardiovascular Outcomes Research, Barts Health NHS Trust, EC1A 4AS - London/GB
  • 4 Institute Of Cardiovascular Sciences, University College London, WC1E 6DD - London/GB
  • 5 Myocardial Ischaemia National Audit Project, School of Medicine, Swansea University, SA2 8QA - Swansea/GB
  • 6 Cancer Division, University College London Hospitals, NW1 2BU - London/GB
  • 7 Cardiovascular Biomedical Research Unit - Leicester Nihr Biomedical Research Centre - Department Of Cardiovascular Sciences, University of Leicester, LE1 7RH - Leicester/GB
  • 8 Department Of Medicine - Breast Unit, The Royal Marsden Hospital NHS Foundation Trust, SM2 5PT - Sutton/GB

Resources

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Abstract 1831P

Background

The co-existence of cardiovascular disease (CVD) in cancer patients may explain treatment and outcomes disparities. However, CVD prevalence in cancer patients is unknown. We described CVD prevalence in adults with curable tumours and investigated factors associated with CVD.

Methods

From the UK National Cancer Registration and Analysis Service we retrieved data on patients with stage I-III breast cancer (BC), stage I-III colon/rectal cancer (CC/RC), stage I-III prostate cancer (PC), stage I-IIIA non-small cell lung cancer (NSCLC), stage I-IV diffuse large B cell lymphoma (DLBCL) and stage I-IV Hodgkin lymphoma (HL) in England in 2013-2018. We identified CVD from Hospital Episode Statistics and National Institute for Cardiovascular Outcomes Research datasets. We investigated CVD rates in tumour cohorts and evaluated the impact of patient and disease characteristics on its prevalence.

Results

Among 640,958 patients, mean age was 67.2 years, 47.5% of patients were male, 66.0% had Index of Multiple Deprivation (IMD) 1-3 and 46.7% Charlson comorbidity index (CCI) 0.104,035 (16.2%) had CVD. Men, older patients and those with higher CCI, more advanced stage cancer or higher IMD had higher CVD rates. After age- and sex-standardisation, prevalence was highest for NSCLC (36.2%) and lowest for BC patients (7.8%). After adjustment for age, sex, IMD and CCI, CVD odds were highest in NSCLC patients vs the other cohorts. NSCLC patients had the highest prevalence of ischaemic heart disease (21.8%), peripheral vascular disease (11.1%), congestive cardiac failure (8.5%), cerebrovascular disease (6.2%), valvular heart disease (6.1%), stroke (3.0%) and myocardial infarction (3.8%). BC patients had lower CVD category rates. Odds ratios (OR) of CVD were larger for each cohort compared to BC, particularly for NSCLC. After adjustment for age, sex, stage, IMD and CCI, all cohorts were significantly different to BC (OR 2.57; 95% CI 2.50, 2.64).

Conclusions

There is significant overlap between cancer and CVD although this varies between tumour types. CVD prevalence is key when comparing national and international treatment patterns and cancer outcomes.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Virtual Cardio-Oncology Research Institute.

Funding

Virtual Cardio-Oncology Research Institute.

Disclosure

N.M.L. Battisti: Financial Interests, Personal, Training: Lilly; Financial Interests, Personal, Speaker’s Bureau: Pfizer; Financial Interests, Personal, Training: Pfizer; Financial Interests, Personal, Speaker’s Bureau: AbbVie; Financial Interests, Personal, Training: Genomic Health. A. Ring: Financial Interests, Personal, Advisory Board: Roche; Financial Interests, Personal, Advisory Board: Novartis; Financial Interests, Personal, Advisory Board: Pfizer; Financial Interests, Personal, Advisory Board: MSD; Financial Interests, Personal, Advisory Board: Lilly. All other authors have declared no conflicts of interest.

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