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. 2023 Jul 7;9:30. doi: 10.1186/s40959-023-00181-2

Table 2.

Frequency of cardiovascular toxicities by treatment received

Anthracycline only VEGF inhibitor only Anthracycline and VEGF inhibitor (N = 74)
(N = 891) (N = 200)
N (%) N (%) aHR (95% CI) N (%) aHR (95% CI) p*
Any Cardiovascular Toxicity 230 (25.8) 38 (19.0) 0.72 (0.51–1.01) 22 (29.7) 1.06 (0.70–1.61) 0.15
 Hypertension 172 (21.0) 30 (17.4) 0.84 (0.57–1.24) 21 (30.0) 1.32 (0.85–2.05) 0.27
 Cardiomyopathy/heart failure 12 (1.4) 0 (0) - 0 (0) - *
 Cardiomegaly 3 (0.3) 1 (0.5) - 0 (0) - *
 Pericardial disease 21 (2.4) 2 (1.0) - 0 (0) - *
 Myocardial infarction 4 (0.5) 0 (0) - 0 (0) - *
 Coronary artery disease 1 (0.1) 0 (0) - 0 (0) - *
 Conduction abnormality/dysrhythmia 47 (5.3) 5 (2.5) 0.45 (0.18–1.13) 2 (2.7) 0.48 (0.12–1.95) 0.15
 Cerebrovascular event 3 (0.3) 1 (0.5) - 0 (0) - *
 Valvular degeneration 5 (0.6) 1 (0.5) 0.72 (0.09–5.88) 2 (2.8) 4.47 (0.82–24.43) 0.17
 Peripheral vascular disease 7 (0.8) 0 (0) - 0 (0) - *

Groups were compared using Cox proportional hazard models adjusted for age and sex to evaluate time until onset of the cardiovascular toxicity. The anthracyline only group was used for the reference. Study participants with a baseline diagnosis of the cardiovasular toxicity were removed from the given analysis. E.g. the 30 patients in the VEGF group with hypertension are new onset hypertension after excluding the 28 patients with baseline hypertension

CI Confidence interval

*No statistical comparison was made due to infrequent events