Factor | Coefficient±SE | P value |
Early phase/within 3 years after cancer diagnosis | ||
Cardiotoxic cancer therapeutics | 0.10±0.220 | 0.66 |
Time of first cardiotoxic cancer therapeutic | 0.94±0.039 | <0.001* |
Non-cardiotoxic cancer therapeutics | 0.14±0.220 | 0.51 |
Time of first non-cardiotoxic cancer therapeutic | 0.03±0.051 | 0.59 |
Late phase/(at least) 3 years after cancer diagnosis | ||
Cardiotoxic cancer therapeutics | −0.21±0.250 | 0.40 |
Time of first cardiotoxic cancer therapeutic | −0.06±0.069 | 0.36 |
Non-cardiotoxic cancer therapeutics | 0.44±0.340 | 0.19 |
Time of first non-cardiotoxic cancer therapeutic | 0.06±0.049 | 0.27 |
Time-varying covariate of AF diagnosis and time of AF diagnosis was forced into the model and adjusted for cardiotoxic versus non-cardiotoxic cancer therapeutics. Because cancer therapeutics timing varies from time zero (date of cancer diagnosis), we analysed cardiotoxic versus non-cardiotoxic cancer therapeutics as a time-varying covariate using parametric hazard function modelling. Cardiotoxic cancer therapeutics included anthracyclines, HER2-neu inhibitors, tyrosine kinase inhibitors, targeted chemotherapy and radiation. Non-cardiotoxic chemotherapy included all other chemotherapy such as alkylating agents, antimetabolites and antimicrotubule inhibitors.
*p<0.05.
AF, atrial fibrillation.