Beta-Blocker Use After Pulmonary Embolism in Patients with Cancer: A Real-World Propensity-Matched Study

BackgroundPatients with active malignancy are at heightened risk for pulmonary embolism (PE), yet the prognostic implications of initiating beta-blocker (BB) therapy after PE in this population remain poorly characterized. Given the frequent coexistence of cardiovascular comorbidities, clarifying the safety profile of BB use post-PE in cancer patients is of clinical importance. MethodsWe conducted a retrospective cohort study using the TriNetX Global Health Research Network, a federated database aggregating de-identified electronic health records from over 85 health systems. Adults with active cancer and a new diagnosis of acute PE between January 1, 2015, and May 1, 2024, were included. Patients who received a BB within 30 days of PE diagnosis were assigned to the BB cohort; those who did not formed the comparator group. Propensity score matching (1:1, greedy nearest-neighbor, caliper = 0.01) was applied across baseline covariates. The primary outcome was 5-year all-cause mortality. Secondary outcomes included ICU admission, hospitalization, and incident heart failure. Patients with pre-index occurrence of the outcome were excluded from each respective analysis. Time-to-event analyses began on day 1 post-index using Kaplan-Meier curves and Cox proportional hazards models. Effect estimates were reported as absolute risk differences, odds ratios (OR), risk ratios (RR), and hazard ratios (HR), all with 95% confidence intervals (CI). ResultsAmong 242,034 eligible patients, 19,948 received a beta-blocker within 30 days of PE diagnosis. After matching, 19,743 patients were retained in each cohort with excellent covariate balance (all post-match standardized mean differences <0.10). Over a 5-year period, all-cause mortality occurred in 7,342 of 18,942 BB patients (38.8%) versus 6,757 of 18,848 in the no BB group (35.8%), corresponding to a risk difference of 2.9% (95% CI: 1.9-3.9), RR 1.081 (95% CI: 1.053-1.110), OR 1.133 (95% CI: 1.086-1.181), and HR 1.219 (95% CI: 1.179-1.260). Median survival in the BB group was 1,508 days; median survival was not reached in the no BB group. BB use was also associated with higher rates of ICU admission (RR 1.564, 95% CI: 1.450-1.687), hospitalization (RR 1.118, 95% CI: 1.070-1.167), and incident heart failure (RR 1.080, 95% CI: 1.011-1.155); all associations were statistically significant. ConclusionOur study that showed early beta-blocker use was associated with significantly increased risk of all-cause mortality and multiple adverse clinical outcomes. While rigorous propensity score matching was employed, unmeasured confounding and indication bias remain possible. These findings underscore the need for prospective studies to define the role--and risk--of beta-blocker therapy following thromboembolic events in oncology populations.