Key result
Cardiovascular thrombosis after TACE is linked to ~130% higher mortality in HCC patients.
Why the study?
Cardiovascular thrombosis complications are expected to rise in hepatocellular carcinoma due to shifting etiologies, but its clinical impact after transarterial chemoembolization needed evaluation.
Does the presence of cardiovascular thrombosis worsen overall survival in patients with hepatocellular carcinoma treated with transarterial chemoembolization?
Cohort (n=402)
No
Does the presence of cardiovascular thrombosis worsen overall survival in patients with hepatocellular carcinoma treated with transarterial chemoembolization?
Cardiovascular thrombosis is a major independent prognostic factor that significantly shortens overall survival and post-recurrence survival in patients with hepatocellular carcinoma undergoing transarterial chemoembolization.
CVT after TACE in HCC was associated with halved survival; leaves open whether prevention alters outcomes.
Objectives Progression of hepatocellular carcinoma (HCC) and cardiovascular thrombosis (CVT) has a bidirectional causal relationship. CVT complications will increase in patients with HCC due to etiology shift from viral hepatitis to metabolic dysfunction‐related steatohepatitis. Aim This study aimed to evaluate the clinical impact of CVT, focusing on patients with HCC treated after transarterial chemoembolization. Methods A retrospective cohort study enrolled 402 patients including 79 patients with CVT in a single university hospital. Cox proportional hazard model analysis was performed to identify independent prognostic factors. After adjusting for baseline characteristics by propensity score matching, the survival impact of the CVT complication was evaluated using the Kaplan–Meier curve. Results A multivariate analysis determined that CVT complication was an independent risk factor for overall deaths in patients with HCC (HR = 1.751, IQR 1.203–2.548, p < 0.05). Propensity score matching generated a pair of 54‐patient cohorts. The median survival time of patients with CVT (1106 days) shortened to half compared to those without CVT (2707 days, HR = 2.298, IQR: 1.399–4.169, p = 0.0020). While recurrence‐free survival was not significantly different ( p > 0.05), post‐recurrence survival was shorter in patients with CVT (2150 days vs. 1008 days, HR = 1.945, IQR: 1.150–3.740, p = 0.0188). Conclusions Assuming that the expected life expectancy is only half that of uncomplicated cases of CVT, CVT might be a major prognostic factor in patients with HCC, following tumor burden and functional hepatic reserve.
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FUJITA et al. (2026) conducted a cohort in Patients with hepatocellular carcinoma treated with transarterial chemoembolization, including those with cardiovascular thrombosis (n=402). Cardiovascular thrombosis (CVT) presence vs. No cardiovascular thrombosis was evaluated on Overall survival after TACE (HR 2.298, 95% CI 1.399–4.169, p=0.0020). Cardiovascular thrombosis reduced median overall survival by half after TACE (1106 vs 2707 days) with HR 2.298 (p=0.002) in hepatocellular carcinoma patients.
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