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Combination TACE plus systemic therapy showed no PFS benefit but improved OS in BCLC-C HCC patients compared to TACE alone.

Combination TACE plus systemic therapy showed no PFS benefit but improved OS in BCLC-C HCC patients …
Photo by Isaac Quesada / Unsplash
Key Takeaway
Consider combination therapy for BCLC-C HCC given improved OS, but note comparable PFS and safety versus TACE alone.

This retrospective cohort study included 142 patients with intermediate and advanced-stage hepatocellular carcinoma (BCLC B or C) treated at Hunan Provincial People's Hospital. The intervention involved combination therapy consisting of TACE plus systemic therapy, compared against TACE monotherapy. Follow-up duration was not reported for this analysis.

Regarding progression-free survival, no significant difference was observed between the combination group and the monotherapy group, with median durations of 5.5 versus 6.0 months respectively (P= 0.832). For overall survival in BCLC-C patients specifically, the combination group demonstrated a significant benefit with 17.9 versus 11.0 months (P= 0.048). In BCLC-B patients, overall survival showed no significant difference at 18.3 versus 17.4 months (P= 0.516). Overall overall survival showed a trend toward improvement in the combination group at 24.8 versus 16.7 months (P= 0.282).

Adverse events of Grade 3 or 4 occurred in 7.2% versus 14.9% of patients in the respective groups (P= 0.187), indicating a comparable safety profile. Tolerability was comparable between groups, particularly in patients with preserved liver function. Serious adverse events and discontinuations were not reported.

Key limitations include the single-center design and the retrospective nature of the data. Controversies regarding survival benefits and safety persist in this field. These results highlight the importance of patient selection and warrant further prospective studies to optimize treatment strategies.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedMay 2026
View Original Abstract ↓
BackgroundTransarterial chemoembolization (TACE) is a standard treatment for intermediate-stage hepatocellular carcinoma (HCC), but its efficacy varies due to patient heterogeneity. Combining TACE with systemic therapies, such as targeted agents or immune checkpoint inhibitors, has shown promise in improving outcomes, though controversies regarding survival benefits and safety persist. This study investigates whether synchronized systemic therapy enhances the therapeutic efficacy of TACE in intermediate and advanced-stage HCC.MethodsThis single-center, retrospective study included 142 patients with intermediate and advanced-stage HCC (BCLC B or C) who received TACE as initial treatment between February 2019 and August 2022 at Hunan Provincial People’s Hospital. Patients were divided into two groups: combination therapy (TACE plus systemic therapy, n=41) and TACE monotherapy (n=101). Progression-free survival (PFS), overall survival (OS), treatment response (per mRECIST criteria), and adverse events (AEs) were compared. Cox regression and Kaplan-Meier analyses were used to assess survival outcomes.ResultsNo significant differences were observed in baseline characteristics, except for a higher proportion of Child-Pugh A patients in the combination group (90.2% vs. 67.3%, P= 0.005). Median PFS was similar between the combination and monotherapy groups (5.5 vs. 6.0 months, P= 0.832), with no significant differences in BCLC-B (18.3 vs. 17.4 months, P= 0.516) or BCLC-C (4.1 vs. 3.7 months, P= 0.255) subgroups. However, the combination group showed a trend toward improved OS (24.8 vs. 16.7 months, P= 0.282), with a significant benefit in BCLC-C patients (17.9 vs. 11.0 months, P= 0.048). Grade 3 or 4 AEs were comparable between groups (7.2% vs. 14.9%, P= 0.187).ConclusionCombining systemic therapy with TACE does not improve PFS but may enhance OS in BCLC-C patients. The safety profile is comparable, particularly in patients with preserved liver function. These findings highlight the importance of patient selection and warrant further prospective studies to optimize treatment strategies.
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