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Early antibiotic exposure reduces progression-free survival in unresectable hepatocellular carcinoma patients treated with TACE plus TKI and ICI therapy: a propensity score-matched analysis

Ren L, Suwanbai M, Shi L, Yan S, Deng C, Xie W, Li L, Yang G et al.

BMC gastroenterology, 2026

Abstract

Background/objective: The combination of immune checkpoint inhibitors (ICIs) with transarterial chemoembolization (TACE) and tyrosine kinase inhibitors (TKIs) has emerged as a promising treatment strategy for unresectable HCC; however, the impact of concurrent antibiotic use on treatment efficacy remains controversial and poorly understood. This study aimed to evaluate the impact of early antibiotic (ATB) exposure on the long-term efficacy of TACE, TKI and ICI therapy in patients with unresectable intermediate-to-advanced HCC.

Methods: We conducted a retrospective analysis of patients with hepatitis B virus (HBV)-related advanced HCC who received combination therapy with TACE, TKIs, and ICIs at the Affiliated Hospital of Xuzhou Medical University from January 1, 2019, to December 31, 2024. Patients were classified into the ATB group and non-ATB group based on whether they had received ATB therapy within 30 days prior to or 30 days after ICI initiation. The median follow-up duration was 20 months (interquartile range: 12-28 months). Follow-up assessments were performed every 3 months through outpatient reviews, re-admissions, or telephone contact.

Results: After PSM, 20 matched pairs were analyzed. No significant difference in overall survival (OS) between the ATB and non-ATB groups (median OS:18.2vs24.0 months; P = 0.692). However, progression-free survival (PFS) was significantly shorter in the ATB group (median PFS:7.6vs12.3 months; P = 0.006). Multivariable analysis…

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Evidence Hub reads this as a cohort study, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence.

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