# Hepatic arterial infusion chemotherapy (HAlC) versus sorafenib for hepatocellular carcinoma (HCC) in Barcelona Clinic Liver Cancer (BCLC) B/C: A systematic review and meta-analysis

**Authors:** Zhengqiang Chen, Yaotian Fan, Yuting Luo, Xiwen Ye, Zhen You

PMC · DOI: 10.1371/journal.pone.0342495 · PLOS One · 2026-02-18

## TL;DR

This study compares HAIC and sorafenib for liver cancer treatment, finding HAIC, especially FOLFOX-based, offers better survival and fewer side effects.

## Contribution

The study provides a meta-analysis comparing HAIC and sorafenib for HCC in BCLC B/C stages, revealing FOLFOX-based HAIC as more effective.

## Key findings

- HAIC, especially FOLFOX-based regimens, improves overall survival and oncologic outcomes over sorafenib.
- HAIC shows higher response rates and lower disease progression compared to sorafenib in BCLC B/C HCC patients.
- Adverse events are less frequent with HAIC compared to sorafenib, particularly for grade 3−4 events.

## Abstract

Despite both hepatic arterial infusion chemotherapy (HAIC) and sorafenib being efficacious for hepatocellular carcinoma (HCC), choosing between them for Barcelona Clinic Liver Cancer (BCLC) stages B/C patients remains controversial. This meta-analysis aims to compare their therapeutic outcomes and prognoses in such patients.

Pubmed, EMBASE, and Web of Science databases were searched. The primary outcome of this meta-analysis is Overall Survival (OS), while secondary outcomes include Progression-Free Survival (PFS), tumor response rate, and the incidence of adverse events. The analysis has included a total of 18 studies, comprising 3008 patients in aggregate.

The analysis revealed a combined Hazard Ratio (HR) for OS of 0.57 (95% CI 0.38–0.86) and for PFS of 0.46 (95% CI 0.38–0.57). Subgroup analysis by different HAIC regimens: FOLFOX-based HAIC regimens 0.28 (95% CI: 0.16–0.50), FP regimen 0.68 (95% CI: 0.25–1.87), New-FP regimen 0.60 (95% CI: 0.47–0.77), cisplatin-based HAIC 0.63 (95% CI: 0.47–0.85). The pooled ORs were: Complete Response (CR) 3.88 (95% CI 1.56–9.65), Partial Response (PR)4.72(95% CI 2.44–9.13), Stable Disease (SD) 0.83 (95% CI 0.45–1.53), Progressive Disease (PD) 0.35 (95% CI0.25–0.48, Objective Response Rate (ORR) 5.32 (95% CI 2.54–11.13), Disease Control Rate (DCR) 2.03 (95% CI 1.05–3.92). For adverse events (AEs), the overall incidence Odds Ratios (OR) was 0.53 (95% CI 0.06–4.82) and for grade 3−4 events, 0.49 (95% CI 0.28–0.85).

In Asian and African patients with BCLC stage B/C hepatocellular carcinoma, HAIC—particularly the FOLFOX regimen—confers superior overall survival and oncologic outcomes compared to sorafenib, with higher response and disease control rates and reduced disease progression.

## Linked entities

- **Diseases:** hepatocellular carcinoma (MONDO:0007256)

## Full-text entities

- **Genes:** AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, TENM1 (teneurin transmembrane protein 1) [NCBI Gene 10178] {aka ODZ1, ODZ3, TEN-M1, TEN1, TNM, TNM1}, MAP2K7 (mitogen-activated protein kinase kinase 7) [NCBI Gene 5609] {aka JNKK2, MAPKK7, MEK, MEK 7, MKK7, PRKMK7}, ZHX2 (zinc fingers and homeoboxes 2) [NCBI Gene 22882] {aka AFR1, RAF}
- **Diseases:** toxicity (MESH:D064420), thrombocytopenia (MESH:D013921), hematologic (MESH:D006402), C (OMIM:211750), hypertension (MESH:D006973), neutropenia (MESH:D009503), deaths (MESH:D003643), thrombus (MESH:D013927), portal vein tumor thrombosis (MESH:D012170), metastases (MESH:D009362), anemia (MESH:D000740), gastritis (MESH:D005756), BCLC stage (MESH:D006528), PD (MESH:D018450), Artery Infusion (MESH:D000075662), anorexia (MESH:D000855), hand-foot skin reaction (MESH:D060831), Solid Tumors (MESH:D009369), SD (MESH:D060050), Disease (MESH:D004194), CR (MESH:D001766), diarrhea (MESH:D003967), alopecia (MESH:D000505), nausea (MESH:D009325), rash (MESH:D005076), PR (MESH:D004828)
- **Chemicals:** FOLFOX (MESH:C410216), ethiodized oil (MESH:D004998), cisplatin (MESH:D002945), CZQ (-), epirubicin (MESH:D015251), DDP-H (MESH:C057485), lenvatinib (MESH:C531958), Des (MESH:D004054), toripalimab (MESH:C000656314), bilirubin (MESH:D001663), oxaliplatin (MESH:D000077150), Sorafenib (MESH:D000077157), leucovorin (MESH:D002955), DCP (MESH:C580746), 5-FU (MESH:D005472)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12915927/full.md

## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12915927/full.md

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Source: https://tomesphere.com/paper/PMC12915927