Abstract
Hepatocellular carcinoma (HCC) is one of the most common malignancies and the third leading cause of cancer-related deaths globally. Hepatic arterial infusion chemotherapy (HAIC) treatment is widely accepted as one of the alternative therapeutic modalities for HCC owing to its local control effect and low systemic toxicity. Nevertheless, although accumulating high-quality evidence has displayed the superior survival advantages of HAIC of oxaliplatin, fluorouracil, and leucovorin (HAIC-FOLFOX) compared with standard first-line treatment in different scenarios, the lack of standardization for HAIC procedure and remained controversy limited the proper and safe performance of HAIC treatment in HCC. Therefore, an expert consensus conference was held on March 2023 in Guangzhou, China to review current practices regarding HAIC treatment in patients with HCC and develop widely accepted statements and recommendations. In this article, the latest evidence of HAIC was systematically summarized and the final 22 expert recommendations were proposed, which incorporate the assessment of candidates for HAIC treatment, procedural technique details, therapeutic outcomes, the HAIC-related complications and corresponding treatments, and therapeutic scheme management.
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Data availability
All data included in this study are available upon request by contact with the corresponding author (drmingzhao@outlook.com).
Abbreviations
- AEs:
-
Adverse events
- AFP:
-
Alpha-fetoprotein
- BTC:
-
Betacellulin
- CCL28:
-
C–C motif chemokine ligand 28
- c-TACE:
-
Conventional TACE
- CTLA-4:
-
Cytotoxic T lymphocyte-associated antigen 4
- DCR:
-
Disease control rate
- DEB-TACE:
-
Drug-eluting bead TACE
- EHS:
-
Extrahepatic spread
- FOLFOX:
-
The combined chemotherapeutic regimen of oxaliplatin, leucovorin, and fluorouracil
- GRADE:
-
The grading of recommendations assessment, development, and evaluation system
- HAIC:
-
Hepatic arterial infusion chemotherapy
- HBV:
-
Hepatitis B virus
- HCC:
-
Hepatocellular carcinoma
- ICIs:
-
Immune checkpoint inhibitors
- MTAs:
-
Molecular targeting agents
- MVI:
-
Macrovascular invasion
- OS:
-
Overall survival
- PDGFR:
-
Platelet-derived growth factor receptor
- PD-L1:
-
Programmed cell death 1
- PVTT:
-
Portal vein tumor thrombosis
- RCTs:
-
Randomized controlled trials
- TACE:
-
Transarterial chemoembolization
- TARE:
-
Transarterial radioembolization
- TRAE:
-
Treatment-related adverse events
- TKIs:
-
Tyrosine kinase inhibitors
- VEGFR:
-
Vascular endothelial growth factor receptor
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Conception and design: MZ, NL, and JZY. Provision of study material: NL. Collection and assembly of data: JZY and YMZ. Data analysis and interpretation: JZY and YMZ. Manuscript writing: All authors. Final approval of manuscript: All authors. Accountable for all aspects of the work: All authors.
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Ming Zhao, Zhi Guo, Ying-Hua Zou, Xiao Li, Zhi-Ping Yan, Min-Shan Chen, Wei-Jun Fan, Hai-Liang Li, Ji-Jin Yang, Xiao-Ming Chen, Lin-Feng Xu, Yue-Wei Zhang, Kang-Shun Zhu, Jun-Hui Sun, Jia-Ping Li, Yong Jin, Hai-Peng Yu, Feng Duan, Bin Xiong, Guo-Wen Yin, Hai-Lan Lin, Yi-Long Ma, Hua-Ming Wang, Shan-Zhi Gu, Tong-Guo Si, Xiao-Dong Wang, Chang Zhao, Wen-Chang Yu, Jian-Hai Guo, Jian Zhai, Yong-Hui Huang, Wei-Yu Wang, Hai-Feng Lin, Yang-Kui Gu, Jin-Zhang Chen, Jian-Peng Wang, Yi-Min Zhang, Jun-Zhe Yi, Ning Lyu declare no potential conflicts of interest.
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Zhao, M., Guo, Z., Zou, YH. et al. Arterial chemotherapy for hepatocellular carcinoma in China: consensus recommendations. Hepatol Int 18, 4–31 (2024). https://doi.org/10.1007/s12072-023-10599-6
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DOI: https://doi.org/10.1007/s12072-023-10599-6