Hepatic arterial infusion chemotherapy versus transarterial chemoembolization, potential conversion therapies for single huge hepatocellular carcinoma: a retrospective comparison study

医学 肝细胞癌 内科学 化疗 回顾性队列研究 肿瘤科 放射科
作者
Min Deng,Hao Cai,Benyi He,Renguo Guan,Carol Lee,Rong Guo
出处
期刊:International Journal of Surgery [Elsevier]
被引量:6
标识
DOI:10.1097/js9.0000000000000654
摘要

Background: The treatment efficacy of transarterial chemoembolization (TACE) and hepatic arterial infusion chemotherapy (HAIC) for huge single hepatocellular carcinoma (HCC) has not been fully documented. The aim of this study was to compare TACE and HAIC for patients with solitary nodular HCCs ≥10 cm without vascular invasion and metastasis. Methods: From July 2015 to June 2020, a total of 147 patients with single nodular HCC ≥10 cm without vascular invasion and metastasis receiving TACE (n=77) or HAIC (n=70) were retrospectively enrolled. The tumor response, overall survival (OS), and progression-free survival (PFS) were investigated and compared. The treatment outcome of 2 transarterial interventional therapies was explored. Results: The objective response rate and PFS were higher in patients who received HAIC than in those who received TACE (44.3% vs. 10.4% and 8.9 vs. 4.2 mo, respectively; P =0.001 and P =0.030), whereas the disease control rate and OS were not significantly different (92.9% vs. 84.4% and 21.3 vs. 26.6 mo, respectively; P =0.798 and P =0.749). The decreased levels of alpha‐fetoprotein and protein induced by vitamin K absence or antagonist-II (PIVKA-II) in patients treated with HAIC were significantly higher than those treated with TACE ( P =0.038 and P <0.001). Multivariable analysis showed that the aspartate aminotransferase/platelet ratio index was associated with OS, whereas albumin-bilirubin grade and PIVKA-II were associated with PFS. Conclusions: HAIC has better potential than TACE to control local tumors for huge single HCC without vascular invasion and metastasis and thus may be the preferred conversion therapy for these tumors.
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