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肝细胞癌经动脉化疗栓塞联合分子靶向药物和免疫检查点抑制剂治疗后液化坏死形成增加
Authors Wang Y, Zhou C, Liu J, Shi Q, Huang S, Yang C, Li T, Chen Y, Xiong B
Received 10 July 2021
Accepted for publication 28 August 2021
Published 7 September 2021 Volume 2021:13 Pages 6935—6941
DOI https://doi.org/10.2147/CMAR.S328812
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Professor Harikrishna Nakshatri
Purpose: In clinical practice, we found some of the patients who received transarterial chemoembolization (TACE) with molecular targeted agents (MTGs) plus immune checkpoint inhibitors (ICIs) for hepatocellular carcinoma (HCC) had obvious liquefactive necrosis formation within the tumor and some even progressed to a liver abscess, which seems more frequent than patients who received other treatments. Thus, we aim to identify this condition and analyze the potential risk factors.
Patients and Methods: Medical records of 72 consecutive patients with intermediate (BCLC B) and advanced (BCLC C) HCC who received TACE plus MTGs combined with (n=30) or without (n=42) ICIs were reviewed. Liquefactive necrosis formation was defined as the presence of obvious liquefactive necrosis within the tumor that required intervention.
Results: The liquefactive necrosis rate was higher in the TACE+MTGs+ICIs group than in the TACE+MTGs group (30% vs 4.8%, P=0.006). Moreover, 18.2% (2/11) of the patients with liquefactive necrosis within the tumor had a bacterial infection. We then take the binary logistic regression analysis model to identify the predictors of liquefactive necrosis formation, and which showed the tumor size (P=0.006, OR=1.355, 95% CI: 1.090– 1.684), alpha-fetoprotein level (P=0.036, OR=6.745, 95% CI: 1.130– 40.262) and treatment modality (P=0.015, OR=11.717, 95% CI: 1.617– 84.887) were the independent risk factor for liquefactive necrosis formation within the tumor.
Conclusion: Patients with HCC who received TACE combined with MTGs plus ICIs have increased liquefactive necrosis formation, and the larger tumor size and higher alpha-fetoprotein level were associated with more liquefactive necrosis formation within the tumor.
Keywords: liver cancer, transarterial chemoembolization, molecular targeted agents, immune checkpoint inhibitors, liquefactive necrosis