Purpose: To evaluate the efficacy and safety of postoperative adjuvant hepatic arterial infusion chemotherapy (PA-HAIC) plus programmed death-1 (PD-1) inhibitors versus PA-HAIC alone for hepatocellular carcinoma (HCC) patients with microvascular invasion (MVI).
Methods: This retrospective study included HCC patients with MVI who were treated with either PA-HAIC or PA-HAIC plus PD-1 inhibitors between February 2021 and February 2024. The differences in baseline characteristics, disease-free survival (DFS), and overall survival (OS) were compared between the two groups before and after propensity score-matching (PSM). The treatment-related adverse events (TRAEs) were compared among the two groups after PSM. Cox regression analysis was utilized to determine factors affecting DFS and OS.
Results: A total of 102 patients were included in the study: 65 in the PA-HAIC group and 37 in the PA-HAIC plus PD-1 group. PSM analysis generated 32 matched pairs of patients in the two groups. The HCC patients in the PA-HAIC plus PD-1 group experienced significantly better DFS compared to those in the PA-HAIC group alone (HR: 0.412; P = 0.031). However, there was no significant difference in OS between the two groups (P = 0.124). Multivariate analysis identified the treatment option (PA-HAIC vs. PA-HAIC + PD-1) as an independent predictive factor for DFS of the patients. Furthermore, the results indicated no statistically significant difference in the incidence of TRAEs between the two groups (P < 0.05).
Conclusion: In comparison with PA-HAIC alone, PA-HAIC combined with PD-1 inhibitors could improve the DFS benefits with acceptable safety profiles in HCC patients with MVI.
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http://dx.doi.org/10.1186/s12885-025-13793-x | DOI Listing |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11887270 | PMC |
Cureus
February 2025
Department of Radiology, Krishna Institute of Medical Sciences, Secunderabad, IND.
Background Patients with risk factors such as viral hepatitis-induced liver cirrhosis, advanced-stage primary biliary cirrhosis, hereditary hemochromatosis, metabolic-associated fatty liver disease, and alcoholic liver disease are more likely to develop hepatocellular carcinoma (HCC). Most HCC patients have advanced-stage disease unresponsive to treatment. Therefore, avoiding or treating viral infections and early detection through routine surveillance, such as repeated liver ultrasonography, are the most effective ways to reduce HCC-related mortality.
View Article and Find Full Text PDFJ Hepatocell Carcinoma
March 2025
Department of Laboratory Medicine, Huadong Hospital, Fudan University, Shanghai, People's Republic of China.
Purpose: The prevalence of primary liver cancer (PLC) is rising, yet strategies for its early diagnosis remain inadequate. This study aims to identify novel biomarkers to improve the diagnostic ability of PLC.
Patients And Methods: This study included 94 patients with PLC, 128 patients with benign liver disease (BLD), and 79 normal controls (NC) were included.
J Hepatocell Carcinoma
March 2025
Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.
Hepatocellular carcinoma (HCC) is a complex cancer that generally arises in the context of cirrhosis. Patients with HCC have symptom burden and impact on health-related quality of life (HRQOL) resulting from underlying liver disease, HCC, and cancer treatments. Patient-reported outcome (PRO) measures may improve the management of patients with HCC by accurately capturing the patient perspective, informing prognosis, guiding treatment decisions, and supporting symptom based and palliative care.
View Article and Find Full Text PDFCell Commun Signal
March 2025
Department of Hepatobiliary Surgery, Xijing Hospital, Air Force Medical University, 15 Changle Western Road, Xi'an, Shaanxi, 710032, China.
Mitochondria dysfunction has been closely linked to a wide spectrum of human cancers, whereas the molecular basis has yet to be fully understood. SLC25A35 belongs to the SLC25 family of mitochondrial carrier proteins. However, the role of SLC25A35 in mitochondrial metabolism reprogramming, development and progression in human cancers remains unclear.
View Article and Find Full Text PDFBMC Cancer
March 2025
Department of Guidance and Counseling, Faculty of Education, University of Calabar, Calabar, Nigeria.
Mutations in the TP53 gene had been attributed to the development of liver cancer. Hepatocellular carcinoma (HCC) and liver tumour are liver diseases having high mortality rates in several populations. There is no information on the TP53 gene polymorphism among liver diseases patients in Calabar, Nigeria.
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