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HBV reactivation and its management in HBV-related HCC patients undergoing HAIC-TKI-ICI therapy: A multicenter study
Jiayun Liu1,2,3, Bo Sun1,2,3, Jiahua Zou4
1Department of Radiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
This study aimed to assess hepatitis B virus (HBV) reactivation, its impact on prognosis, and its management in patients with HBV-related hepatocellular carcinoma (HCC), who received hepatic arterial infusion chemotherapy (HAIC) plus tyrosine kinase inhibitors (TKIs), immune checkpoint inhibitors (ICIs), and entecavir (HAIC+TKIs+ICIs+entecavir) treatments. Three hundred and seven patients in five centers with advanced HBV-related HCC, who received the quadruple treatment, were included. The HBV reactivation was observed in 44 (14.3%) patients. HBV-DNA level ≥1 × 104 IU/mL, positive HBeAg, and white blood cell count <4 × 109/L were the independent risk factors of HBV reactivation. The median progression-free survival and median overall survival of patients in the HBV non-reactivation group were significantly longer than those of patients in the HBV reactivation group (p < 0.001, p < 0.001). The additional treatment with tenofovir alafenamide fumarate can effectively manage the HBV reactivation and improve the survival of these HBV reactivated HCC patients.
This study aimed to assess hepatitis B virus (HBV) reactivation, its impact on prognosis, and its management in patients with HBV-related hepatocellular carcinoma (HCC), who received hepatic arterial infusion chemotherapy (HAIC) plus tyrosine kinase inhibitors (TKIs), immune checkpoint inhibitors (ICIs), and entecavir (HAIC+TKIs+ICIs+entecavir) treatments. Three hundred and seven patients in five centers with advanced HBV-related HCC, who received the quadruple treatment, were included. The HBV reactivation was observed in 44 (14.3%) patients. HBV-DNA level ≥1 × 104 IU/mL, positive HBeAg, and white blood cell count <4 × 109/L were the independent risk factors of HBV reactivation. The median progression-free survival and median overall survival of patients in the HBV non-reactivation group were significantly longer than those of patients in the HBV reactivation group (p < 0.001, p < 0.001). The additional treatment with tenofovir alafenamide fumarate can effectively manage the HBV reactivation and improve the survival of these HBV reactivated HCC patients.
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