PMID- 38074645 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20231211 IS - 2234-943X (Print) IS - 2234-943X (Electronic) IS - 2234-943X (Linking) VI - 13 DP - 2023 TI - Anlotinib combined with transarterial chemoembolization for unresectable hepatocellular carcinoma associated with hepatitis B virus: a retrospective controlled study. PG - 1235786 LID - 10.3389/fonc.2023.1235786 [doi] LID - 1235786 AB - PURPOSE: To investigate the efficacy and safety of combined treatment of anlotinib and transarterial chemoembolization (TACE) in patients with unresectable hepatocellular carcinoma (uHCC) associated with hepatitis B virus (HBV) infection. METHODS: We retrospectively collected the data of 96 uHCC patients associated with HBV infection who received either TACE only (TO group; n = 64) or anlotinib combined with TACE (TA group; n = 32) from January 2017 to January 2021. The primary endpoint was overall survival (OS). The secondary outcomes included progression-free survival (PFS), tumor response according to modified Response Evaluation Criteria in Solid Tumors (mRECIST) and RECIST 1.1, and adverse events (AEs). RESULTS: The median OS and median PFS were significantly longer in the TA group compared to the TO group (17.6 months vs. 9.4 months, p = 0.018; 6.7 months vs. 3.8 months, p = 0.003, respectively). In addition, the overall objective response rate (ORR) and disease control rate (DCR) numerically increased in the TA group (mRECIST, ORR 65.6% vs. 46.9%, p = 0.064, DCR 90.6% vs. 85.9%, p = 0.382; RECIST 1.1, ORR 46.9% vs. 15.6%, p = 0.001, DCR 90.6% vs. 85.9%, p = 0.382, respectively). It was worth noting that no treatment-related mortality occurred during the study. The most common AEs included elevated transaminases (56.3%), decreased appetite (46.9%), and abdominal pain (37.5%) in the TA group. Although the incidence rate of grade 3/4 AEs was higher in the TA group, all of them were controllable. CONCLUSIONS: The combination of anlotinib and TACE has shown promising results in improving outcomes for patients with HBV-related uHCC, as compared to TACE monotherapy. In addition, this combination therapy has demonstrated a controllable safety profile. However, further validation is urgently needed through randomized controlled trials with large sample sizes. CI - Copyright (c) 2023 Chen, Cai, Wu, Tang, Chen, Wang, Zhuang and Guo. FAU - Chen, Song AU - Chen S AD - Department of Minimally Invasive Interventional Therapy, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou, China. FAU - Cai, Hongjie AU - Cai H AD - Department of Interventional Radiology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China. FAU - Wu, Zhiqiang AU - Wu Z AD - Department of Interventional Radiology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China. FAU - Tang, Shuangyan AU - Tang S AD - Department of Interventional Radiology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China. FAU - Chen, Ludan AU - Chen L AD - Department of Interventional Radiology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China. FAU - Wang, Fan AU - Wang F AD - Department of Interventional Radiology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China. FAU - Zhuang, Wenquan AU - Zhuang W AD - Department of Interventional Radiology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China. FAU - Guo, Wenbo AU - Guo W AD - Department of Interventional Radiology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China. LA - eng PT - Journal Article DEP - 20231122 PL - Switzerland TA - Front Oncol JT - Frontiers in oncology JID - 101568867 PMC - PMC10702964 OTO - NOTNLM OT - anlotinib OT - combination therapy OT - hepatitis B virus OT - transarterial chemoembolization OT - unresectable hepatocellular carcinoma COIS- The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2023/12/11 06:45 MHDA- 2023/12/11 06:46 PMCR- 2023/01/01 CRDT- 2023/12/11 05:46 PHST- 2023/06/06 00:00 [received] PHST- 2023/11/06 00:00 [accepted] PHST- 2023/12/11 06:46 [medline] PHST- 2023/12/11 06:45 [pubmed] PHST- 2023/12/11 05:46 [entrez] PHST- 2023/01/01 00:00 [pmc-release] AID - 10.3389/fonc.2023.1235786 [doi] PST - epublish SO - Front Oncol. 2023 Nov 22;13:1235786. doi: 10.3389/fonc.2023.1235786. eCollection 2023.