Drug-eluting bead transarterial chemoembolization combined with apatinib/camrelizumab for the treatment of advanced hepatocellular carcinoma with hepatic arterioportal shunts.

IF 1.8 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING British Journal of Radiology Pub Date : 2024-12-01 DOI:10.1093/bjr/tqae166
Yanqiao Ren, Bo Sun, Licheng Zhu, Lei Chen, Tao Sun, Xiangjun Dong, Chuansheng Zheng
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Abstract

Objective: To evaluate the efficacy and safety of drug eluting bead transarterial chemoembolization (D-TACE) combined with apatinib/camrelizumab in patients with advanced hepatocellular carcinoma (HCC) and hepatic arterioportal shunts (APSs).

Methods: From January 2021 to December 2022, the consecutive medical records of patients with advanced HCC and APS receiving D-TACE combined with apatinib/camrelizumab were reviewed for eligibility. Overall survival (OS), progression-free survival (PFS), tumour response, and adverse events (AEs) were assessed.

Results: A total of 23 patients were included in this study, with a median follow-up of 11 months (range, 2-26 months). Eight patients (34.8%) achieved partial response; 13 (56.5%), stable disease; and 2 (8.7%), progressive disease. The objective response and disease control rates were 34.8% and 91.3%, respectively. The OS and PFS rates were 11 and 7 months, respectively. Multivariate analysis indicated that the tumour number was an independent prognostic factor for PFS. AEs occurred in 19 patients after oral apatinib treatment and in 8 patients after camrelizumab treatment. No treatment-related death occurred during the study period.

Conclusions: D-TACE combined with apatinib/camrelizumab showed meaningful efficacy and controllable AEs in these patients, making it a promising treatment option.

Advances in knowledge: (1) We investigated a new treatment strategy for patients with advanced HCC and hepatic APS and (2) D-TACE combined with apatinib/camrelizumab demonstrated meaningful efficacy and manageable AEs, making it a promising treatment option.

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药物洗脱珠经动脉化疗栓塞联合阿帕替尼/康瑞珠单抗治疗伴肝动脉门静脉分流的晚期肝细胞癌。
研究目的本研究旨在评估药物洗脱珠经动脉化疗栓塞术(D-TACE)联合阿帕替尼/康瑞珠单抗治疗肝动脉主动脉分流术(APS)晚期肝细胞癌(HCC)患者的疗效和安全性:从2021年1月至2022年12月,对接受D-TACE联合阿帕替尼/康瑞珠单抗治疗的APS晚期肝细胞癌患者的连续病历进行资格审查。对总生存期(OS)、无进展生存期(PFS)、肿瘤反应和不良事件(AEs)进行了评估:本研究共纳入 23 例患者,中位随访时间为 11 个月(2-26 个月)。其中,8 例患者(34.8%)达到 PR,13 例患者(56.5%)达到 SD,2 例患者(8.7%)达到 PD。客观反应率和疾病控制率分别为34.8%和91.3%。OS和PFS分别为11个月和7个月。多变量分析表明,肿瘤数目是影响PFS的独立预后因素。19名患者在口服阿帕替尼后出现了不良反应,8名患者在接受康瑞珠单抗治疗后出现了不良反应。没有发生与治疗相关的死亡:D-TACE联合阿帕替尼/坎瑞珠单抗治疗晚期HCC患者APS疗效显著,AEs可控,可能是一种有前景的治疗方案:-1.我们研究了肝动脉门体分流晚期HCC患者的一种新治疗策略;2.D-TACE联合阿帕替尼/坎瑞珠单抗对APS晚期HCC患者具有显著疗效和可控AEs,可能是一种有前景的治疗方案。
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来源期刊
British Journal of Radiology
British Journal of Radiology 医学-核医学
CiteScore
5.30
自引率
3.80%
发文量
330
审稿时长
2-4 weeks
期刊介绍: BJR is the international research journal of the British Institute of Radiology and is the oldest scientific journal in the field of radiology and related sciences. Dating back to 1896, BJR’s history is radiology’s history, and the journal has featured some landmark papers such as the first description of Computed Tomography "Computerized transverse axial tomography" by Godfrey Hounsfield in 1973. A valuable historical resource, the complete BJR archive has been digitized from 1896. Quick Facts: - 2015 Impact Factor – 1.840 - Receipt to first decision – average of 6 weeks - Acceptance to online publication – average of 3 weeks - ISSN: 0007-1285 - eISSN: 1748-880X Open Access option
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