Efficacy of sorafenib plus transcatheter arterial chemoembolization in treating hepatocellular carcinoma with portal vein tumor thrombosis: A meta-analysis.

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY Acta Pharmaceutica Pub Date : 2024-09-14 Print Date: 2024-09-01 DOI:10.2478/acph-2024-0019
Li Xu, Shanshan Chen, Haijun Cao, Zemin Feng, Chao Yang
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Abstract

This meta-analysis aimed to evaluate the efficacy of sorafenib plus transcatheter arterial chemoembolization (TACE) in treating hepato-cellular carcinoma (HCC) with portal vein tumor thrombosis (PVTT). Twelve randomized controlled trials published until 28th Sep 2022 were finally included. Of the total 1746 patients, of whom 458 received sorafenib and TACE treatment (Group S+TACE), and 1288 only underwent TACE (Group TACE), were enrolled. Outcomes including time to progression (TTP), objective response rate (ORR), disease control rate (DCR), overall survival (OS), survival rate (SR), and adverse reactions, were extracted. The OS (HR: 0.596, 95 %CI: 0.507-0.685, p < 0.001; I2 = 0.0 %) and TTP (HR: 0.379, 95 %CI: 0.205-0.553, p < 0.001; I2 = 4.5 %) in the S+TACE group were longer than those in the TACE group. The ORR (RR: 2.101, 95 %CI: 1.555-2.839, p < 0.001; I2 = 0.0 %), DCR (RR: 1.547, 95 %CI: 1.126-2.126, p = 0.007; I2 = 79.6 %) and SR (RR: 1.416, 95 %CI: 1.183-1.694, p < 0.001; I2 = 83.8 %) in the S+TACE group were higher than those in the TACE group. Compared with the TCAE group, the higher odds of HFSR, oral ulcer, and diarrhea among patients with HCC complicated by PVTT were discovered in the S+TACE group. The marginal significance was found in ascites and gastrointestinal bleeding between the two groups. Sorafenib plus TACE has good efficacy and mild adverse reactions, which may be worthy of clinical promotion.

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索拉非尼联合经导管动脉化疗栓塞治疗伴门静脉肿瘤血栓形成的肝癌的疗效:荟萃分析
这项荟萃分析旨在评估索拉非尼联合经导管动脉化疗栓塞术(TACE)治疗伴有门静脉肿瘤血栓(PVTT)的肝细胞癌(HCC)的疗效。最终纳入了截至 2022 年 9 月 28 日发表的 12 项随机对照试验。共纳入1746例患者,其中458例接受索拉非尼和TACE治疗(S+TACE组),1288例仅接受TACE治疗(TACE组)。研究结果包括进展时间(TTP)、客观反应率(ORR)、疾病控制率(DCR)、总生存期(OS)、生存率(SR)和不良反应。S+TACE组的OS(HR:0.596,95 %CI:0.507-0.685,p < 0.001;I2 = 0.0 %)和TTP(HR:0.379,95 %CI:0.205-0.553,p < 0.001;I2 = 4.5 %)均长于TACE组。S+TACE组的ORR(RR:2.101,95 %CI:1.555-2.839,p < 0.001;I2 = 0.0 %)、DCR(RR:1.547,95 %CI:1.126-2.126,p = 0.007;I2 = 79.6 %)和SR(RR:1.416,95 %CI:1.183-1.694,p < 0.001;I2 = 83.8 %)均高于TACE组。与 TCAE 组相比,S+TACE 组的 HFSR、口腔溃疡和腹泻发生率更高。在腹水和消化道出血方面,两组间的差异不显著。索拉非尼联合TACE疗效好,不良反应轻,值得临床推广。
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来源期刊
Acta Pharmaceutica
Acta Pharmaceutica PHARMACOLOGY & PHARMACY-
CiteScore
5.20
自引率
3.60%
发文量
20
审稿时长
>12 weeks
期刊介绍: AP is an international, multidisciplinary journal devoted to pharmaceutical and allied sciences and contains articles predominantly on core biomedical and health subjects. The aim of AP is to increase the impact of pharmaceutical research in academia, industry and laboratories. With strong emphasis on quality and originality, AP publishes reports from the discovery of a drug up to clinical practice. Topics covered are: analytics, biochemistry, biopharmaceutics, biotechnology, cell biology, cell cultures, clinical pharmacy, drug design, drug delivery, drug disposition, drug stability, gene technology, medicine (including diagnostics and therapy), medicinal chemistry, metabolism, molecular modeling, pharmacology (clinical and animal), peptide and protein chemistry, pharmacognosy, pharmacoepidemiology, pharmacoeconomics, pharmacodynamics and pharmacokinetics, protein design, radiopharmaceuticals, and toxicology.
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