Unleashing the potential: transarterial chemoembolization combined with intra-arterial infusion of bevacizumab for unresectable hepatocellular carcinoma.

IF 2.8 3区 医学 Q2 ONCOLOGY Clinical & Translational Oncology Pub Date : 2024-12-01 Epub Date: 2024-05-27 DOI:10.1007/s12094-024-03498-1
Qu Xie, Yanzhen Yang, Weiyuan Hao, Cong Luo
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Abstract

Background: The purpose of this study is to compare the efficacy and safety of transarterial chemoembolization (TACE) alone with transarterial chemoembolization combined with the arterial infusion of bevacizumab (TACE + Bev) in patients with unresectable hepatocellular carcinoma (uHCC).

Methods: A retrospective analysis was conducted on 446 uHCC patients treated with TACE or TACE + Bev between January 2021 and March 2023. The study evaluated objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and adverse events in both treatment groups.

Results: Finally, the TACE group comprised 295 patients, and the TACE + Bev group comprised 151 patients. Patients in the TACE + Bev group exhibited significantly prolonged median PFS (7.9 months vs. 10.3 months, P = 0.013) and median OS (16.1 months vs. 21.4 months, P = 0.041), improved ORR (26.8% vs. 37.7%, P = 0.017) and DCR (71.5% vs. 80.8%, P = 0.033) compared to the TACE group. Multifactorial Cox analysis identified alpha-fetoprotein (AFP) > 400 ng/ml as an independent prognostic factor for PFS and OS. Meanwhile, portal vein cancer thrombosis and distant metastasis are poor prognostic factors for OS. The overall incidence of adverse events was similar between the two groups.

Conclusion: In comparison with the TACE group, the TACE + Bev group demonstrated efficacy in improving outcomes for patients with uHCC with a manageable safety profile.

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释放潜能:经动脉化疗栓塞术联合动脉内输注贝伐单抗治疗不可切除的肝细胞癌。
研究背景本研究旨在比较单独经动脉化疗栓塞术(TACE)与经动脉化疗栓塞术联合动脉输注贝伐单抗(TACE + Bev)对不可切除肝细胞癌(uHCC)患者的疗效和安全性:对2021年1月至2023年3月期间接受TACE或TACE + Bev治疗的446例uHCC患者进行了回顾性分析。研究评估了两个治疗组的客观反应率(ORR)、疾病控制率(DCR)、无进展生存期(PFS)、总生存期(OS)和不良事件:最终,TACE组有295名患者,TACE + Bev组有151名患者。与 TACE 组相比,TACE + Bev 组患者的中位 PFS(7.9 个月 vs. 10.3 个月,P = 0.013)和中位 OS(16.1 个月 vs. 21.4 个月,P = 0.041)明显延长,ORR(26.8% vs. 37.7%,P = 0.017)和 DCR(71.5% vs. 80.8%,P = 0.033)有所改善。多因素 Cox 分析发现,甲胎蛋白(AFP)> 400 ng/ml 是 PFS 和 OS 的独立预后因素。同时,门静脉癌栓和远处转移是OS的不良预后因素。两组患者的不良反应总发生率相似:结论:与 TACE 组相比,TACE + Bev 组在改善 uHCC 患者预后方面具有疗效,且安全性可控。
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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
240
审稿时长
1 months
期刊介绍: Clinical and Translational Oncology is an international journal devoted to fostering interaction between experimental and clinical oncology. It covers all aspects of research on cancer, from the more basic discoveries dealing with both cell and molecular biology of tumour cells, to the most advanced clinical assays of conventional and new drugs. In addition, the journal has a strong commitment to facilitating the transfer of knowledge from the basic laboratory to the clinical practice, with the publication of educational series devoted to closing the gap between molecular and clinical oncologists. Molecular biology of tumours, identification of new targets for cancer therapy, and new technologies for research and treatment of cancer are the major themes covered by the educational series. Full research articles on a broad spectrum of subjects, including the molecular and cellular bases of disease, aetiology, pathophysiology, pathology, epidemiology, clinical features, and the diagnosis, prognosis and treatment of cancer, will be considered for publication.
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