A multicenter, randomized, parallel-controlled clinical trial protocol to evaluate the safety and efficacy of irreversible electroporation compared with radiofrequency ablation for the treatment of small hepatocellular carcinoma.

IF 2.5 3区 医学 Q3 ONCOLOGY World Journal of Surgical Oncology Pub Date : 2024-12-20 DOI:10.1186/s12957-024-03614-z
Chao Cheng, Min Xu, Jinhua Pan, Qiang Chen, Kai Li, Dong Xu, Xiang Jing, Qiang Lu, Hong Yang, Qiyu Zhao, Zhuang Deng, Tian'an Jiang
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Abstract

Background: At present, the main clinical application of local ablation therapy, such as radiofrequency ablation (RFA), is to heat the tissue to a certain temperature. However, high temperature will cause thermal damage. Irreversible electroporation (IRE) is a novel minimally invasive local ablation technology for tumors. By high-frequency pulse, the tumor cell membrane can be irretrievably perforated, resulting in the destruction of the intracellular environment, which can preserve important structures in the treatment area. However, there are no randomized controlled clinical trials comparing the efficacy of IRE with traditional local ablation in the treatment of liver cancer.

Aims: This study aims to conduct a randomized controlled clinical trial comparing the efficacy of IRE with RFA in the treatment of liver cancer.

Methods: We will conduct a multicenter, randomized, parallel-controlled non-inferiority clinical trial to compare the efficacy and safety of IRE and RFA for hepatocellular carcinoma (HCC). One hundred and ninety patients with HCC from five academic medical centers will be enrolled. The patients will be randomized into treatment arm (IRE) and control arm (RFA). The primary outcome is the progress -free survival (PFS) and the key secondary outcome is the Overall survival (OS).

Results: Forty-eight patients had been recruited from 5 centers, of which, 33 patients (median age, 59.1 years) with 38 tumors had completed the 1-month follow-up and 21 patients have complete the 3-month follow up, with 2.3 months median follow up period. The mean largest tumor diameter is 3.9 cm. No end point was observed for PFS or OS in both groups, and the complete ablation rate was 100% in both groups. The lesions in the IRE group showed obvious shrinkage 1 month after procedure. One major adverse event (AE) was occurred in the control group.

Conclusion: This is the first randomized controlled clinical trial to compare the clinical effects of IRE and RFA. The preliminary results suggest that both RFA and IRE are effective in the treatment of HCC, which can provide strong evidence for the use of IRE in HCC and provide more options for the treatment of patients with HCC.

Clinical trial registration: ClinicalTrials. gov, identifier NCT05451160.

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一项多中心、随机、平行对照的临床试验方案,以评估不可逆电穿孔与射频消融治疗小肝癌的安全性和有效性。
背景:目前,射频消融(RFA)等局部消融治疗的主要临床应用是将组织加热到一定温度。但高温会造成热损伤。不可逆电穿孔(IRE)是一种新型的肿瘤微创局部消融技术。高频脉冲可使肿瘤细胞膜不可挽回地穿孔,破坏细胞内环境,而细胞内环境可保存治疗区域的重要结构。然而,目前尚无随机对照临床试验比较IRE与传统局部消融治疗肝癌的疗效。目的:本研究旨在进行一项随机对照临床试验,比较IRE与RFA治疗肝癌的疗效。方法:我们将进行一项多中心、随机、平行对照的非劣效性临床试验,比较IRE和RFA治疗肝细胞癌(HCC)的疗效和安全性。来自5个学术医疗中心的190名HCC患者将被纳入研究。患者将被随机分为治疗组(IRE)和对照组(RFA)。主要终点是无进展生存期(PFS),关键的次要终点是总生存期(OS)。结果:共纳入5个中心48例患者,其中33例患者(中位年龄59.1岁),38例肿瘤完成1个月随访,21例患者完成3个月随访,中位随访时间为2.3个月。平均最大肿瘤直径为3.9 cm。两组均未观察到PFS或OS的终点,两组的完全消融率均为100%。IRE组术后1个月病灶明显缩小。对照组发生1例主要不良事件(AE)。结论:这是第一个比较IRE和RFA临床效果的随机对照临床试验。初步结果提示RFA和IRE治疗HCC均有效,可为IRE在HCC中的应用提供有力证据,为HCC患者的治疗提供更多选择。临床试验注册:临床试验。. gov,标识符NCT05451160。
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来源期刊
CiteScore
4.70
自引率
15.60%
发文量
362
审稿时长
3 months
期刊介绍: World Journal of Surgical Oncology publishes articles related to surgical oncology and its allied subjects, such as epidemiology, cancer research, biomarkers, prevention, pathology, radiology, cancer treatment, clinical trials, multimodality treatment and molecular biology. Emphasis is placed on original research articles. The journal also publishes significant clinical case reports, as well as balanced and timely reviews on selected topics. Oncology is a multidisciplinary super-speciality of which surgical oncology forms an integral component, especially with solid tumors. Surgical oncologists around the world are involved in research extending from detecting the mechanisms underlying the causation of cancer, to its treatment and prevention. The role of a surgical oncologist extends across the whole continuum of care. With continued developments in diagnosis and treatment, the role of a surgical oncologist is ever-changing. Hence, World Journal of Surgical Oncology aims to keep readers abreast with latest developments that will ultimately influence the work of surgical oncologists.
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