Efficacy and Safety Analysis of Transarterial Chemoembolization Plus Donafenib With or Without Immune Checkpoint Inhibitors for Unresectable Hepatocellular Carcinoma: A Prospective, Single-Arm, Single-Center, Phase II Clinical Study.

IF 4.2 3区 医学 Q2 ONCOLOGY
Journal of Hepatocellular Carcinoma Pub Date : 2024-06-27 eCollection Date: 2024-01-01 DOI:10.2147/JHC.S473617
Jinpeng Li, Yan Li, Jinlong Song, Lujun Zhao
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Abstract

Purpose: To observe and assess the efficacy and safety of donafenib combined with transarterial chemoembolization (TACE) to treat unresectable hepatocellular carcinoma (HCC).

Patients and methods: This prospective, single-arm, single-center, phase II clinical study enrolled 36 patients with initial unresectable HCC who had not undergone any systemic treatment. The patients received donafenib plus TACE (n = 26) or donafenib plus TACE plus programmed death receptor 1 inhibitors (n = 10). The primary endpoint was short-term efficacy, with secondary endpoints including progression-free survival (PFS), time to response (TTR), disease control rate (DCR), and adverse events. The tumor feeding artery diameter was also measured.

Results: Efficacy evaluation of all 36 patients revealed 6 cases of complete response, 19 of partial response, 8 of stable disease, and 3 of progressive disease. Six (16.7%) patients successfully underwent conversion surgery, all achieving R0 resection, and 2 (5.6%) achieved a complete pathological response. The objective response rate (ORR) was 69.4% and the DCR was 91.7%. The median PFS was 10.7 months, the median overall survival was not reached, and the median TTR was 1.4 months. The median survival rates at 6, 12, and 18 months were 85.0%, 77.6%, and 71.3%, respectively. The median PFS rates at 6, 12, and 18 months were 65.3%, 45.6%, and 34.2%, respectively. Treatment-related adverse events (TRAEs) occurred in all 25 subjects, including 4 (11.3%) grade 3 TRAEs. No grade 4 or 5 TRAEs occurred. The tumor feeding artery diameter was significantly decreased following treatment (P = 0.036). Multivariable analysis revealed the sum of baseline target lesion diameters, best tumor response, and combined immunotherapy as independent predictors of PFS.

Conclusion: TACE plus donafenib reduced the tumor feeding artery diameter in patients with unresectable HCC. The safety profile was good, and a high ORR was achieved.

经动脉化疗栓塞术加多纳非尼与或不加免疫检查点抑制剂治疗不可切除肝细胞癌的疗效和安全性分析:一项前瞻性、单臂、单中心、II 期临床研究。
目的:观察和评估多那非尼联合经动脉化疗栓塞术(TACE)治疗不可切除性肝细胞癌(HCC)的疗效和安全性:这项前瞻性、单臂、单中心、II期临床研究共招募了36例未接受过任何系统治疗的初治不可切除肝细胞癌患者。患者接受了多纳非尼加TACE治疗(26例)或多纳非尼加TACE加程序性死亡受体1抑制剂治疗(10例)。主要终点是短期疗效,次要终点包括无进展生存期(PFS)、反应时间(TTR)、疾病控制率(DCR)和不良事件。此外,还测量了肿瘤供血动脉的直径:对所有 36 例患者的疗效评估显示,完全应答 6 例,部分应答 19 例,病情稳定 8 例,病情进展 3 例。6例(16.7%)患者成功接受了转换手术,全部实现了R0切除,2例(5.6%)实现了完全病理反应。客观反应率(ORR)为 69.4%,DCR 为 91.7%。中位生存期为10.7个月,中位总生存期未达标,中位TTR为1.4个月。6、12和18个月的中位生存率分别为85.0%、77.6%和71.3%。6、12和18个月的中位生存率分别为65.3%、45.6%和34.2%。所有25名受试者均发生了治疗相关不良事件(TRAE),其中包括4例(11.3%)3级TRAE。没有出现 4 级或 5 级 TRAE。治疗后,肿瘤供血动脉直径明显缩小(P = 0.036)。多变量分析显示,基线靶病变直径之和、最佳肿瘤反应和联合免疫疗法是预测PFS的独立因素:结论:TACE加多那非尼能缩小不可切除HCC患者的肿瘤供血动脉直径。结论:TACE联合多纳非尼可减少无法切除的HCC患者的肿瘤供血动脉直径,安全性良好,并获得了较高的ORR。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.50
自引率
2.40%
发文量
108
审稿时长
16 weeks
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