Department of Abdominal Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Abdominal Oncology Ward, Division of Medical Oncology, Cancer Center, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China.
Cancer Med. 2024 Apr;13(8):e7131. doi: 10.1002/cam4.7131.
More than half of neuroendocrine tumor (NET) patients will experience liver metastasis, and interventional therapy represented by transarterial embolization (TAE) is the main local treatment method. Surufatinib is recommended as a standard systemic treatment for advanced NETs. The efficacy and safety of surufatinib combined with TAE in the treatment of liver metastasis are undetermined. This study was conducted to compare the clinical outcome of surufatinib combined with TAE versus surufatinib monotherapy in liver metastatic NETs.
This is a prospective, multicenter, open-label, and randomized controlled trial. Patients diagnosed with liver metastatic NETs will be enrolled. Participants are randomly assigned in a 1:1 ratio to either the experimental group or the control group. Patients will be treated with surufatinib plus TAE in the experimental group, while patients in the control group will receive surufatinib monotherapy. The primary endpoint is progression-free survival (PFS) assessed by a blinded independent image review committee (BIIRC). The secondary endpoints are investigator-assessed PFS, liver-specific objective response rate (ORR), objective response rate (ORR), disease control rate (DCR), overall survival (OS), and incidence of adverse events.
This is the first prospective study to investigate the efficacy of surufatinib combined with TAE. We expect this trial to propose a new and effective treatment strategy for liver metastatic NETs.
超过一半的神经内分泌肿瘤(NET)患者会发生肝转移,经动脉栓塞术(TAE)为代表的介入治疗是主要的局部治疗方法。索凡替尼被推荐为晚期 NET 的标准系统治疗药物。尚不确定索凡替尼联合 TAE 与索凡替尼单药治疗肝转移 NET 的疗效和安全性。本研究旨在比较索凡替尼联合 TAE 与索凡替尼单药治疗肝转移 NET 的临床结局。
这是一项前瞻性、多中心、开放标签、随机对照试验。将招募诊断为肝转移 NET 的患者。参与者以 1:1 的比例随机分配到实验组或对照组。实验组患者接受索凡替尼联合 TAE 治疗,对照组患者接受索凡替尼单药治疗。主要终点是由盲法独立影像评估委员会(BIIRC)评估的无进展生存期(PFS)。次要终点包括研究者评估的 PFS、肝脏特异性客观缓解率(ORR)、客观缓解率(ORR)、疾病控制率(DCR)、总生存期(OS)和不良事件发生率。
这是第一项研究索凡替尼联合 TAE 疗效的前瞻性研究。我们期望这项试验能为肝转移 NET 提出一种新的有效治疗策略。