Gao Wenfeng, Xiong Yiqi, Mei Tingting, Pocha Christine, Adhoute Xavier, Lucatelli Pierleone, Zhang Yonghong
Interventional Therapy Center for Oncology, Beijing You'an Hospital, Capital Medical University, Beijing, China.
Avera Medical Group Hepatology, University of South Dakota, Sioux Falls, SD, USA.
J Gastrointest Oncol. 2025 Jun 30;16(3):1050-1059. doi: 10.21037/jgo-2025-337. Epub 2025 Jun 27.
Most patients with hepatocellular carcinoma (HCC) have progressed to the intermediate or advanced stage when diagnosed and are ineligible for curative therapies. The currently available therapeutic options, including ablation, radioembolization, transarterial chemoembolization (TACE), and systemic treatment with tyrosine kinase inhibitors (TKIs), provide limited survival benefits. Studies have suggested that the combination treatment may provide better therapeutic outcomes as compared to individual treatments. However, studies of regorafenib in combination with local treatment in patients after failure of first-line treatment are still lacking, and the efficacy of this regimen has not been thoroughly investigated. Therefore, the purpose of our study was to determine the efficacy and safety of TACE combined with regorafenib as second-line therapy in patients with unresectable HCC.
Patients with HCC at Barcelona Clinic Liver Cancer (BCLC) stage B or C who received the combined treatment of TACE, ablation, and regorafenib or regorafenib plus anti-PD-1 immune checkpoint inhibitors (ICIs) in Beijing You'an Hospital between April 2020 to June 2023 were reviewed. The primary endpoint was overall survival (OS), while progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), and toxicity were the secondary endpoints.
A total of 73 patients were enrolled in our study, including 63 (86.3%) males and 10 (13.7%) females. Among these patients, 16 (21.9%) had portal vein tumor thrombosis (PVTT), and 33 (45.2%) had extrahepatic metastasis. There were 53 (72.6%) patients with multiple tumors and 23 (31.5%) with large tumors (>30 mm). All patients received TACE combined with regorafenib, while 37 (50.7%) additionally received ICIs and 36 (49.3%) did not. The majority (n=61, 83.6%) of patients in our cohort received ablation therapy. There were 22 (30.1%) patients with an alpha fetoprotein (AFP) level >400 U/L. The average follow-up of the cohort was 24.6 months, the median PFS was 7.06 months [95% confidence interval (CI): 4.77-9.36 months], and the median OS was 24.0 months (95% CI: 6.25-41.75 months). According to the modified Response Evaluation Criteria in Solid Tumors, the ORR was 58.9%, and the DCR was 91.8%. No adverse events (AEs) were reported in the 11 patients in the study. The most common any-grade treatment-related AEs were hand-foot syndrome (34.25%), diarrhea (23.29%), and hypertension (21.92%). Grade ≥3 treatment-related AEs occurred in 12.3% of the patients. The most common grade 3 treatment-related AE was hypertension (5.48%).
TACE combined with ablation and regorafenib is an effective, safe, and promising second-line treatment option for patients with unresectable HCC after progression from first-line therapy.
大多数肝细胞癌(HCC)患者在确诊时已进展至中晚期,不符合根治性治疗条件。目前可用的治疗选择,包括消融、放射性栓塞、经动脉化疗栓塞(TACE)以及酪氨酸激酶抑制剂(TKIs)的全身治疗,所带来的生存获益有限。研究表明,联合治疗与单一治疗相比可能带来更好的治疗效果。然而,一线治疗失败后瑞戈非尼联合局部治疗在患者中的研究仍然缺乏,且该方案的疗效尚未得到充分研究。因此,我们研究的目的是确定TACE联合瑞戈非尼作为不可切除HCC患者二线治疗的疗效和安全性。
回顾2020年4月至2023年6月在北京佑安医院接受TACE、消融联合瑞戈非尼或瑞戈非尼加抗PD-1免疫检查点抑制剂(ICIs)联合治疗的巴塞罗那临床肝癌(BCLC)B期或C期HCC患者。主要终点是总生存期(OS),而无进展生存期(PFS)、客观缓解率(ORR)、疾病控制率(DCR)和毒性是次要终点。
我们的研究共纳入73例患者,其中男性63例(86.3%),女性10例(13.7%)。在这些患者中,16例(21.9%)有门静脉癌栓(PVTT),33例(45.2%)有肝外转移。有53例(72.6%)患者有多发性肿瘤,23例(31.5%)有大肿瘤(>30mm)。所有患者均接受TACE联合瑞戈非尼治疗,其中37例(50.7%)额外接受了ICIs,36例(49.3%)未接受。我们队列中的大多数患者(n=61,83.6%)接受了消融治疗。有22例(30.1%)患者甲胎蛋白(AFP)水平>400U/L。该队列的平均随访时间为24.6个月,中位PFS为7.06个月[95%置信区间(CI):4.77-9.36个月],中位OS为24.0个月(95%CI:6.25-41.75个月)。根据改良的实体瘤疗效评价标准,ORR为58.9%,DCR为91.8%。研究中的11例患者未报告不良事件(AE)。最常见的任何级别的治疗相关AE是手足综合征(34.25%)、腹泻(23.29%)和高血压(21.92%)。≥3级治疗相关AE发生在12.3%的患者中。最常见的3级治疗相关AE是高血压(5.48%)。
TACE联合消融和瑞戈非尼是一线治疗进展后不可切除HCC患者的一种有效、安全且有前景的二线治疗选择。