Huang Jin-Tao, Hu Di, Hong Xin, Zhou Wen-Jie, Shen Jian, Lv Peng-Hua, Zhu Xiao-Li
Department of Interventional Radiology, The First Affiliated Hospital of Soochow University, Suzhou, China.
Department of Interventional Radiology, Affiliated Hospital 2 of Nantong University, Nantong, China.
Eur Radiol Exp. 2025 Feb 18;9(1):21. doi: 10.1186/s41747-025-00563-4.
The objective of this study was to evaluate the therapeutic effectiveness and safety of transarterial chemoembolization (TACE) combined with programmed cell death-1 (PD-1) inhibitors and lenvatinib in the treatment of unresectable intrahepatic cholangiocarcinoma (uICC).
This multicenter retrospective study screened patients with uICC who underwent TACE in combination with PD-1 inhibitors and lenvatinib between January 2019 and June 2023. Tislelizumab or camrelizumab (200 mg) was intravenously administered every three weeks. The daily dose of lenvatinib was 8 mg for patients weighing < 60 kg and 12 mg for those weighing ≥ 60 kg. In cases of disease progression, the therapeutic strategy was adjusted based on the clinical condition and individual patient's treatment preferences. Options included transitioning to standard or supportive care or continuing treatment with TACE in combination with PD-1 inhibitors and lenvatinib. The primary outcomes were overall survival (OS) and progression-free survival (PFS), while secondary outcomes included the objective response rate (ORR), disease control rate (DCR), and the incidence of adverse events (AEs).
A total of 59 patients with uICC were included. Over a median follow-up period of 32.3 months, the median OS and PFS were 25.8 months (95% confidence interval [CI]: 17.9-33.7) and 9.5 months (95% CI: 7.9-11.0), respectively. The ORR was 55.9%, and the DCR was 96.6%. Grade 3 or four AEs were observed in 15 of 59 patients (25.4%).
TACE combined with PD-1 inhibitors and lenvatinib demonstrated a promising therapeutic potential with a manageable safety profile for patients with uICC.
The combination of TACE, PD-1 inhibitors, and lenvatinib represents a novel therapeutic option for patients with uICC.
TACE plus PD-1 inhibitors and lenvatinib represent a promising therapeutic strategy for uICC. The safety profile of TACE plus PD-1 inhibitors and lenvatinib was manageable. This study demonstrated improved outcomes compared to prior standard-of-care treatments.
本研究的目的是评估经动脉化疗栓塞术(TACE)联合程序性细胞死亡蛋白1(PD-1)抑制剂和乐伐替尼治疗不可切除肝内胆管癌(uICC)的疗效和安全性。
这项多中心回顾性研究筛选了2019年1月至2023年6月期间接受TACE联合PD-1抑制剂和乐伐替尼治疗的uICC患者。替雷利珠单抗或卡瑞利珠单抗(200mg)每三周静脉注射一次。乐伐替尼的日剂量对于体重<60kg的患者为8mg,对于体重≥60kg的患者为12mg。在疾病进展的情况下,根据临床情况和患者个体的治疗偏好调整治疗策略。选择包括转为标准治疗或支持治疗,或继续使用TACE联合PD-1抑制剂和乐伐替尼进行治疗。主要结局为总生存期(OS)和无进展生存期(PFS),次要结局包括客观缓解率(ORR)、疾病控制率(DCR)和不良事件(AE)的发生率。
共纳入59例uICC患者。在中位随访期32.3个月时,中位OS和PFS分别为25.8个月(95%置信区间[CI]:17.9-33.7)和9.5个月(95%CI:7.9-11.0)。ORR为55.9%,DCR为96.6%。59例患者中有15例(25.4%)观察到3级或4级AE。
TACE联合PD-1抑制剂和乐伐替尼对uICC患者显示出有前景的治疗潜力,且安全性可控。
TACE、PD-1抑制剂和乐伐替尼的联合应用为uICC患者提供了一种新的治疗选择。
TACE加PD-1抑制剂和乐伐替尼是一种有前景的uICC治疗策略。TACE加PD-1抑制剂和乐伐替尼的安全性可控。与先前的标准治疗相比,本研究显示出更好的结局。