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经动脉化疗栓塞、仑伐替尼和 PD-1 抑制剂联合治疗显著改善肝细胞癌伴胆管癌栓患者的肿瘤反应:一例报告
Authors Fu Y, Wu J, Wu J , Li Y , Zeng Z, Liu D, Li H, Ou X, Lin Z, Wei S, Song H, Yan M
Received 10 December 2024
Accepted for publication 4 April 2025
Published 13 April 2025 Volume 2025:17 Pages 793—799
DOI http://doi.org/10.2147/CMAR.S511319
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Antonella D'Anneo
Yangkai Fu,1 Junyi Wu,1,2 Jiayi Wu,1,2 Yinan Li,1 Zhenxin Zeng,1 Deyi Liu,1 Han Li,1 Xiangye Ou,1 Zhongtai Lin,1 Shaoming Wei,1 Huachun Song,1 Maolin Yan1,2
1Shengli Clinical Medical College of Fujian Medical University, Fuzhou, Fujian Province, People’s Republic of China; 2Department of Hepatobiliary Pancreatic Surgery, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, Fujian Province, People’s Republic of China
Correspondence: Maolin Yan, The Shengli Clinical Medical College of Fujian Medical University, Department of Hepatobiliary Pancreatic Surgery, Fujian Provincial Hospital, Dongjie Road 134, Fuzhou, Fujian Province, 350001, People’s Republic of China, Email yanmaolin74@163.com
Abstract: Combination therapy plays a critical role in optimizing surgical outcomes for patients with locally advanced hepatocellular carcinoma (HCC) complicated by bile duct tumor thrombus (BDTT). Current neoadjuvant strategies integrate local and systemic modalities to reduce tumor burden and recurrence rate. However, the combination of transarterial chemoembolization (TACE), lenvatinib, and PD-1 inhibitors (triple therapy) as a neoadjuvant regimen for HCC with BDTT has not been previously reported. Here, we present the case of a 61-year-old man with HBV-associated HCC and BDTT, initially deemed high-risk for direct resection due to tumor size (7 cm) and biliary involvement. The patient underwent one session of TACE followed by two months of lenvatinib (12 mg/day) and sintilimab (200 mg every 3 weeks). Post-treatment contrast-enhanced MRI revealed complete resolution of BDTT and partial response of the primary tumor. Subsequent right hemihepatectomy confirmed extensive tumor necrosis (> 90%) with negative margins. At 15-month follow-up, surveillance imaging showed no recurrence. The patient experienced only grade 1 hypertension, managed without treatment interruption. This case highlights the potential of triple therapy as a neoadjuvant approach to downstage advanced HCC with BDTT, enabling curative resection while maintaining a manageable safety profile. Further studies are warranted to validate its efficacy in larger cohorts and define optimal treatment protocols.
Keywords: hepatocellular carcinoma, bile duct tumor thrombus, combination therapy, lenvatinib, immunotherapy