The Combination of D-TACE-HAIC, Lenvatinib, and PD-1 Inhibitors Shows Significant Clinical Efficacy in Patients with Unresectable Hepatocellular Carcinoma.

IF 2.6 4区 医学 Q3 ONCOLOGY Cancer Management and Research Pub Date : 2025-02-06 eCollection Date: 2025-01-01 DOI:10.2147/CMAR.S481242
Yintao Wu, Jianyong Zhu, Hong Zhang, Nianxin Xia
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Abstract

Purpose: This study was developed to compare the efficacy of combined D-TACE-HAIC + lenvatinib + PD-1 inhibitor treatment to that of TACE + sorafenib treatment for patients with intermediate and advanced HCC.

Patients and methods: Here, a retrospective analysis of patients with unresectable HCC who underwent transarterial chemoembolization (TACE) from March 2018 to March 2022 at the our hospital was conducted. In total, 60 patients underwent treatment with drug-eluting beads-TACE-hepatic arterial infusion chemotherapy (D-TACE-HAIC) combined with lenvatinib and PD-1 inhibitors (Group A), while 21 underwent combined TACE and sorafenib treatment (Group B).

Results: In this study cohort, the rate of surgical conversion in Group A was significantly higher than that in Group B (33.3% vs 9.5%). As per the Revised Evaluation Criteria for Clinical Efficacy in Solid Tumors (mRECIST) criteria, the objective remission rate in Group A was significantly higher than that in Group B (86.6% vs 33.4%). Group A also exhibited significantly higher rates of overall adverse events including hypertension, abdominal pain, leukopenia, thrombocytopenia, and hypoproteinemia as compared to Group B, although the incidence of hand-foot syndrome in Group A was significantly reduced as compared to Group B (13.3% vs 42.8%). The median progression-free and overall survival (PFS and OS) of patients in Group A were 13.2 and 28.8 months, with both being significantly higher than the corresponding intervals in Group B (5.7 and 10.8 months, respectively). Cox multivariate analyses identified combination D-TACE-HAIC + lenvatinib+ PD-1 inhibitor treatment as being independently associated with patient PFS and OS.

Conclusion: In summary, D-TACE-HAIC + lenvatinib + PD-1 inhibitor treatment exhibits a favorable safety profile, outperforming TACE + sorafenib treatment for unresectable HCC patients while improving overall rates of translational efficacy, increasing rates of surgical conversion, prolonging patient survival, and conferring long-term survival benefits.

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D-TACE-HAIC、Lenvatinib和PD-1抑制剂联合治疗不可切除肝癌临床疗效显著。
目的:本研究旨在比较D-TACE-HAIC + lenvatinib + PD-1抑制剂联合治疗中晚期HCC患者与TACE +索拉非尼治疗的疗效。患者与方法:回顾性分析2018年3月至2022年3月在我院行经动脉化疗栓塞术(TACE)的不可切除HCC患者。共60例患者采用药物洗脱珠-TACE-肝动脉输注化疗(D-TACE-HAIC)联合lenvatinib和PD-1抑制剂治疗(A组),21例患者采用TACE联合索拉非尼治疗(B组)。结果:在本研究队列中,A组的手术转化率显著高于B组(33.3% vs 9.5%)。根据修订的实体瘤临床疗效评价标准(mRECIST)标准,A组的客观缓解率明显高于B组(86.6% vs 33.4%)。与B组相比,A组也表现出明显更高的总体不良事件发生率,包括高血压、腹痛、白细胞减少、血小板减少和低蛋白血症,尽管A组的手足综合征发生率明显低于B组(13.3%对42.8%)。A组患者的中位无进展生存期和总生存期(PFS和OS)分别为13.2和28.8个月,均显著高于B组患者的相应生存期(分别为5.7和10.8个月)。Cox多变量分析发现,D-TACE-HAIC + lenvatinib+ PD-1抑制剂联合治疗与患者PFS和OS独立相关。结论:总之,D-TACE-HAIC + lenvatinib + PD-1抑制剂治疗具有良好的安全性,在不可切除的HCC患者中优于TACE +索拉非尼治疗,同时提高了总体转化效率,增加了手术转换率,延长了患者生存期,并获得了长期生存益处。
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来源期刊
Cancer Management and Research
Cancer Management and Research Medicine-Oncology
CiteScore
7.40
自引率
0.00%
发文量
448
审稿时长
16 weeks
期刊介绍: Cancer Management and Research is an international, peer reviewed, open access journal focusing on cancer research and the optimal use of preventative and integrated treatment interventions to achieve improved outcomes, enhanced survival, and quality of life for cancer patients. Specific topics covered in the journal include: ◦Epidemiology, detection and screening ◦Cellular research and biomarkers ◦Identification of biotargets and agents with novel mechanisms of action ◦Optimal clinical use of existing anticancer agents, including combination therapies ◦Radiation and surgery ◦Palliative care ◦Patient adherence, quality of life, satisfaction The journal welcomes submitted papers covering original research, basic science, clinical & epidemiological studies, reviews & evaluations, guidelines, expert opinion and commentary, and case series that shed novel insights on a disease or disease subtype.
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