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经导管动脉化疗栓塞联合 PD-1 抑制剂和仑伐替尼治疗伴有门静脉癌栓的肝细胞癌。

Transcatheter arterial chemoembolization combined with PD-1 inhibitors and Lenvatinib for hepatocellular carcinoma with portal vein tumor thrombus.

机构信息

Cancer Center, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.

出版信息

World J Gastroenterol. 2024 Feb 28;30(8):843-854. doi: 10.3748/wjg.v30.i8.843.

DOI:10.3748/wjg.v30.i8.843
PMID:38516240
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10950640/
Abstract

BACKGROUND

Hepatocellular carcinoma (HCC) patients complicated with portal vein tumor thrombus (PVTT) exhibit poor prognoses and treatment responses.

AIM

To investigate efficacies and safety of the combination of PD-1 inhibitor, transcatheter arterial chemoembolization (TACE) and Lenvatinib in HCC subjects comorbid with PVTT.

METHODS

From January 2019 to December 2020, HCC patients with PVTT types I-IV were retrospectively enrolled at Beijing Ditan Hospital. They were distributed to either the PTL or TACE/Lenvatinib (TL) group. The median progression-free survival (mPFS) was set as the primary endpoint, while parameters like median overall survival, objective response rate, disease control rate (DCR), and toxicity level served as secondary endpoints.

RESULTS

Forty-one eligible patients were finally recruited for this study and divided into the PTL ( = 18) and TL ( = 23) groups. For a median follow-up of 21.8 months, the DCRs were 88.9% and 60.9% in the PTL and TL groups ( = 0.046), res-pectively. Moreover, mPFS indicated significant improvement (HR = 0.25; < 0.001) in PTL-treated patients (5.4 months) compared to TL-treated (2.7 months) patients. There were no treatment-related deaths or differences in adverse events in either group.

CONCLUSION

A triplet regimen of PTL was safe and well-tolerated as well as exhibited favorable efficacy over the TL regimen for advanced-stage HCC patients with PVTT types I-IV.

摘要

背景

肝细胞癌(HCC)合并门静脉癌栓(PVTT)的患者预后和治疗反应较差。

目的

探讨 PD-1 抑制剂联合经导管动脉化疗栓塞(TACE)和仑伐替尼治疗合并 PVTT 的 HCC 患者的疗效和安全性。

方法

回顾性纳入 2019 年 1 月至 2020 年 12 月在北京地坛医院就诊的 HCC 合并 PVTT Ⅰ-Ⅳ型患者,按治疗方案分为 TACE+培美曲塞组(PTL 组)和 TACE+仑伐替尼组(TL 组)。以中位无进展生存期(mPFS)为主要研究终点,以中位总生存期、客观缓解率(ORR)、疾病控制率(DCR)和毒性水平等为次要研究终点。

结果

本研究共纳入 41 例患者,PTL 组 18 例,TL 组 23 例。中位随访时间为 21.8 个月,PTL 组和 TL 组的 DCR 分别为 88.9%和 60.9%( = 0.046)。PTL 组 mPFS 为 5.4 个月,明显长于 TL 组的 2.7 个月(HR = 0.25; < 0.001)。两组均无治疗相关死亡和不良事件差异。

结论

PTL 三联方案治疗 HCC 合并 PVTT Ⅰ-Ⅳ型患者安全、耐受良好,疗效优于 TL 方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae0/10950640/d84be850d7f2/WJG-30-843-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae0/10950640/0712caaa7ea1/WJG-30-843-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae0/10950640/3abb459d2b72/WJG-30-843-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae0/10950640/d84be850d7f2/WJG-30-843-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae0/10950640/0712caaa7ea1/WJG-30-843-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae0/10950640/3abb459d2b72/WJG-30-843-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae0/10950640/d84be850d7f2/WJG-30-843-g003.jpg

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