Combined transarterial chemoembolization and tislelizumab for patients with unresectable hepatocellular carcinoma.

IF 1.8 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Bin-Bin Tan, Ying Fu, Ming-Hua Shao, Hai-Lei Chen, Ping Liu, Chao Fan, Hui Zhang
{"title":"Combined transarterial chemoembolization and tislelizumab for patients with unresectable hepatocellular carcinoma.","authors":"Bin-Bin Tan, Ying Fu, Ming-Hua Shao, Hai-Lei Chen, Ping Liu, Chao Fan, Hui Zhang","doi":"10.4240/wjgs.v16.i9.2829","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Hepatocellular carcinoma (HCC) often presents as unresectable, necessitating effective treatment modalities. Combining transarterial chemoembolization (TACE) with immunotherapy and targeted therapy has shown promise, yet real-world evidence is needed.</p><p><strong>Aim: </strong>To investigate effectiveness and safety of TACE with tislelizumab ± targeted therapy for unresectable HCC in real-world setting.</p><p><strong>Methods: </strong>This retrospective study included patients with unresectable HCC receiving combined treatment of TACE and tislelizumab. The clinical outcomes included progression-free survival (PFS), overall survival (OS), objective response rate (ORR), and disease control rate (DCR). All patients were evaluated according to the mRECIST criteria. The adverse event (AE) was also assessed.</p><p><strong>Results: </strong>In this study of 56 patients with median follow-up of 10.9 months, 7 had previous immunotherapy. Tislelizumab was administered before TACE in 21 (37.50%) and after in 35 (62.50%) patients, with 91.07% receiving concurrent targeted therapy. Median PFS was 14.0 (95%CI: 7.0-18.00) months, and OS was 28 (95%CI: 2.94-53.05) months. Patients with prior immunotherapy had shorter PFS (6 vs. 18 months, <i>P</i> = 0.006). Overall ORR and DCR were 82.14% and 87.50%. Grade ≥ 3 treatment-related AEs included increased alanine aminotransferase (8.93%), aspartate aminotransferase (10.71%), and total bilirubin (3.57%).</p><p><strong>Conclusion: </strong>The combination of TACE and tislelizumab, with or without targeted therapy, demonstrated promising efficacy and safety in unresectable HCC, especially in immunotherapy-naive patients, warranting further prospective validation studies.</p>","PeriodicalId":23759,"journal":{"name":"World Journal of Gastrointestinal Surgery","volume":"16 9","pages":"2829-2841"},"PeriodicalIF":1.8000,"publicationDate":"2024-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11438790/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"World Journal of Gastrointestinal Surgery","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.4240/wjgs.v16.i9.2829","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Hepatocellular carcinoma (HCC) often presents as unresectable, necessitating effective treatment modalities. Combining transarterial chemoembolization (TACE) with immunotherapy and targeted therapy has shown promise, yet real-world evidence is needed.

Aim: To investigate effectiveness and safety of TACE with tislelizumab ± targeted therapy for unresectable HCC in real-world setting.

Methods: This retrospective study included patients with unresectable HCC receiving combined treatment of TACE and tislelizumab. The clinical outcomes included progression-free survival (PFS), overall survival (OS), objective response rate (ORR), and disease control rate (DCR). All patients were evaluated according to the mRECIST criteria. The adverse event (AE) was also assessed.

Results: In this study of 56 patients with median follow-up of 10.9 months, 7 had previous immunotherapy. Tislelizumab was administered before TACE in 21 (37.50%) and after in 35 (62.50%) patients, with 91.07% receiving concurrent targeted therapy. Median PFS was 14.0 (95%CI: 7.0-18.00) months, and OS was 28 (95%CI: 2.94-53.05) months. Patients with prior immunotherapy had shorter PFS (6 vs. 18 months, P = 0.006). Overall ORR and DCR were 82.14% and 87.50%. Grade ≥ 3 treatment-related AEs included increased alanine aminotransferase (8.93%), aspartate aminotransferase (10.71%), and total bilirubin (3.57%).

Conclusion: The combination of TACE and tislelizumab, with or without targeted therapy, demonstrated promising efficacy and safety in unresectable HCC, especially in immunotherapy-naive patients, warranting further prospective validation studies.

联合经动脉化疗栓塞术和替赛利珠单抗治疗无法切除的肝细胞癌患者。
背景:肝细胞癌(HCC)通常无法切除,因此需要有效的治疗方法。经动脉化疗栓塞术(TACE)与免疫疗法和靶向疗法的联合治疗已显示出前景,但还需要真实世界的证据。目的:在真实世界环境中研究TACE与替舒利珠单抗和靶向疗法联合治疗不可切除HCC的有效性和安全性:这项回顾性研究纳入了接受TACE和替舒利珠单抗联合治疗的不可切除HCC患者。临床结果包括无进展生存期(PFS)、总生存期(OS)、客观反应率(ORR)和疾病控制率(DCR)。所有患者均按照 mRECIST 标准进行评估。同时还评估了不良事件(AE):在这项中位随访期为 10.9 个月的 56 例患者中,有 7 例曾接受过免疫治疗。21名患者(37.50%)在TACE前使用了Tislelizumab,35名患者(62.50%)在TACE后使用了Tislelizumab,91.07%的患者同时接受了靶向治疗。中位 PFS 为 14.0(95%CI:7.0-18.00)个月,OS 为 28(95%CI:2.94-53.05)个月。既往接受过免疫治疗的患者的 PFS 较短(6 个月对 18 个月,P = 0.006)。总体ORR和DCR分别为82.14%和87.50%。治疗相关的≥3级AE包括丙氨酸氨基转移酶升高(8.93%)、天门冬氨酸氨基转移酶升高(10.71%)和总胆红素升高(3.57%):无论是否进行靶向治疗,TACE和替舒利珠单抗联合治疗不可切除的HCC,尤其是免疫治疗无效的患者,均显示出良好的疗效和安全性,值得进一步开展前瞻性验证研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
5.00%
发文量
111
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信