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阿替利珠单抗联合贝伐单抗与经动脉化疗栓塞术治疗不可切除肝细胞癌的疗效:一项真实世界研究

Efficacy of Atezolizumab Plus Bevacizumab Combined with Transarterial Chemoembolization for Unresectable Hepatocellular Carcinoma: A Real-World Study.

作者信息

Shen Xiao, Zhang Jin-Xing, Liu Jin, Liu Sheng, Shi Hai-Bin, Cheng Yuan, Zhang Qing-Qiao, Yin Guo-Wen, Zu Qing-Quan

机构信息

Department of Interventional Radiology, The First Affiliated Hospital with Nanjing Medical University, Nanjing, 210029, People's Republic of China.

Department of Clinical Medicine Research Institution, The First Affiliated Hospital with Nanjing Medical University, Nanjing, 210029, People's Republic of China.

出版信息

J Hepatocell Carcinoma. 2024 Oct 21;11:1993-2003. doi: 10.2147/JHC.S478604. eCollection 2024.

DOI:10.2147/JHC.S478604
PMID:39465042
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11505562/
Abstract

PURPOSE

Transarterial chemoembolization (TACE), when used in combination with immunotherapy and antiangiogenic therapy, has been shown to have synergistic anticancer effects. The aim of this study was to further assess the efficacy and safety of TACE combined with atezolizumab and bevacizumab in the treatment of unresectable hepatocellular carcinoma (HCC) in the real world.

METHODS

Between August 2021 and September 2023, clinical information was collected from consecutive HCC patients who received treatment via TACE-Atezo/Bev at four tertiary institutions. This study evaluated the objective response rate (ORR), overall survival (OS), and progression-free survival (PFS) as outcomes. Predictors for OS and PFS were also analyzed. Treatment-related adverse events (TRAEs) were recorded and assessed.

RESULTS

Ninety-two patients were enrolled in this study, with a median follow-up duration of 14.1 months. The ORRs based on the modified Response Evaluation Criteria in Solid Tumors (RECIST) and RECIST 1.1 criteria were 54.3% and 41.3%, respectively. The median OS and PFS of the patients were 15.9 months [95% confidence interval (CI), 14.5-17.2 months] and 9.1 months (95% CI, 7.4-10.8 months), respectively. Multivariate analyses revealed that the Eastern Cooperative Oncology Group score and neutrophil‒lymphocyte ratio were independent risk factors for OS, whereas tumor size and extrahepatic metastasis were independent risk factors for PFS. Grade 3/4 TRAEs occurred in 16.3% (15/92) of the patients and were controlled conservatively.

CONCLUSION

The combination of Atezo/Bev with TACE demonstrated acceptable synergistic therapeutic effects and manageable safety profiles in patients with unresectable HCC.

摘要

目的

经动脉化疗栓塞术(TACE)与免疫治疗和抗血管生成治疗联合使用时,已显示出协同抗癌作用。本研究的目的是在现实世界中进一步评估TACE联合阿替利珠单抗和贝伐单抗治疗不可切除肝细胞癌(HCC)的疗效和安全性。

方法

2021年8月至2023年9月期间,收集了四家三级医疗机构中连续接受TACE-Atezo/Bev治疗的HCC患者的临床信息。本研究将客观缓解率(ORR)、总生存期(OS)和无进展生存期(PFS)作为观察指标。还分析了OS和PFS的预测因素。记录并评估治疗相关不良事件(TRAEs)。

结果

本研究共纳入92例患者,中位随访时间为14.1个月。基于实体瘤改良疗效评价标准(RECIST)和RECIST 1.1标准的ORR分别为54.3%和41.3%。患者的中位OS和PFS分别为15.9个月[95%置信区间(CI),14.5 - 17.2个月]和9.1个月(95%CI,7.4 - 10.8个月)。多因素分析显示,东部肿瘤协作组评分和中性粒细胞与淋巴细胞比值是OS的独立危险因素,而肿瘤大小和肝外转移是PFS的独立危险因素。16.3%(15/92)的患者发生3/4级TRAEs,并得到了保守控制。

结论

Atezo/Bev与TACE联合使用对不可切除HCC患者显示出可接受的协同治疗效果和可控的安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e23/11505562/ce80310a0d10/JHC-11-1993-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e23/11505562/0906e58baeba/JHC-11-1993-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e23/11505562/ce80310a0d10/JHC-11-1993-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e23/11505562/0906e58baeba/JHC-11-1993-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e23/11505562/ce80310a0d10/JHC-11-1993-g0002.jpg

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