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

被引:0
|
作者
Shen, Xiao [1 ]
Zhang, Jin-Xing [1 ]
Liu, Jin [2 ]
Liu, Sheng [1 ]
Shi, Hai-Bin [1 ]
Cheng, Yuan [3 ]
Zhang, Qing-Qiao [4 ]
Yin, Guo-Wen [5 ]
Zu, Qing-Quan [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Intervent Radiol, 300 Guangzhou Rd, Nanjing 210029, Peoples R China
[2] Nanjing Med Univ, Affiliated Hosp 1, Dept Clin Med Res Inst, Nanjing 210029, Peoples R China
[3] Nanjing Univ, Jinling Hosp, Affiliated Hosp, Dept Med Oncol,Med Sch, Nanjing 210002, Peoples R China
[4] Xuzhou Med Univ, Affiliated Hosp, Dept Intervent Radiol & Vasc Surg, Xuzhou 221006, Peoples R China
[5] Nanjing Med Univ, Affiliated Canc Hosp, Dept Intervent Radiol, Nanjing 210009, Peoples R China
关键词
atezolizumab; bevacizumab; efficacy; hepatocellular carcinoma; transarterial chemoembolization; LENVATINIB; SAFETY;
D O I
10.2147/JHC.S478604
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
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页码:1993 / 2003
页数:11
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