Efficacy of Atezolizumab Plus Bevacizumab-Transcatheter Arterial Chemoembolization Sequential Therapy for Patients with Intermediate-Stage Hepatocellular Carcinoma

被引:0
|
作者
Moriyama, Etsuko [1 ]
Shimose, Shigeo [1 ]
Niizeki, Takashi [1 ]
Iwamoto, Hideki [1 ,2 ]
Tanaka, Masatoshi [3 ]
Shirono, Tomotake [1 ]
Noda, Yu [1 ]
Nakano, Masahito [1 ]
Kuromatsu, Ryoko [1 ]
Koga, Hironori [1 ]
Kawaguchi, Takumi [1 ]
机构
[1] Kurume Univ, Sch Med, Dept Med, Div Gastroenterol, Fukuoka 8300011, Japan
[2] Iwamoto Internal Med Clin, Kitakyushu 8020832, Japan
[3] Yokokura Hosp, Clin Res Ctr, Miyama, Fukuoka 8390295, Japan
关键词
atezolizumab plus bevacizumab; hepatocellular carcinoma; TACE; TRANSARTERIAL CHEMOEMBOLIZATION; ANGIOGENESIS; MANAGEMENT; INHIBITORS; SORAFENIB; PROGNOSIS; GRADE; JAPAN; TACE;
D O I
10.3390/curroncol31100432
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This retrospective study aimed to evaluate the impact of atezolizumab plus bevacizumab-transcatheter arterial chemoembolization (TACE) sequential therapy in unresectable hepatocellular carcinoma (HCC), especially in patients with intermediate-stage HCC. A total of 212 patients were enrolled and categorized into the Atez/Bev-TACE sequential therapy (n = 23) or Atez/Bev monotherapy group (n = 189) between 2020 and 2024. Of these, patients with intermediate-stage HCC were categorized into the Atez/Bev-TACE sequential (n = 18) or Atez/Bev monotherapy group (n = 91). The best objective response rate, disease control rate, and median progression-free survival (PFS) after TACE were 73.9%, 82.6%, and 6.1 months, respectively. The PFS after TACE was significantly higher in the Atez/Bev sequential therapy group than in the no-Atez/Bev-administration group after TACE (6.9 months vs. 5.0 months, p = 0.025). The median overall survival (OS) was significantly higher in the Atez/Bev-TACE sequential therapy group than in the Atez/Bev monotherapy group for intermediate-stage HCC (34.9 months vs. 17.8 months; p = 0.016). Independent factors associated with OS were low alpha-fetoprotein levels, modified albumin-bilirubin 1 or 2a levels, and Atez/Bev-TACE sequential therapy. Atez/Bev-TACE sequential therapy improved prognosis compared with Atez/Bev monotherapy in patients with intermediate-stage HCC. Moreover, Atez/Bev should be readministered after TACE.
引用
收藏
页码:5821 / 5831
页数:11
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