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在阿替利珠单抗联合贝伐单抗治疗中降低贝伐单抗剂量可延长肝细胞癌患者疾病控制的治疗持续时间。

Dose-Reduction of Bevacizumab in Atezolizumab plus Bevacizumab Therapy Extends Treatment duration with Disease Control in Patients with Hepatocellular Carcinoma.

作者信息

Sakai Miwa, Iwamoto Hideki, Shimose Shigeo, Niizeki Takashi, Nakano Masahito, Shirono Tomotake, Noda Yu, Moriyama Etsuko, Suzuki Hiroyuki, Koga Hironori, Kuromatsu Ryoko, Kawaguchi Takumi

机构信息

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan,

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.

出版信息

Oncology. 2025;103(4):265-276. doi: 10.1159/000541082. Epub 2024 Sep 12.

Abstract

INTRODUCTION

Atezolizumab (ATZ) and bevacizumab (BEV) combination therapy is widely used in patients with unresectable hepatocellular carcinoma (HCC). However, combination therapy is typically interrupted or discontinued owing to BEV-related adverse events. In this study, we examined the effects of BEV dose-reduction on the treatment of unresectable HCC using propensity score matching (PSM).

METHOD

Overall, 119 patients with HCC who were treated with ATZ + BEV between November 2020 and October 2022 were enrolled retrospectively at our institute. The therapeutic effects and safety of BEV dose-reduction and non-dose reduction after PSM were compared. Decision-tree analysis was used to investigate treatment duration in the patients.

RESULTS

Significant differences were not observed between the two groups after PSM. The objective response rate (ORR) and disease control rate (DCR) assessed by modified RECIST did not differ significantly between the two groups (BEV non-dose-reduction/dose-reduction: ORR; 46/34%, DCR; 80/91%). Progression-free survival (PFS) and overall survival (OS) also did not differ significantly between the two groups (BEV non-dose-reduction/dose-reduction: PFS; 5.6/8.6 months, OS; 18.6/15.5 months). The median duration of treatment in the BEV dose-reduction group was significantly longer than that in the non-dose-reduction group (BEV non-dose-reduction/dose-reduction: 4.8/9.1 months, p = 0.038). Decision-tree analysis revealed that dose-reduction of BEV was the first distinguish factor for the extension of treatment duration with ATZ + BEV.

CONCLUSION

BEV dose-reduction can be effectively used in maintaining the treatment duration of ATZ + BEV while maintaining therapeutic effects and safety in real-world clinical practice.

摘要

引言

阿替利珠单抗(ATZ)和贝伐珠单抗(BEV)联合疗法广泛应用于不可切除肝细胞癌(HCC)患者。然而,联合治疗通常因与BEV相关的不良事件而中断或停止。在本研究中,我们使用倾向评分匹配(PSM)研究了BEV剂量减少对不可切除HCC治疗的影响。

方法

总体而言,2020年11月至2022年10月期间在我院接受ATZ + BEV治疗的119例HCC患者被纳入回顾性研究。比较PSM后BEV剂量减少和未减少的治疗效果和安全性。采用决策树分析研究患者的治疗持续时间。

结果

PSM后两组之间未观察到显著差异。改良RECIST评估的客观缓解率(ORR)和疾病控制率(DCR)在两组之间无显著差异(BEV未减量/减量:ORR;46/34%,DCR;80/91%)。两组之间的无进展生存期(PFS)和总生存期(OS)也无显著差异(BEV未减量/减量:PFS;5.6/8.6个月,OS;18.6/15.5个月)。BEV减量组的中位治疗持续时间显著长于未减量组(BEV未减量/减量:4.8/9.1个月,p = 0.038)。决策树分析显示,BEV剂量减少是延长ATZ + BEV治疗持续时间的首要区分因素。

结论

在真实世界的临床实践中,BEV剂量减少可有效用于维持ATZ + BEV的治疗持续时间,同时维持治疗效果和安全性。

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