Fever following Treatment with Atezolizumab plus Bevacizumab Predicts Liver Injury in Patients with Unresectable Hepatocellular Carcinoma: A Prospective Observational Analysis.

IF 11.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Liver Cancer Pub Date : 2025-06-14 DOI:10.1159/000546967
Takanori Ito, Takafumi Yamamoto, Kazuki Nishida, Yumiko Kobayashi, Kazuyuki Mizuno, Takaya Suzuki, Shinya Yokoyama, Kenta Yamamoto, Norihiro Imai, Yoji Ishizu, Takashi Honda, Masatoshi Ishigami, Toshinari Koya, Sayori Nakashima, Takehito Naito, Satoshi Yasuda, Teiji Kuzuya, Hidenori Toyoda, Yuichi Ando, Sachiyo Yoshio, Hiroki Kawashima
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引用次数: 0

Abstract

Introduction: Liver injury is a treatment-related adverse event (liver-TRAE), one of the most common complications of atezolizumab plus bevacizumab (Atez/Bev) therapy, when treating unresectable hepatocellular carcinoma (uHCC). Fever following immune checkpoint inhibitor (ICI) therapy may predict ICI-induced liver injury in various malignancy types. However, the association between fever and liver-TRAEs in patients with uHCC treated with Atez/Bev has not been investigated. We prospectively evaluated the relationship between the onset of liver-TRAEs and preceding fever and sought to identify circulating biomarkers that predict liver injury in patients with Atez/Bev-treated uHCC.

Methods: The primary outcome of this prospective, multicenter study was the association between liver-TRAEs (grade ≥2) and the presence of ICI-induced fever before the onset of liver injury. We used a multiplex bead-based immunoassay to evaluate 40 circulating proteins in the serum before and at 1, 3, and 6 weeks after initial Atez/Bev treatment.

Results: Among 99 patients receiving Atez/Bev, grade ≥2 liver-TRAEs occurred in 10 (10.1%) during the follow-up period (median, 14.7 months). The incidences of liver-TRAEs associated with fever before liver injury were 27.8% (n = 5/18) and 6.2% (n = 5/81) in the fever and non-fever groups, respectively. Multivariable analysis showed that the presence of fever was a significant risk factor for liver-TRAEs (odds ratio 7.57; 95% confidence interval, 1.83-33.89; p = 0.006). Furthermore, the prognosis was worse in the liver-TRAE (grade ≥2) group (p = 0.065 for progression-free survival and p = 0.074 for overall survival). Among patients with preceding fever, the liver-TRAE group had significantly lower CXCL-5 levels before treatment, higher IL-6 levels at 1 and 3 weeks, and lower CXCL-5, IFN-γ, and IL-10 levels at 6 weeks (p < 0.05).

Conclusion: Fever during Atez/Bev treatment may predict liver-TRAEs, which leads to poor prognosis in patients with uHCC. Altered inflammatory cytokine and chemokine levels may help predict liver-TRAEs in patients with fever after Atez/Bev therapy.

阿特唑单抗联合贝伐单抗治疗后发热预测不可切除肝细胞癌患者肝损伤:一项前瞻性观察分析。
简介:肝损伤是治疗相关不良事件(Liver - trae),是阿特唑单抗联合贝伐单抗(Atez/Bev)治疗不可切除肝细胞癌(uHCC)时最常见的并发症之一。免疫检查点抑制剂(ICI)治疗后发热可以预测ICI诱导的各种恶性肿瘤类型的肝损伤。然而,在接受Atez/Bev治疗的uHCC患者中,发烧与肝脏trae之间的关系尚未被调查。我们前瞻性地评估了肝脏traes发作与先前发热之间的关系,并试图确定预测Atez/ bev治疗的uHCC患者肝损伤的循环生物标志物。方法:这项前瞻性、多中心研究的主要结局是肝traes(≥2级)与肝损伤发生前ici诱导的发热之间的关系。我们使用了一种基于多重头部的免疫分析法来评估在初始Atez/Bev治疗前、1周、3周和6周血清中的40种循环蛋白。结果:在99例接受Atez/Bev治疗的患者中,在随访期间(中位14.7个月),10例(10.1%)发生≥2级肝脏trae。肝损伤前发热伴肝trae的发生率在发热组和非发热组分别为27.8% (n = 5/18)和6.2% (n = 5/81)。多变量分析显示,发热是肝traes的重要危险因素(优势比7.57;95%置信区间为1.83 ~ 33.89;P = 0.006)。此外,肝- trae(≥2级)组的预后更差(无进展生存期p = 0.065,总生存期p = 0.074)。在既往有发热的患者中,肝trae组治疗前CXCL-5水平显著降低,治疗1周和治疗3周时IL-6水平显著升高,治疗6周时CXCL-5、IFN-γ和IL-10水平显著降低(p < 0.05)。结论:Atez/Bev治疗期间发热可预测肝脏trae,导致hcc患者预后不良。炎性细胞因子和趋化因子水平的改变可能有助于预测Atez/Bev治疗后发热患者的肝脏trae。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Liver Cancer
Liver Cancer Medicine-Oncology
CiteScore
20.80
自引率
7.20%
发文量
53
审稿时长
16 weeks
期刊介绍: Liver Cancer is a journal that serves the international community of researchers and clinicians by providing a platform for research results related to the causes, mechanisms, and therapy of liver cancer. It focuses on molecular carcinogenesis, prevention, surveillance, diagnosis, and treatment, including molecular targeted therapy. The journal publishes clinical and translational research in the field of liver cancer in both humans and experimental models. It publishes original and review articles and has an Impact Factor of 13.8. The journal is indexed and abstracted in various platforms including PubMed, PubMed Central, Web of Science, Science Citation Index, Science Citation Index Expanded, Google Scholar, DOAJ, Chemical Abstracts Service, Scopus, Embase, Pathway Studio, and WorldCat.
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