中性粒细胞与淋巴细胞比值可预测接受阿替利珠单抗联合贝伐单抗治疗的肝细胞癌患者的免疫相关不良事件。
Neutrophil-to-Lymphocyte Ratio Predicts Immune-related Adverse Events in Patients With Hepatocellular Carcinoma Treated With Atezolizumab Plus Bevacizumab.
作者信息
Kuwano Akifumi, Yada Masayoshi, Tanaka Kosuke, Koga Yuta, Nagasawa Shigehiro, Masumoto Akihide, Motomura Kenta
机构信息
Department of Hepatology, Aso Iizuka Hospital, Fukuoka, Japan.
出版信息
Cancer Diagn Progn. 2024 Jan 3;4(1):34-41. doi: 10.21873/cdp.10282. eCollection 2024 Jan-Feb.
BACKGROUND/AIM: Atezolizumab in combination with bevacizumab is an approved systemic chemotherapy regimen for advanced hepatocellular carcinoma (HCC). However, immune checkpoint inhibitors (ICIs), such as atezolizumab, frequently lead to immune-related adverse events (irAEs). The identification of biomarkers that can predict the occurrence of irAEs is crucial for the optimal management of patients undergoing ICI treatment.
PATIENTS AND METHODS
Between October 2020 and June 2023, we conducted a study involving 69 patients with advanced HCC who received treatment with atezolizumab plus bevacizumab. We conducted an analysis of blood-based biomarkers to identify independent risk factors associated with irAEs.
RESULTS
In our study, 12 out of 69 patients (17.4%) experienced irAEs. Our investigation into blood-based biomarkers revealed that a neutrophil-to-lymphocyte ratio (NLR) <2.04 at three weeks after the initiation of treatment had high predictive power (area under the curve: 0.77) for irAEs. Furthermore, multivariate logistic analysis identified NLR at three weeks (hazard ratio=0.23; p=0.037) and non-viral infection (hazard ratio=4.47; p=0.037) as independent factors contributing to the occurrence of irAEs. Patients who developed irAEs demonstrated a more favorable overall response rate (75.0% vs. 28.1%, p=0.005), disease control rate (91.6% vs. 52.6%, p=0.016), and progression-free survival (12.1 months vs. 6.0 months, p=0.010) than those who did not experience irAEs.
CONCLUSION
An NLR <2.04 at three weeks after the initiation of treatment may serve as a valuable biomarker for predicting irAEs in patients with HCC undergoing atezolizumab plus bevacizumab therapy.
背景/目的:阿替利珠单抗联合贝伐单抗是一种已获批用于晚期肝细胞癌(HCC)的全身化疗方案。然而,免疫检查点抑制剂(ICI),如阿替利珠单抗,经常会导致免疫相关不良事件(irAE)。识别能够预测irAE发生的生物标志物对于接受ICI治疗的患者的最佳管理至关重要。
患者与方法
在2020年10月至2023年6月期间,我们开展了一项研究,纳入了69例接受阿替利珠单抗加贝伐单抗治疗的晚期HCC患者。我们对基于血液的生物标志物进行了分析,以确定与irAE相关的独立危险因素。
结果
在我们的研究中,69例患者中有12例(17.4%)发生了irAE。我们对基于血液的生物标志物的研究表明,治疗开始后三周时中性粒细胞与淋巴细胞比值(NLR)<2.04对irAE具有较高的预测能力(曲线下面积:0.77)。此外,多因素逻辑分析确定治疗后三周时的NLR(风险比=0.23;p=0.037)和非病毒感染(风险比=4.47;p=0.037)是导致irAE发生的独立因素。发生irAE的患者与未发生irAE的患者相比,总体缓解率更高(75.0%对28.1%,p=0.005)、疾病控制率更高(91.6%对52.6%,p=0.016)以及无进展生存期更长(12.1个月对6.0个月,p=0.010)。
结论
治疗开始后三周时NLR<2.04可能是预测接受阿替利珠单抗加贝伐单抗治疗的HCC患者发生irAE的有价值的生物标志物。