中性粒细胞与淋巴细胞比值的动态变化对预测免疫检查点抑制剂加靶向疗法治疗不可切除肝细胞癌反应的影响

IF 4.2 3区 医学 Q2 ONCOLOGY
Journal of Hepatocellular Carcinoma Pub Date : 2024-08-05 eCollection Date: 2024-01-01 DOI:10.2147/JHC.S468843
Jianming Yang, Yu Zhang, Yewu Chen, Yang Yang, Yinan Deng
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引用次数: 0

摘要

背景和目的:免疫检查点抑制剂(ICIs)加靶向治疗的多种方案是不可切除肝细胞癌(uHCC)一线治疗的常用处方。在此,我们旨在研究中性粒细胞与淋巴细胞比值(NLR)的动态变化与肿瘤对 ICIs 和靶向疗法联合治疗 uHCC 的反应之间的相关性:这项回顾性研究共纳入了61例接受ICIs和靶向疗法治疗的uHCC患者。评估治疗前和治疗后3-6周的NLR,计算动态NLR变化(ΔNLR)。多变量逻辑回归和 Cox 回归模型分别用于探讨动态 NLR 变化与肿瘤反应或无进展生存期(PFS)之间的关系。此外,我们还评估了甲胎蛋白(AFP)变化与动态 NLR 变化相结合与单独 AFP 变化相结合的预测效果:结果:接受进展性疾病(PD)治疗的患者在治疗后3-6周的NLR和ΔNLR显著增加,而基线NLR在不同肿瘤反应之间无显著差异。治疗后 NLR 和 AFP 的增加都是进展期的独立预测因素(NLR 增加:OR,2.28;95% AFP;OR,2.28;95% NLR;OR,2.28):OR,2.28;95% CI,1.47-3.88,P <0.001;AFP 增高:OR,1.46;95% CI,1.47-3.88,P <0.001:OR,1.46;95% CI,1.03-2.17,P = 0.043),并与更差的 PFS 相关(NLR 增加:HR,4.08;95% CI,1.03-2.17,P = 0.043):HR,4.08;95% CI,1.99-8.36,P<0.001;AFP 增高:HR,2.10;95% CI,1.99-8.36,P<0.001:HR,2.10;95% CI,1.04-4.24,P = 0.039)。接受者操作特征曲线(ROC)和净再分类指数(NRI)显示,动态NLR和AFP变化的组合在预测PD(AUC:0.83 vs 0.68,P = 0.034;NRI:0.340,P = 0.048)和PFS(AUC:0.80 vs 0.70,P = 0.166;NRI:0.431,P = 0.042)方面优于单独的AFP变化:结论:NLR的动态变化可能是预测ICIs加靶向疗法对uHCC治疗反应的有效指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dynamic Changes of Neutrophil-to-Lymphocyte Ratio on Predicting Response of Immune Checkpoint Inhibitors Plus Targeted Therapies for Unresectable Hepatocellular Carcinoma.

Backgrounds and aims: Multiple regimens of immune checkpoint inhibitors (ICIs) plus targeted therapies are commonly prescribed as first-line treatments for unresectable hepatocellular carcinoma (uHCC). Here, we aimed to investigate the correlation between dynamic changes of neutrophil-to-lymphocyte ratio (NLR) and tumor response to the combination of ICIs and targeted therapies for uHCC.

Methods: Sixty-one patients who received ICIs plus targeted therapies for uHCC were enrolled in this retrospective study. The NLR before and at 3-6 weeks after treatments were assessed to calculate the dynamic NLR changes (ΔNLR). Multivariate logistic regression and Cox regression models were used to explore the relationship between dynamic NLR changes and tumor response or progression-free survival (PFS), respectively. Furthermore, we assessed the predictive effect of alpha-fetoprotein (AFP) changes in combination with dynamic NLR changes compared to AFP changes alone.

Results: The NLR at 3-6 weeks and ΔNLR after treatments significantly increased in patients who underwent progressive disease (PD), while the baseline NLR showed no significant difference between different tumor responses. Increased NLR and AFP after treatments were both independent predictors of PD (For NLR increase: OR, 2.28; 95% CI, 1.47-3.88, P < 0.001; For AFP increase: OR, 1.46; 95% CI, 1.03-2.17, P = 0.043), and correlated with worse PFS (for NLR increase: HR, 4.08; 95% CI, 1.99-8.36, P < 0.001; for AFP increase: HR, 2.10; 95% CI, 1.04-4.24, P = 0.039). The receiver operating characteristic (ROC) curve and net reclassification index (NRI) showed that the combination of dynamic NLR and AFP changes was better than AFP changes alone on predicting PD (AUC: 0.83 vs 0.68, P = 0.034; NRI: 0.340, P = 0.048) and PFS (AUC: 0.80 vs 0.70, P = 0.166; NRI: 0.431, P = 0.042).

Conclusion: Dynamic changes of NLR might be an effective predictor of the therapeutic response to ICIs plus targeted therapies for uHCC.

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来源期刊
CiteScore
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自引率
2.40%
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