Grenda Anna, Kuźnar-Kamińska Barbara, Kalinka Ewa, Krawczyk Paweł, Sawicki Marek, Filip Agata, Chmielewska Izabela, Frąk Małgorzata, Krzyżanowska Natalia, Milanowski Janusz
Department of Pneumonology, Oncology and Allergology, Medical University of Lublin, Lublin, Poland.
Department of Pulmonology, Allergology and Pulmonary Oncology, Poznan University of Medical Sciences, Poznań, Poland.
Front Immunol. 2024 Feb 26;15:1344858. doi: 10.3389/fimmu.2024.1344858. eCollection 2024.
Expression of PD-L1 on cancer cells is the only validated predictive factor for immunotherapy in NSCLC (Non-Small Cell Lung Cancer) patients. However, on this basis, it is difficult to predict the occurrence of resistance to immune checkpoint inhibitors (ICIs). MicroRNAs are widely studied as biomarkers of cancers. Our study was designed to determine whether microRNAs can be sensitive predictive factors in the qualification of NSCLC patients to first-line immunotherapy or chemoimmunotherapy.
The two-stage research on validation group (n=20) and study group (n=35) of patients with advanced NSCLC was conducted. Analysis of microRNAs expression by qPCR in plasma collected prior to the start of immunotherapy (pembrolizumab) or chemoimmunotherapy (combination of pembrolizumab with chemotherapy) was made. Broad-spectrum analysis of microRNAs expression was used in the studied group. Three microRNAs selected in that group as important for the effectiveness of ICIs were then examined in the validation group.
In the studied group, significantly higher expression of miRNA-126-3p, miR-144-3p and miR-146-5p was observed in patients with long PFS compared to those with short PFS. In the validation group, low miRNA-126 expression indicated lower median progression-free survival and overall survival (2.3 vs. 5.0 months and 5.2 vs 11.2, respectively). These patients had a significantly higher risk of progression (HR= 2.92, 95% CI: 1.01 to 8.40, p=0.04) and death (HR=3.64, 95% CI: 1.22 to 10.84, p=0.02).
Our study showed that the expression of miR-126 in blood plasma may be a predictive factor for the effectiveness of first-line immunotherapy or chemoimmunotherapy in advanced NSCLC patients.
癌细胞上程序性死亡受体配体1(PD-L1)的表达是目前唯一已得到验证的非小细胞肺癌(NSCLC)患者免疫治疗预测因子。然而,基于此,很难预测免疫检查点抑制剂(ICI)耐药的发生。微小RNA作为癌症生物标志物得到了广泛研究。我们的研究旨在确定微小RNA是否可以作为NSCLC患者一线免疫治疗或化疗免疫治疗资格的敏感预测因子。
对晚期NSCLC患者的验证组(n=20)和研究组(n=35)进行两阶段研究。在免疫治疗(帕博利珠单抗)或化疗免疫治疗(帕博利珠单抗与化疗联合)开始前采集的血浆中,通过定量聚合酶链反应(qPCR)分析微小RNA表达。研究组采用微小RNA表达的广谱分析。然后在验证组中检测该组中选择的对ICI疗效重要的三种微小RNA。
在研究组中,与无进展生存期(PFS)短的患者相比,PFS长的患者中miRNA-126-3p、miR-144-3p和miR-146-5p的表达显著更高。在验证组中,低miRNA-126表达表明无进展生存期和总生存期的中位数较低(分别为2.3个月对5.0个月和5.2个月对11.2个月)。这些患者的疾病进展风险(风险比[HR]=2.92,95%置信区间[CI]:1.01至8.40,p=0.04)和死亡风险(HR=3.64,95%CI:1.22至10.84,p=0.02)显著更高。
我们的研究表明,血浆中miR-126的表达可能是晚期NSCLC患者一线免疫治疗或化疗免疫治疗疗效的预测因子。