对表皮生长因子受体-TKIs耐药的晚期非小细胞肺癌患者使用PD-1/L1抑制剂和含铂双药化疗的疗效和安全性比较研究。

IF 1.7 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL American journal of translational research Pub Date : 2024-08-15 eCollection Date: 2024-01-01 DOI:10.62347/FEVG6730
Chunhui Shi, Xiaochun Liu, Jing Zhao, Wenjiang Xu, Rui Zhang, Zhongqin He
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引用次数: 0

摘要

目的评估程序性死亡-1/程序性死亡配体1(PD-1/L1)抑制剂联合含铂化疗治疗对表皮生长因子受体-酪氨酸激酶抑制剂(EGFR-TKIs)耐药的晚期非小细胞肺癌(NSCLC)患者的疗效和安全性:宝鸡市中医医院对2018年10月至2021年5月期间接受治疗的133例EGFR-TKIs耐药的晚期NSCLC患者进行了回顾性分析。队列分为两组:一组接受免疫检查点抑制剂(ICIs)加化疗和抗血管生成药物治疗(ICIs+BCP组),另一组仅接受ICIs治疗(ICIs组)。收集的基线数据包括人口统计学因素、吸烟状况、PD-L1肿瘤比例评分(TPS)、表皮生长因子受体突变、东部合作肿瘤学组(ECOG)评分以及二线治疗前的常规血液指标。每两个疗程进行一次计算机断层扫描(CT),以评估疗效:与 ICIs 组相比,ICIs+BCP 组的总生存期(OS)有显著的统计学改善(P=0.001)。Cox生存分析揭示了年龄(P=0.012)、PD-L1 TPS表达(PConclusion:ICIs与BCP联合治疗可延长对EGFR-TKIs耐药的NSCLC患者的OS。这项研究强调了个性化治疗方案和生物标志物评估对改善耐药病例预后的重要性。
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A comparative study of the efficacy and safety of PD-1/L1 inhibitor and platinum-containing dual-agent chemotherapy in patients with advanced non-small cell lung cancer resistant to EGFR-TKIs.

Objective: To assess the efficacy and safety of combining Programmed Death-1/Programmed Death-Ligand 1 (PD-1/L1) inhibitors with platinum-containing chemotherapy for treating late-stage Non-Small Cell Lung Cancer (NSCLC) patients who have developed resistance to Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitors (EGFR-TKIs).

Methods: A retrospective analysis was conducted at Baoji Traditional Chinese Medicine Hospital involving 133 patients with advanced NSCLC who had shown resistance to EGFR-TKIs and were treated from October 2018 to May 2021. The cohort was categorized into two groups: one treated with immune checkpoint inhibitors (ICIs) plus chemotherapy and antiangiogenic agents (ICIs+BCP group), and the other treated with ICIs alone (ICIs group). Baseline data collected included demographic factors, smoking status, PD-L1 Tumor Proportion Score (TPS), EGFR mutation, Eastern Cooperative Oncology Group (ECOG) score, and routine blood markers prior to second-line therapy. Computed Tomography (CT) scans were performed every two treatment courses to evaluate the treatment efficacy.

Results: The ICIs+BCP group exhibited a statistically significant improvement in Overall Survival (OS) compared to the ICIs group (P=0.001). Cox survival analysis uncovered age (P=0.012), PD-L1 TPS expression (P<0.001), treatment regimen (P=0.006), Neutrophil-to-Lymphocyte Ratio (NLR) (P=0.024), and Platelet-to-Lymphocyte Ratio (PLR) (P=0.005) as independent factors influencing OS in patients with advanced NSCLC resistant to primary-line EGFR-TKI therapy. The nomogram model, based on these prognostic factors, exhibited Area Under the Curve (AUC) values of 0.823 and 0.769, indicating its predictive accuracy for 1-year and 2-year survival, respectively.

Conclusion: Combining ICIs with BCP prolongs OS in patients with NSCLC resistant to EGFR-TKIs. This study underscores the importance of personalized treatment plans and biomarker evaluations to improve outcomes in drug-resistant cases.

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American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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