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一项关于阿片类药物使用对晚期非小细胞肺癌患者免疫检查点抑制剂疗效负面影响的新研究

英文原题:A novel investigation into the negative impact of opioid use on the efficacy of immune checkpoint inhibitors in advanced non-small cell lung cancer patients.

查看英文原题

A novel investigation into the negative impact of opioid use on the efficacy of immune checkpoint inhibitors in advanced non-small cell lung cancer patients.

PubMed 2024/02/06(内容时间) Int Immunopharmacol Q1 · IF 5.6(JCR 2025)

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研究概要

阿片类药物的使用与接受 ICI 治疗的 NSCLC 患者的不良临床结局相关。提倡精准疼痛管理,并建议在这些患者中谨慎使用阿片类药物。OTGs 有潜力成为 NSCLC 患者的预后生物标志物,其在肿瘤免疫中的作用需要进一步研究。

研究思路结论见上方概要

免疫检查点抑制剂(ICIs)有效改善了晚期非小细胞肺癌(NSCLC)的临床结局。阿片类药物常用于癌症患者的疼痛缓解。本研究旨在阐明阿片类药物使用对接受ICI治疗的晚期NSCLC患者预后的影响。

2023年7月前,利用在线数据库进行了系统性文献综述。采用荟萃分析阐明阿片类药物使用与接受ICI治疗的NSCLC患者总生存期(OS)或无进展生存期(PFS)的相关性,两者均通过风险比(HR)及95%置信区间(CI)确定。随后,利用一个纳入181例NSCLC患者的独立队列进行验证。最后,基于TCGA队列进行全面的生物信息学分析,以探究阿片类药物靶基因(OTGs)在NSCLC患者中的预后意义及其与免疫浸润的相关性。

本meta分析共纳入8项研究,涉及1174例患者。在ICI治疗的NSCLC患者中,阿片类药物的使用与较差的PFS(HR = 2.16,95 %CI:1.26-3.71)和OS(HR = 2.02,95 %CI:1.54-2.63)呈负相关。回顾性验证证实了上述结果,并确定阿片类药物的使用是整个队列和ICI亚组中PFS和OS的独立不良预测因素。生物信息学分析确定了14个预后OTGs(CYP17A1、PDYN、PYCARD、FGA、NTSR1、FABP1、HPCA、PENK、PDGFB、LIN7A、FKBP5、TYMS、CACNA1H和LDHA),其中大多数与NSCLC中的免疫浸润相关。基于14个OTGs构建了一个风险模型,并发现该模型能有效分层训练集和验证集中的临床结局,且独立于年龄、性别和TNM分期系统。该模型还与活化树突状细胞、中性粒细胞和TIL(肿瘤浸润淋巴细胞)的浸润显著相关。最后,基于该模型、年龄、性别和TNM分期构建了一个列线图,可以很好地预测NSCLC患者的1年、3年和5年生存率。

展开英文摘要原文

Immune checkpoint inhibitors (ICIs) have effectively improved the clinical outcome of advanced non-small cell lung cancer (NSCLC). Opioids are commonly used for pain relief in cancer patients. This study aims to clarify the prognostic impact of opioid use in advanced NSCLC patients receiving ICI therapy.

A systematic literature review was carried out using online databases before July 2023. The meta-analysis was used to clarify the correlation of opioid use with the overall survival (OS) or progression-free survival (PFS) of ICI-treated NSCLC patients, both of which were determined using hazard ratios (HRs) coupled with 95 % confidence intervals (CIs). Then, an independent cohort enrolling 181 NSCLC patients was utilized for validation. Finally, a comprehensive bioinformatics analysis based on TCGA cohort was performed to investigate the prognostic significance of opioid target genes (OTGs) and their correlation with immune infiltration in NSCLC patients.

A total of 8 studies enrolling 1174 patients were included in the meta-analysis. Opioid use was negatively associated with worse PFS (HR = 2.16, 95 %CI: 1.26-3.71) and OS (HR = 2.02, 95 %CI: 1.54-2.63) in ICI-treated NSCLC patients. The retrospective validation confirmed the above result and identified opioid use as an independent unfavorable predictor for PFS and OS in both the entire cohort and ICI subgroup. The bioinformatic analysis identified 14 prognostic OTGs (CYP17A1, PDYN, PYCARD, FGA, NTSR1, FABP1, HPCA, PENK, PDGFB, LIN7A, FKBP5, TYMS, CACNA1H and LDHA), most of which were correlated with immune infiltration in NSCLC. A risk model was constructed based on 14 OTGs and found to effectively stratify the clinical outcome in both the training and validation set, independent of age, gender and TNM staging system. The model was also significantly correlated with infiltration of activated dendritic cells, neutrophils and tumor infiltrating lymphocytes. Finally, a nomogram was constructed based on the model, age, gender and TNM stage, which could predict well the 1-, 3- and 5-year survival of NSCLC patients.

Opioid use is correlated with the poor clinical outcome in ICI-treated NSCLC patients. Precise pain management is highly advocated and opioids are recommended to be cautiously used in these patients. OTGs have the potential to be prognostic biomarkers for NSCLC patients and their role in tumor immunity needs to be further investigated.

论文信息

作者
Guo H、Li Y、Lin J、Li D、Yang J、Wang J、Mao J、Wang Y
第一作者单位
Department of Oncology, The Affiliated Hospital of Yangzhou University, Yangzhou University, Yangzhou, Jiangsu, China.China
通讯作者单位
Department of Oncology, The Affiliated Hospital of Yangzhou University, Yangzhou University, Yangzhou, Jiangsu, China. Electronic address: yyxxbb8904@163.com.China
文献类型
荟萃分析 · 系统综述
期刊
International immunopharmacology2024 Mar 10
原文标识
PubMed 38325047 · DOI 10.1016/j.intimp.2024.111611