• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

具有驱动基因突变的非小细胞肺癌中的炎症参数。

Inflammatory parameters in NSCLC with driver mutation.

作者信息

Buyukbayram Mehmet Emin, Hannarici Zekeriya, Yilmaz Ali, Turhan Aykut, Caglar Alperen Akansel, Esdur Pınar Coban, Bilici Mehmet, Tekin Salim Basol

机构信息

Department of Medical Oncology, Atatürk University Faculty of Medicine, Erzurum, 25100, Turkey.

Department of Medical Oncology, Nev Hospital, Sanliurfa, 63000, Turkey.

出版信息

Lung Cancer Manag. 2024 May 16;13(1):LMT66. doi: 10.2217/lmt-2023-0014. eCollection 2024.

DOI:10.2217/lmt-2023-0014
PMID:38818368
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11137794/
Abstract

The tumor microenvironment of NSCLC with driver mutations, such as , and , is less inflammatory. This retrospective study included 38 patients with NSCLC driver mutations. The relationship between clinical and inflammatory markers concerning progression-free survival and overall survival was analyzed based on Kaplan-Meier curves. The mean age of the patients was 59.8 ± 11.9. Progression-free survival and overall survival were significantly longer in patients under 65 years of age and with low neutrophil-lymphocyte ratio, low systemic immune-inflammation index and high lymphocyte count (p < 0.05). Unlike tumor biology, peripheral inflammatory parameters, such as neutrophil-lymphocyte ratio, systemic immune-inflammation index and lymphocyte count may be associated with survival in NSCLC patients with driver mutations.

摘要

具有驱动基因突变(如 、 和 )的非小细胞肺癌的肿瘤微环境炎症较轻。这项回顾性研究纳入了38例患有非小细胞肺癌驱动基因突变的患者。基于Kaplan-Meier曲线分析了与无进展生存期和总生存期相关的临床和炎症标志物之间的关系。患者的平均年龄为59.8±11.9岁。65岁以下、中性粒细胞与淋巴细胞比值低、全身免疫炎症指数低且淋巴细胞计数高的患者无进展生存期和总生存期明显更长(p<0.05)。与肿瘤生物学不同,外周炎症参数,如中性粒细胞与淋巴细胞比值、全身免疫炎症指数和淋巴细胞计数可能与患有驱动基因突变的非小细胞肺癌患者的生存期相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3912/11137794/2d8624b227b6/ILMT_A_2339770_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3912/11137794/624e9561b288/ILMT_A_2339770_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3912/11137794/2d8624b227b6/ILMT_A_2339770_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3912/11137794/624e9561b288/ILMT_A_2339770_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3912/11137794/2d8624b227b6/ILMT_A_2339770_F0002_C.jpg

相似文献

1
Inflammatory parameters in NSCLC with driver mutation.具有驱动基因突变的非小细胞肺癌中的炎症参数。
Lung Cancer Manag. 2024 May 16;13(1):LMT66. doi: 10.2217/lmt-2023-0014. eCollection 2024.
2
Clinical features and therapeutic options in non-small cell lung cancer patients with concomitant mutations of EGFR, ALK, ROS1, KRAS or BRAF.非小细胞肺癌患者同时存在 EGFR、ALK、ROS1、KRAS 或 BRAF 突变的临床特征和治疗选择。
Cancer Med. 2019 Jun;8(6):2858-2866. doi: 10.1002/cam4.2183. Epub 2019 Apr 24.
3
Molecular heterogeneity of anti-PD-1/PD-L1 immunotherapy efficacy is correlated with tumor immune microenvironment in East Asian patients with non-small cell lung cancer.抗 PD-1/PD-L1 免疫疗法疗效的分子异质性与东亚非小细胞肺癌患者的肿瘤免疫微环境相关。
Cancer Biol Med. 2020 Aug 15;17(3):768-781. doi: 10.20892/j.issn.2095-3941.2020.0121.
4
Outcomes of Gamma Knife Radiosurgery for Brain Metastases From Anaplastic Lymphoma Kinase Rearrangement-Positive and EGFR Mutation-Positive Non-Small Cell Lung Cancer.伽玛刀放射外科治疗间变性淋巴瘤激酶重排阳性和表皮生长因子受体突变阳性非小细胞肺癌脑转移瘤的疗效
Cureus. 2021 Dec 13;13(12):e20398. doi: 10.7759/cureus.20398. eCollection 2021 Dec.
5
Low peripheral blood derived neutrophil-to-lymphocyte ratio (dNLR) is associated with increased tumor T-cell infiltration and favorable outcomes to first-line pembrolizumab in non-small cell lung cancer.外周血中性粒细胞与淋巴细胞比值(dNLR)较低与非小细胞肺癌一线帕博利珠单抗治疗时肿瘤 T 细胞浸润增加和预后改善相关。
J Immunother Cancer. 2021 Nov;9(11). doi: 10.1136/jitc-2021-003536.
6
[The efficacy and prognostic factors of immunotherapy in advanced non-small cell lung cancer patients with different driver gene mutations].[免疫疗法在不同驱动基因突变的晚期非小细胞肺癌患者中的疗效及预后因素]
Zhonghua Yi Xue Za Zhi. 2022 Apr 5;102(13):922-929. doi: 10.3760/cma.j.cn112137-20211025-02352.
7
Epidermal Growth Factor Receptor Mutation (EGFR) Testing for Prediction of Response to EGFR-Targeting Tyrosine Kinase Inhibitor (TKI) Drugs in Patients with Advanced Non-Small-Cell Lung Cancer: An Evidence-Based Analysis.表皮生长因子受体突变(EGFR)检测对晚期非小细胞肺癌患者使用表皮生长因子受体靶向酪氨酸激酶抑制剂(TKI)药物疗效的预测:一项循证分析
Ont Health Technol Assess Ser. 2010;10(24):1-48. Epub 2010 Dec 1.
8
Genomic Signature of Driver Genes Identified by Target Next-Generation Sequencing in Chinese Non-Small Cell Lung Cancer.中国非小细胞肺癌中靶向下一代测序鉴定的驱动基因的基因组特征。
Oncologist. 2019 Nov;24(11):e1070-e1081. doi: 10.1634/theoncologist.2018-0572. Epub 2019 Mar 22.
9
Integration of comprehensive genomic profiling, tumor mutational burden, and PD-L1 expression to identify novel biomarkers of immunotherapy in non-small cell lung cancer.综合基因组分析、肿瘤突变负担和 PD-L1 表达的整合,以鉴定非小细胞肺癌免疫治疗的新型生物标志物。
Cancer Med. 2021 Apr;10(7):2216-2231. doi: 10.1002/cam4.3649. Epub 2021 Mar 2.
10
To be, or not to be: the dilemma of immunotherapy for non-small cell lung cancer harboring various driver mutations.是或否:携带有各种驱动基因突变的非小细胞肺癌的免疫治疗困境。
J Cancer Res Clin Oncol. 2023 Sep;149(12):10027-10040. doi: 10.1007/s00432-023-04919-4. Epub 2023 Jun 1.

引用本文的文献

1
Spatial imaging features derived from SUVmax location in resectable NSCLC are associated with tumor aggressiveness.来自可切除非小细胞肺癌中SUVmax位置的空间成像特征与肿瘤侵袭性相关。
Eur J Nucl Med Mol Imaging. 2025 Aug 21. doi: 10.1007/s00259-025-07528-0.

本文引用的文献

1
Investigation of the prognostic role of systemic immunoinflammatory index in patients with acute pancreatitis.探讨全身免疫炎症指数在急性胰腺炎患者中的预后作用。
Ulus Travma Acil Cerrahi Derg. 2023 Mar;29(3):316-320. doi: 10.14744/tjtes.2023.96554.
2
Clinical characteristics of non-small cell lung cancer patients with EGFR mutations and ALK&ROS1 fusions.具有 EGFR 突变和 ALK&ROS1 融合的非小细胞肺癌患者的临床特征。
Clin Respir J. 2022 Mar;16(3):216-225. doi: 10.1111/crj.13472. Epub 2022 Jan 26.
3
Systemic Immune-Inflammation Index (SII) Can Be an Early Indicator for Predicting the Severity of Acute Pancreatitis: A Retrospective Study.
全身免疫炎症指数(SII)可作为预测急性胰腺炎严重程度的早期指标:一项回顾性研究。
Int J Gen Med. 2021 Dec 8;14:9483-9489. doi: 10.2147/IJGM.S343110. eCollection 2021.
4
The value of innovation: association between improvements in survival of advanced and metastatic non-small cell lung cancer and targeted and immunotherapy.创新的价值:晚期和转移性非小细胞肺癌生存率的提高与靶向治疗和免疫治疗之间的关联
BMC Med. 2021 Sep 15;19(1):209. doi: 10.1186/s12916-021-02070-w.
5
Usefulness of the neutrophil-to-lymphocyte ratio in predicting the severity of COVID-19 patients: a retrospective cohort study.中性粒细胞与淋巴细胞比值对预测 COVID-19 患者严重程度的作用:一项回顾性队列研究。
Sao Paulo Med J. 2022 Jan-Feb;140(1):81-86. doi: 10.1590/1516-3180.2021.0298.R1.27052021.
6
Systemic immune-inflammation index predicts prognosis in patients with different EGFR-mutant lung adenocarcinoma.系统免疫炎症指数可预测不同 EGFR 突变型肺腺癌患者的预后。
Medicine (Baltimore). 2021 Feb 12;100(6):e24640. doi: 10.1097/MD.0000000000024640.
7
Peripheral blood markers predictive of outcome and immune-related adverse events in advanced non-small cell lung cancer treated with PD-1 inhibitors.PD-1 抑制剂治疗晚期非小细胞肺癌的外周血标志物预测疗效和免疫相关不良事件。
Cancer Immunol Immunother. 2020 Sep;69(9):1813-1822. doi: 10.1007/s00262-020-02585-w. Epub 2020 Apr 29.
8
Clinical Management of Non-Small Cell Lung Cancer with Concomitant EGFR Mutations and ALK Rearrangements: Efficacy of EGFR Tyrosine Kinase Inhibitors and Crizotinib.具有 EGFR 突变和 ALK 重排的非小细胞肺癌的临床处理:EGFR 酪氨酸激酶抑制剂和克唑替尼的疗效。
Target Oncol. 2019 Apr;14(2):169-178. doi: 10.1007/s11523-019-00628-6.
9
Low lymphocyte count and high monocyte count predicts poor prognosis of gastric cancer.淋巴细胞计数低和单核细胞计数高预示着胃癌的预后不良。
BMC Gastroenterol. 2018 Oct 11;18(1):148. doi: 10.1186/s12876-018-0877-9.
10
Prognostic value of pretreatment prognostic nutritional index in non-small cell lung cancer: A systematic review and meta-analysis.治疗前预后营养指数在非小细胞肺癌中的预后价值:一项系统评价和荟萃分析
Int J Biol Markers. 2018 Nov;33(4):372-378. doi: 10.1177/1724600818799876. Epub 2018 Oct 3.