文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
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
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
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 @ 2025

在晚期肺腺癌中,对于 EGFR 外显子 19 缺失和 21 位 Leu858Arg 突变的患者,采用 eHSP90α 作为一线治疗药物。

eHSP90α in front-line therapy in EGFR exon 19 deletion and 21 Leu858Arg mutations in advanced lung adenocarcinoma.

机构信息

Department of Research, Guangxi Medical University Cancer Hospital, Guangxi Medical University, Guangxi Zhuang Autonomous Region, Nanning, 530021, China.

Guangxi Cancer Molecular Medicine Engineering Research Center, Guangxi Zhuang Autonomous Region, Nanning, 530021, China.

出版信息

BMC Cancer. 2024 Jul 12;24(1):835. doi: 10.1186/s12885-024-12573-3.


DOI:10.1186/s12885-024-12573-3
PMID:38997622
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11245848/
Abstract

PURPOSE: Extracellular heat shock protein 90 AA1(eHSP90α) is intricately linked to tumor progression and prognosis. This study aimed to investigate the difference in the value of eHSP90α in post-treatment response assessment and prognosis prediction between exon 19 deletion(19DEL) and exon 21 Leu858Arg(L858R) mutation types in lung adenocarcinoma(LUAD). METHODS: We analyzed the relationship between the expression of eHSP90α and clinicopathological features in 89 patients with L858R mutation and 196 patients with 19DEL mutation in LUAD. The Kaplan-Meier survival curve was used to determine their respective cut-off values and analyze the relationship between eHSP90α expression and the survival time of the two mutation types. The area under the curve (AUC) was used to evaluate the diagnostic performance of biomarkers. Then, the prognostic model was developed using the univariate-Cox multivariate-Cox and LASSO-multivariate logistic methods. RESULTS: In LUAD patients, eHSP90α was positively correlated with carcinoembryonic antigen(CEA), carbohydrate antigen 125(CA125), and carbohydrate antigen 153(CA153). The truncated values of eHSP90α in L858R and 19DEL patients were 44.5 ng/mL and 40.8 ng/mL, respectively. Among L858R patients, eHSP90α had the best diagnostic performance (AUC = 0.765), and higher eHSP90α and T helper cells(Th cells) expression were significantly related to shorter overall survival(OS) and worse treatment response. Also, high eHSP90a expression and short progression-free survival(PFS) were significantly correlated. Among 19DEL patients, CEA had the best diagnostic efficacy (AUC = 0.734), and CEA and Th cells were independent prognostic factors that predicted shorter OS. Furthermore, high CA125 was significantly associated with short PFS and poor curative effect. CONCLUSIONS: eHSP90α has a better prognostic value in LUAD L858R patients than 19DEL, which provides a new idea for clinical diagnosis and treatment.

摘要

目的:细胞外热休克蛋白 90AA1(eHSP90α)与肿瘤的进展和预后密切相关。本研究旨在探讨肺腺癌(LUAD)中exon19 缺失(19DEL)和 exon21 Leu858Arg(L858R)突变类型中,eHSP90α在治疗后反应评估和预后预测中的价值差异。

方法:我们分析了 89 例 L858R 突变和 196 例 19DEL 突变 LUAD 患者中 eHSP90α的表达与临床病理特征的关系。Kaplan-Meier 生存曲线用于确定这两种突变类型的各自截断值,并分析 eHSP90α表达与两种突变类型生存时间的关系。采用曲线下面积(AUC)评估生物标志物的诊断性能。然后,使用单因素 Cox 多因素 Cox 和 LASSO 多因素逻辑方法建立预后模型。

结果:在 LUAD 患者中,eHSP90α与癌胚抗原(CEA)、糖抗原 125(CA125)和糖抗原 153(CA153)呈正相关。L858R 和 19DEL 患者 eHSP90α截断值分别为 44.5ng/ml 和 40.8ng/ml。在 L858R 患者中,eHSP90α具有最佳的诊断性能(AUC=0.765),较高的 eHSP90α和辅助性 T 细胞(Th 细胞)表达与总生存期(OS)较短和治疗反应较差显著相关。此外,高 eHSP90a 表达与较短的无进展生存期(PFS)显著相关。在 19DEL 患者中,CEA 具有最佳的诊断效果(AUC=0.734),CEA 和 Th 细胞是预测 OS 较短的独立预后因素。此外,高 CA125 与较短的 PFS 和较差的疗效显著相关。

结论:与 19DEL 相比,eHSP90α在 LUAD L858R 患者中具有更好的预后价值,为临床诊断和治疗提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb3/11245848/7243f9b5f410/12885_2024_12573_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb3/11245848/0fd0b60f600f/12885_2024_12573_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb3/11245848/7a2b9aff0d3c/12885_2024_12573_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb3/11245848/796116c8ddc3/12885_2024_12573_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb3/11245848/7243f9b5f410/12885_2024_12573_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb3/11245848/0fd0b60f600f/12885_2024_12573_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb3/11245848/7a2b9aff0d3c/12885_2024_12573_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb3/11245848/796116c8ddc3/12885_2024_12573_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb3/11245848/7243f9b5f410/12885_2024_12573_Fig3_HTML.jpg

相似文献

[1]
eHSP90α in front-line therapy in EGFR exon 19 deletion and 21 Leu858Arg mutations in advanced lung adenocarcinoma.

BMC Cancer. 2024-7-12

[2]
MET overexpression correlated with prognosis of EGFR-mutant treatment‑naïve advanced lung adenocarcinoma: a real‑world retrospective study.

Clin Transl Oncol. 2024-7

[3]
Are exon 19 deletions and L858R different in early stage lung adenocarcinoma?

J Cancer Res Clin Oncol. 2018-1

[4]
Comparison of therapeutic effects of EGFR-tyrosine kinase inhibitors on 19Del and L858R mutations in advanced lung adenocarcinoma and effect on cellular immune function.

Thorac Cancer. 2017-12-9

[5]
Prognostic implication of EGFR mutation status and subtype in resected lung adenocarcinoma patients irrespective of therapy.

Clin Transl Oncol. 2018-7-18

[6]
Efficacy observation and prognosis analysis of EGFR-TKIs alone versus EGFR-TKIs plus chemotherapy in advanced lung adenocarcinoma with EGFR Exon 19 Deletion, Exon 21 L858R mutation: A historical cohort study.

Medicine (Baltimore). 2023-6-30

[7]
Prognostic implications of combining EGFR-TKIs and radiotherapy in Stage IV lung adenocarcinoma with 19-Del or 21-L858R mutations: A real-world study.

Cancer Med. 2024-4

[8]
[Comparison of clinical outcomes of patients with non-small cell lung cancer harboring different types of epidermal growth factor receptor sensitive mutations after first-line EGFR-TKI treatment].

Zhonghua Zhong Liu Za Zhi. 2016-3-23

[9]
Clinical outcomes of EGFR-TKI treatment and genetic heterogeneity in lung adenocarcinoma patients with EGFR mutations on exons 19 and 21.

Chin J Cancer. 2016-3-21

[10]
EGFR Exon 19 Deletion is Associated With Favorable Overall Survival After First-line Gefitinib Therapy in Advanced Non-Small Cell Lung Cancer Patients.

Am J Clin Oncol. 2018-4

引用本文的文献

[1]
Elevated plasma HSP90α as a prognostic marker in EGFR-mutant non-small cell lung cancer.

Oncol Lett. 2025-7-22

本文引用的文献

[1]
Cancer statistics, 2024.

CA Cancer J Clin. 2024

[2]
GW4869 Can Inhibit Epithelial-Mesenchymal Transition and Extracellular HSP90α in Gefitinib-Sensitive NSCLC Cells.

Onco Targets Ther. 2023-11-8

[3]
Comparison of the Efficacy of EGFR-TKIs Combined with Antiangiogenic Agents between Patients with Exon 19 Deletion and Patients with Exon 21 Leu858 Arg Mutation: A Systematic Review and Meta-Analysis.

J Oncol. 2022-10-20

[4]
Analysis of the prognostic, diagnostic and immunological role of HSP90α in malignant tumors.

Front Oncol. 2022-9-8

[5]
High Expression of Plasma Extracellular HSP90α is Associated With the Poor Efficacy of Chemotherapy and Prognosis in Small Cell Lung Cancer.

Front Mol Biosci. 2022-7-11

[6]
Plasma heat shock protein 90alpha as a biomarker for the diagnosis of liver cancer: in patients with different clinicopathologic characteristics.

World J Surg Oncol. 2021-8-4

[7]
Plasma Levels of Heat Shock Protein 90 Alpha Associated With Colorectal Cancer Development.

Front Mol Biosci. 2021-7-8

[8]
Plasma HSP90AA1 Predicts the Risk of Breast Cancer Onset and Distant Metastasis.

Front Cell Dev Biol. 2021-5-24

[9]
Plasma Heat Shock Protein 90 Alpha: A Valuable Predictor of Early Chemotherapy Effectiveness in Advanced Non-Small-Cell Lung Cancer.

Med Sci Monit. 2021-1-9

[10]
Efficacy of Osimertinib Plus Bevacizumab vs Osimertinib in Patients With EGFR T790M-Mutated Non-Small Cell Lung Cancer Previously Treated With Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitor: West Japan Oncology Group 8715L Phase 2 Randomized Clinical Trial.

JAMA Oncol. 2021-3-1

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索