• 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

无驱动基因突变的转移性肺腺癌的一线治疗。

First-Line Therapies for Metastatic Lung Adenocarcinoma Without a Driver Mutation.

机构信息

Fox Chase Cancer Center, Philadelphia, PA.

出版信息

J Oncol Pract. 2018 Sep;14(9):529-535. doi: 10.1200/JOP.18.00250.

DOI:10.1200/JOP.18.00250
PMID:30205771
Abstract

Lung cancer is the leading cause of cancer-related death worldwide. The majority of these cancers are non-small-cell lung cancer, of which adenocarcinoma is the most common histologic subtype. Most patients are diagnosed at advanced stages when systemic treatment is needed. Whereas prognosis has improved for patients with targetable driver mutations, the majority of patients do not possess tumors with such molecular mutations. Platinum-based chemotherapy has traditionally been the mainstay of treatment, although in recent years immunotherapy has emerged as a treatment option and can result in robust and durable treatment responses in a subset of patients. Recent clinical trials on novel immunotherapy combinations and immunochemotherapy combinations may broaden the number of patients that may benefit from checkpoint inhibitors and elicit responses in those who otherwise may not have experienced a response to monotherapy with an immunotherapy drug. This review will outline the currently available therapies for the first-line treatment of metastatic adenocarcinoma that do not possess a driver mutation and provide a recommended approach and algorithm by which to select the best first-line therapy.

摘要

肺癌是全球癌症相关死亡的主要原因。这些癌症大多数是非小细胞肺癌,其中腺癌是最常见的组织学亚型。大多数患者在需要全身治疗时被诊断为晚期。虽然对于可靶向驱动突变的患者,预后已经有所改善,但大多数患者的肿瘤没有这种分子突变。铂类化疗一直是治疗的主要方法,尽管近年来免疫疗法已成为一种治疗选择,并且可以在一部分患者中产生强大且持久的治疗反应。最近关于新型免疫疗法联合和免疫化疗联合的临床试验可能会扩大可能从检查点抑制剂中获益的患者数量,并在那些否则可能对免疫疗法药物单药治疗没有反应的患者中引起反应。这篇综述将概述目前用于治疗无驱动突变的转移性腺癌的一线治疗方法,并提供一种推荐的方法和算法,以选择最佳的一线治疗方法。

相似文献

1
First-Line Therapies for Metastatic Lung Adenocarcinoma Without a Driver Mutation.无驱动基因突变的转移性肺腺癌的一线治疗。
J Oncol Pract. 2018 Sep;14(9):529-535. doi: 10.1200/JOP.18.00250.
2
Treatment options beyond immunotherapy in patients with wild-type lung adenocarcinoma: a Delphi consensus.免疫治疗之外的治疗选择:野生型肺腺癌患者的德尔菲共识。
Clin Transl Oncol. 2020 May;22(5):759-771. doi: 10.1007/s12094-019-02191-y. Epub 2019 Jul 31.
3
Chemotherapy combined with bevacizumab for the treatment of advanced lung adenocarcinoma cancer harboring EGFR-ANXA2, EGFR-RAD51, ATR and BRCA2 mutations: A case report.化疗联合贝伐珠单抗治疗携带 EGFR-ANXA2、EGFR-RAD51、ATR 和 BRCA2 突变的晚期肺腺癌:一例报告。
Thorac Cancer. 2020 Feb;11(2):456-460. doi: 10.1111/1759-7714.13286. Epub 2019 Dec 22.
4
Survival outcome according to KRAS mutation status in newly diagnosed patients with stage IV non-small cell lung cancer treated with platinum doublet chemotherapy.在接受铂类双联化疗的新诊断IV期非小细胞肺癌患者中,根据KRAS突变状态得出的生存结果。
Oncotarget. 2015 Oct 6;6(30):30287-94. doi: 10.18632/oncotarget.4711.
5
Efficacy of pemetrexed and carboplatin with or without bevacizumab in lung adenocarcinoma patients with EGFR non-T790M mutations after progression on first-line EGFR-tyrosine kinase inhibitors.培美曲塞和卡铂联合或不联合贝伐珠单抗治疗 EGFR 酪氨酸激酶抑制剂一线治疗进展后 EGFR 非 T790M 突变的肺腺癌患者的疗效。
Thorac Cancer. 2018 Sep;9(9):1151-1155. doi: 10.1111/1759-7714.12814. Epub 2018 Jul 20.
6
Management of advanced non-small cell lung cancers with known mutations or rearrangements: latest evidence and treatment approaches.已知存在突变或重排的晚期非小细胞肺癌的管理:最新证据与治疗方法
Ther Adv Respir Dis. 2016 Apr;10(2):113-29. doi: 10.1177/1753465815617871. Epub 2015 Nov 30.
7
Afatinib as first-line treatment for advanced lung adenocarcinoma patients harboring HER2 mutation: A case report and review of the literature.阿法替尼一线治疗 HER2 突变阳性晚期肺腺癌患者 1 例报告及文献复习
Thorac Cancer. 2018 Dec;9(12):1788-1794. doi: 10.1111/1759-7714.12906. Epub 2018 Oct 31.
8
EPHA5 mutation predicts the durable clinical benefit of immune checkpoint inhibitors in patients with lung adenocarcinoma.Epha5 突变可预测肺腺癌患者免疫检查点抑制剂的持久临床获益。
Cancer Gene Ther. 2021 Aug;28(7-8):864-874. doi: 10.1038/s41417-020-0207-6. Epub 2020 Aug 6.
9
Iodine-125 radioactive particles antagonize hyperprogressive disease following immunotherapy: A case report.碘-125放射性粒子拮抗免疫治疗后的超进展性疾病:一例报告
Medicine (Baltimore). 2020 Oct 30;99(44):e22933. doi: 10.1097/MD.0000000000022933.
10
Hyperprogression after first dose of immunotherapy in a patient with radioresistant metastasis from nonsmall cell lung cancer.免疫治疗第一剂后,对一位放射抗拒性非小细胞肺癌转移患者出现超进展。
Anticancer Drugs. 2019 Nov;30(10):1067-1070. doi: 10.1097/CAD.0000000000000837.

引用本文的文献

1
Cytotoxicity and Binding to DNA, Lysozyme, Ribonuclease A, and Human Serum Albumin of the Diiodido Analog of Picoplatin.匹铂二碘代类似物对DNA、溶菌酶、核糖核酸酶A和人血清白蛋白的细胞毒性及结合作用
Inorg Chem. 2025 May 12;64(18):8895-8905. doi: 10.1021/acs.inorgchem.4c05424. Epub 2025 May 1.
2
Comprehensive transcriptome, miRNA and kinome profiling identifies new treatment options for personalized lung cancer therapy.综合转录组、微小RNA和激酶组分析为个性化肺癌治疗确定新的治疗方案。
Clin Transl Med. 2025 Mar;15(3):e70177. doi: 10.1002/ctm2.70177.
3
Editorial: Lung adenocarcinoma: from genomics to immunotherapy.
社论:肺腺癌:从基因组学到免疫治疗
Front Genet. 2024 Apr 9;15:1399127. doi: 10.3389/fgene.2024.1399127. eCollection 2024.
4
NPAS2 dampens chemo-sensitivity of lung adenocarcinoma cells by enhancing DNA damage repair.NPAS2 通过增强 DNA 损伤修复来降低肺腺癌细胞的化疗敏感性。
Cell Death Dis. 2024 Jan 30;15(1):101. doi: 10.1038/s41419-023-06256-3.
5
Tumor-related exosomal circ_0001715 promotes lung adenocarcinoma cell proliferation and metastasis via enhancing M2 macrophage polarization by regulating triggering receptor expressed on myeloid cells-2.肿瘤相关外泌体 circ_0001715 通过调节髓系细胞表达的触发受体 2 增强 M2 巨噬细胞极化促进肺腺癌细胞增殖和转移。
Thorac Cancer. 2024 Jan;15(3):227-238. doi: 10.1111/1759-7714.15182. Epub 2023 Dec 12.
6
Transcriptional analysis of landmark molecular pathways in lung adenocarcinoma results in a clinically relevant classification with potential therapeutic implications.肺腺癌标志性分子通路的转录组分析可产生具有潜在治疗意义的临床相关分类。
Mol Oncol. 2024 Feb;18(2):453-470. doi: 10.1002/1878-0261.13550. Epub 2023 Dec 21.
7
Single-cell mass cytometric analysis of peripheral immunity and multiplex plasma marker profiling of non-small cell lung cancer patients receiving PD-1 targeting immune checkpoint inhibitors in comparison with platinum-based chemotherapy.单细胞质量细胞分析外周免疫和非小细胞肺癌患者接受 PD-1 靶向免疫检查点抑制剂与铂类化疗的多重血浆标志物分析。
Front Immunol. 2023 Oct 13;14:1243233. doi: 10.3389/fimmu.2023.1243233. eCollection 2023.
8
Dishevelled Segment Polarity Protein 3: A Novel Prognosis-related Marker in Pan-driver-gene-negative Lung Adenocarcinoma.无序节段极性蛋白3:泛驱动基因阴性肺腺癌中的一种新型预后相关标志物。
J Cancer. 2023 Sep 18;14(16):3028-3038. doi: 10.7150/jca.87722. eCollection 2023.
9
Blood Immune Cells as Biomarkers in Long-Term Surviving Patients with Advanced Non-Small-Cell Lung Cancer Undergoing a Combined Immune/Chemotherapy.血液免疫细胞作为接受免疫/化疗联合治疗的晚期非小细胞肺癌长期存活患者的生物标志物
Cancers (Basel). 2023 Oct 6;15(19):4873. doi: 10.3390/cancers15194873.
10
Targeted EGFR Nanotherapy in Non-Small Cell Lung Cancer.非小细胞肺癌中的靶向表皮生长因子受体纳米疗法
J Funct Biomater. 2023 Sep 9;14(9):466. doi: 10.3390/jfb14090466.