• 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

培美曲塞在晚期非小细胞肺癌二线化疗中的作用。

The role of pemetrexed in second-line chemotherapy for advanced non-small cell lung cancer.

机构信息

Pacific Cancer Centre, Singapore.

出版信息

Curr Drug Targets. 2010 Jan;11(1):58-60. doi: 10.2174/138945010790031036.

DOI:10.2174/138945010790031036
PMID:19839927
Abstract

Despite improvements in first-line therapy for advanced NSCLC all patients with metastatic disease will progress at some point. Patients with favorable prognostic factors such as good performance status, non-squamous histology, stable weight, and perhaps female gender are more likely to receive second-line chemotherapy. Currently the United States FDA recognizes three single agents (docetaxel, erlotinib, and pemetrexed) as established for providing a benefit in patients who have experienced progression after first-line therapy. This review focus on the role of PEM in the treatment of advanced NSCLC in patients who have experienced disease progression during or after first-line therapy. The multi-targeted antifolate pemetrexed is equivalent to docetaxel for second-line therapy and with less toxicity.

摘要

尽管晚期非小细胞肺癌的一线治疗有所改善,但所有转移性疾病患者都将在某个时候进展。预后良好的因素,如良好的体能状态、非鳞状组织学、稳定的体重,以及可能的女性性别,更有可能接受二线化疗。目前,美国食品和药物管理局 (FDA) 认可三种单一药物(多西紫杉醇、厄洛替尼和培美曲塞)在一线治疗后进展的患者中提供获益。本综述重点关注培美曲塞在一线治疗期间或之后疾病进展的晚期非小细胞肺癌患者中的治疗作用。多靶点抗叶酸培美曲塞在二线治疗中与多西紫杉醇等效,且毒性更小。

相似文献

1
The role of pemetrexed in second-line chemotherapy for advanced non-small cell lung cancer.培美曲塞在晚期非小细胞肺癌二线化疗中的作用。
Curr Drug Targets. 2010 Jan;11(1):58-60. doi: 10.2174/138945010790031036.
2
Advances in the treatment of second-line non-small-cell lung cancer.
Lung Cancer. 2005 Oct;50 Suppl 1:S15-7. doi: 10.1016/s0169-5002(05)81554-5.
3
Pemetrexed: a multitargeted antifolate.培美曲塞:一种多靶点抗叶酸药物。
Clin Ther. 2005 Sep;27(9):1343-82. doi: 10.1016/j.clinthera.2005.09.010.
4
Pemetrexed: a new cytotoxic agent in the development for first-line non-small-cell lung cancer.培美曲塞:一种正在开发用于一线非小细胞肺癌的新型细胞毒性药物。
Lung Cancer. 2005 Oct;50 Suppl 1:S18-9. doi: 10.1016/s0169-5002(05)81555-7.
5
A dose-escalation study of pemetrexed and docetaxel in non-small-cell lung cancer.培美曲塞和多西他赛治疗非小细胞肺癌的剂量递增研究。
Cancer Chemother Pharmacol. 2011 Aug;68(2):415-22. doi: 10.1007/s00280-010-1508-5. Epub 2010 Nov 11.
6
Pemetrexed versus docetaxel in second line non-small-cell lung cancer: results and subsets analyses of a multi-center, randomized, exploratory trial in Chinese patients.培美曲塞对比多西他赛二线治疗非小细胞肺癌:一项多中心、随机、探索性临床试验在中国患者中的结果和亚组分析。
Pulm Pharmacol Ther. 2012 Oct;25(5):364-70. doi: 10.1016/j.pupt.2012.06.008. Epub 2012 Jul 3.
7
Pemetrexed disodium for the treatment of NSCLC: an update.培美曲塞二钠治疗非小细胞肺癌:最新进展
Drugs Today (Barc). 2008 Sep;44(9):669-78. doi: 10.1358/dot.2008.44.9.1250412.
8
Second-line chemotherapy in the treatment of advanced non-small cell lung cancer (NSCLC).晚期非小细胞肺癌(NSCLC)治疗中的二线化疗
J Chemother. 2004 Nov;16 Suppl 4:104-7. doi: 10.1179/joc.2004.16.Supplement-1.104.
9
[Impact of histology on efficacy of pemetrexed: pemetrexed in second-line setting and as maintenance therapy after first-line treatment in Chinese patients with advanced NSCLC].[组织学对培美曲塞疗效的影响:中国晚期非小细胞肺癌患者二线应用培美曲塞及一线治疗后维持治疗的情况]
Zhonghua Zhong Liu Za Zhi. 2014 Jan;36(1):29-33.
10
The role of pemetrexed in advanced non small-cell lung cancer: special focus on pharmacology and mechanism of action.培美曲塞在晚期非小细胞肺癌中的作用:特别关注药理学和作用机制。
Curr Drug Targets. 2010 Jan;11(1):37-47. doi: 10.2174/138945010790030974.

引用本文的文献

1
Role of gefitinib in the targeted treatment of non-small-cell lung cancer in Chinese patients.吉非替尼在中国患者非小细胞肺癌靶向治疗中的作用。
Onco Targets Ther. 2016 Mar 9;9:1291-302. doi: 10.2147/OTT.S80635. eCollection 2016.