• 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

克服个性化癌症治疗实施挑战。

Overcoming implementation challenges of personalized cancer therapy.

机构信息

Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1400 Pressler Street, Unit 1484, Houston, TX 77030, USA.

出版信息

Nat Rev Clin Oncol. 2012 Sep;9(9):542-8. doi: 10.1038/nrclinonc.2012.127. Epub 2012 Jul 31.

DOI:10.1038/nrclinonc.2012.127
PMID:22850751
Abstract

Personalized cancer therapy is based on the precept that detailed molecular characterization of the patient's tumour and its microenvironment will enable tailored therapies to improve outcomes and decrease toxicity. The goal of personalized therapy is to target aberrations that drive tumour growth and survival, by administering the right drug combination for the right person. This is becoming increasingly achievable with advances in high-throughput technologies to characterize tumours and the expanding repertoire of molecularly targeted therapies. However, there are numerous challenges that need to be surpassed before delivering on the promise of personalized cancer therapy. These include tumour heterogeneity and molecular evolution, costs and potential morbidity of biopsies, lack of effective drugs against most genomic aberrations, technical limitations of molecular tests, and reimbursement and regulatory hurdles. Critically, the 'hype' surrounding personalized cancer therapy must be tempered with realistic expectations, which, today, encompass increased survival times for only a portion of patients.

摘要

个体化癌症治疗的基础是,对患者肿瘤及其微环境进行详细的分子特征分析,从而能够制定出针对性的治疗方案,改善疗效并降低毒性。个体化治疗的目标是通过为合适的患者施用合适的药物组合,靶向驱动肿瘤生长和存活的异常。随着高通量技术在肿瘤特征分析以及分子靶向治疗方案的扩展方面取得进展,这一目标正变得越来越可行。然而,在实现个体化癌症治疗的承诺之前,还有许多挑战需要克服。这些挑战包括肿瘤异质性和分子进化、活检的成本和潜在发病率、针对大多数基因组异常的有效药物的缺乏、分子检测的技术限制以及报销和监管障碍。关键的是,围绕个体化癌症治疗的“炒作”必须与现实的期望相协调,目前,个体化癌症治疗仅能延长一部分患者的生存时间。

相似文献

1
Overcoming implementation challenges of personalized cancer therapy.克服个性化癌症治疗实施挑战。
Nat Rev Clin Oncol. 2012 Sep;9(9):542-8. doi: 10.1038/nrclinonc.2012.127. Epub 2012 Jul 31.
2
Successes and limitations of targeted cancer therapy in breast cancer.乳腺癌靶向治疗的成功与局限
Prog Tumor Res. 2014;41:15-35. doi: 10.1159/000355896. Epub 2014 Feb 17.
3
Pharmacogenomic biomarkers for personalized cancer treatment.用于癌症个体化治疗的药物基因组生物标志物。
J Intern Med. 2015 Feb;277(2):201-217. doi: 10.1111/joim.12321.
4
Genomics and the History of Precision Oncology.基因组学与精准肿瘤学的历史
Surg Oncol Clin N Am. 2020 Jan;29(1):35-49. doi: 10.1016/j.soc.2019.08.003. Epub 2019 Oct 29.
5
Personalized cancer medicine: molecular diagnostics, predictive biomarkers, and drug resistance.个体化癌症医学:分子诊断、预测生物标志物和耐药性。
Clin Pharmacol Ther. 2013 Mar;93(3):252-9. doi: 10.1038/clpt.2012.237. Epub 2012 Dec 7.
6
Future of personalized medicine in oncology: a systems biology approach.肿瘤个性化医学的未来:系统生物学方法。
J Clin Oncol. 2010 Jun 1;28(16):2777-83. doi: 10.1200/JCO.2009.27.0777. Epub 2010 Apr 20.
7
Large-scale pharmacogenomic studies and drug response prediction for personalized cancer medicine.大规模的药物基因组学研究和药物反应预测,以实现个体化癌症治疗。
J Genet Genomics. 2021 Jul 20;48(7):540-551. doi: 10.1016/j.jgg.2021.03.007. Epub 2021 Apr 14.
8
Precision Medicine in Pediatric Oncology.儿科肿瘤学中的精准医学
Surg Oncol Clin N Am. 2020 Jan;29(1):63-72. doi: 10.1016/j.soc.2019.08.005. Epub 2019 Oct 29.
9
Counterpoint: Successes in the Pursuit of Precision Medicine: Biomarkers Take Credit.反驳观点:精准医学追求中的成功:生物标志物居功至伟。
J Natl Compr Canc Netw. 2017 Jul;15(7):863-866. doi: 10.6004/jnccn.2017.0127.
10
Beyond the limitation of targeted therapy: Improve the application of targeted drugs combining genomic data with machine learning.超越靶向治疗的局限:将基因组数据与机器学习相结合,改善靶向药物的应用。
Pharmacol Res. 2020 Sep;159:104932. doi: 10.1016/j.phrs.2020.104932. Epub 2020 May 28.

引用本文的文献

1
Precise Electromagnetic Modulation of the Cell Cycle and Its Applications in Cancer Therapy.细胞周期的精确电磁调制及其在癌症治疗中的应用。
Int J Mol Sci. 2025 May 7;26(9):4445. doi: 10.3390/ijms26094445.
2
The Growth Modulation Index (GMI) as an Efficacy Outcome in Cancer Clinical Trials: A Scoping Review with Suggested Reporting Guidelines.癌症临床试验中作为疗效指标的生长调节指数(GMI):一项带有建议报告指南的范围综述
Curr Oncol Rep. 2025 May;27(5):516-532. doi: 10.1007/s11912-025-01667-1. Epub 2025 Mar 29.
3
Breast cancer treatment modalities, treatment delays, and survival in Brunei Darussalam.

本文引用的文献

1
The BATTLE trial: personalizing therapy for lung cancer.BATTLE 试验:为肺癌患者实施个体化治疗。
Cancer Discov. 2011 Jun;1(1):44-53. doi: 10.1158/2159-8274.CD-10-0010. Epub 2011 Jun 1.
2
Sequential application of anticancer drugs enhances cell death by rewiring apoptotic signaling networks.抗癌药物的序贯应用通过重新布线细胞凋亡信号网络增强细胞死亡。
Cell. 2012 May 11;149(4):780-94. doi: 10.1016/j.cell.2012.03.031.
3
The clonal and mutational evolution spectrum of primary triple-negative breast cancers.原发性三阴性乳腺癌的克隆和突变进化图谱。
文莱达鲁萨兰国的乳腺癌治疗方式、治疗延误及生存率
BMC Cancer. 2025 Mar 20;25(1):510. doi: 10.1186/s12885-025-13861-2.
4
Editorial: design considerations for future personalized vaccination approaches.社论:未来个性化疫苗接种方法的设计考量
Nanomedicine (Lond). 2025 Feb;20(4):329-334. doi: 10.1080/17435889.2024.2419816. Epub 2024 Nov 18.
5
Circulating tumor DNA as prognostic markers of relapsed breast cancer: a systematic review and meta-analysis.循环肿瘤DNA作为复发性乳腺癌的预后标志物:一项系统综述和荟萃分析。
J Natl Cancer Cent. 2024 Jan 23;4(1):63-73. doi: 10.1016/j.jncc.2024.01.003. eCollection 2024 Mar.
6
A nationwide survey of the current status of radiation oncology teaching in Spanish medical schools.一项关于西班牙医学院校放射肿瘤学教学现状的全国性调查。
Rep Pract Oncol Radiother. 2024 Feb 16;28(6):794-800. doi: 10.5603/rpor.98741. eCollection 2023.
7
Computational Approaches: A New Frontier in Cancer Research.计算方法:癌症研究的新前沿。
Comb Chem High Throughput Screen. 2024;27(13):1861-1876. doi: 10.2174/0113862073265604231106112203.
8
The EDN1/EDNRA/β‑arrestin axis promotes colorectal cancer progression by regulating STAT3 phosphorylation.EDN1/EDNRA/β-arrestin 轴通过调节 STAT3 磷酸化促进结直肠癌的进展。
Int J Oncol. 2023 Jan;62(1). doi: 10.3892/ijo.2022.5461. Epub 2022 Dec 1.
9
Clinical prospects of WRN inhibition as a treatment for MSI tumours.WRN抑制作为微卫星高度不稳定(MSI)肿瘤治疗方法的临床前景。
NPJ Precis Oncol. 2022 Nov 15;6(1):85. doi: 10.1038/s41698-022-00319-y.
10
Integrated Molecular Analysis Reveals 2 Distinct Subtypes of Pure Seminoma of the Testis.综合分子分析揭示睾丸纯精原细胞瘤的两种不同亚型。
Cancer Inform. 2022 Oct 31;21:11769351221132634. doi: 10.1177/11769351221132634. eCollection 2022.
Nature. 2012 Apr 4;486(7403):395-9. doi: 10.1038/nature10933.
4
Intratumor heterogeneity and branched evolution revealed by multiregion sequencing.多区域测序揭示的肿瘤内异质性和分支进化。
N Engl J Med. 2012 Mar 8;366(10):883-892. doi: 10.1056/NEJMoa1113205.
5
Inhibition of PI3K/mTOR leads to adaptive resistance in matrix-attached cancer cells.PI3K/mTOR 的抑制会导致基质附着癌细胞产生适应性耐药。
Cancer Cell. 2012 Feb 14;21(2):227-39. doi: 10.1016/j.ccr.2011.12.024.
6
An emerging toolkit for targeted cancer therapies.一种用于靶向癌症治疗的新兴工具包。
Genome Res. 2012 Feb;22(2):177-82. doi: 10.1101/gr.136044.111.
7
Clinical and economic aspects of KRAS mutational status as predictor for epidermal growth factor receptor inhibitor therapy in metastatic colorectal cancer patients.KRAS 基因突变状态作为转移性结直肠癌患者表皮生长因子受体抑制剂治疗预测因子的临床和经济方面。
Oncology. 2011;81(5-6):359-64. doi: 10.1159/000334919. Epub 2012 Jan 13.
8
Loss of human epidermal growth factor receptor 2 (HER2) expression in metastatic sites of HER2-overexpressing primary breast tumors.人表皮生长因子受体 2(HER2)过表达的原发性乳腺癌转移部位 HER2 表达缺失。
J Clin Oncol. 2012 Feb 20;30(6):593-9. doi: 10.1200/JCO.2010.33.8889. Epub 2011 Nov 28.
9
Whole cancer genome sequencing by next-generation methods.下一代方法进行全癌症基因组测序。
Am J Clin Pathol. 2011 Oct;136(4):527-39. doi: 10.1309/AJCPR1SVT1VHUGXW.
10
Outcomes of research biopsies in phase I clinical trials: the MD anderson cancer center experience.I 期临床试验中研究性活检的结果:MD 安德森癌症中心的经验。
Oncologist. 2011;16(9):1292-8. doi: 10.1634/theoncologist.2011-0043. Epub 2011 Aug 22.