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用于癌症治疗和预防的分子靶向药物的趋同发展。

The convergent development of molecular-targeted drugs for cancer treatment and prevention.

作者信息

Lippman Scott M, Heymach John V

机构信息

Department of Thoracic/Head and Neck Medical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030-4009, USA.

出版信息

Clin Cancer Res. 2007 Jul 15;13(14):4035-41. doi: 10.1158/1078-0432.CCR-07-0063.

DOI:10.1158/1078-0432.CCR-07-0063
PMID:17634526
Abstract

Advances in our understanding of multistep and field carcinogenesis are erasing the clear demarcation of intraepithelial neoplasia from invasive neoplasia. The growing ability to define a very high risk of cancer is forging important commonalities between prevention and therapy, such as in potential prognostic/predictive markers, agents, and side effects that patients would be willing to tolerate, and the logistics of definitive trials. The emergence of promising new molecular-targeted agents and new technologies for screening and early detection provides new opportunities for applying clinical trial designs that integrate therapy and prevention end points. Such trials may be used to facilitate targeted drug development and help identify strategies for both cancer prevention and advanced cancer therapy. These several advances are creating a convergence of cancer therapy with cancer prevention that promises to streamline the development of targeted drugs and improve the control of major cancers.

摘要

我们对多步骤和场致癌作用认识的进展正在消除上皮内瘤变与浸润性肿瘤之间明确的界限。定义癌症极高风险的能力不断增强,正在形成预防与治疗之间的重要共性,比如在潜在的预后/预测标志物、药物以及患者愿意耐受的副作用方面,还有确定性试验的后勤保障。有前景的新型分子靶向药物以及用于筛查和早期检测的新技术的出现,为应用整合治疗和预防终点的临床试验设计提供了新机会。此类试验可用于促进靶向药物的开发,并有助于确定癌症预防和晚期癌症治疗的策略。这几方面的进展正在使癌症治疗与癌症预防趋于融合,有望简化靶向药物的开发并改善对主要癌症的控制。

相似文献

1
The convergent development of molecular-targeted drugs for cancer treatment and prevention.用于癌症治疗和预防的分子靶向药物的趋同发展。
Clin Cancer Res. 2007 Jul 15;13(14):4035-41. doi: 10.1158/1078-0432.CCR-07-0063.
2
The convergence of cancer prevention and therapy in early-phase clinical drug development.癌症预防与治疗在早期临床药物研发中的融合。
Cancer Cell. 2004 Oct;6(4):321-6. doi: 10.1016/j.ccr.2004.09.021.
3
Surrogate end-point biomarkers in chemopreventive drug development.化学预防药物研发中的替代终点生物标志物
IARC Sci Publ. 2001;154:13-26.
4
Oral cancer prevention and the evolution of molecular-targeted drug development.口腔癌预防与分子靶向药物研发的进展
J Clin Oncol. 2005 Jan 10;23(2):346-56. doi: 10.1200/JCO.2005.09.128.
5
Assessing intraepithelial neoplasia and drug safety in cancer-preventive drug development.评估癌症预防药物研发中的上皮内瘤变及药物安全性。
Nat Rev Cancer. 2007 Jul;7(7):508-18. doi: 10.1038/nrc2154.
6
Chemoprevention: from research to clinical oncology.化学预防:从研究到临床肿瘤学
Eur J Cancer. 2005 Sep;41(13):1833-41. doi: 10.1016/j.ejca.2005.06.007.
7
Point: Surrogate end point biomarkers are likely to be limited in their usefulness in the development of cancer chemoprevention agents against sporadic cancers.观点:替代终点生物标志物在开发针对散发性癌症的癌症化学预防药物方面的作用可能有限。
Cancer Epidemiol Biomarkers Prev. 2003 Jul;12(7):589-92.
8
Counterpoint: Because some surrogate end point biomarkers measure the neoplastic process they will have high utility in the development of cancer chemopreventive agents against sporadic cancers.反驳观点:由于一些替代终点生物标志物可测量肿瘤形成过程,因此它们在开发针对散发性癌症的癌症化学预防剂方面将具有很高的实用性。
Cancer Epidemiol Biomarkers Prev. 2003 Jul;12(7):593-6.
9
Reducing the "risk" of chemoprevention: defining and targeting high risk--2005 AACR Cancer Research and Prevention Foundation Award Lecture.降低化学预防的“风险”:定义并定位高风险人群——2005年美国癌症研究协会癌症研究与预防基金会奖讲座
Cancer Res. 2006 Mar 15;66(6):2893-903. doi: 10.1158/0008-5472.CAN-05-4573.
10
Chemoprevention of head and neck cancer.头颈部癌症的化学预防
J Med Assoc Thai. 1996 Mar;79(3):185-93.

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