期刊文献+

New evidence-based adaptive clinical trial methods for optimally integrating predictive biomarkers into oncology clinical development programs 被引量:1

New evidence-based adaptive clinical trial methods for optimally integrating predictive biomarkers into oncology clinical development programs
下载PDF
导出
摘要 Predictive biomarkers are important to the future of oncology; they can be used to identify patient populations who will benefit from therapy, increase the value of cancer medicines, and decrease the size and cost of clinical trials while increasing their chance of success. But predictive biomarkers do not always work. When unsuccessful, they add cost, complexity, and time to drug development. This perspective describes phases 2 and 3 development methods that efficiently and adaptively check the ability of a biomarker to predict clinical outcomes. In the end, the biomarker is emphasized to the extent that it can actually predict. Predictive biomarkers are important to the future of oncology; they can be used to identify patient populations who will benefit from therapy, increase the value of cancer medicines, and decrease the size and cost of clinical trials while increasing their chance of success. But predictive biomarkers do not always work. When unsuccessful, they add cost, complexity, and time to drug development. This perspective describes phases 2 and 3 development methods that efficiently and adaptively check the ability of a biomarker to predict clinical outcomes. In the end, the biomarker is emphasized to the extent that it can actually predict.
出处 《Chinese Journal of Cancer》 SCIE CAS CSCD 2013年第5期233-241,共9页
关键词 生物标志物 临床试验 药物开发 预测 试验方法 肿瘤 自适应 基础 Predictive biomarkers, adaptive clinical trials, evidence-based approach
  • 相关文献

参考文献30

  • 1Cobleigh MA, Vogel CL, Tripathy D, et al. Multinational study of the efficacy and safety of humanized anti-HER2 monoclonal antibody in women who have HER2-overexpressing metastatic breast cancer that has progressed after chemotherapy for metastatic disease. J Clin Oncol, 1999,17:2639-2648.
  • 2Slamon D J, Leyland-Jones B, Shak S, et al. Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2. N Engl J Med, 2001,344:783-792.
  • 3Paez JG, Janne PA, Lee JC, et al. EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science, 2004,30:1497-1500.
  • 4Pao W, Miller V, Zakowski M, et al. EGF receptor gene mutations are common in lung cancers from "never smokers"and are associated with sensitivity of tumors to gefitinib and erlotinib. Proc Natl Acad Sci USA, 2004,101:13306-13311.
  • 5Amado RG, Wolf M, Peeters M, et al. Wild-type KRAS is required for panitumumab efficacy in patients with metastatic colorectal cancer. J Clin Oncol, 2006,26:1626-;634.
  • 6Lievre A, Bachet JB, Le Corre D, et al. KRAS mutation status is predictive of response to cetuximab therapy in colorectal cancer. Cancer Res, 2006,66:3992-3995.
  • 7Bokemeyer C, Bondarenko I, Hartmann JT, et al. KRAS status and efficacy of first-line treatment of patients with metastatic colorectal cancer (mCRC) with FLFOX with or without cetuximab: the OPUS experience. J Clin Oncol, 2008,26 Suppl 15:4000.
  • 8Van Cutsem E, Lang I, D'haens G, et al. KRAS status andefficacy in the first-line treatment of patients with metastatic colorectal cancer (mCRC) treated with FOLFIRI with or without cetuximab: The CRYSTAL experience. J Clin Oncol 2008:26 Suppl 15:2.
  • 9Yan L, Beckman RA. Pharmacogenetics and pharmaco- genomics in oncology therapeutic antibody development. Biotechniques, 2005,39:565-568.
  • 10Ransohoff DF, Gourlay ML Sources of bias in specimens for research about molecular markers for cancer. J Clin Oncol, 2010,28:698-704.

同被引文献6

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部