Progress in chemoprevention drug development: The promise of molecular biomarkers for prevention of intraepithelial neoplasia and cancer - A plan to move forward

被引:201
作者
Kelloff, Gary J.
Lippman, Scott M.
Dannenberg, Andrew J.
Sigman, Caroline C.
Pearce, Homer L.
Reid, Brian J.
Szabo, Eva
Jordan, V. Craig
Spitz, Margaret R.
Mills, Gordon B.
Papadimitrakopoulou, Vali A.
Lotan, Reuben
Aggarwal, Bharat B.
Bresalier, Robert S.
Kim, Jeri
Arun, Banu
Lu, Karen H.
Thomas, Melanie E.
Rhodes, Helen E.
Brewer, Molly A.
Follen, Michele
Shin, Dong M.
Parnes, Howard L.
Siegfried, Jill M.
Evans, Alison A.
Blot, William J.
Chow, Wong-Ho
Blount, Patricia L.
Maley, Carlo C.
Wang, Kenneth K.
Lam, Stephen
Lee, J. Jack
Dubinett, Steven M.
Engstrom, Paul F.
Meyskens, Frank L., Jr.
O'Shaughnessy, Joyce
Hawk, Ernest T.
Levin, Bernard
Nelson, William G.
Hong, Waun Ki
机构
[1] NCI, Rockville, MD 20852 USA
[2] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
[3] Cornell Univ, Weill Med Coll, New York, NY USA
[4] CCS Associates, Mountain View, CA USA
[5] Eli Lilly & Co, Indianapolis, IN 46285 USA
[6] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
[7] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[8] Wistar Inst Anat & Biol, Philadelphia, PA 19104 USA
[9] Univ Arizona, Tucson, AZ USA
[10] Emory Univ, Atlanta, GA 30322 USA
[11] Univ Pittsburgh, Pittsburgh, PA USA
[12] Int Epidemiol Inst, Rockville, MD USA
[13] Mayo Clin, Rochester, MN USA
[14] British Columbia Canc Agcy, Vancouver, BC V5Z 4E6, Canada
[15] Univ Calif Los Angeles, Los Angeles, CA USA
[16] Univ Calif Irvine, Irvine, CA USA
[17] Texas Oncol PA, US Oncol, Baylor Sammons Canc Ctr, Dallas, TX USA
[18] Johns Hopkins Univ, Baltimore, MD USA
关键词
D O I
10.1158/1078-0432.CCR-06-1104
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This article reviews progress in chemopreventive drug development, especially data and concepts that are new since the 2002 AACR report on treatment and prevention of intraepithelial neoplasia. Molecular biomarker expressions involved in mechanisms of carcinogenesis and genetic progression models of intraepithelial neoplasia are discussed and analyzed for how they can inform mechanism-based, molecularly targeted drug development as well as risk stratification, cohort selection, and end-point selection for clinical trials. We outline the concept of augmenting the risk, mechanistic, and disease data from histopathologic intraepithelial neoplasia assessments with molecular biomarker data. Updates of work in 10 clinical target organ sites include new data on molecular progression, significant completed trials, new agents of interest, and promising directions for future clinical studies. This overview concludes with strategies for accelerating chemopreventive drug development, such as integrating the best science into chemopreventive strategies and regulatory policy, providing incentives for industry to accelerate preventive drugs, fostering multisector cooperation in sharing clinical samples and data, and creating public-private partnerships to foster new regulatory policies and public education.
引用
收藏
页码:3661 / 3697
页数:37
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