Progress in Chemoprevention Drug Development: The Promise of Molecular Biomarkers for Prevention of Intraepithelial Neoplasia and Cancer—A Plan to Move Forward

Author:

Kelloff Gary J.1,Lippman Scott M.2,Dannenberg Andrew J.3,Sigman Caroline C.4,Pearce Homer L.5,Reid Brian J.6,Szabo Eva1,Jordan V. Craig7,Spitz Margaret R.2,Mills Gordon B.2,Papadimitrakopoulou Vali A.2,Lotan Reuben2,Aggarwal Bharat B.2,Bresalier Robert S.2,Kim Jeri2,Arun Banu2,Lu Karen H.2,Thomas Melanie E.2,Rhodes Helen E.2,Brewer Molly A.8,Follen Michele2,Shin Dong M.9,Parnes Howard L.1,Siegfried Jill M.10,Evans Alison A.7,Blot William J.11,Chow Wong-Ho1,Blount Patricia L.6,Maley Carlo C.12,Wang Kenneth K.13,Lam Stephen14,Lee J. Jack2,Dubinett Steven M.15,Engstrom Paul F.7,Meyskens Frank L.16,O'Shaughnessy Joyce17,Hawk Ernest T.1,Levin Bernard2,Nelson William G.18,Hong Waun Ki2,

Affiliation:

1. 1National Cancer Institute, Bethesda, Maryland;

2. 2University of Texas M.D. Anderson Cancer Center, Houston, Texas;

3. 3Weill Medical College of Cornell University, New York, New York;

4. 4CCS Associates, Mountain View, California;

5. 5Eli Lilly & Co., Indianapolis, Indiana;

6. 6Fred Hutchinson Cancer Research Center, Seattle, Washington;

7. 7Fox Chase Cancer Center;

8. 9University of Arizona, Tucson, Arizona;

9. 10Emory University, Atlanta, Georgia;

10. 11University of Pittsburgh, Pittsburgh, Pennsylvania;

11. 12International Epidemiology Institute, Rockville, Maryland;

12. 8The Wistar Institute, Philadelphia, Pennsylvania;

13. 13Mayo Clinic, Rochester, Minnesota;

14. 14British Columbia Cancer Agency, Vancouver, British Columbia, Canada;

15. 15University of California at Los Angeles, Los Angeles, California;

16. 16University of California at Irvine, Irvine, California;

17. 17Baylor Sammons Cancer Center, Texas Oncology, PA, U.S. Oncology, Dallas, Texas; and

18. 18Johns Hopkins University, Baltimore, Maryland

Abstract

AbstractThis 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.

Publisher

American Association for Cancer Research (AACR)

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