This is a proposal for a randomized trial designed to study the long- term chemopreventive effects of low-dose 13-cis retinoic acid (13-cRA) and of the relatively non-toxic micronutrients beta-carotene and retinol in suppressing premalignant oral lesions (oral leukoplakia). The study's primary hypothesis--i.e., that daily supplementation with oral beta-carotene and retinol will be as effective or more effective than low-dose 13-cRA in producing and maintaining remission in oral leukoplakia--will be tested through assessment of response in the two groups using standard clinical and histologic criteria and measurement of micronuclei frequency. The expression and modulation of a series of biologic biomarkers will be tested through careful correlations between marker expression and modulation and outcome in the two treatment groups. We also plan to prospectively assess and biochemically validate (by assaying for cotinine, retinyl palmitate, and beta-carotene serum levels) the roles of tobacco cessation and dietary intake in the natural history or oral leukoplakia. Preclinical, epidemiologic and early clinical data support the role of retinoids and carotenoids in suppressing upper aerodigestive tract (UADT) and lung carcinogenesis. This proposed long-term, phase III trial has evolved directly from our other two studies of 13-cRA in oral leukoplakia. The first study, now concluded, was in the form of a prospective, randomized trial and established the significant activity of 13-cRA. Preliminary data from the second study indicate the efficacy of low-dose 13-cRA (0.5 mg/kg/d) as short-term (9 month) maintenance therapy and the feasibility of analyzing a limited panel of biomarkers from small tissue samples, which is critical in chemoprevention trials. The proposed study will be significant even if it establishes only that the relatively nontoxic natural agents being tested are effective chemopreventive drugs against oral leukoplakia, as this would imply that they have high potential for chemoprevention of other UADT and lung epithelial cancers. Equally significant, however, will be progress in the laboratory toward the identification of biologic markers as indicators of intermediate endpoints within the multistep carcinogenic process.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA052051-06A1
Application #
6237124
Study Section
Project Start
1997-02-01
Project End
1997-11-30
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
6
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Texas MD Anderson Cancer Center
Department
Type
DUNS #
001910777
City
Houston
State
TX
Country
United States
Zip Code
77030
Hildebrandt, Michelle A T; Lippman, Scott M; Etzel, Carol J et al. (2012) Genetic variants in the PI3K/PTEN/AKT/mTOR pathway predict head and neck cancer patient second primary tumor/recurrence risk and response to retinoid chemoprevention. Clin Cancer Res 18:3705-13
Lee, J Jack; Wu, Xifeng; Hildebrandt, Michelle A T et al. (2011) Global assessment of genetic variation influencing response to retinoid chemoprevention in head and neck cancer patients. Cancer Prev Res (Phila) 4:185-93
Wang, Jianming; Lippman, Scott M; Lee, J Jack et al. (2010) Genetic variations in regulator of G-protein signaling genes as susceptibility loci for second primary tumor/recurrence in head and neck squamous cell carcinoma. Carcinogenesis 31:1755-61
Zhang, Xiaofan; Yang, Hushan; Lee, J Jack et al. (2010) MicroRNA-related genetic variations as predictors for risk of second primary tumor and/or recurrence in patients with early-stage head and neck cancer. Carcinogenesis 31:2118-23
Wu, Xifeng; Spitz, Margaret R; Lee, J Jack et al. (2009) Novel susceptibility loci for second primary tumors/recurrence in head and neck cancer patients: large-scale evaluation of genetic variants. Cancer Prev Res (Phila) 2:617-24
William Jr, William N; Lee, J Jack; Lippman, Scott M et al. (2009) High-dose fenretinide in oral leukoplakia. Cancer Prev Res (Phila) 2:22-6
Papadimitrakopoulou, Vassiliki A; Lee, J Jack; William Jr, William N et al. (2009) Randomized trial of 13-cis retinoic acid compared with retinyl palmitate with or without beta-carotene in oral premalignancy. J Clin Oncol 27:599-604
Kawaguchi, Hidetoshi; El-Naggar, Adel K; Papadimitrakopoulou, Vali et al. (2008) Podoplanin: a novel marker for oral cancer risk in patients with oral premalignancy. J Clin Oncol 26:354-60
Wu, Xifeng; Gu, Jian; Dong, Qiong et al. (2006) Joint effect of mutagen sensitivity and insulin-like growth factors in predicting the risk of developing secondary primary tumors and tumor recurrence in patients with head and neck cancer. Clin Cancer Res 12:7194-201
Lippman, Scott M; Lee, J Jack (2006) Reducing the ""risk"" of chemoprevention: defining and targeting high risk--2005 AACR Cancer Research and Prevention Foundation Award Lecture. Cancer Res 66:2893-903

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