Chemoprevention of colorectal neoplasia: The potential for personalized medicine

被引:75
作者
Arber, Nadir [1 ,2 ]
Levin, Bernard [3 ]
机构
[1] Tel Aviv Sourasky Med Ctr, Integrated Canc Prevent Ctr, IL-64239 Tel Aviv, Israel
[2] Tel Aviv Univ, IL-64239 Tel Aviv, Israel
[3] Univ Texas MD Anderson Canc Ctr, Div Canc Prevent & Populat Sci, Houston, TX USA
关键词
D O I
10.1053/j.gastro.2008.02.012
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
CRC development is a multi-step process that span 10 to 15 years, thereby providing an opportunity for early detection and even prevention. The poor survival rate of advanced CRC has prompted the emphasis on prevention of this disease. CRC screening and removal of adenomas is an effective intervention, and is the cornerstone of prevention. However, screening efforts have had limited impact due to less than optimal compliance with guidelines. Chemoprevention involves the long-term use of a variety of oral agents that can delay, prevent or even reverse the development of adenomas in the large bowel, thus interfering with the multi-step progessing from adenoma to carcinoma. This effect is of particular importance to individuals with a hereditary prediposition to colorectal neoplasia and to those who are especially susceptile to the environmental causes of CRC. NSAIDs have drawn the most attention as chemoprevention agents. Sulindac and celecoxib are effective in promoting poly regression in high risk individuals with Familial Adenomatous Polyposis (FAP). In the more common sporadic setting the APROVe (refecoxib), APC and PreSAP (Celecoxib) trials have shown a significant reduction in adenoma recurrence but important concerns exist regarding cardiovascular toxicity associated with selective COX-2 inhibitors. These landmark studies are very important, as they provide a proof of concept that we can prevent high risk adenomas that can lead to CRC development. The ideal chemopreventive agent remains to be discovered with great emphasis on need not to harm. Possibly, combinations of agents will maximize effectiveness while limiting drug toxicity. Finally, personalized approaches will include the ability to predict risk and toxicity.
引用
收藏
页码:1224 / 1237
页数:14
相关论文
共 126 条
[61]   A large cohort study of long-term daily use of adult-strength aspirin and cancer incidence [J].
Jacobs, Eric J. ;
Thun, Michael J. ;
Bain, Elizabeth B. ;
Rodriguez, Carmen ;
Henley, S. Jane ;
Calle, Eugenia E. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2007, 99 (08) :608-615
[62]   Selenium and colorectal adenoma:: Results of a pooled analysis [J].
Jacobs, ET ;
Jiang, RY ;
Alberts, DS ;
Greenberg, ER ;
Gunter, EW ;
Karagas, MR ;
Lanza, E ;
Ratnasinghe, L ;
Reid, ME ;
Schatzkin, A ;
Smith-Warner, SA ;
Wallace, K ;
Martínez, ME .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (22) :1669-1675
[63]   Ursodeoxycholate/sulindac combination treatment effectively prevents intestinal adenomas in a mouse model of polyposis [J].
Jacoby, RF ;
Cole, CE ;
Hawk, ET ;
Lubet, RA .
GASTROENTEROLOGY, 2004, 127 (03) :838-844
[64]   PROSTAGLANDINS AND CANCER - UPDATE [J].
JAFFE, BM .
PROSTAGLANDINS, 1974, 6 (06) :453-461
[65]   Primary care:: Chemoprevention of colorectal cancer [J].
Jänne, PA ;
Mayer, RJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (26) :1960-1968
[66]   Cancer statistics, 2007 [J].
Jemal, Ahmedin ;
Siegel, Rebecca ;
Ward, Elizabeth ;
Murray, Taylor ;
Xu, Jiaquan ;
Thun, Michael J. .
CA-A CANCER JOURNAL FOR CLINICIANS, 2007, 57 (01) :43-66
[67]   Risk factors for colorectal neoplasia in inflammatory bowel disease: A nested case-control study from copenhagen county, denmark and olmsted county, minnesota [J].
Jess, Tine ;
Loftus, Edward V., Jr. ;
Velayos, Fernando S. ;
Winther, Karen V. ;
Tremaine, William J. ;
Zinsmeister, Alan R. ;
Harmsen, W. Scott ;
Langholz, Ebbe ;
Binder, Vibeke ;
Munkholm, Pia ;
Sandborn, William J. .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2007, 102 (04) :829-836
[68]  
KELLOFF GJ, 2006, CLIN CANCER RES, V66, P6851
[69]   Dietary calcium, phosphorus, vitamin D, dairy products and the risk of colorectal adenoma and cancer among French women of the E3N-EPIC prospective study [J].
Kesse, E ;
Boutron-Ruault, MC ;
Norat, T ;
Riboli, E ;
Clavel-Chapelon, F .
INTERNATIONAL JOURNAL OF CANCER, 2005, 117 (01) :137-144
[70]   Tamoxifen and breast cancer incidence among women with inherited mutations in BRCA1 and BRCA2 -: National Surgical Adjuvant Breast and Bowel Project (NSABP-P1) Breast Cancer Prevention Trial [J].
King, MC ;
Wieand, S ;
Hale, K ;
Lee, M ;
Walsh, T ;
Owens, K ;
Tait, J ;
Ford, L ;
Dunn, BK ;
Costantino, J ;
Wickerham, L ;
Wolmark, N ;
Fisher, B .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (18) :2251-2256