Chemoprevention of hereditary colon cancers: time for new strategies

被引:59
|
作者
Ricciardiello, Luigi [1 ]
Ahnen, Dennis J. [2 ]
Lynch, Patrick M. [3 ]
机构
[1] Univ Bologna, Dept Med & Surg Sci, Via Massarenti 9, I-40124 Bologna, Italy
[2] Univ Colorado, Sch Med & Gastroenterol Rockies, Dept Med, 5001 E 17th Ave Pkwy, Denver, CO 80220 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Gastroenterol Hepatol & Nutr, 1515 Holcombe Blvd, Houston, TX 77054 USA
关键词
FAMILIAL ADENOMATOUS POLYPOSIS; SELECTIVE CYCLOOXYGENASE-2 INHIBITOR; POUCH-ANAL ANASTOMOSIS; COLORECTAL-CANCER; LYNCH SYNDROME; DOUBLE-BLIND; RECTAL POLYPS; EICOSAPENTAENOIC ACID; RESISTANT STARCH; RANDOMIZED-TRIAL;
D O I
10.1038/nrgastro.2016.56
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Colorectal cancer (CRC) is potentially preventable. Chemoprevention, a focus of research for the past three decades, aims to prevent or delay the onset of cancer through the regression or prevention of colonic adenomas. Ideal pharmacological agents for chemoprevention should be cheap and nontoxic. Although data indicate that aspirin can reduce the risk of CRC in the general population, the highest return from chemopreventive strategies would be expected in patients with the highest risk of developing the disease, particularly those with a defined hereditary predisposition. Despite compelling data showing that a large number of chemopreventive agents show promise in preclinical CRC models, clinical studies have yielded conflicting results. This Review provides a historical and methodological perspective of chemoprevention in familial adenomatous polyposis and Lynch syndrome, and summarizes the current status of CRC chemoprevention in humans. Our goal is to critically focus on important issues of trial design, with particular attention on the choice of appropriate trial end points, how such end points should be measured, and which patients are the ideal candidates to be included in a chemopreventive trial.
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页码:352 / 361
页数:10
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