散发性结直肠癌的化学预防策略:综述。

IF 2.5 Q2 GASTROENTEROLOGY & HEPATOLOGY
Translational gastroenterology and hepatology Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI:10.21037/tgh-24-97
Savanna Monson, Pin-Jung Chen, Alexandra Gangi, Kevin Waters, Sandrine Billet, Andrew Hendifar, Shelly Lu, Jason A Zell, Jun Gong
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引用次数: 0

摘要

背景与目的:在全球范围内,结直肠癌(CRC)是第三大最常诊断的癌症。众所周知,结直肠癌起源于癌前息肉,即腺瘤。虽然有遗传综合征(如家族性腺瘤性息肉病综合征)具有较高的CRC终生风险,但大多数CRC病例是散发的。散发性结直肠癌是通过正常结肠上皮向浸润性癌转化过程中早期和频繁发生的分子事件发展而来的。散发性结直肠癌的预防(即结直肠癌化学预防)由于其巨大的公共卫生负担,在过去几十年中一直是一个感兴趣的话题。本研究的目的是回顾在随机对照试验(RCTs)中研究的各种化学预防药物,以评估其预防散发性结直肠癌的有效性和安全性。方法:本文综述了近期使用潜在化学预防药物预防散发性结直肠癌形成的随机对照试验,无论是直接预防还是通过非甾体抗炎药(NSAIDs)、维生素和矿物质以及代谢药物等干预措施减少其已知前体如腺瘤或异常隐窝灶(ACF)来预防结直肠癌的形成。主要内容和发现:在散发性结直肠癌化学预防方面进行了多项随机对照试验。非甾体抗炎药已被证明在散发性结直肠癌化学预防方面很有前景,但由于心血管风险增加,特别是塞来昔布和罗非昔布,其应用受到限制。结论:初步建立散发性结直肠癌化学预防策略的研究正在积极进行。根据以往的试验,研究人群的选择、终点的选择、安全性和耐受性、替代生物标志物的可用性以及针对腺瘤-癌序列的新的作用机制仍然是未来所有散发性结直肠癌化学预防试验需要考虑的重要问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chemopreventive strategies for sporadic colorectal cancer: a narrative review.

Background and objective: Globally, colorectal cancer (CRC) is the third most commonly diagnosed cancer. CRC is known to arise from precancerous polyps known as adenomas. Although there are genetic syndromes (i.e., familial adenomatous polyposis syndrome) that carry a high lifetime risk of CRC, the majority of CRC cases are sporadic. Sporadic CRC develops via molecular events that occur early and frequently in the transformation of the normal colon epithelium to invasive cancer. Prevention of sporadic CRC (i.e., CRC chemoprevention) has been a topic of interest in the past decades due to its large public health burden. The objective of this study is to review various chemopreventive agents studied in randomized controlled trials (RCTs) to evaluate their effectiveness and safety in preventing sporadic CRC.

Methods: This review focuses on recent RCTs using potential chemopreventive agents to prevent sporadic CRC formation, either directly or through reduction of its known precursors such as adenomas or aberrant crypt foci (ACF) through interventions including nonsteroidal anti-inflammatory drugs (NSAIDs), vitamins and minerals, and metabolic agents.

Key content and findings: Multiple RCTs have been conducted in sporadic CRC chemoprevention. NSAIDs have proven promising in sporadic CRC chemoprevention but have been limited due to increased cardiovascular risk, particularly for celecoxib and rofecoxib.

Conclusions: There is active investigation into establishing the first sporadic CRC chemoprevention strategy. Building from previous trials, the choice of study population, selection of endpoints, safety and tolerability, availability of surrogate biomarkers, and novel mechanisms of action targeting the adenoma-carcinoma sequence remain important points to consider for all future trials of sporadic CRC chemoprevention.

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