Monson Savanna, Chen Pin-Jung, Gangi Alexandra, Waters Kevin, Billet Sandrine, Hendifar Andrew, Lu Shelly, Zell Jason A, Gong Jun
Department of Medicine, Division of Medical Oncology, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Department of Surgery, Division of Surgical Oncology, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Transl Gastroenterol Hepatol. 2025 Jan 7;10:11. doi: 10.21037/tgh-24-97. eCollection 2025.
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.
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.
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.
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.
在全球范围内,结直肠癌(CRC)是第三大最常被诊断出的癌症。已知CRC由称为腺瘤的癌前息肉发展而来。尽管存在一些遗传综合征(如家族性腺瘤性息肉病综合征),其携带者患CRC的终生风险很高,但大多数CRC病例是散发性的。散发性CRC通过正常结肠上皮向浸润性癌转变过程中早期且频繁发生的分子事件发展而来。由于散发性CRC带来巨大的公共卫生负担,在过去几十年中,预防散发性CRC(即CRC化学预防)一直是一个备受关注的话题。本研究的目的是回顾在随机对照试验(RCT)中研究的各种化学预防剂,以评估它们在预防散发性CRC方面的有效性和安全性。
本综述聚焦于近期使用潜在化学预防剂预防散发性CRC形成的RCT,这些化学预防剂可直接预防,或通过干预措施(包括非甾体抗炎药(NSAIDs)、维生素和矿物质以及代谢剂)减少其已知前体(如腺瘤或异常隐窝灶(ACF))来预防。
在散发性CRC化学预防方面已进行了多项RCT。NSAIDs在散发性CRC化学预防中已被证明有前景,但由于心血管风险增加而受到限制,尤其是塞来昔布和罗非昔布。
目前正在积极研究以确立首个散发性CRC化学预防策略。基于以往试验,对于散发性CRC化学预防的所有未来试验而言,研究人群的选择、终点的选定、安全性和耐受性、替代生物标志物的可用性以及针对腺瘤 - 癌序列的新作用机制仍是需要考虑的重要要点。