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Cancer Prevention with Resistant Starch in Lynch Syndrome Patients in the CAPP2-Randomized Placebo Controlled Trial: Planned 10-Year Follow-up

医学 结直肠癌 安慰剂 内科学 随机对照试验 癌症 入射(几何) 林奇综合征 置信区间 胃肠病学 癌症登记处 外科 病理 DNA错配修复 替代医学 光学 物理
作者
John C. Mathers,Faye Elliott,Finlay Macrae,Jukka‐Pekka Mecklin,Gabriela Möslein,Fiona E. McRonald,Lucio Bertario,D. Gareth Evans,Anne‐Marie Gerdes,Judy Ho,Annika Lindblom,Patrick J. Morrison,Jem Rashbass,Raj Ramesar,Toni T. Seppälä,Huw Thomas,Harsh Sheth,Kirsi Pylvänäinen,Lynn Reed,Gillian M. Borthwick
出处
期刊:Cancer Prevention Research [American Association for Cancer Research]
卷期号:15 (9): 623-634 被引量:52
标识
DOI:10.1158/1940-6207.capr-22-0044
摘要

ABSTRACT: The CAPP2 trial investigated the long-term effects of aspirin and resistant starch on cancer incidence in patients with Lynch syndrome (LS). Participants with LS were randomized double-blind to 30 g resistant starch (RS) daily or placebo for up to 4 years. We present long-term cancer outcomes based on the planned 10-year follow-up from recruitment, supplemented by National Cancer Registry data to 20 years in England, Wales, and Finland. Overall, 463 participants received RS and 455 participants received placebo. After up to 20 years follow-up, there was no difference in colorectal cancer incidence (n = 52 diagnosed with colorectal cancer among those randomized to RS against n = 53 on placebo) but fewer participants had non-colorectal LS cancers in those randomized to RS (n = 27) compared with placebo (n = 48); intention-to-treat (ITT) analysis [HR, 0.54; 95% confidence interval (CI), 0.33-0.86; P = 0.010]. In ITT analysis, allowing for multiple primary cancer diagnoses among participants by calculating incidence rate ratios (IRR) confirmed the protective effect of RS against non-colorectal cancer LS cancers (IRR, 0.52; 95% CI, 0.32-0.84; P = 0.0075). These effects are particularly pronounced for cancers of the upper GI tract; 5 diagnoses in those on RS versus 21 diagnoses on placebo. The reduction in non-colorectal cancer LS cancers was detectable in the first 10 years and continued in the next decade. For colorectal cancer, ITT analysis showed no effect of RS on colorectal cancer risk (HR, 0.92; 95% CI, 0.62-1.34; P = 0.63). There was no interaction between aspirin and RS treatments. In conclusion, 30 g daily RS appears to have a substantial protective effect against non-colorectal cancer cancers for patients with LS. PREVENTION RELEVANCE: Regular bowel screening and aspirin reduce colorectal cancer among patients with LS but extracolonic cancers are difficult to detect and manage. This study suggests that RS reduces morbidity associated with extracolonic cancers. See related Spotlight, p. 557.
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