Hereditary cancer due to pathological mutations in the mismatch repair gene family is now known as Lynch syndrome and affects at least 1 in 1,000 people, resulting in a 30-50% cancer risk most often involving the colorectum and endometrium. Annual or biennial colonoscopy reduces cancer deaths and many offer gynaecological surveillance, but most other associated cancers are not amenable to early detection. As microsatellite instability testing and tumour immunohistochemistry become routine, case finding will improve. Our recent demonstration that 600 mg aspirin per day for at least 2 years reduces the cancer burden by 63% after a 3-year lag period reinforces the need to identify gene carriers and introduce them to chemoprevention. CaPP3 will test different doses of aspirin in at least 3,000 gene carriers to determine whether low-dose aspirin is as effective.

译文

由于错配修复基因家族的病理突变引起的遗传性癌症现在被称为Lynch综合征,至少1,000人中有1人受到影响,导致30-50% 的癌症风险最常涉及结直肠和子宫内膜。每年或两年一次的结肠镜检查可减少癌症死亡,并且许多提供妇科监测,但大多数其他相关癌症不适合早期发现。随着微卫星不稳定性测试和肿瘤免疫组织化学成为常规,病例发现将得到改善。我们最近的证明,每天600毫克阿司匹林持续至少2年,在3年的滞后期后,癌症负担减轻了63%,这加强了鉴定基因携带者并将其引入化学预防的必要性。CaPP3将在至少3,000基因携带者中测试不同剂量的阿司匹林,以确定低剂量阿司匹林是否同样有效。

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