Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
Curr Gastroenterol Rep. 2020 Jun 3;22(7):32. doi: 10.1007/s11894-020-00770-6.
Participation goals for colorectal cancer (CRC) screening in the USA have not been met. Non-invasive screening strategies may improve CRC screening participation. We highlight recent literature on stool-based screening performance and expectations for emerging non-invasive screening tests.
Stool-based CRC screening detects screen-relevant colorectal neoplasia and outperforms a currently available plasma assay. Though modestly sensitive for CRC, adherence to annual fecal immunochemical testing (FIT) is sub-optimal. Multi-target stool DNA (MT-sDNA) has greater adherence, superior sensitivity for screen-relevant lesions (including those in the proximal colon and sessile serrated architecture), and equivalent specificity to FIT over a 3-year period. Stool-based CRC screening tests are anticipated to reduce the incidence and mortality of CRC through detection of early-stage cancers and high-risk polyps. These endpoints in performance will need to be met by emerging blood sample-based tests in order have meaningful impact in clinical practice.
美国的结直肠癌(CRC)筛查参与率尚未达到目标。非侵入性筛查策略可能会提高 CRC 筛查的参与率。我们重点介绍了最近关于基于粪便的筛查性能以及对新兴非侵入性筛查测试的期望的文献。
基于粪便的 CRC 筛查可检测出与筛查相关的结直肠肿瘤,其性能优于目前可用的血浆检测。尽管粪便免疫化学检测(FIT)对 CRC 的敏感性适中,但对其的依从性并不理想。多靶点粪便 DNA(MT-sDNA)的依从性更高,对与筛查相关的病变(包括近端结肠和无蒂锯齿状结构)的敏感性更高,并且在 3 年期间的特异性与 FIT 相当。通过检测早期癌症和高危息肉,基于粪便的 CRC 筛查测试有望降低 CRC 的发病率和死亡率。为了在临床实践中产生有意义的影响,这些基于血液样本的新兴检测方法需要在性能方面达到这些终点。