video: A brief introduction of our study, ctDNA methylation in colorectal cancer. This material relates to a paper that appeared in the Jan. 1, 2020, issue of Science Translational Medicine, published by AAAS. The paper, by H. Luo at Collaborative Innovation Center for Cancer Medicine in Guangzhou, P.R. China; and colleagues was titled, "Circulating tumor DNA methylation profiles enable early diagnosis, prognosis prediction, and screening for colorectal cancer."
A new machine learning platform can identify patients with colorectal cancer and helps predict their disease severity and survival, according to a study involving samples from thousands of subjects. The noninvasive method adds to recent advances in technologies that analyze circulating tumor DNA (ctDNA) and could help spot colorectal cancers in at-risk patients at earlier stages. Like many other malignancies, colorectal cancers are most treatable if they are detected before they have metastasized to other tissues. Colonoscopies are the "gold standard" for diagnosis, but they are uncomfortable and invasive and can lead to complications, which leaves patients less willing to undergo screening. Huiyan Luo and colleagues leveraged machine learning techniques to develop a less invasive diagnostic method that can detect colorectal cancer in at-risk patients. Their technology works by screening for methylation markers, which are DNA modifications that are frequently found in tumors. The scientists first created a diagnostic model based on nine methylation markers associated with colorectal cancer, which they identified by studying plasma samples from 801 patients with colorectal cancer as well as 1,021 controls. This model accurately distinguished patients from healthy individuals with a sensitivity and specificity of 87.5% and 89.9%, respectively, and outperformed a clinically available blood test named CEA. Furthermore, a modified prognostic model helped predict the patients' risk of death over a follow-up period of 26.6 months on average, especially when combined with established clinical characteristics such as tumor location. One methylation marker was particularly useful, as screening for it alone spotted cases of colorectal cancer and precancerous lesions in a prospective study of 1,493 at-risk individuals. Luo et al. conclude that studies with longer follow-up periods will be needed to further assess their model's reliability for clinicians and patients.