作者
David Haan,Anna Bergamaschi,Verena Friedl,Gulfem D. Guler,Yuhong Ning,Roman E. Reggiardo,Michael Kesling,Micah Collins,Bill Gibb,Kyle Hazen,Steven Bates,Michael Antoine,Carolina Fraire,Vanessa Lopez,Roger Malta,Maryam Nabiyouni,Albert Nguyen,Tierney Phillips,Michael A. Riviere,Anna Leighton,Christopher K. Ellison,Erin McCarthy,Aaron Scott,Lauren Gigliotti,Eric Nilson,Judith Sheard,Melissa Peters,Kelly Bethel,Shimul Chowdhury,Wayne Volkmuth,Samuel Levy
摘要
Early detection of pancreatic cancer (PaC) can drastically improve survival rates. Approximately 25% of subjects with PaC have type 2 diabetes diagnosed within 3 years prior to the PaC diagnosis, suggesting that subjects with type 2 diabetes are at high risk of occult PaC. We have developed an early-detection PaC test, based on changes in 5-hydroxymethylcytosine (5hmC) signals in cell-free DNA from plasma.Blood was collected from 132 subjects with PaC and 528 noncancer subjects to generate epigenomic and genomic feature sets yielding a predictive PaC signal algorithm. The algorithm was validated in a blinded cohort composed of 102 subjects with PaC, 2048 noncancer subjects, and 1524 subjects with non-PaCs.5hmC differential profiling and additional genomic features enabled the development of a machine learning algorithm capable of distinguishing subjects with PaC from noncancer subjects with high specificity and sensitivity. The algorithm was validated with a sensitivity for early-stage (stage I/II) PaC of 68.3% (95% confidence interval [CI], 51.9%-81.9%) and an overall specificity of 96.9% (95% CI, 96.1%-97.7%).The PaC detection test showed robust early-stage detection of PaC signal in the studied cohorts with varying type 2 diabetes status. This assay merits further clinical validation for the early detection of PaC in high-risk individuals.