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A Revolutionary Blood Test Offers Hope in Colorectal Cancer Screening

Written by Andrew Le, MD

UpdatedApril 11, 2024

A groundbreaking study published by the New England Journal of Medicine unveils a cell-free DNA blood-based test that could potentially transform the current approach to colorectal cancer screening. Colorectal cancer, the third most common cancer affecting U.S. adults, boasts a high cure rate when detected early. However, screening adherence has been a stumbling block, with over a third of adults falling behind recommended testing schedules. This novel blood test could increase screening compliance and ultimately save lives by catching cancer sooner.

Experts including Daniel C. Chung, M.D., and a team of venerable colleagues, evaluated the test within a group deemed eligible for colorectal cancer screening. Screening effectively reduces colorectal cancer incidence and mortality, but current methods often dissuade individuals from participating regularly due to various barriers such as fear of invasive procedures and access to care.

The study, named the ECLIPSE (Evaluation of the ctDNA LUNAR Test in an Average Patient Screening Episode), assessed over 10,000 individuals. The results were promising: an 83.1% sensitivity in detecting colorectal cancer and a 89.6% specificity in identifying advanced neoplasia, which includes both colorectal cancer and serious pre-cancerous lesions. Early-stage cancers, which are most crucial to identify for treatment efficacy, showed even higher sensitivity rates.

While this new test highlights an encouraging advancement in non-invasive screening, it's important to note a lower sensitivity of 13.2% for advanced precancerous lesions. Unlike direct visualization methods like colonoscopies that can detect and remove these lesions, the blood test's ability to identify them remains limited. Despite this, the test offers an additional, more accessible, and potentially less intimidating option for colorectal cancer screening. It represents a meaningful stride in public health, potentially encouraging wider screening participation.

The study sample reflected a diverse demographic and took place across various U.S. sites, suggesting promising implications for widespread implementation. With FDA benchmarks for colorectal cancer sensitivity and advanced neoplasia specificity surpassed, this blood-based test shows potential for substantial impact on early detection and prevention efforts.

A broader adherence to colorectal cancer screenings, fostered by this simple blood test, could lead to earlier detection, more effective treatments, and ultimately, a decrease in colorectal cancer mortality. As the medical community awaits further research to assess the real-world effectiveness, and economic implications of this novel method, the study's findings offer a beacon of hope in the fight against colorectal cancer.

Discover more about this transformative breakthrough in colorectal cancer screening by accessing the full article from the New England Journal of Medicine at https://www.nejm.org/doi/full/10.1056/NEJMoa2304714.

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References

Chung, D. C., Gray II, D. M., Singh, H., Issaka, R. B., Raymond, V. M., Eagle, C., Hu, S., Chudova, D. I., Talasaz, A. A., Greenson, J. K., Sinicrope, F. A., Gupta, S., & Grady, W. M. (2024). A Cell-free DNA Blood-Based Test for Colorectal Cancer Screening. The New England Journal of Medicine, 390(11), 973-983. https://doi.org/10.1056/NEJMoa2304714