Posted by Kate Murphy on February 20th, 2008
Scientists have developed and validated a blood test for ovarian cancer that is more than 95 percent accurate in finding the disease.
Using a panel of six biomarkers, the team was able to identify ovarian cancer in 95.3 percent of women who had recently been diagnosed with the disease. None of the healthy controls were positive for the combination marker panel.
Ovarian cancer is a particularly deadly disease since it is hard to recognize and diagnose early when it is most curable. In 2007, 22,430 women will be diagnosed with ovarian cancer and 15,280 will die. A simple screening test for early detection would save many lives.
The assay tested for concentrations of leptin, prolactin, osteopontin, insulin-like growth factor II, macrophage inhibitory factor, and CA-125. Although CA-125 is currently used as a test for ovarian cancer, it is not as accurate as the six-marker panel. None of the biomarkers individually effectively diagnosed cancer, but used together they were both very sensitive in finding cancer and specific in not leading to false positive results.
The research team at the Yale School of Medicine wrote,
We describe the first blood biomarker test with a sensitivity of 95.3% and a specificity of 99.4% for the detection of ovarian cancer. Six markers provided a significant improvement over CA-125 alone for ovarian cancer detection. Validation was performed with a blinded cohort. This novel multiplex platform has the potential for efficient screening in patients who are at high risk for ovarian cancer.
Further testing involving over 2000 women is now underway.
Women who have a genetic mutation for colorectal and related cancers known as Lynch syndrome or HNPCC have about a 10 to 12 percent risk of developing ovarian cancer during their lifetimes.
SOURCE: Visintin et al. Clinical Cancer Research, Volume 14, Issue 4, February 15, 2008.
An additional article by Peter M. Crosta about the study appears online in Medical News Today.