The OvaPrint test searches for DNA fragments circulating in the blood that have been methylated at certain nucleic acids.
in cells that can alter the way genes are expressed in the body — and can also be used as a biological marker of disease.
, OvaPrint identifies high-grade serous ovarian carcinoma (HGSOC) when the cancer is new and relatively easy to treat, unlike most existing tests for ovarian cancer. HGSOC is the most common type of ovarian cancer. It is also the most lethal form, in part because clinicians do not have effective ways to screen women for it during the cancer’s early stages, when it’s easiest to treat. For patients with a pelvic mass (an abnormal lump or growth in the lower abdomen), it is difficult to detect whether the growth is benign or cancerous ahead of surgery. Unlike many other
, biopsies are typically not an option. That makes it hard for doctors to choose the best course of treatment.
When ovarian cancer is found in its initial stages, patients have a more than 90 percent chance of living for five years or more. Their chances drop to less than 40 percent if the cancer is detected in advanced stages.”Early detection saves lives,” said Bodour Salhia, co-leader of the Genomic and Epigenomic Regulation Research Programme at University of South California (USC), US.
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“If we can accurately identify early-stage ovarian cancer, we can change the outcome of the disease and really crank up survival rates. In addition, the test has the potential to improve treatment, because the surgical approach to removing a pelvic mass differs depending on whether it’s benign or not,” said Salhia, also an Associate Professor at the Keck School of Medicine at USC. For the study, published in the journal Clinical Cancer Research , the team focused solely on the HGSOC subtype of ovarian cancer in this study, rather than looking at all subtypes at once.
The researchers collected more than 370 tissue and blood samples, comparing samples from patients who had been diagnosed with ovarian cancer in its early stages with samples collected from patients with normal ovaries or benign tumors.
Source: IANS
