New blood test can identify multiple types of cancer

Washington: A new kind of blood test has been developed by researchers which is capable of screening multiple types of cancer.

Moreover, it has a high degree of accuracy, according to the results presented at the European Society for Medical Oncology (ESMO) 2109 Congress.

The test, developed by GRAIL Inc., uses next-generation sequencing technology to probe DNA for tiny chemical tags (methylation) that influence whether genes are active or inactive.

When applied to nearly 3,600 blood samples – some from patients with cancer, some from people who had not been diagnosed with cancer at the time of the blood draw – the test successfully picked up a cancer signal from the cancer patient samples, and correctly identified the tissue from where cancer began (the tissue of origin).

The test’s specificity – its ability to return a positive result only when cancer is actually present – was high, as was its ability to pinpoint the organ or tissue of origin, researchers found.

The new test looks for DNA, which cancer cells shed into the bloodstream when they die. In contrast to “liquid biopsies,” which detect genetic mutations or other cancer-related alterations in DNA, the technology focuses on modifications to DNA known as methyl groups.

Methyl groups are chemical units that can be attached to DNA, in a process called methylation, to control which genes are “on” and which are “off.”
Abnormal patterns of methylation turn out to be, in many cases, more indicative of cancer – and cancer type – than mutations are.

The new test zeroes in on portions of the genome where abnormal methylation patterns are found in cancer cells.

“Our previous work indicated that methylation-based assays outperform traditional DNA-sequencing approaches to detecting multiple forms of cancer in blood samples,” said the study’s lead author, Geoffrey Oxnard, MD, of Dana-Farber.

In the study, investigators analyzed cell-free DNA (DNA that had once been confined to cells but had entered the bloodstream upon the cells’ death) in 3,583 blood samples, including 1,530 from patients diagnosed with cancer and 2,053 from people without cancer.

The patient samples comprised more than 20 types of cancer, including hormone receptor-negative breast, colorectal, esophageal, gallbladder, gastric, head and neck, lung, lymphoid leukemia, multiple myeloma, ovarian, and pancreatic cancer.

The overall specificity was 99.4 per cent, meaning only 0.6 per cent of the results incorrectly indicated that cancer was present.

The sensitivity of the assay for detecting pre-specified high mortality cancer (the per cent of blood samples from these patients that tested positive for cancer) was 76 per cent.

Within this group, the sensitivity was 32 per cent for patients with stage I cancer; 76 per cent for those with stage II; 85 per cent for stage III; and 93 per cent for stage IV.

Sensitivity across all cancer types was 55 per cent, with similar increases in detection by stage. For the 97 per cent of samples that returned a tissue of origin result, the test correctly identified the organ or tissue of origin in 89 per cent of cases.