A new test for bowel cancer could be on the horizon, according to a study published in the British Journal of Cancer.
The test detects an enzyme, called Tumour M2-PK, which is a by-product of tumour growth. The enzyme leaks from the cancerous tissue into the bowel and can then be found in faeces.
The researchers, based at Giessen University in Germany, found that levels of the enzyme in faeces not only confirmed a diagnosis, but also signalled how advanced the disease was.
The UK Government is currently considering the introduction of a national bowel-screening programme. One of the tests under consideration is the Faecal Occult Blood Test (FOBT), which is a method of detecting blood in the faeces – a symptom of bowel cancer. The researchers hope Tumour M2-PK could offer a better tool to detect the disease.
Previous research estimates that about 1,200 bowel cancer deaths would be prevented each year in England alone if the current FOBT was introduced. There are over 35,000 cases and over 16,000 deaths from bowel cancer every year in the UK.
However, the FOBT cannot distinguish whether the blood in the faeces is caused by a tumour or a minor condition such as piles.
A false positive result can also be caused by certain foods and drinks. Only about six out of every 100 people with a single positive FOBT will have bowel cancer.
This level of false results means that many people who do not have cancer might undergo invasive procedures, such as a colonoscop*(2) , unneccesarily.
The test also fails to pick up all cases of bowel cancer, as not all tumours bleed. Only about 25 – 50 per cent of bowel cancers will be detected by FOBT.
The researchers believe that an additional test for Tumour M2-PK could be key to improving the accuracy of screening. They obtained faecal samples from patients who were to undergo colonoscopies for various reasons.
The sample was taken prior to the procedure and levels of Tumour M2-PK recorded. The colonoscopy established that 60 patients had bowel cancer and 144 did not. The researchers found that the levels of Tumour M2-PK were much higher in the 60 patients with the disease.