A new three-in-one blood test could pave the way to precision-personalised treatment for advanced prostate cancer, say scientists.
The test has the potential to transform the way the disease is tackled by targeting specific gene mutations, it is claimed.
By looking for cancer DNA in blood samples, researchers were able to identify men with defective BRCA genes who were likely to benefit from a class of drugs called Parp inhibitors.
Finally, the same test was used to pick up signs of evolving cancer showing the first signs of drug resistance.
Prof Johann de Bono, who led the team at the Institute of Cancer Research in London, said: “We were able to develop a powerful, three-in-one test that could in future be used to help doctors select treatment, check whether it is working and monitor the cancer in the longer term.
“We think it could be used to make clinical decisions about whether a Parp inhibitor is working within as little as four to eight weeks of starting therapy.
“Not only could the test have a major impact on treatment of prostate cancer, but it could also be adapted to open up the possibility of precision medicine to patients with other types of cancer as well.”
In future, the test could allow the Parp inhibitor olaparib to become a standard treatment for advanced prostate cancer, by targeting those most likely to benefit, picking up early signs that the drug might not be working, and monitoring for emerging resistance.
Parp inhibitors such as olaparib block an enzyme used by cancer cells with defective BRCA 1 and 2 genes to repair their DNA.
When Parp is disabled, the cells die. The drugs do not generally work on cancer cells with functioning BRCA genes, because these are primary DNA repair tools that make Parp unnecessary. While some patients respond to the drugs for years, others either fail to respond at an early stage or develop resistant cancer.
The new test, described in the journal Cancer Discovery, was developed with the help of 49 patients enrolled in TOPARP-A, a Phase II clinical trial investigating the effectiveness of olaparib.
Patients whose cancer DNA blood levels were lowered by olaparib survived an average of 17 months compared with 10.1 months for those whose levels remained high.
The scientists also conducted a detailed investigation of the genetic changes in cancer DNA among men who stopped responding to olaparib. They found that the cells acquired genetic changes that cancelled out the DNA repair defects making them susceptible to the drug.
Prof Paul Workman, chief executive of the Institute of Cancer Research, said: “Blood tests for cancer promise to be truly revolutionary. They are cheap and simple to use, but most importantly, because they aren’t invasive, they can be employed or applied to routinely monitor patients to spot early if treatment is failing – offering patients the best chance of surviving their disease.
“This test is particularly exciting because it is multi-purpose, designed for use both before and after treatment, and using both the absolute amounts of cancer DNA in the bloodstream and also a readout of the specific mutations within that genetic material.
“We believe it can usher in a new era of precision medicine for prostate cancer.”
Each year, around 47,000 men in the UK are diagnosed with prostate cancer and more than 11,000 die from the disease.
Dr Matthew Hobbs, deputy director of research at the charity Prostate Cancer UK, which funded the research, said: “It’s clear that we need to move away from the current one-size-fits-all approach to much more targeted treatment methods.
“The results from this study and others like it are crucial as they give an important understanding of the factors that drive certain prostate cancers, or make them vulnerable to specific treatments.”