The research, published in the journal Nature Genetics, in the future aims to enable the prediction of the trajectory of tumour growth in patients, allowing clinicians to pre-empt disease course and tailor treatment regimens accordingly.
The model was developed in collaboration with researchers from Barts Cancer Institute’s Centre for Tumour Biology, led by Professor Trevor Graham, the Institute of Cancer research, led by Dr Andrea Sottoriva, and University College London, led by Dr Chris Barnes.
Professor Graham from Queen Mary’s Barts Cancer Institute said: “Forecasting of the future offers a real opportunity for clinical benefit that is based on anticipatory action.
“It would be a great advantage to know if a tumour is going to change in a certain way and so be able to administer the most effective treatment in light of the prediction. This work is in its infancy, and the possibilities that this research may have as it matures are very exciting.”
As tumours grow and become more advanced, different mutations – changes to the genetic code – occur in different cancer cells. Some of these changes may confer an advantage for the cell, making it more suited to survive in its environment. Following the principles of Darwin’s theory of Evolution, such cells will be favoured and able to replicate, creating more cells with the same mutation. In this way, different populations of cells with different mutations build up, creating tumours that are highly genetically diverse.
Although it is known that such changes take place as cancer develops, knowing exactly what changes occur and when has proven difficult as tumour samples are often only analysed in the laboratory after they are large enough to be detected in a patient. Therefore, the history of how tumours grow has remained invisible to researchers. The present study, majoritively funded by The Wellcome Trust, endeavoured to fill in this missing history.
By interpreting the genetic sequences of tumour cells, the computer system is able to read the ‘secret diary’ of mutations hidden in the genome, learning how the cancer has changed over time. Notably, the study revealed that mutations acquired by cells that drive the progression of cancer – known as driver mutations – allow the cells to grow up to 30 per cent faster in some cases than cells without the mutation.
The computer system used this genetic information with defined algorithms to predict future changes that may occur as the cancer continues to evolve.
How a cancer changes over time underlies a patient’s prognosis, as such changes may determine response to treatment. This study, also supported by Cancer Research UK, makes steps towards the ‘mechanistic forecasting’ of future disease course and offers great potential for personalised medicine.
Before this research can become a clinical reality, the team first need to verify that the predictions of the system are correct by testing it in pre-clinical models and analysing tumour samples of patients that are under long-term surveillance.
Mr Marc Williams, first author of the paper, added: “We are measuring changes that occur in cancer that have proven difficult to quantify. Such changes may be important in the evolutionary dynamics of individual cancers. Hopefully with these kinds of measurements we will be able to make important predictions of what the future evolutionary trajectory of cancer could be. This is the long-term aim.”
Source: Queen Mary University of London