Analysing a patient’s complete set of genetic material “can transform cancer care” in the NHS by helping doctors provide more personalised treatments, say scientists, following the largest study of its kind.
Combining clinical health data with information gathered from whole-genome sequencing tests – which determine a person’s genetic make-up – can provide cancer patients with tailored care, researchers found.
Precision drugs can target genetic mutations or faults, which often play a key role in the development of cancer.
Knowing details of a patient’s illness as well as their genetic make-up can help clinicians choose the best treatment for patients.
The team looked at data collected from more than 13,000 cancer patients covering more than 30 types of tumours – abnormal masses of tissue – over a five-year period.
It found that more than 90 per cent of brain tumours and over 50 per cent of colon and lung cancers showed genetic changes that could help doctors make key decisions about surgery or specific treatments patients might need.
The data also revealed inherited risks in more than 10 per cent of ovarian cancers, offering crucial insights for clinical care, the researchers said.
“This study shows how we can transform cancer care from a ‘one size fits all’ approach into precision healthcare and defines specific genomic signatures that predict treatment response and outcomes, which may usher in expanded use of whole genomes for cancer care,” Professor Sir Mark Caulfield, vice principal for health at Queen Mary University of London, said.
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The researchers said their work, published in the journal Nature Medicine, supports the increased use of genomic testing in cancer care.
The NHS offers whole-genome sequencing as part of routine care for patients with certain rare diseases and cancer, including all childhood cancers.
Its long-term plan aims to make this more widely available – through the NHS Genomic Medicine Service.
The patients were part of the 100,000 Genomes Project – a groundbreaking initiative launched in the UK with the goal of sequencing and analysing the genomes of 100,000 individuals, including patients with rare diseases and cancer.
A whole genome sequencing test looks at the 3.2 billion letters that make up a person's DNA – but its main focus is to look for changes in genes related to cancer.
This technique is used to compare DNA from a patients’ tumours to the DNA in their healthy tissues, the researchers said.
The study, led by Genomics England, NHS England, Queen Mary University of London, Guy’s and St Thomas’ NHS Foundation Trust and the University of Westminster, was able to identify specific genetic changes in the cancer associated with better – or worse – survival rates.
The researchers said the cost of whole genome sequencing testing is dropping, which in turn, will “influence the type of testing that gets done in NHS”.
The findings are “an important milestone in genomic medicine”, said Dr Nirupa Murugaesu, principal clinician – cancer genomics and clinical studies at Genomics England, and oncology consultant and cancer genomics lead at Guy’s and St Thomas’ NHS Foundation Trust.
“We are showing how cancer genomics can be incorporated into mainstream cancer care across a national health system and the benefits that can bring patients,” she said.
“By collecting long-term clinical data alongside genomic data, the study has created a first-of-its-kind resource for clinicians to better predict outcomes and tailor treatments, which will allow them to inform, prepare, and manage the expectations of patients more effectively.”
“This groundbreaking research demonstrates the power of genomics and is already helping to transform care, allowing patients to receive more tailored treatment and driving improved diagnosis,” Health Minister Andrew Stephenson said.
“But we won’t stop there. We want to harness this innovation to improve care for patients and affirm our position as a life sciences superpower – leading to quicker and more targeted interventions.”