A dramatic breakthrough in breast cancer research will lead to a revolution in the way the disease will be diagnosed and treated in years to come, leading cancer specialists said yesterday.
Researchers have discovered that breast cancer patients can be subdivided into ten different groups each with a unique genetic fingerprint that will determine the type of drugs and treatment that could lead to a cure.
Instead of looking at breast cancer as a single disease with a limited number of treatments, the scientists believe that it is now more accurate to view it as a range of illnesses with a wide variety of potential therapies that can be tailored to individual patients.
The discovery was made by analysing the tumours of some 2,000 women with breast cancer in a large Anglo-Canadian research effort, the biggest so far into understanding the genetics of a disease that kills nearly 12,000 people a year in Britain alone.
The study has also identified several new genes that are implicated in triggering or controlling breast cancer, which the scientists believe will become valuable targets for the development of novel anti-cancer drugs.
Harpal Kumar, chief executive of the charity Cancer Research UK, said that the landmark study will change the way clinical trials on new drugs and treatments are undertaken now that the complexities of the disease are more accurately understood.
“This in the years to come will have an enormous impact in the way we think about both diagnosing and treating women with breast cancer, and that should enable us to contine the progress we’ve made in breast cancer over the past 25 years,” Dr Kumar said.
The study, published in the journal Nature, involved more than a dozen research centres in Britain, Canada and Norway.
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