A new test could pick out women with advanced breast cancer who are likely to benefit from an exciting new targeted therapy for more than a year.
Analysing levels of a molecule called cyclin E1 in tumour biopsies could be used to guide breast cancer treatment – helping delay chemotherapy for some women and ensuring others are closely monitored for any signs of progression.
Researchers found that testing for cyclin E1 could predict the chances of a year or more of successful treatment with a drug called palbociclib – a drug hailed by doctors as the biggest advance in breast cancer treatment for 20 years.
Palbociclib targets weaknesses in cancer cells specifically, and so has far fewer side-effects than conventional chemotherapy – allowing women to live well with their cancer.
It comes as NICE last week recommended the use of palbociclib on the NHS through the Cancer Drugs Fund, for women with advanced oestrogen receptor-positive breast cancer who have received hormone therapy.
Hormone therapy works against around 70 per cent of breast cancers and is one of the most common first treatments for people with advanced breast cancer – so the new approval could significantly increase the number of women who can benefit from palbociclib on the NHS.
The study by the team at The Institute of Cancer Research, London, and The Royal Marsden NHS Foundation Trust, showed that women with low levels of cyclin E1 in their tumours responded to palbociclib given in combination with hormone treatment for nearly twice as long as women with high levels.
Following her initial breast cancer diagnosis and successful treatment in 2012, Christine was shocked to discover that her cancer had spread to her brain in 2018. Thanks to palbociclib, Christine is now living well with cancer, including a new-found passion for cycling.
Exciting new targeted therapy
The study found that the combination of palbociclib and hormone treatment had some benefit for women irrespective of their test results, delaying the need for chemotherapy for at least three months, even in the shortest responders.
But the researchers suggest that women with higher levels of cyclin E1 in their tumours should be monitored especially closely, since they can be expected to stop responding much more quickly than others.
Researchers in the Breast Cancer Now Toby Robins Research Centre at The Institute of Cancer Research (ICR) looked at tumour samples from two different trials involving palbociclib – 302 patients from PALOMA-3, a trial which assessed the drug in combination with hormone therapy for advanced cancer, and the POP trial which looked at palbociclib used on its own before surgery in 61 patients with breast cancers that hadn’t yet spread.
In the PALOMA-3 trial, women with low levels of cyclin E1 responded to combination treatment for an average of 14.1 months before their tumour started growing again, compared with only 7.6 months in women with high levels, and 4 months among those who received a placebo plus hormone therapy.
In the POP trial, palbociclib treatment stopped the tumour growing in 80 per cent of women if low levels of cyclin E1 were present, whereas palbociclib only stopped the tumour growing in 36 per cent of women it high levels of cyclin E1 were present.
Importance of biopsies to guide treatment
Strategies to overcome cancer’s lethal ability to survive and resist treatment are a major focus by researchers at the ICR, who are poised to outsmart cancer with the world’s first anti-evolution ‘Darwinian’ drug discovery programme.
To facilitate this, the research institution is constructing a £75 million state of the art building – the Centre for Cancer Drug Discovery. It will house a series of pioneering projects to deliver long-term control and effective cures, just as comparable approaches have achieved with HIV.
Palbociclib targets two proteins called CDK4 and CDK6 that are involved in a series of checks that control when a cell can replicate its DNA. By blocking these two proteins from doing their jobs, cancer cells can’t multiply.
Cyclin E1 is also involved in the checkpoints that dictate when a cell can multiply, and the researchers hypothesise that high levels of cyclin E1 allow cells to bypass other checks and keep multiplying, uncontrolled.
Previous studies hadn’t been able to identify a marker which indicated how successful palbociclib would be, or to spot resistance arising, so the team widened the search and analysed the activity of 2,534 different cancer-related genes.
Cyclin E1 appeared to be the most significant predictive indicator of how a patient will respond to palbociclib, and they identified possible others including associated protein CDK2.
Interestingly, the effect of cyclin E1 on treatment response was stronger in biopsies from metastatic tumours than primary tumour biopsies taken at diagnosis.
The difference highlights the importance of taking biopsies of recurrent breast cancer to guide treatment as tumours evolve to become drug resistant.
Although the researchers show cyclin E1 is an indicator of response to palbociclib in two different treatment settings, it will still need to be validated as a test to guide treatment in clinical trials designed specifically to assess its success.
‘Delaying the need for chemotherapy’
Professor Nicholas Turner, Professor of Molecular Oncology at The Institute of Cancer Research, London, and Consultant Medical Oncologist at The Royal Marsden NHS Foundation Trust, said:
“Palbociclib is a targeted drug that allows women to live a normal life for longer – but when their cancer evolves and develops resistance, they can stop responding to the treatment.
“We’ve developed a way of identifying which women with advanced breast cancer stand to benefit for more than a year from the targeted treatment palbociclib, and which are likely to stop responding much more quickly.
“Nearly all the women on the PALOMA-3 trial benefited from the drug for at least a few months, delaying the need for chemotherapy. But some women will progress more quickly, and may require additional monitoring so we can switch treatments as soon as the drug stops working.
“We validated our findings using data from a second trial, but we will need to assess our test further to see how effectively it can guide treatment before it could start to be used routinely in patients.”
‘I take my pill and I get on with my life’
Christine O’Connell, 46, from south-west London, was diagnosed with secondary breast cancer in February 2018. She said:
“I have seen first-hand the difference a targeted treatment can make. I’m on the 19th cycle of palbociclib and my cancer is currently stable. I take my pill every morning, and I get on with my life. I still cycle 3-4 times a week, which I could never have done had I been on conventional therapy.
“Palbociclib allows me to live a good life with cancer – and I want all cancer patients to have this hope and optimism for the future.”
Professor Paul Workman, Chief Executive of The Institute of Cancer Research, London, said:
“At the ICR, we believe precision cancer medicine should be driven by a test for every treatment – ensuring that only patients who are likely to benefit from a drug are treated with it, and that patients who are likely to quickly relapse are closely monitored for signs of resistance.
“Our researchers have developed a test which could ensure the exciting new drug palbociclib is used more effectively in the clinic, and that where necessary women can be moved promptly from it onto alternative treatments.
“This kind of targeted, test-driven approach can reduce costs for the NHS, improve quality of life for patients and spare some people treatment that will not benefit them or which has stopped working.”