Discovery Revives Abandoned Breast Cancer Therapy

Lund University

A new study led by Lund University in Sweden has solved a years-old mystery: which patients with aggressive breast cancer are helped by a targeted cancer treatment that had been under development but was shelved. The study is important since it brings hope that the development of the drug can continue and that it will make it all the way to these patients.

Despite the efforts of the North American researchers, many years of research and development and millions of dollars spent, a medicine named ganitumab that had shown promising results against breast cancer in animal trials was shelved. The drug was also clinically tested, but in spite of some success, the question of which breast cancer patients were helped by the treatment remained unanswered.

When developing new cancer therapies, it is often the case that not all patients with the same disease are helped by the same treatment. That is why clear diagnostic markers are needed. It was not possible, however, to find clear indicators that could show healthcare professionals which individuals actually benefitted from the treatment. The medicine blocks a receptor (IGFIR) on the tumour which, when activated, can lead to the tumour growing and spreading.

"It was a great disappointment to many of us in the field. We saw clear results in pre-clinical trials, but when we looked at entire patient cohorts it was not possible to draw firm conclusions. So, when I saw the results from the research group in Sweden, whose analysis came up with the answer as to which marker identified those who benefited from the drug, I was very pleasantly surprised," says Michael Pollak, professor at McGill University in Canada and one of the co-authors of the study.

Fortunately, the researchers in the USA had made all their data from the I-SPY2 trial available - perhaps other researchers would be able to solve the problem?

Christopher Godina, a post-doctoral researcher at Lund University and a junior doctor at Skåne University Hospital, was drawn to all the data collected after the clinical trials in Sweden and Canada. In the clinical studies, patients had been given the new drug before surgical treatment for breast cancer, but Christopher Godina looked at the data from a new perspective.

He mapped out the way in which various genes are expressed in the tumours and the ongoing processes around the cancerous tumour and compared this with patient outcomes. This involves advanced bioinformatics calculations, combining biology, computer science and mathematics to analyse biological data, focussing here on genetic, molecular and clinical data.

The aim was to see if it was possible to find any marker that the patients who were helped by the treatment had in common. Surprisingly, it did not matter whether or not the tumour had the receptor the medicine is supposed to block on the cell surface.

"We found a biomarker, IGFBP7, that helps us to show which patients may benefit from this treatment. In the group with lowest levels of the marker, almost 50 per cent (in 15 out of 32 patients) of aggressive tumours disappeared completely before surgery and 66 per cent of the most aggressive triple negative tumours disappeared (in 12 out of 18 patients). This was certainly not the biomarker we expected to provide the answer, and that might be why the riddle hasn't been solved before," says Christopher Godina, first author of the study.

The result was surprising. Previously, it was thought that tumours which contained a lot of this particular protein, IGFBP7, could be treated with the medicine. The reverse turned out to be true: the drug is effective for those whose tumours contained little of the protein. The study, recently published in the scientific journal NPJ Precision Oncology, shows that it is possible to identify the group of patients who will be helped by the treatment.

"A quarter of all patients with aggressive breast cancer may benefit from the treatment. The discovery is potentially something of a breakthrough after several unsuccessful attempts to show which patients benefit from this treatment," says Helena Jernström, professor at Lund University and one of the researchers behind the study. It is also possible that patients with types of cancer other than breast cancer may be helped by the medicine.

The researchers say that this result demonstrates the value of open data. If the American researchers had not made their results available, it would have been difficult to solve the mystery.

"In this case, it was possible for others to analyse the results and see if they could find something that the earlier researchers had missed. So, it all stems from their openness. We hope that this will now lead the drug companies that have shelved this medicine for cancer treatment to resume its development," concludes Christopher Godina.

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