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A tumour test could help to identify ovarian cancer patients with predicted poor survival, and down the track inform new therapeutical approaches, the results of a major international collaboration have shown.

The research paper led by UNSW Medicine – involving 125 authors across 86 organizations, including Ï㽶ÊÓƵ of Southern California (USC), Ï㽶ÊÓƵ of Cambridge, Ï㽶ÊÓƵ of British Columbia, Huntsman Cancer Institute (HCI) at the Ï㽶ÊÓƵ of Utah (U of U), Mayo Clinic, and Peter MacCallum Cancer Center in Melbourne – .

In 2020, it is predicted that 21,750 women in the U.S. will be diagnosed with ovarian cancer, and 13,940 will die from the disease, according to the American Cancer Society. Ovarian cancer has poor survival and the type studied in this paper – high grade serous ovarian cancer – is the most common and worst survival type. It is the eighth most commonly occurring cancer in women, with nearly 300,000 global new cases in 2018.

"We conducted an analysis of 3,769 tumour samples from women with ovarian cancer and found we were able to reliably use a piece of tumour to determine how good a woman’s survival chances would be five years after diagnosis," says lead author Professor Susan Ramus from UNSW Medicine.

The researchers found their gene expression test was substantively better at predicting survival than using a patient’s age and cancer stage.

"It has been difficult to identify factors that are associated with ovarian cancer survival beyond age and stage, and this gene expression-based test holds promise to help with stratifying women for more tailored treatments," says , a senior author on the paper. Doherty is a cancer epidemiologist at HCI and associate professor of population health sciences at the U of U.

"When women were divided into five groups, we found that the women whose tumour gene expression was associated with the best prognosis had nine years survival, whereas the women in the poorest survival group have two years survival, which is a very big difference," Professor Ramus says.

"Our vision is that clinicians could use our test at diagnosis to identify the group of patients who wouldn't do well on the current treatments and potentially offer them alternatives – for example, we may be able to put those patients into clinical trials and offer them different treatments that may improve their survival."

For the study, the team used a training set of samples and a test set – nearly 4000 samples in total.

"Using novel statistical approaches, we analysed data from six previous gene expression studies, which helped us identify genes likely to be involved in high grade serous ovarian cancer survival," says the paper’s first author, Joshua Millstein, PhD, from USC.

After putting together a panel of about 500 candidate genes, the team measured gene expression in the 4000 samples using the NanoString platform.

"To predict survival from gene expression, we chose one of four machine learning methods, an approach called "elastic net", which performed the best in the training data," Millstein says.

"We used the training set to determine what genes could be used in the prediction, and then we tested them to see whether we got the same results in the other set," Professor Ramus says.

Professor Ramus is the co-founder of the Ovarian Tumour Tissue Analysis (OTTA) consortium, an international group of researchers that are working on a number of different large-scale projects, using the samples compiled by the consortium to address important clinical questions.

"The consortium is unique in this space because it has access to thousands of samples – which is a lot of samples for a rare disease like ovarian cancer.

"That’s what enabled us to develop this prognostic tool – other groups have tried before to look at prognosis, but nothing has been used clinically. At the moment, only patient age and stage are used to determine survival, so something like our tool is sorely needed."

The researchers say they selected genes for analysis that had known drug targets.

"Some of the genes we identified as being predictors for good or poor survival may be potential targets for new treatments. At the moment the majority of ovarian cancer patients get the same treatment – it's not like breast cancer or other cancers where they look at your tumour and select from a range of treatments. So this is a way to stratify patients and potentially give more personalized treatment down the track."

To validate the findings further, the research team wants to include the test in a prospective study and clinical trials.

"Potentially, we could incorporate it within a clinical trial so that the women who are predicted to have poor survival could get alternative treatments as rapidly as possible."

The researchers hope their test will be ready for clinical use in the near future.

The study is available online and was funded by the National Cancer Institute (NCI), USA. Doherty’s support includes NCI R01CA168758, P30CA250971 and Huntsman Cancer Foundation. A full list of funding for the study authors is available through the .