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Medicine Matters oncology

So my name is Dr. Maha Hussain, I am a medical oncologist and Professor of Medicine, Deputy Director for the Robert H. Lurie Comprehensive Cancer Center at Northwestern Medicine in Chicago. I am delighted to be here to present the results of PROfound, which is a randomized phase III clinical trial evaluating olaparib compared to a standard hormonal agent, such as abiraterone, prednisone, or enzalutamide in men with metastatic castration resistant prostate cancer and whose tumors harbor DNA repair damage response defects.



PROfound is the first biomarker preselected trial applying precision medicine therapy in prostate cancer. And we are hoping for even more progress in the field.



What proportion of men do these results apply to?

I'm going to say, in general, from practicality as it relates to the positivity of the genes and eligibility and what have you, I'm going to say somewhere about the 25% to 30% of men will be eligible for these treatments.



How easy is it to assess the presence of these defects?

A lot of these assays are routine now, however, it's going to depend on which country is the assay approved for, and what the agency, like the FDA, requires in terms of companion diagnostic. So for example, right now we go to with Tempus, Foundation, and so on if we're trying to screen patients for genomics. And then use the findings to actually prescribe a drug recognizing fully that in prostate cancer, none of these drugs are approved by say, in the US, by the FDA, and I'm sure the European agency, same story. So it's going to be driven by what they will-- what companion diagnostic will be. My guess is that the Foundation Medicine is going to be the assay that they will tie it to.



Does liquid biopsy have a role in detecting these alterations?

I think liquid biopsy is emerging as a very promising technology. I have to say, I'm a bit conservative. I would like to see a prospective validation of at least, I'm not going to say equivalence, but comparability, and more important outcomes. So not just that it matches, but that actually what you're measuring, and you're pre-selecting patients for based on when you test it prospectively, it's translating to potential benefits.