Michael Savin, MD
The path of biosimilars in oncology has been challenging, explained Michael Savin, MD, adding that although clinical trials for these agents are extensive and expensive to run, it will lead to more cost-effective measures in the field going forward.
, Savin discussed the emergence of biosimilars in oncology, and why there are still obstacles with incorporating them into clinical practice.
OncLive: What are your thoughts on the wave of biosimilars?
: It is an interesting field. It's been hard to get practicing oncologists engaged with it over the years, but that's changing now. We are getting to be more experienced with biosimilars; there has also been so much progress in seeing “me too” kind of drugs that actually are highly effective. Therefore, we are becoming more and more comfortable with the concept of a biosimilar—not just molecularly similar, but a biosimilar agent that targets pathways.
Part of the problem was that a few years ago when we were doing this, we didn't understand these pathways at all. We knew there were hormone receptors and we had a notion of how they drove the cells, but we didn’t have it at the level that we do now.
Can you highlight the early research with biosimilars that you were a part of?
That particular agent was a colon cancer biosimilar, and it turned out that it was made by the manufacturers who actually made the brand of drug used in this country, but we couldn’t get it going. Boehringer Ingelheim was the manufacturer. The drug was a receptor-blocking agent and we got this study going, but we didn’t accrue to it very well.
The Europeans are way ahead of us on this; they have been using biosimilars for a long time. They are more cost-driven than we are, and in a way that helps. Twenty or 30 years ago, tamoxifen was a very expensive drug, and a very expensive drug then was defined as 0 or 0 a month. Now, we prescribe drugs that are thousands of dollars or tens of thousands of dollars a month, and we’re bankrupting ourselves in the process. We are accomplishing wonderful things, but at enormous costs. We have to be cognizant of those costs and try to figure out how to reign them in. Biosimilars may be one of the tools.
Now that we are gaining more knowledge and experience with biosimilars, is the research driven by the desire to bring down those costs?
We are looking at trying to get more and more agents. We kind of jokingly talk about “me too” drugs and say, “Well this company has come out with something that kind of does the same thing.” On the other hand, you can look at this and say, ultimately, this may be a cost-control measure, even if it doesn’t start out that way.
There are several trastuzumab biosimilars in development. If they all get approved, do you sort of have to pick the best version?
It’s a tough question, and that is where a lot of the resistance comes from: how you see the data. What you worry about is not that it’ll hit the correct target or that kind of thing, what you worry about is that the dynamics or interactions with that target may be different. You know the degree to which it binds to the target and how easily it can come off of the target. However, will it work better than the agent we already have that does work?
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