In case you missed it: Jeffery Scott, MD, chief medical officer of Integra Connect, discussed what role biosimilars will play in a value-based system on a recent podcast episode of Not So Different.
As the healthcare delivery model transitions from a fee-for-service (FFS) model to a value-based model, biosimilars may begin to play a much larger role.
The American healthcare system has largely operated under the FFS model, but a value-based model places more emphasis on cost-saving practices when clinically appropriate and using less-expensive alternatives to branded medications.
In a recent podcast interview broadcast on Not So Different, Jeffery Scott, MD, chief medical officer of Integra Connect, a company that uses cloud-based technologies and services that help specialty care providers optimize their performance in the ongoing shift to value-based models, talked about the future of the value-based system, what’s holding it back, where it’s already working, and what role biosimilars will play in a value-based system.
“The key about value-based contracting would be trying to identify products that offer the best care or in the setting of multiple entities that have similar outcomes, contracting, to drive down the total cost of care by choosing the one that you get a contract on,” Scott said.
A value-based model is already being used in some areas of the healthcare space, most notably Veterans Affairs (VA). Although the VA, like Medicare, is paid for with taxpayer money, the VA is separate and has the ability to negotiate its prices with industry, according to Scott.
“The prices paid to the VA and other DOD, the Department of Defense, facilities are, are not calculated as part of the average selling price. So this would allow the VA to lower cost of care through negotiations since anything that they pay is related to the cost of the drug, not a markup,” Scott said.
According to Scott, a system like the one the VA has would allow physicians to lower out-of-pocket costs for patients. However, several things are holding the value-based system back, with contracts being one of the most prominent.
So far, the value-based system has had very little impact on the oncology space because there are not currently contracts based on value, according to Scott. For example, United Healthcare has signed a deal that forces physicians to use the branded version of pegfilgrastim, Neulasta (which is produced by Amgen).
“And the community, we deal with Part B and D in the Medicare plans,” Scott said. “The Part B Medicare for the injectable drugs sets a market reimbursement at average selling price plus 6%. Short of a change in the Medicare Modernization Act of 2003 or a Medicare waiver, it would be a challenge for any value-based contract.”
According to Scott, any discount provided would impact the rest of the market because it would lower reimbursement, thus taking the ASP lower.
While Scott believes biosimilars have an important role to play in a value-based market, healthcare needs to go beyond biosimilars to provide true savings to the patient.
“When I think of a value-based contract, I think of an opportunity for us not to just lower the acquisition cost to the practice, but commensurate to that, lower the cost that the payer has to pay,” Scott said.
According to Scott, over 60% of the total costs of care come from drugs, most of which are new immunotherapies (IO). IO can have an amazing impact on patients but also contribute to massive growth in cost, he noted.
“Now, across the IO class, multiple drugs appear to be similar. I think there's an opportunity for payers and the IO companies to start to have discussions, for example, that could lead to a preferred choice of therapy and exchange to a lower cost,” Scott said.
“I think if there's a way to maintain the physician margin while lowering the cost of care to the payer, there'll be a lot of interest in that contracts and those types of contracts,” Scott said.
From Amjevita to Zarxio: A Decade of US Biosimilar Approvals
March 6th 2025Since the FDA’s groundbreaking approval of Zarxio in 2015, the US biosimilars market has surged to 67 approvals across 18 originators—though the journey has been anything but smooth, with adoption facing hurdles along the way.
How AI Can Help Address Cost-Related Nonadherence to Biologic, Biosimilar Treatment
March 9th 2025Despite saving billions, biosimilars still account for only a small share of the biologics market—what's standing in the way of broader adoption and how can artificial intelligence (AI) help change that?
Biosimilar Approvals Streamlined With Advanced Statistics Amidst Differing Regulatory Requirements
February 25th 2025The FDA and European Medicines Agency (EMA) mandate high similarity between biosimilars and reference products, but their regulatory processes differ, especially with multiple reference products.
Will the FTC Be More PBM-Friendly Under a Second Trump Administration?
February 23rd 2025On this episode of Not So Different, we explore the Federal Trade Commission’s (FTC) second interim report on pharmacy benefit managers (PBMs) with Joe Wisniewski from Turquoise Health, discussing key issues like preferential reimbursement, drug pricing transparency, biosimilars, shifting regulations, and how a second Trump administration could reshape PBM practices.
Similar Survival, Safety for Bevacizumab Biosimilar vs Originator in Colorectal Cancer
February 8th 2025A retrospective observational study found no significant differences in progression-free survival or safety in patients with colorectal cancers in Japan treated with ABP 215, Amgen’s bevacizumab biosimilar, or reference bevacizumab (Avastin), and estimated cost savings of 800,000 Japanese yen (approximately $5100) per patient with the biosimilar.