Biosimilars included were approved for cancers, hematology, inflammation disorders, and autoimmune disorders, according to the study authors. As of analysis in January 2021, epoetin alfa had 1 biosimilar and the other reference products had at least 2 biosimilars ranging to 5 for trastuzumab. A total of 1.7 million claims were analyzed from 190,364 individuals.
In the first analysis for the trends in annual out-of-pocket cost, investigators used a total of 1.3 claims in the first 4 years before and after biosimilar competition for each drug. However, only filgrastim and infliximab had the full 4 years of post-competition data. For other biosimilars, at least 2 years of data were included. Infliximab was the most common biologic prescribed at 31% of patient-years and epoetin alfa only made up 3% of patient years, according to the study authors.
For approximately 49% of patient-years, patients had an annual out-of-pocket spending of above 0, averaging all 7 drugs, patients with nonzero out-of-pocket costs were greater both before and after biosimilars entered the market. Further, investigators found that patients had a higher mean nonzero annual out-of-pocket cost both before and after biosimilar competition.
Two biologics (rituximab and trastuzumab) were the only drugs that showed significantly lower mean nonzero annual out-of-pocket spending after 2 years of biosimilar competition, according to the study authors. The other drugs were either higher or did not have significant changes.
Key Takeaways
- The study reveals that out-of-pocket costs haven't significantly decreased after biosimilar competition for most drugs. In some cases, costs even increased.
- Only two drugs (rituximab and trastuzumab) showed a decrease in out-of-pocket costs after biosimilars entered the market.
- The study also found that patients using biosimilars were more likely to have some out-of-pocket expense compared to those using the original biologic, although the average cost was slightly lower for biosimilars.
In the second analysis for out-of-pocket costs for biosimilars compared to the reference product, investigators included 586,493 claims for any of the 7 biologics after biosimilars were available. Approximately 25% were a biosimilar, according to the study authors. Overall, investigators found that 28% of the reference biologic claims and 17% of biosimilars has nonzero out-of-pocket costs, but after adjustment, biosimilars were more likely to have nonzero out-of-pocket claims compared to the reference product. The study authors added that there was variation among the 7 drugs, with some claims for the biosimilar more likely to have nonzero out-of-pocket costs (infliximab) and some where the reference product was more likely to have nonzero out-of-pocket claims (bevacizumab).
Furthermore, investigators found that the mean out-of-pocket costs were lower for biosimilars at $707 compared to the reference product at $911, according to the study authors.
Reference
Feng K, Russo M, Maini L, Kesselheim AS, Rome BN. Patient Out-of-Pocket Costs for Biologic Drugs After Biosimilar Competition. JAMA Health Forum. 2024;5(3):e235429. doi:10.1001/jamahealthforum.2023.5429