Pharmacists will have the opportunity to use their knowledge of biosimilars to reinforce their benefits, safety, and efficacy.
This article was originally published on Pharmacy Times®. This version has been edited. To read the full article, click here.
Rheumatoid arthritis (RA), an autoimmune inflammatory disease that attacks the synovial tissues in the joints, is the most common form of autoimmune arthritis, affecting 1.3 million people in the United States.1 Rheumatologists often employ disease-modifying anti-rheumatic drugs (DMARDs) to slow disease progression, but many patients have an incomplete response. For those people, biologic DMARDs are usually prescribed, but these drugs are too costly for many, putting optimal disease management out of reach for this population.2
To meet the need for more affordable biologIcs, biosimilar DMARDs were developed, reducing costs to allow more patients to access these critical therapies. So far, 4 biosimilars for the RA reference product Remicade have received FDA approval, but only 3 are currently available on the US market: Inflectra, Renflexis, and Avolsa.4
Although these medications have no clinically meaningful differences with their reference biologics and offer significant cost advantages, adoption of these products by rheumatologists has been slow.5 Educating providers and patients about the biosimilar approval process could decrease patient resistance and increase the likelihood of rheumatologists embracing biosimilars.
Several more RA biosimilars will be released soon, and stakeholders remain cautiously optimistic. The impact of these biosimilars could be massive, both in terms of cost savings and health outcomes, so it is worthwhile to examine how pharmacists can help overcome obstacles blocking the uptake of these life-changing therapies.
Education is key to acceptance
Both rheumatologists and patients have been slow to accept biosimilars due to the lack of awareness around the biosimilar streamlined approval process. Providers may not know that biosimilars have no clinically meaningful differences from the original product, which may lead to concerns that biosimilars might not be as effective or safe as brand products.
Patients also have concerns, especially if they switch to a biosimilar from a drug they have taken for a long time. Often when this happens, the nocebo effect comes into play. This is when adverse effects (AEs) or symptoms are experienced with a drug just because the patient believes they may occur.9
These symptoms may not actually materialize because the treatment is not working, but the patient believes that is what is happening. In other specialties like oncology, this situation is not as big an issue because the provider can use scans and lab tests to verify what is actually happening, but rheumatologists usually rely on qualitative factors, such as asking the patient about pain level or range of motion.
This is discouraging to rheumatologists, as these patients strongly believe they have experienced treatment failure with the biosimilar. Some patients may also refuse to even try a biosimilar because they do not understand the drug is highly similar to the more expensive brand product with no clinically meaningful differences in the safety and efficacy.
Pharmacists can lead the way
The public has a high level of trust in pharmacists, as demonstrated by more than 30 years of polling from Gallup, which for decades has placed pharmacists among the most trusted professions.10 Consequently, pharmacists can play a key role with helping rheumatologists and patients understand and accept the new RA biosimilars entering the market.
Pharmacists will have the opportunity to use their knowledge of biosimilars to reinforce their benefits, safety, and efficacy. Rather than just telling patients they will be getting a product similar to what they had in the past, the pharmacist can explain in detail they will be receiving a product just as clinically safe and effective as the one they have been taking, and it will actually cost less than the brand product. Additionally, they will be able to answer any questions that may arise.
The pharmacist’s skill set is tailor-made for the roll out of products such as biosimilars, and there is little doubt they can do a fantastic job of getting providers and patients on board with these complex products. Pharmacists have been tackling problems like this for years and have a proven track record of affecting change.
For example, when generics were launched in the late 1990s, there was a high level of patient distrust around their use. Pharmacists were able to educate patients to the point where today when patients fill a prescription, many request a generic. If history is any indication, pharmacists will be able to achieve comparable results with biosimilars.
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References
AAM Report: Generics and Biosimilars Savings Reach $445 Billion in 2023, Part 1
September 18th 2024Savings from generic and biosimilar drugs totaled $445 billion in 2023, showing promise for the growth of both markets and highlighting the success of expansion policies for these products, according to a new report from the Association for Accessible Medicines (AAM).
Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
Real-World Study Shows Comparable Outcomes Between CT-P13, Remicade in RA
September 14th 2024A real-world study of the biosimilar infliximab-dyyb (CT-P13; Inflectra) in rheumatoid arthritis (RA) reported the majority of patients who initiated CT-P13 switched from the reference product (Remicade) or another biologic or targeted synthetic disease-modifying antirheumatic drug.
Breaking Barriers in Osteoporosis Care: New Denosumab Biosimilars Wyost, Jubbonti Approved
June 16th 2024In this episode, The Center for Biosimilars® delves into the FDA approval of the first denosumab biosimilars, Wyost and Jubbonti (denosumab-bbdz), and discuss their potential to revolutionize osteoporosis treatment with expert insights from 2 rheumatologists.
Survey of Clinicians: Lower Cost of Biosimilars Is the Main Driver of Treatment Choice in IBD
September 7th 2024Researchers surveyed clinicians from 63 countries and found that adalimumab and infliximab biosimilars, primarily chosen for their lower cost, are widely available and have improved access to biologic treatment in inflammatory bowel disease (IBD).
Switching From Originator Etanercept to Biosimilar Version Proves Safe, Effective in RA
September 5th 2024Patients with rheumatoid arthritis who switched from the etanercept originator to a biosimilar exhibited similar disease activity and drug persistence compared with those who remained on the originator, indicating that nonmedical switching does not negatively impact treatment outcomes.