The Psoriasis Stratification to Optimize Relevant Therapy (PSORT) study assessed real-world levels of self-reported non-adherence to traditional systemic and biologic therapies used for psoriasis, and evaluated psychological and biomedical factors associated with non-adherence using multivariable analyses.
Conventional systemic and biologic therapies are highly effective in the treatment of moderate to severe psoriasis; however, treatment effectiveness is much lower in routine clinical practice than in clinical trials. Medication non-adherence is a missed opportunity for therapeutic benefit. Although patients go to their doctors for assistance in treating their symptoms, according to the study, approximately half of medications are not taken as prescribed.
This study, Psoriasis Stratification to Optimize Relevant Therapy (PSORT), assessed real-world levels of self-reported non-adherence to traditional systemic and biologic therapies used for psoriasis, and evaluated psychological and biomedical factors associated with non-adherence using multivariable analyses. Researchers defined non-adherence as either being intentional, in which patients knowingly make the decision not to follow the prescribed medication regimen, or unintentional, such as forgetting to take the medication. Of the 811 patients included in the study, 617 self-administered systemic therapy, and 22.4% were classified as non-adherent (12% intentionally, 10.9% unintentionally).
In the traditional systemic treatment group, (35.3%; n = 286), methotrexate was the most common treatment product (52%; n = 141). In the biologic treatement group, (64.7%, n = 525) adalimumab was the most common prescribed biologic (52.5%, n= 258), followed by ustekinumab (32.6%; n = 160) and etanercept (14.9%; n = 73). A significant proportion of patients using self-administered oral conventional systemic or subcutaneous biologic therapies (etanercept, adalimumab) were classified as non-adherent (22.4%); 12% were classified as intentionally and 10.9% were classified as unintentionally non-adherent.
The study reports that the multivariable model showed that being on a conventional systemic (odds ratio [OR], 4.34; 95% CI, 2.38-7.91), having strong medication concerns (OR, 1.92; 95% CI, 1.09-3.39), having a weaker routine or habit for taking systemic therapy (OR, 0.94; 95% CI, 0.91-0.97), a longer treatment duration (OR, 1.04; 95% CI, 1.02-1.06) and a younger age (OR, 0.97; 95% CI, 0.95-0.99), were associated with being classified as overall non-adherent.
The researchers concluded that a significant number of patients with psoriasis who were prescribed self-administered systemic therapies reported both intentional and unintentional non-adherence with their treatment regimen. This study emphasizes the need to assess adherence when determining factors that could be influencing treatment response, rather than the prescribed treatment simply being ineffective.
Breaking Down Biosimilar Barriers: Interchangeability
November 14th 2024Part 3 of this series for Global Biosimilars Week, penned by Dracey Poore, director of biosimilars at Cardinal Health, explores the critical topic of interchangeability, examining its role in shaping biosimilar adoption and the broader implications for accessibility.
Biosimilars Development Roundup for October 2024—Podcast Edition
November 3rd 2024On this episode of Not So Different, we discuss the GRx+Biosims conference, which included discussions on data transparency, artificial intelligence (AI), and collaboration to enhance the global supply chain for biosimilars and generic drugs, as well as the evolving requirements for biosimilar devices.
Overcoming Challenges to Improve Access and Reduce Costs
November 12th 2024Biosimilars hold the potential to dramatically lower health care costs and improve access to life-changing treatments, but realizing this potential will require urgent policy reforms, market competition, and better education for both providers and patients.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
Challenges, Obstacles, and Future Directions for Anti-TNF Biosimilars in IBD
November 9th 2024A review article on tumor necrosis factor (TNF)-α inhibitors in inflammatory bowel disease (IBD) outlined current use of anti-TNF originators and biosimilars, their efficacy and safety, the benefits and challenges of biosimilars, and the future of biosimilars in IBD.
Skyrizi Overtakes Humira: “Product Hopping” Leaves Biosimilar Market in Limbo
November 7th 2024For the first time, Skyrizi (risankizumab-rzaa) has replaced Humira (reference adalimumab) as AbbVie’s sales driver, largely due to companies encouraging “product hopping” to avoid competition, creating concerns for the sustainability of the burgeoning adalimumab biosimilar market.