Results of a recent survey demonstrate that Asian physicians are less confident in using biosimilars than their European peers are.
The European Crohn’s and Colitis Organisation (ECCO) has surveyed its members in 2013 and 2015 concerning their knowledge of and views on biosimilars, and in 2017, researchers from Asia adopted the same survey questions to gather information on the views of members of the Asian Organization of Crohn’s and Colitis (AOCC). Results of the survey, published in Intestinal Research, demonstrate that Asian physicians are less confident in using biosimilars than their European peers are.
The 17-question, multiple-choice, anonymous web survey gathered responses from 151 physicians from Korea, Japan, China, Hong Kong, Malaysia, Taiwan, Singapore, and India. Most participants were gastroenterologists (96.6%), and most (77.5%) had cared for patients with inflammatory bowel disease (IBD) for more than 5 years.
The survey found that 49.6% of respondents had access to biosimilars and had already prescribed them, while 26.4% had access to biosimilars but had not prescribed them, and 19% had no access to biosimilars (in 2015, the corresponding percentages among ECCO members were 60%, 22%, and 18%, respectively).
In terms of provider education, most respondents (66.2%) were aware that a biosimilar is not identical to the originator. Some (8%) thought that a biosimilar was a different agent altogether (comparable to the difference between adalimumab and infliximab). Furthermore, 19.9% believed that biosimilars have different activities than the originator, while 38.4% thought that biosimilars would have different immunogenicity than the originator. While these patterns of education are similar to ECCO members’ responses, a lower percentage of AOCC respondents (77.5%) than ECCO members (92.4% in 2015) considered cost savings as a main advantage of biosimilars.
Like ECCO members (85% in 2015), most AOCC respondents (87.8%) disagreed with automatic substitution of a biosimilar by a pharmacist, but unlike ECCO members (44.4% in 2015), only 19.2% of AOCC respondents believed that biosimilars could be used interchangeably with their references. Similarly, fewer AOCC respondents (39.1%) than ECCO members (50.8% in 2015) were comfortable with the extrapolation of indications.
Finally, only 6.0% of the survey respondents said they would be confident prescribing a biosimilar, compared with 28.8% of ECCO members in the 2015 survey.
“Asian gastroenterologists are generally well informed about biosimilars,” write the paper’s authors. “However, compared with ECCO members in 2015, Asian gastroenterologists had more concerns and less confidence about the use of biosimilars clinical practice. Thus, IBD-specific data on comparison of efficacy, safety, and immunogenicity in Asian patients are needed.”
Reference
Park SK, Hisamatsu T, Ran Z, Wei SC, Park DI. Knowledge and viewpoints on biosimilar monoclonal antibodies from members of the Asian Organization of Crohn’s and Colitis: comparison with European Crohn’s and Colitis members [published online November 12, 2018]. Intest Res. doi: 10.5217/ir.2018.00084.
Boosting Health Care Sustainability: The Role of Biosimilars in Latin America
November 21st 2024Biosimilars could improve access to biologic treatments and health care sustainability in Latin America, but their adoption is hindered by misconceptions, regulatory gaps, and weak pharmacovigilance, requiring targeted education and stronger regulations.
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.
Breaking Down Biosimilar Barriers: Payer and PBM Policies
November 13th 2024Part 2 of this series for Global Biosimilars Week dives into the complexities of payer and pharmacy benefit manager (PBM) policies, how they impact biosimilar accessibility, and how addressing these issues may look under a second Trump term.
Biosimilars Gastroenterology Roundup for May 2024—Podcast Edition
June 2nd 2024On this episode of Not So Different, we review the biggest gastroenterology biosimilar stories from May 2024, covering new data from conferences and journals on infliximab and adalimumab products that demonstrate positive clinical results and confirm the safety of these biosimilars, as well as the feasibility of switching to them.
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.