Kashyap Patel, MD, CEO of Carolina Blood and Cancer Care, told The Center for Biosimilars® in an interview that, as his practice has begun to implement the Oncology Care Model, it has moved 100% of its patients to biosimilar filgrastim, Zarxio, from the reference filgrastim, Neupogen.
The Oncology Care Model (OCM), a reimbursement model developed by CMS’ Center for Medicare and Medicaid Innovation, allows oncology practices to enter into payment arrangements that include financial and performance accountability for episodes of cancer care. The model is intended to improve health outcomes and produce higher quality care at the same cost or a lower cost to Medicare, and one practice participating in the model has seen firsthand that biosimilars have a role to play in achieving those objectives.
Kashyap Patel, MD, CEO of Carolina Blood and Cancer Care, told The Center for Biosimilars® in an interview that, as his practice has begun to implement OCM, it has moved 100% of its patients to biosimilar filgrastim, Zarxio, from the reference filgrastim, Neupogen. With an approximate 15% difference in cost between the 2 products, the change has saved the practice—and Medicare—valuable resources, and Patel sees the potential for savings to be even greater once biosimilar anticancer therapies reach the US marketplace.
With the cost savings that his practice has been able to achieve so far under OCM, Patel says that his clinic has been able to institute drop-in hours for patients who have any health concerns—even concerns that aren’t related to their cancer treatment. “The patients love it,” he said, and the practice has been able to refer patients to other specialists to address comorbidities that are impacting their overall health.
To date, Patel says that his patients have not had concerns about using biosimilar filgrastim instead of its reference; in Patel’s rural South Carolina practice, “Some of my patients are still using flip phones,” he said; they aren’t particularly concerned about the nuances of biosimilarity or the technicalities of the biosimilar approval pathway. Instead, they care about whether a treatment has been FDA approved and whether it is effective in treating their condition.
“If I were practicing in Manhattan or in Beverly Hills,” he said, these conversations might be different, but even when anticancer biosimilars like trastuzumab and bevacizumab reach the clinic, Patel expects that mutual patient—provider respect will be the most important factor in patients’ acceptance of biosimilar drugs.
Provider education, said Patel, is a bigger hurdle than patient awareness in bringing biosimilars into the clinic to reduce costs and better implement OCM. Patel pointed to results of a National Comprehensive Cancer Network survey that assessed clinician awareness of biosimilars and found that only 3% of respondents rated themselves “extremely familiar” with biosimilars. In Patel’s view, awareness hasn’t gotten much better since that survey. Yet, he emphasized, oncologists have to start discussing these issues, given the high financial toxicity surrounding cancer care and the potential for biosimilars to bring down costs for patients and the healthcare system as a whole.
It’s not just the oncologist who has to become more knowledgeable about biosimilars: Nurses, said Patel, are a cornerstone of patient care.
“[Patients] spend 6 hours with the infusion nurse while they may spend 15 minutes with me,” he said, adding that it’s “human nature” for some patients to be reticent about asking their physician questions about their treatments. Many patients, he said, may be more willing to talk with an infusion nurse about any concerns with their therapies. As the anticancer biosimilars begin to make their way into the clinic, Patel plans to work on greater nurse education to help support and reassure patients as they undergo treatment.
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 Oncology Roundup for June 2024—Podcast Edition
July 7th 2024On this episode of Not So Different, we review biosimilar news coming out of June, with clinical trial results from conferences and a study showcasing how to overcome economic and noneconomic barriers to oncology biosimilars.
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.