Video: Every Case Tells a Story| Webinar: ACR/CHEST ILD Guidelines in Practice

An official publication of the ACR and the ARP serving rheumatologists and rheumatology professionals

  • Conditions
    • Axial Spondyloarthritis
    • Gout and Crystalline Arthritis
    • Myositis
    • Osteoarthritis and Bone Disorders
    • Pain Syndromes
    • Pediatric Conditions
    • Psoriatic Arthritis
    • Rheumatoid Arthritis
    • Sjögren’s Disease
    • Systemic Lupus Erythematosus
    • Systemic Sclerosis
    • Vasculitis
    • Other Rheumatic Conditions
  • FocusRheum
    • ANCA-Associated Vasculitis
    • Axial Spondyloarthritis
    • Gout
    • Psoriatic Arthritis
    • Rheumatoid Arthritis
    • Systemic Lupus Erythematosus
  • Guidance
    • Clinical Criteria/Guidelines
    • Ethics
    • Legal Updates
    • Legislation & Advocacy
    • Meeting Reports
      • ACR Convergence
      • Other ACR meetings
      • EULAR/Other
    • Research Rheum
  • Drug Updates
    • Analgesics
    • Biologics/DMARDs
  • Practice Support
    • Billing/Coding
    • EMRs
    • Facility
    • Insurance
    • QA/QI
    • Technology
    • Workforce
  • Opinion
    • Patient Perspective
    • Profiles
    • Rheuminations
      • Video
    • Speak Out Rheum
  • Career
    • ACR ExamRheum
    • Awards
    • Career Development
  • ACR
    • ACR Home
    • ACR Convergence
    • ACR Guidelines
    • Journals
      • ACR Open Rheumatology
      • Arthritis & Rheumatology
      • Arthritis Care & Research
    • From the College
    • Events/CME
    • President’s Perspective
  • Search

High Cost of Specialty Drugs Demands Action

Mary Beth Nierengarten  |  Issue: August 2021  |  July 6, 2021

As the costs of specialty drugs continue to rise and patient access to them becomes more challenging, physicians are increasingly called on to argue for treatments supported by medical evidence but difficult to access due to decisions outside their control. Medicine as big business is not new. However, the growing influence of pharmacy benefit managers (PBMs) highlights the clashing priorities between a profit-driven business model and a care-driven medical model.

Many PBM practices, including formulary construction, copay accumulators and non-medical switching, affect the cost of, and access to, specialty drugs and can have detrimental effects on patient care (see Table 1). Yet these decisions are made far from clinical settings, often without input from providers.

ad goes here:advert-1
ADVERTISEMENT
SCROLL TO CONTINUE

Rheumatologists are on the front lines of this conflict given the importance of specialty drugs, particularly biologic agents and biosimilars, in the treatment of rheumatic conditions and the administrative hoops providers have to jump through to prescribe these drugs for their patients.

“Rheumatologists understand very well that most of the medications we prescribe are going to be subject to prior authorization and step therapy,” says Angus Worthing, MD, a rheumatologist at Arthritis & Rheumatism Associates, Washington, D.C. “But I’m not sure everyone knows these things are mainly a profit scheme for PBMs and can increase the incentive to raise drug prices.”

Dr. Worthing

Dr. Worthing serves as vice president of the Alliance for Transparent & Affordable Prescriptions, a coalition of providers and patients that works to address PBMs’ impact on drug costs and patient access to affordable care. Understanding how PBMs negotiate drug prices and formulary access is critical, he says, given the impact these negotiations have on downstream practices, such as prior authorization and step therapy.

Dr. Gewanter

Unlike physicians, whose professional oath and duty are to make decisions in their patients’ best interest, a PBM has a fiduciary duty to the corporation it works for: “The first rule for any corporation is to make money for its shareholders,” says Harry L. Gewanter, MD, FAAP, MACR, clinical associate professor of pediatrics, Children’s Hospital of Richmond, Virginia Commonwealth University. “No matter what PBMs or payers say, any care patients get is a secondary side effect.” Dr. Gewanter works closely with the Biologics Prescribers Collaborative, an organization that promotes the safe use of both originator and biosimilar biologic medications.

A major problem with PBMs and insurers is the lack of transparency in negotiations regarding which drugs are placed on a formulary and which tier the medication is on. Dr. Gewanter underscores that the list price, or wholesale acquisitions price, used for negotiations with PBMs does not accurately reflect the net cost to PBMs after price concessions they receive in the form of rebates and discounts or the cost patients see. “Unlike medical charges, where patient copays are based on the negotiated net price, patients’ pharmacy copays are based on the list price—[not the PBM’s negotiated cost],” he says.

Page: 1 2 3 4 | Single Page
Share: 

Filed under:Legislation & AdvocacyPractice Support Tagged with:drug pricingpharmacy benefit managers (PBMs)

Related Articles

    Marching to the Biosimilar Beat: Questions on Rollout Remain

    September 7, 2023

    The availability of biosimilars for the treatment of patients with rheumatic diseases exploded in 2023. Here’s where we stand and what to expect going forward.

    Biosimilars Debate Heats up over Cost Savings, Safety Concerns

    Biosimilars Debate Heats up over Cost Savings, Safety Concerns

    April 15, 2016

    After years of speculation about potential cost savings and debates on safety, biosimilars are about to step onto the stage of rheumatic disease treatment. On Feb. 9, the Arthritis Advisory Committee of the U.S. Food and Drug Administration (FDA) met in Washington, D.C., and recommended the approval of CT-P13, a proposed biosimilar to infliximab (Remicade),…

    The Biosimilars Debate Heats Up: Potential cost savings weighed against patient health & safety

    March 1, 2016

    After years of speculation about potential cost savings and debates on safety, biosimilars are about to step onto the stage of rheumatic disease treatment. On Feb. 9, the Arthritis Advisory Committee of the U.S. Food and Drug Administration (FDA) met in Washington, D.C., and recommended the approval of CT-P13, a proposed biosimilar to infliximab (Remicade),…

    Report on EU’s Experience with Biosimilar Drugs Released: Will U.S. Experience Be Similar?

    October 17, 2017

    As questions about biosimilar medications swirl among U.S. rheumatologists, a recently released report sheds some light on the European experience with biosimilars—and may offer some important insights for the U.S. market. The report, Biosimilars in the EU: Information Guide for Healthcare Professionals, was released in late April by the European Medicines Agency (EMA) and the…

  • About Us
  • Meet the Editors
  • Issue Archives
  • Contribute
  • Advertise
  • Contact Us
  • Copyright © 2025 by John Wiley & Sons, Inc. All rights reserved, including rights for text and data mining and training of artificial technologies or similar technologies. ISSN 1931-3268 (print). ISSN 1931-3209 (online).
  • DEI Statement
  • Privacy Policy
  • Terms of Use
  • Cookie Preferences