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. 2020 May;13(2):72–73.

Dose Modification of Subcutaneous Tocilizumab in Patients with Rheumatoid Arthritis

Jennie H Best 1, Ibrahim Abbass 2, Lenore Tominna 3, William Reiss 4
PMCID: PMC7370831  PMID: 32724501

TO THE EDITOR,

In their study published in American Health & Drug Benefits in December 2019, Punekar and colleagues analyzed US claims and electronic health record data and reported that more than 33% of patients with rheumatoid arthritis who initiated treatment with subcutaneous (SC) tocilizumab administered every other week, increased the dose to every-week dosing.1

As the authors noted, according to the prescribing information approved by the US Food and Drug Administration, SC tocilizumab is administered every 2 weeks or every week, based on the patient's weight and clinical response.1,2 The authors conclude that this dose optimization of tocilizumab from every 2 weeks to every week “could result in increased economic burden.”1

We acknowledge the authors' efforts to analyze treatment patterns of patients receiving tocilizumab; however, the authors do not provide any data to support this conclusion. There are many factors that drive the direct and indirect costs related to biologic therapy use in patients with rheumatoid arthritis; the frequency of drug administration is only one component of direct costs. Other factors include concomitant treatment for rheumatoid arthritis, the number of previous treatments, adverse events, and inadequate or suboptimal response to treatment.35 Indirect costs, such as low productivity, lost wages, and caregiver burden, also contribute to the increased economic burden.6

In their study, Punekar and colleagues did not evaluate the economic burden associated with tocilizumab alone or in comparison with other biologic drugs. Inadequate response to rheumatoid arthritis treatment has been shown to be associated with increased costs in patients with rheumatoid arthritis.3 Multiple studies have demonstrated greater persistence with tocilizumab compared with other biologics.711

The ability to optimize biologic drug dosing to achieve treatment targets provides patients and physicians with more flexibility and therapy options, which can potentially reduce the costs of care. In addition, dose optimization allows physicians to adapt to the clinical needs of the patient. Accordingly, we believe that the authors' conclusion that an increased dose frequency of tocilizumab may increase economic burden is not supported by the data.

Sincerely,

Jennie H. Best, PhD

Ibrahim Abbass, RPh, PhD

Lenore Tominna, PharmD

William Reiss, PharmD

Genentech, Inc., South San Francisco, CA

All the authors are employees and shareholders of Genentech.

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Contributor Information

Jennie H. Best, Genentech, Inc., South San Francisco, CA.

Ibrahim Abbass, Genentech, Inc., South San Francisco, CA.

Lenore Tominna, Genentech, Inc., South San Francisco, CA.

William Reiss, Genentech, Inc., South San Francisco, CA.

References

  • 1. Punekar R, Choi J, Boklage S, et al. Real-world dose modification patterns of subcutaneous tocilizumab among patients with rheumatoid arthritis. Am Health Drug Benefits. 2019;12(8):400–409. [PMC free article] [PubMed] [Google Scholar]
  • 2. Actemra (tocilizumab) injection, for intravenous or subcutaneous use [prescribing information]. South San Francisco, CA: Genentech; June 2019. [Google Scholar]
  • 3. Strand V, Tundia N, Song Y, et al. Economic burden of patients with inadequate response to targeted immunomodulators for rheumatoid arthritis. J Manag Care Spec Pharm. 2018;24:344–352. [DOI] [PMC free article] [PubMed] [Google Scholar]
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  • 8. Ebina K, Hashimoto M, Yamamoto W, et al. Drug retention and discontinuation reasons between seven biologics in patients with rheumatoid arthritis – the ANSWER cohort study-. PLoS One. 2018;13:e0194130. doi.org/10.1371/journal.pone.0194130. [DOI] [PMC free article] [PubMed] [Google Scholar]
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Am Health Drug Benefits. 2020 May;13(2):72–73.

THE AUTHORS RESPOND:

Rajeshwari Punekar 1, Jeannie Choi 2, Susan H Boklage 3, Melitza Iglesias-Rodriguez 4, Kamala Nola 5

We thank Dr Best and her colleagues for their interest in our recently published study1 and appreciate the opportunity to clarify the issues that were raised.

We agree with our colleagues that “there are many factors that drive the direct and indirect costs related to biologic therapy use in patients with rheumatoid arthritis.” Having said that, the evaluation of the economic burden associated with subcutaneous (SC) tocilizumab dose escalation was not the objective of the study. The main objective of the study, as stated in the article, was to understand the real-world dose modification patterns of SC tocilizumab in the treatment of patients with rheumatoid arthritis in the United States.

Therefore, in the discussion section of the article, we have clearly stated that “the impact of SC tocilizumab dose escalation on costs was not formally examined in our study” (page 407), and we suggested an examination of the economic implications of SC tocilizumab dose escalation as a potential area for future research.

Given the direct drug cost increases associated with dose escalation of SC tocilizumab, previous literature on the economic implications of dose escalation,2,3 and expressed need for further study in this area, we believe that an appropriate characterization of the research and conclusions have been provided.

Sincerely,

Rajeshwari Punekar, MPH, PhD, Sanofi, Bridgewater, NJ

Jeannie Choi, PharmD, Independent Researcher, MD

Susan H. Boklage, MS, MPH, Regeneron Pharmaceuticals

Melitza Iglesias-Rodriguez, MD, Tarrytown, NY

Kamala Nola, PharmD, MS, Lipscomb College of Pharmacy, Nashville, TN

References

  • 1. Punekar R, Choi J, Boklage S, et al. Real-world dose modification patterns of subcutaneous tocilizumab among patients with rheumatoid arthritis. Am Health Drug Benefits. 2019;12(8):400–409. [PMC free article] [PubMed] [Google Scholar]
  • 2. Nadkarni A, McMorrow D, Patel C, et al. Incidence of dose escalation and impact on biologic costs among patients with rheumatoid arthritis treated with three intravenous agents. J Comp Eff Res. 2017;6:671–682. [DOI] [PubMed] [Google Scholar]
  • 3. Garces K, Thorne C, Boire G, et al. Comparison of dose escalation and costs of dose escalation between patients with rheumatoid arthritis initiating biologic treatment with etanercept, adalimumab, or infliximab. Value Health. 2016;19:A229–A230. Abstract PMS29. [Google Scholar]

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