Long-Term Treatment Patterns Among Patients With Psoriasis Treated With Ixekizumab or Adalimumab: A Real-World Study

April 2022 | Volume 21 | Issue 4 | Original Article | 399 | Copyright © April 2022


Published online March 28, 2022

Andrew Blauvelt MD MBA,a Nianwen Shi PhD,b Mwangi J. Murage PhD MPH,c Terri Lynn Ridenour MBA BSN,c Carolyn R. Lew PhD,b Najwa Somani MD,c Baojin Zhu PhD,c Nicole M. Zimmerman MS,b Scott A. Kern RN,c Russel T. Burge PhDc,d

aOregon Medical Research Center, Portland, OR
bIBM Watson Health, Cambridge, MA
cEli Lilly and Company, Indianapolis, IN
dUniversity of Cincinnati, Cincinnati, OH

LIMITATIONS

The study relied on diagnostic codes and pharmacy prescriptions in claims, which are subject to data coding limitations and data entry errors. Also, treatment pattern analyses were built on the assumption that patients took medications as prescribed, ie, there was no confirmation that patients took the medications as directed. Pre-period number of unique biologics (as a proxy for treatment resistance) and pre-period obesity were measured and included in multivariate models. IPTW and multivariable modeling were employed to address observable imbalances between patient cohorts, but residual differences not captured in claims may remain. Lastly, the chosen databases are limited to only those individuals with commercial health coverage or private Medicare supplemental coverage.

CONCLUSION

In summary, compared to ADA, IXE use for the treatment of psoriasis is associated with significantly better long-term persistence on therapy, a greater adherence to treatment, and a lower risk of treatment discontinuation in real-world settings. The results of this study supplement the data derived from randomized controlled trials for IXE and ADA to provide important information on their effectiveness in routine clinical practice and will help to inform decisions by both healthcare providers and payers in their treatment selection for patients with moderate-to-severe psoriasis.

DISCLOSURES

Dr Andrew Blauvelt has served as a scientific adviser and/or clinical study investigator for AbbVie, Abcentra, Aligos, Almirall, Amgen, Arcutis, Arena, Aslan, Athenex, Boehringer Ingelheim, Bristol-Myers Squibb, Dermavant, Eli Lilly and Company, Evommune, Forte, Galderma, Incyte, Janssen, Landos, Leo, Novartis, Pfizer, Rapt, Regeneron, Sanofi Genzyme, Sun Pharma, and UCB Pharma. Dr. Nianwen Shi, Dr Carolyn R. Lew, and Nicole M. Zimmerman are employees of IBM Watson Health that was compensated by Eli Lilly and Company for conducting this research. Dr Najwa Somani, Scott A. Kern, Dr Russel Burge, Terri Ridenour, Dr Baojin Zhu, and Dr Mwangi Murage are fulltime employees and stockholders of Eli Lilly and Company.

ACKNOWLEDGMENT

Authors thank Bilal Atiya, an employee of Eli Lilly and Company for providing inputs during study design and critical review and Uma Jyothi Kommoju, an employee of Eli Lilly Services India Private Limited for providing writing support.
Funding: This study was sponsored by Eli Lilly and Company, Indianapolis, IN, US.

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AUTHOR CORRESPONDENCE

Mwangi J. Murage PhD MPH murage_mwangi_james@lilly.com