Treatment persistence and maintenance dose titration among ulcerative colitis patients on biologics: a pooled study of three United States claim databases

Curr Med Res Opin. 2022 Jul;38(7):1093-1101. doi: 10.1080/03007995.2022.2071041. Epub 2022 May 23.

Abstract

Objective: This real-world study evaluated biologic treatment patterns in patients with moderate-to-severe ulcerative colitis (UC).

Methods: IQVIA PharMetrics, IBM MarketScan, and Optum Clinformatics were pooled to identify UC patients with ≥1 claim for UC and ≥1 claim for adalimumab (ADA), golimumab (GOL), infliximab (IFX), or vedolizumab (VDZ). The index date for each biologic was the first claim for that biologic. Patients could be included in >1 cohort if they switched biologics during the identification period. Continuous eligibility for medical/pharmacy benefits was required for 12 months before (baseline) and after (follow-up) the index date. Patients lacking claims for any biologic during baseline were categorized as bio-naïve; those with any biologic claim were categorized as bio-experienced. Persistence was defined as the proportion of patients that remained on the index biologic without a gap between claims of >28 days for ADA, >56 days for GOL, and >112 days for IFX and VDZ. Dose titration was assessed among patients with ≥2 maintenance doses during follow-up among ADA, GOL, and VDZ patients.

Results: In total, 6,106 bio-naïve UC patients and 1,027 bio-experienced UC patients were identified. Patients treated with VDZ and IFX had the highest persistence followed by ADA and GOL patients for bio-naïve and bio-experienced, respectively. ADA patients had a numerically higher proportion of patients with 50% dose escalation, followed by VDZ and GOL; 50% dose reduction was observed in ≤1% patients.

Conclusions: In this descriptive study of UC patients without confounder adjustment, VDZ persistence was numerically highest followed by IFX, GOL, and ADA across both populations.

Keywords: Ulcerative colitis; bio-experienced; bio-naïve; dose titration; persistence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adalimumab / therapeutic use
  • Biological Products* / therapeutic use
  • Colitis, Ulcerative* / drug therapy
  • Humans
  • Infliximab / therapeutic use
  • Retrospective Studies
  • Treatment Outcome
  • Tumor Necrosis Factor-alpha
  • United States

Substances

  • Biological Products
  • Tumor Necrosis Factor-alpha
  • Infliximab
  • Adalimumab