Cure8

Why This Matters

This study models comparative cost-effectiveness across many advanced therapy sequences for moderate–severe ulcerative colitis in Japan; its findings could influence how health systems and clinicians consider first- and second-line choices among newer agents like etrasimod and upadacitinib.

Who Should Pay Attention

Clinicians, health-system decision makers, researchers, and patients interested in advanced therapy sequencing or drug-cost/value considerations for ulcerative colitis in Japan.

Study Snapshot

Story typeResearch paper
Evidence typeResearch paper
Source depthMetadata only

What To Know

This modeling study compared cost-effectiveness of 79 advanced treatment sequences for moderately to severely active ulcerative colitis in Japan.

Using a hybrid decision-tree + Markov model adapted to Japanese practice, the authors report that first-line etrasimod followed by second-line upadacitinib was the most cost-effective sequence under the study's assumptions and the Japanese willingness-to-pay threshold.

The analysis included multiple available advanced therapies (oral S1P modulators like etrasimod and ozanimod; JAK inhibitors including upadacitinib and tofacitinib; biologics such as anti-TNF agents adalimumab, golimumab, infliximab; vedolizumab; and ustekinumab) and modeled lifetime clinical and economic outcomes with treatment switching rules.

Results are model-based and intended to inform sequencing considerations alongside clinical judgement, safety, and patient preferences.

Key limitations noted by the authors include reliance on network meta-analysis inputs, model assumptions about treatment effects and sequencing, and adaptation to the Japanese healthcare setting; real-world effectiveness, safety, and individual patient factors can change optimal choices.

Keep In Mind

These are model-based findings using published trial/network-meta inputs and Japanese cost parameters; they do not replace individualized clinical decision-making. The analysis depends on assumptions about treatment effects, switching rules, and costs; results may differ with new data or in other healthcare settings.

Source Details

Review the original publication for the complete reporting, methods, and context.

Read Original Source
Research paper Evidence type derived from source or registry metadata.
PublicationAdvances in Therapy
PublisherSpringer Science and Business Media LLC
AuthorsKazumasa Kamei, Miwa Enami, Hiroyuki Matsuda +5 more
Study typeJournal Article
Indexed viaCrossref
Source typeResearch paper
PublishedSep 8, 2026, 12:00 AM
Content availableMetadata only

Funding disclosed by the source: Pfizer Japan

This Cure8 brief is based on source text from the linked article. Cure8 is informational only and is not a substitute for professional medical advice, diagnosis, or treatment.

Related Reading

Browse latest news →