About this benchmarkRheumatoid arthritis · USRheumatologists · USAI answers generated with a US rheumatologist persona4 AI systemsPre-ACR baseline, 30 October 2026

03 · Patient Profiles

Does AI favour the same therapies for every patient?

The same therapy. Different patient contexts. Different AI positioning.

Upadacitinib

Not a controlled comparison

The two profiles contain different questions and different comparators. This is not a controlled comparison, and it says nothing about clinical value or superiority.

After TNF-inhibitor failure

120 comparative answers · 30 questions in this profile

Favoured in 16 of 32

  • Favoured16 · 50%
  • Equal11
  • Conditional4
  • Other1
  • Comparator favoured0

Cardiovascular & thromboembolic risk

68 comparative answers · 17 questions in this profile

Favoured in 0 of 24

  • Favoured0 · 0%
  • Equal5
  • Conditional8
  • Other4
  • Comparator favoured7

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Patient profile

MTX intolerance / monotherapy

Clinical context

Comparative questions framed around patients who cannot take methotrexate, mostly about monotherapy.

MTX intolerance / monotherapy: tocilizumab is favoured in 18 of the 24 answers in which it was compared.

Therapies assessed

  1. TocilizumabFavoured in 18 of 24

    • Favoured18 · 75%
    • Equal1
    • Conditional2
    • Other3
    • Comparator favoured0
  2. AbataceptFavoured in 1 of 12

    • Favoured1 · 8%
    • Equal2
    • Conditional1
    • Other2
    • Comparator favoured6
  3. AdalimumabFavoured in 1 of 12

    • Favoured1 · 8%
    • Equal2
    • Conditional2
    • Other0
    • Comparator favoured7
  4. EtanerceptFavoured in 2 of 8Small base

    • Favoured2 · 25%
    • Equal0
    • Conditional1
    • Other1
    • Comparator favoured4
  5. SarilumabFavoured in 3 of 8Small base

    • Favoured3 · 38%
    • Equal1
    • Conditional1
    • Other2
    • Comparator favoured1

After TNF-inhibitor failure

Clinical context

Comparative questions framed around patients whose disease responded inadequately to a TNF inhibitor.

After TNF-inhibitor failure: upadacitinib is favoured in 16 of 32 comparisons and rituximab in 14 of 48.

Therapies assessed

  1. RituximabFavoured in 14 of 48

    • Favoured14 · 29%
    • Equal11
    • Conditional14
    • Other9
    • Comparator favoured0
  2. UpadacitinibFavoured in 16 of 32

    • Favoured16 · 50%
    • Equal11
    • Conditional4
    • Other1
    • Comparator favoured0
  3. BaricitinibFavoured in 7 of 32

    • Favoured7 · 22%
    • Equal11
    • Conditional3
    • Other4
    • Comparator favoured7
  4. TofacitinibFavoured in 0 of 32

    • Favoured0 · 0%
    • Equal12
    • Conditional2
    • Other6
    • Comparator favoured12
  5. AbataceptFavoured in 3 of 28

    • Favoured3 · 11%
    • Equal12
    • Conditional0
    • Other3
    • Comparator favoured10
  6. SarilumabFavoured in 0 of 24

    • Favoured0 · 0%
    • Equal10
    • Conditional3
    • Other4
    • Comparator favoured7
  7. TocilizumabFavoured in 6 of 24

    • Favoured6 · 25%
    • Equal9
    • Conditional1
    • Other7
    • Comparator favoured1

Pregnancy planning

Clinical context

Comparative questions framed around patients planning pregnancy.

Pregnancy planning: certolizumab pegol is favoured in 5 of 8 comparisons.

Therapies assessed

  1. Certolizumab pegolFavoured in 5 of 8Small base

    • Favoured5 · 63%
    • Equal0
    • Conditional2
    • Other1
    • Comparator favoured0
  2. AdalimumabFavoured in 0 of 8Small base

    • Favoured0 · 0%
    • Equal1
    • Conditional0
    • Other3
    • Comparator favoured4
  3. EtanerceptFavoured in 1 of 8Small base

    • Favoured1 · 13%
    • Equal1
    • Conditional2
    • Other2
    • Comparator favoured2
  4. HydroxychloroquineFavoured in 2 of 8Small base

    • Favoured2 · 25%
    • Equal2
    • Conditional3
    • Other1
    • Comparator favoured0

Cardiovascular & thromboembolic risk

Clinical context

Comparative questions framed around patients with cardiovascular or thromboembolic risk.

Cardiovascular and thromboembolic risk: no JAK inhibitor is favoured in any comparison; tocilizumab is favoured in 8 of 16, abatacept in 6 of 12 and sarilumab in 6 of 12.

Therapies assessed

  1. TocilizumabFavoured in 8 of 16

    • Favoured8 · 50%
    • Equal4
    • Conditional3
    • Other1
    • Comparator favoured0
  2. AbataceptFavoured in 6 of 12

    • Favoured6 · 50%
    • Equal0
    • Conditional5
    • Other1
    • Comparator favoured0
  3. SarilumabFavoured in 6 of 12

    • Favoured6 · 50%
    • Equal1
    • Conditional5
    • Other0
    • Comparator favoured0
  4. UpadacitinibFavoured in 0 of 24

    • Favoured0 · 0%
    • Equal5
    • Conditional8
    • Other4
    • Comparator favoured7
  5. BaricitinibFavoured in 0 of 20

    • Favoured0 · 0%
    • Equal0
    • Conditional8
    • Other0
    • Comparator favoured12
  6. TofacitinibFavoured in 0 of 20

    • Favoured0 · 0%
    • Equal0
    • Conditional6
    • Other1
    • Comparator favoured13
  7. EtanerceptFavoured in 7 of 16

    • Favoured7 · 44%
    • Equal4
    • Conditional4
    • Other1
    • Comparator favoured0
  8. AdalimumabFavoured in 4 of 12

    • Favoured4 · 33%
    • Equal4
    • Conditional4
    • Other0
    • Comparator favoured0

Across profiles

Follow a therapy across the four profiles.

Not a controlled comparison

Each profile has its own questions and comparators. Read a therapy across profiles as a description of AI answers in different contexts, never as a controlled comparison or a ranking.

Follow a therapy across the four profiles.
TherapyMTX intolerance / monotherapyAfter TNF-inhibitor failurePregnancy planningCardiovascular & thromboembolic risk
AbataceptFavoured in 1 of 12Favoured in 3 of 28Not shownFavoured in 6 of 12
TocilizumabFavoured in 18 of 24Favoured in 6 of 24Not shownFavoured in 8 of 16
TofacitinibNot shownFavoured in 0 of 32Not shownFavoured in 0 of 20
AdalimumabFavoured in 1 of 12Not shownFavoured in 0 of 8Small baseFavoured in 4 of 12
UpadacitinibNot shownFavoured in 16 of 32Not shownFavoured in 0 of 24
BaricitinibNot shownFavoured in 7 of 32Not shownFavoured in 0 of 20
EtanerceptFavoured in 2 of 8Small baseNot shownFavoured in 1 of 8Small baseFavoured in 7 of 16
SarilumabFavoured in 3 of 8Small baseFavoured in 0 of 24Not shownFavoured in 6 of 12

“Not shown” means the therapy was not compared in that profile, or was compared fewer than 8 times there.

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What this means

Why profile intelligence matters to brand, medical and market-access teams

Positioning, evidence communication and access arguments are built for specific patients. In this benchmark, the therapies AI answers favour differ between the four profiles shown, so a single market-wide reading can hide where a therapy is favoured and where it is not.

What limits this reading

Four profiles are shown. Each has its own questions, comparators and bases, and profiles overlap, so no figure is added across them and none is a controlled comparison.

The Theralexis capability

A Theralexis assessment measures the patient profiles that matter to your portfolio, with the comparators and questions you choose.

Your portfolio

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About this benchmark

What was measured

AI representation analysis of 1,816 answers to US rheumatologist-style open questions and 960 answers to comparative questions from four web-enabled AI systems (ChatGPT, Claude, Gemini, Perplexity), collected 30 October 2026 with a US rheumatologist persona. Visibility = share of answers naming a therapy. Neither visibility, order of mention nor head-to-head verdicts indicate clinical efficacy, safety, preference or recommendation.

Pre-ACR baseline (v1.1 corrected analytical view, 30 Oct 2026). Re-measured after ACR Convergence 2026.

Full methodology

Sources and scope
Publisher
Theralexis
Market
Rheumatoid arthritis · United States
Persona
AI answers generated with a US rheumatologist persona
Open questions
454 questions · 1,816 answers
Comparative questions
240 questions · 960 answers
Measured
Published
AI systems
ChatGPT (GPT-5.4-mini), Claude (Claude Haiku 4.5), Gemini (Gemini 3.1 Flash-Lite), Perplexity (Sonar)
Head-to-head judge
gpt-4.1-mini