🔹With how quickly drug-development 💊 and treatment strategies ♟️ change, AGA will review new lit. 📄 and update recommendations as needed every 6 months 📝.
Stay tuned for updates in the future!
10/10
🔹With how quickly drug-development 💊 and treatment strategies ♟️ change, AGA will review new lit. 📄 and update recommendations as needed every 6 months 📝.
Stay tuned for updates in the future!
10/10
👍 Early advanced therapy
❌ No step-up 🪜 therapy
✳️16.🤷♂️Knowledge gap re: treating to a target of mucosal healing vs clinical remission. More data needed!
👍 Early advanced therapy
❌ No step-up 🪜 therapy
✳️16.🤷♂️Knowledge gap re: treating to a target of mucosal healing vs clinical remission. More data needed!
👍 Consider stopping IMM if in steroid-free remission >6mo
❌ Don’t stop TNF
Should involve shared decision making, consideration of disease severity + history, comorbidities, and risk of immunogenicity
8/10
👍 Consider stopping IMM if in steroid-free remission >6mo
❌ Don’t stop TNF
Should involve shared decision making, consideration of disease severity + history, comorbidities, and risk of immunogenicity
8/10
🔹 IFX + thiopurine > IFX or thiopurine alone, particularly if no prior thiopurine use.
🤷♂️Knowledge gaps: Combo therapy with MTX, ADA+ IMM, or non-TNF biologics + IMM
7/10
🔹 IFX + thiopurine > IFX or thiopurine alone, particularly if no prior thiopurine use.
🤷♂️Knowledge gaps: Combo therapy with MTX, ADA+ IMM, or non-TNF biologics + IMM
7/10
❌ Thiopurines for induction
👍 Okay to use thiopurines for maintenance
👍Methotrexate SQ for induction or maintenance
❌Methotrexate PO for induction or maintenance
6/10
❌ Thiopurines for induction
👍 Okay to use thiopurines for maintenance
👍Methotrexate SQ for induction or maintenance
❌Methotrexate PO for induction or maintenance
6/10
🔑High🪣or med🪣 > lower🪣 🔑
You need to factor in the patient when making tx choices, not just focus on which efficacy bucket each medication is in.
Consider age 👨🦳, pregnancy status 🤰, comorbidities 🤒, functional status 👩🦽, prior med exposures, & patient preferences.
5/10
🔑High🪣or med🪣 > lower🪣 🔑
You need to factor in the patient when making tx choices, not just focus on which efficacy bucket each medication is in.
Consider age 👨🦳, pregnancy status 🤰, comorbidities 🤒, functional status 👩🦽, prior med exposures, & patient preferences.
5/10
✳️3. Bio naive: Higher 🪣> Lower 🪣
Higher🪣: IFX, ADA, VDZ, UST, RIS, MIR, GUS
Lower🪣: CTP, UPA
✳️4. Exposed: Higher 🪣 or Med 🪣 > Lower 🪣
Higher🪣: ADA, RIS, GUS, UPA
Med🪣: UST, MIR
Lower🪣: VDZ, CTP
4/10
✳️3. Bio naive: Higher 🪣> Lower 🪣
Higher🪣: IFX, ADA, VDZ, UST, RIS, MIR, GUS
Lower🪣: CTP, UPA
✳️4. Exposed: Higher 🪣 or Med 🪣 > Lower 🪣
Higher🪣: ADA, RIS, GUS, UPA
Med🪣: UST, MIR
Lower🪣: VDZ, CTP
4/10
Strong rec: IFX, ADA, UST, RIS, GUS, MIR, UPA
Conditional rec: CTP, VDZ
Considerations:
1. Biosimilar = originator
2. SQ = IV
3. If severe disease, consider extended induction, dose esc, and higher maintenance doses.
3/10
Strong rec: IFX, ADA, UST, RIS, GUS, MIR, UPA
Conditional rec: CTP, VDZ
Considerations:
1. Biosimilar = originator
2. SQ = IV
3. If severe disease, consider extended induction, dose esc, and higher maintenance doses.
3/10
📍Thresholds for clinically meaningful benefits across txs: >10% vs. pbo & >5% vs. other 💊
📍For those with no prior adv tx exposure, meds were stratified into higher vs lower efficacy. For adv tx-exposed, higher-, medium-, and lower-eff. buckets were used.
2/10
📍Thresholds for clinically meaningful benefits across txs: >10% vs. pbo & >5% vs. other 💊
📍For those with no prior adv tx exposure, meds were stratified into higher vs lower efficacy. For adv tx-exposed, higher-, medium-, and lower-eff. buckets were used.
2/10