Ulcerative colitis (UC) is the most common type of inflammatory bowel disease, affecting almost 2 million people in the United States. The disease is characterized by inflammation and ulceration of the colon. It’s typical for patients to have relapsing and remitting symptoms of bloody stools, stomach cramping and urgency of bowel movements.
UC can significantly affect quality of life and be associated with psychological conditions. Complications include dehydration, toxic megacolon, and a higher risk of dysplasia and colorectal cancer. Proper management is important to manage symptoms and prevent potential complications. The first biologic therapy was approved for the treatment of UC in 2005 with quite a few more advanced therapies approved over the last 20 years.
In this Guidelines Side-by-Side, we have compared the latest clinical practice guidelines, from the American Gastroenterology Association (AGA) and the American College of Gastroenterology (ACG) on ulcerative colitis, focusing on pharmacologic treatment of moderate to severe UC. The recommendations made are meant to guide clinical practice, taking into consideration the unique desires and needs of individual patients.
Guidelines for Comparison
| Item | AGA | ACG |
|---|---|---|
| Authoring Organization | American Gastroenterological Association | American College of Gastronenterology |
| Publication Date | November 2024 | June 2025 |
| Graded Recommendations | Yes | Yes |
| Uses GRADE | Yes | Yes |
| Links | Summary Pocket Guide Full Text Patient Summary | Summary Full Text |
Key Takeaways
- The guideline from the AGA is a living guideline reviewed and updated every 6 months. The most current update focused on pharmacologic management of moderate to severe UC. Fourteen recommendations were made intended for patients with moderate to severe UC being managed as an outpatient. Advanced therapies for initiation and maintenance of remission, medications for patients naive to advanced therapies, and medications for patients who have been exposed to advanced therapies were discussed. This article only reviewed the recommendations for initiation and maintenance of remission.
- In contrast the ACG guideline was more all-encompassing with 54 recommendations and 57 key concept statements. Recommendations for diagnosis, assessment, monitoring, prognosis, management of mild to moderate UC, management of moderate to severe UC, and management of hospitalized patients with acute severe UC were all included. This article covers the management of patients with moderate to severe UC.
- The ACG made recommendations for the use of oral budesonide and oral systemic corticosteroids for induction of remission, while the update from the AGA did not address these medications.
- Some areas that differed in these two guidelines include:
- Infliximab was suggested for combination use with an immunomodulator by the AGA while the ACG also recommended combination therapy, they specifically recommended a thiopurine be used with infliximab.
- The ACG and AGA recommended golimumab and adalimumab for induction and maintenance, but the AGA also suggested these be used in combination with an immunomodulator.
- Vedolizumab was recommended by both societies for induction and maintenance. The ACG adds that this drug is recommended over adalimumab.
- Filgotinib was not addressed by the ACG, but was recommended for induction and maintenance by the AGA.
- These guidelines were otherwise in agreement with the exception of some differences in the strength of the recommendation which can be viewed in the table below.
| Therapy | AGA | ACG |
|---|---|---|
| Oral budesonide MMX | Not addressed. | Recommended for induction. |
| Oral systemic corticosteroids | Not addressed. | Recommended for induction. NOT recommended for maintenance. |
| infliximab | Recommended for induction and maintenance. Suggested to be used in combination with an immunomodulator over monotherapy. | Recommended for induction and maintenance. Recommended as combination therapy with a thiopurine. |
| golimumab | Recommended for induction and maintenance. Suggested to be used in combination with an immunomodulator over monotherapy. | Recommended for induction and maintenance. |
| adalimumab | Suggested for induction and maintenance.. Suggested to be used in combination with an immunomodulator over monotherapy. | Recommended for induction and maintenance. |
| vedolizumab | Recommended for induction and maintenance. | Recommended for induction and maintenance. Vedolizumab recommended over adalimumab for induction and maintenance. |
| tofacitinib | Recommended for induction and maintenance. | Recommended for induction and maintenance. |
| upadacitinib | Recommended for induction and maintenance. | Recommended for induction and maintenance. |
| ustekinumab | Recommended for induction and maintenance. | Recommended for induction and maintenance. |
| ozanimod | Recommended for induction and maintenance. | Recommended for induction and maintenance. |
| etrasimod | Recommended for induction and maintenance. | Recommended for induction and maintenance. |
| risankizumab | Recommended for induction and maintenance. | Recommended for induction and maintenance. |
| guselkumab | Recommended for induction and maintenance. | Recommended for induction and maintenance. |
| mirikizumab | Suggested for induction and maintenance. | Recommended for induction and maintenance. |
| filgotinib | Suggested for induction and maintenance. | Not addressed. |
| thiopurine | NOT suggested as monotherapy for induction. Suggested for maintenance of remission, typically induced by corticosteroids. | NOT recommended as monotherapy for induction. Suggested for maintenance of remission induced by corticosteroid. |
| methotrexate | NOT suggested as monotherapy for induction or maintenance. | NOT recommended as monotherapy for induction or maintenance. |
| 5-ASA | Suggests stopping therapy in patients who have failed 5-ASA and have escalated to therapy with immunomodulators or advanced therapies. | Suggests NOT using in patients who failed therapy on 5-ASA who are using advanced therapies with biologics or JAK inhibitors for induction. Suggest NOT using for maintenance concomitantly with anti-TNF therapy in patient who previously failed 5-ASA. |
Comparison of Recommendations
| Therapy | AGA | ACG |
|---|---|---|
| oral budesonide MMX | Not Addressed. | In patients with moderately active UC, we recommend oral budesonide MMX for induction of remission. |
| oral systemic corticosteroids | Not Addressed. | In patients with moderately to severely active UC of any extent, we recommend oral systemic corticosteroids to induce remission. In patients with prior moderately to severely active UC, we recommend against systemic corticosteroids for maintenance of remission. |
| Anti-TNF therapy (infliximab, golimumab, adalimumab) | ||
| infliximab | In adult outpatients with moderate-to-severe UC, the AGA recommends the use of infliximab, golimumab, vedolizumab, tofacitinib, upadacitinib, ustekinumab, ozanimod, etrasimod, risankizumab, and guselkumab over no treatment. In adult outpatients with moderate-to-severe UC, the AGA suggests the use of infliximab in combination with an immunomodulator over infliximab or an immunomodulator alone. | In patients with moderately to severely active UC, we recommend anti-tumor necrosis factor (TNF) therapy using infliximab for induction of remission. When infliximab is used as induction therapy for patients with moderately to severely active UC, we recommend combination therapy with a thiopurine. We recommend continuing anti-TNF therapy using adalimumab, golimumab, or infliximab (IV or SC dosing) for maintenance of remission after anti-TNF induction in patients with prior moderately to severely active UC. |
| golimumab | In adult outpatients with moderate-to-severe UC, the AGA recommends the use of infliximab, golimumab, vedolizumab, tofacitinib, upadacitinib, ustekinumab, ozanimod, etrasimod, risankizumab, and guselkumab over no treatment. In adult outpatients with moderate-to-severe UC, the AGA suggests the use of adalimumab or golimumab in combination with an immunomodulator over adalimumab, golimumab or immunomodulator monotherapy. | In patients with moderately to severely active UC, we recommend anti-TNF therapy using adalimumab or golimumab for induction of remission. We recommend continuing anti-TNF therapy using adalimumab, golimumab, or infliximab (IV or SC dosing) for maintenance of remission after anti-TNF induction in patients with prior moderately to severely active UC. |
| adalimumab | In adult outpatients with moderate-to-severe UC, the AGA suggests the use of adalimumab, filgotinib or mirikizumab over no treatment. In adult outpatients with moderate-to-severe UC, the AGA suggests the use of adalimumab or golimumab in combination with an immunomodulator over adalimumab, golimumab or immunomodulator monotherapy. | In patients with moderately to severely active UC, we recommend anti-TNF therapy using adalimumab or golimumab for induction of remission We recommend continuing anti-TNF therapy using adalimumab, golimumab, or infliximab (IV or SC dosing) for maintenance of remission after anti-TNF induction in patients with prior moderately to severely active UC. We recommend continuing vedolizumab as compared with no treatment for maintenance of remission (intravenous [IV] or subcutaneous [SC] dosing) in patients with prior moderately to severely active UC now in remission after vedolizumab induction. In patients with moderately to severely active UC, we recommend vedolizumab as compared with adalimumab for induction and maintenance of remission. |
| JAK Inhibitors (tofacitinib, upadacitinib, filgotinib) | ||
| tofacitinib | In adult outpatients with moderate-to-severe UC, the AGA recommends the use of infliximab, golimumab, vedolizumab, tofacitinib, upadacitinib, ustekinumab, ozanimod, etrasimod, risankizumab, and guselkumab over no treatment. | In patients with moderately to severely active UC, we recommend the Janus kinase (JAK) inhibitor tofacitinib for induction of remission. We recommend continuing tofacitinib or upadacitinib as compared with no treatment for maintenance of remission in patients with prior moderately to severely active UC now in remission after induction with tofacitinib or upadacitinib. |
| upadacitinib | In adult outpatients with moderate-to-severe UC, the AGA recommends the use of infliximab, golimumab, vedolizumab, tofacitinib, upadacitinib, ustekinumab, ozanimod, etrasimod, risankizumab, and guselkumab over no treatment. | In patients with moderately to severely active UC, we recommend the JAK inhibitor upadacitinib for induction of remission. We recommend continuing tofacitinib or upadacitinib as compared with no treatment for maintenance of remission in patients with prior moderately to severely active UC now in remission after induction with tofacitinib or upadacitinib. |
| filgotinib | In adult outpatients with moderate-to-severe UC, the AGA suggests the use of adalimumab, filgotinib or mirikizumab over no treatment. | — |
| IL12/23p40 Antibody | ||
| ustekinumab | In adult outpatients with moderate-to-severe UC, the AGA recommends the use of infliximab, golimumab, vedolizumab, tofacitinib, upadacitinib, ustekinumab, ozanimod, etrasimod, risankizumab, and guselkumab over no treatment. | In patients with moderately to severely active UC, we recommend the interleukin (IL)-12/23p40 antibody ustekinumab for induction of remission. We recommend continuing ustekinumab for maintenance of remission as compared to no treatment in patients who responded to the induction dose of this medication. |
| S1P Receptor Modulators | ||
| ozanimod | In adult outpatients with moderate-to-severe UC, the AGA recommends the use of infliximab, golimumab, vedolizumab, tofacitinib, upadacitinib, ustekinumab, ozanimod, etrasimod, risankizumab, and guselkumab over no treatment. | In patients with moderately to severely active UC, we recommend sphingosine-1-phosphate (S1P) receptor modulators, ozanimod and etrasimod, for induction of remission. We recommend continuing S1P receptor modulators ozanimod or etrasimod for maintenance of remission as compared with no treatment after induction of remission with these agents. |
| etrasimod | In adult outpatients with moderate-to-severe UC, the AGA recommends the use of infliximab, golimumab, vedolizumab, tofacitinib, upadacitinib, ustekinumab, ozanimod, etrasimod, risankizumab, and guselkumab over no treatment. | In patients with moderately to severely active UC, we recommend sphingosine-1-phosphate (S1P) receptor modulators, ozanimod and etrasimod, for induction of remission. We recommend continuing S1P receptor modulators ozanimod or etrasimod for maintenance of remission as compared with no treatment after induction of remission with these agents. |
| IL23p19 Inhibitors | ||
| risankizumab | In adult outpatients with moderate-to-severe UC, the AGA recommends the use of infliximab, golimumab, vedolizumab, tofacitinib, upadacitinib, ustekinumab, ozanimod, etrasimod, risankizumab, and guselkumab over no treatment. | In patients with moderately to severely active UC, we recommend the IL23p19 inhibitor guselkumab, mirikizumab, or risankizumab for induction of remission We recommend continuing guselkumab, mirikizumab, or risankizumab as compared with no treatment for maintenance of remission in patients who respond to the induction dosing of the same treatment. |
| guselkumab | In adult outpatients with moderate-to-severe UC, the AGA recommends the use of infliximab, golimumab, vedolizumab, tofacitinib, upadacitinib, ustekinumab, ozanimod, etrasimod, risankizumab, and guselkumab over no treatment. | In patients with moderately to severely active UC, we recommend the IL23p19 inhibitor guselkumab, mirikizumab, or risankizumab for induction of remission. We recommend continuing guselkumab, mirikizumab, or risankizumab as compared with no treatment for maintenance of remission in patients who respond to the induction dosing of the same treatment. |
| mirikizumab | In adult outpatients with moderate-to-severe UC, the AGA suggests the use of adalimumab, filgotinib or mirikizumab over no treatment. | In patients with moderately to severely active UC, we recommend the IL23p19 inhibitor guselkumab, mirikizumab, or risankizumab for induction of remission. We recommend continuing guselkumab, mirikizumab, or risankizumab as compared with no treatment for maintenance of remission in patients who respond to the induction dosing of the same treatment. |
| Immune Surpassants | ||
| thiopurine | In adult outpatients with moderate-to-severe UC, the AGA suggests AGAINST using thiopurine monotherapy for induction of remission. In adult outpatients with moderate-to-severe UC in remission, the AGA suggests using thiopurine monotherapy, rather than no treatment, for maintenance of remission, typically induced by corticosteroids. | In patients with moderately to severely active UC, we recommend against monotherapy with thiopurines or methotrexate for induction of remission. For patients with prior moderately to severely active UC now in remission because of corticosteroid induction, we suggest thiopurines for maintenance of remission as compared with no treatment or corticosteroids. |
| methotrexate | In adult outpatients with moderate-to-severe UC, the AGA suggests AGAINST using methotrexate monotherapy, for induction or maintenance of remission. | In patients with moderately to severely active UC, we recommend against monotherapy with thiopurines or methotrexate for induction of remission. In patients with prior moderately to severely active UC now in remission, we suggest against using methotrexate for maintenance of remission. |
| Anti-inflammatory | ||
| 5-ASA | In adult outpatients with moderate-to-severe UC, who have failed 5-ASAs, and have escalated to therapy with immunomodulators or advanced therapies, the AGA suggests stopping 5-ASAs. | In patients with moderately to severely active UC who have failed 5-ASA therapy and in whom advanced therapies with biologics or JAK inhibitors are used for induction of remission, we suggest against using 5-ASA for added clinical efficacy. |
This concludes our Guidelines Side-by-Side on ulcerative colitis. Don’t forget to sign up for alerts to stay informed on the latest published guidelines and articles.
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