Javascript must be enabled to continue!
728 Second-Line Biologic Therapy After Vedolizumab
View through CrossRef
INTRODUCTION:
Vedolizumab (VDZ), an anti-integrin monoclonal antibody approved for the treatment of Crohn's disease (CD) and ulcerative colitis (UC), is increasingly being utilized as first-line biologic therapy in bio-naïve inflammatory bowel disease (IBD) patients (pts) with moderate-to-severe disease. While prior studies have described the efficacy of VDZ after anti-TNF failure, there is little guidance on the use of alternative biologics following initial VDZ therapy. This study describes the clinical response of IBD pts treated with a second (2nd) biologic following VDZ discontinuation.
METHODS:
We performed a retrospective review of all bio-naïve IBD pts started on VDZ as first-line therapy at a large multicenter gastroenterology private practice since drug approval in 2014. Pts were identified who failed initial VDZ treatment and were switched to a 2nd biologic agent. Data collection included demographics, diagnosis, therapy, and disease activity scores using the partial Mayo score (pMayo) for UC pts and the Harvey-Bradshaw Index (HBI) for CD pts. Clinical remission was assessed for those pts with ≥6 months of data and defined as pMayo less than 2 or HBI less than 5.
RESULTS:
A total of 135 IBD pts receiving VDZ as first-line biologic therapy were identified, of which VDZ was discontinued in 30 (22%). Our study cohort included 25 pts who received a 2nd line biologic following VDZ failure (11 primary non-response, 14 secondary non-response). Second-line biologic agents included 19 infliximab, 3 adalimumab, 2 ustekinumab, and 1 tofacitinib. Baseline demographics of the 25 pts were as follows: mean age 47 ± 18 years, male gender 13 (52%), UC 19 (76%), CD 6 (24%), time to 2nd biologic 8.2 ± 4.5 weeks. Disease severity scores prior to and following initiation of the 2nd line biologic are depicted in Figure 1. Clinical remission assessment was available for 18 of 25 patients. Remission was achieved in 11 of 18 pts (61%), driven by UC pts treated with infliximab [Figure 2]. Overall, pts treated with anti-TNF agents following VDZ had higher rates of remission compared to those treated with other biologics.
CONCLUSION:
Biologic-naïve IBD pts treated initially with VDZ have high treatment persistence. In addition, rates of remission with 2nd-line biologic therapy are significantly greater than expected when first-line failure is VDZ. Further studies are warranted to determine the optimal order in which advanced therapies should be initiated.
Ovid Technologies (Wolters Kluwer Health)
Title: 728 Second-Line Biologic Therapy After Vedolizumab
Description:
INTRODUCTION:
Vedolizumab (VDZ), an anti-integrin monoclonal antibody approved for the treatment of Crohn's disease (CD) and ulcerative colitis (UC), is increasingly being utilized as first-line biologic therapy in bio-naïve inflammatory bowel disease (IBD) patients (pts) with moderate-to-severe disease.
While prior studies have described the efficacy of VDZ after anti-TNF failure, there is little guidance on the use of alternative biologics following initial VDZ therapy.
This study describes the clinical response of IBD pts treated with a second (2nd) biologic following VDZ discontinuation.
METHODS:
We performed a retrospective review of all bio-naïve IBD pts started on VDZ as first-line therapy at a large multicenter gastroenterology private practice since drug approval in 2014.
Pts were identified who failed initial VDZ treatment and were switched to a 2nd biologic agent.
Data collection included demographics, diagnosis, therapy, and disease activity scores using the partial Mayo score (pMayo) for UC pts and the Harvey-Bradshaw Index (HBI) for CD pts.
Clinical remission was assessed for those pts with ≥6 months of data and defined as pMayo less than 2 or HBI less than 5.
RESULTS:
A total of 135 IBD pts receiving VDZ as first-line biologic therapy were identified, of which VDZ was discontinued in 30 (22%).
Our study cohort included 25 pts who received a 2nd line biologic following VDZ failure (11 primary non-response, 14 secondary non-response).
Second-line biologic agents included 19 infliximab, 3 adalimumab, 2 ustekinumab, and 1 tofacitinib.
Baseline demographics of the 25 pts were as follows: mean age 47 ± 18 years, male gender 13 (52%), UC 19 (76%), CD 6 (24%), time to 2nd biologic 8.
2 ± 4.
5 weeks.
Disease severity scores prior to and following initiation of the 2nd line biologic are depicted in Figure 1.
Clinical remission assessment was available for 18 of 25 patients.
Remission was achieved in 11 of 18 pts (61%), driven by UC pts treated with infliximab [Figure 2].
Overall, pts treated with anti-TNF agents following VDZ had higher rates of remission compared to those treated with other biologics.
CONCLUSION:
Biologic-naïve IBD pts treated initially with VDZ have high treatment persistence.
In addition, rates of remission with 2nd-line biologic therapy are significantly greater than expected when first-line failure is VDZ.
Further studies are warranted to determine the optimal order in which advanced therapies should be initiated.
Related Results
Vedolizumab levels are associated with clinical remission in pouchitis
Vedolizumab levels are associated with clinical remission in pouchitis
Abstract
Background
Pouchitis is the most common complication in ulcerative colitis (UC) patients following ileal pouch anal anastomosis (IPAA). Recent studies have demons...
P586 Vedolizumab in Mild to Moderate Crohn’s Disease Patients Naïve to Biological Therapy: a Multicentric Observational Study
P586 Vedolizumab in Mild to Moderate Crohn’s Disease Patients Naïve to Biological Therapy: a Multicentric Observational Study
Abstract
Background
Vedolizumab, a human monoclonal antibody that blocks integrin α4-β7, was approved for the management of Infl...
P1163 Treatment-based risk stratification of serious and opportunistic infections in IBD patients from an tertiary center in brazil: a comparison between advanced therapies and non-biologic exposure in real world setting
P1163 Treatment-based risk stratification of serious and opportunistic infections in IBD patients from an tertiary center in brazil: a comparison between advanced therapies and non-biologic exposure in real world setting
Abstract
Background
The risks of serious and opportunistic (OIs) infections associated with advanced therapies for IBD is one of...
Comparative Safety of Ustekinumab and Vedolizumab in Older Patients with Inflammatory Bowel Disease: A Bicentric Cohort Study
Comparative Safety of Ustekinumab and Vedolizumab in Older Patients with Inflammatory Bowel Disease: A Bicentric Cohort Study
Introduction: Data about the safety of vedolizumab and ustekinumab are lacking in older patients with inflammatory bowel disease. The objective was to compare the safety of vedoliz...
A systematic review of vedolizumab in treating pediatric ulcerative colitis: efficacy and safety insights
A systematic review of vedolizumab in treating pediatric ulcerative colitis: efficacy and safety insights
Background:
Ulcerative colitis (UC) in pediatric patients often results in corticosteroid (CS) dependency, with many individuals developing resistance to conven...
Vedolizumab in Mild-to-Moderate Crohn’s Disease Patients Naïve to Biological Therapy: A Multicentric Observational Study
Vedolizumab in Mild-to-Moderate Crohn’s Disease Patients Naïve to Biological Therapy: A Multicentric Observational Study
Abstract
Background
In real-world experience, the number of patients using vedolizumab as first-line biological therapy was low....
Adalimumab, Infliximab, and Vedolizumab in Treatment of Ulcerative Colitis: A Long-Term Retrospective Study in a Tertiary Referral Center
Adalimumab, Infliximab, and Vedolizumab in Treatment of Ulcerative Colitis: A Long-Term Retrospective Study in a Tertiary Referral Center
Abstract
Background
Biological therapies have changed the landscape of pharmacological management of ulcerative colitis (UC). Ho...
Vedolizumab in patients with inflammatory bowel diseases of in real clinical practice
Vedolizumab in patients with inflammatory bowel diseases of in real clinical practice
Vedolizumab is currently the only selective biological drug for the treatment of inflammatory bowel diseases (IBD). Its effectiveness and safety has been shown in clinical trials. ...

